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Biblioteca

MARC Lista (tabellare)
Atlas of Brain and Spine Oncology Imaging [[electronic resource] /] / edited by Sasan Karimi
Atlas of Brain and Spine Oncology Imaging [[electronic resource] /] / edited by Sasan Karimi
Edizione [1st ed. 2013.]
Pubbl/distr/stampa New York, NY : , : Springer New York : , : Imprint : Springer, , 2013
Descrizione fisica 1 online resource (246 p.)
Disciplina 616.994810754
Collana Atlas of Oncology Imaging
Soggetto topico Radiology
Neuroradiology
Oncology  
Imaging / Radiology
Diagnostic Radiology
Oncology
ISBN 1-283-94620-3
1-4614-5653-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Adult Brain Tumors -- Pediatric Brain Tumors -- Sellar and Parasellar Masses -- Neoplastic Disease of the Spine.
Record Nr. UNINA-9910437995103321
New York, NY : , : Springer New York : , : Imprint : Springer, , 2013
Materiale a stampa
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Atlas of Dermatological Manifestations of Gastrointestinal Disease [[electronic resource] /] / edited by George Y. Wu, Nathan Selsky, Jane M. Grant-Kels
Atlas of Dermatological Manifestations of Gastrointestinal Disease [[electronic resource] /] / edited by George Y. Wu, Nathan Selsky, Jane M. Grant-Kels
Edizione [1st ed. 2013.]
Pubbl/distr/stampa New York, NY : , : Springer New York : , : Imprint : Springer, , 2013
Descrizione fisica 1 online resource (191 p.)
Disciplina 616.3/3
Soggetto topico Gastroenterology 
Dermatology
Internal medicine
Gastroenterology
Internal Medicine
ISBN 1-299-33656-6
1-4614-6191-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Oropharyngeal Cancer: Gastrointestinal Features -- Bazex’s Syndrome: Dermatological Features (Acrokeratosis Paraneoplastica) -- Plummer-Vinson Syndrome: Gastrointestinal Features -- Plummer-Vinson Syndrome: Dermatological Features -- Esophageal Cancer: Gastrointestinal Features -- Howel-Evans Syndrome: Dermatological Features (Familial Keratoderma with Carcinoma of the Esophagus) -- Scleroderma: Gastrointestinal Features -- Scleroderma: Systemic Sclerosis -- Epidermolysis Bullosa Acquisita: Gastrointestinal Features -- Epidermolysis Bullosa Acquisita: Dermatological Features -- Pemphigus Vulgaris: Gastrointestinal Features -- Pemphigus Vulgaris: Dermatological Features -- Dermatomyositis: Gastrointestinal Features -- Dermatomyositis: Dermatological Features -- Pernicious anemia: Gastrointestinal Features -- Vitiligo -- Celiac Disease: Gastrointestinal Features -- Dermatitis Herpetiformis -- Crohn’s Disease: Gastrointestinal Features -- Cutaneous Crohn’s Disease -- Bowel Bypass Syndrome: Gastrointestinal Features -- Bowel-Associated Dermatosis–Arthritis Syndrome -- Blue Rubber Bleb Nevus Syndrome: Gastrointestinal Features -- Blue Rubber Bleb Nevus Syndrome: Dermatological Features -- Henoch–Schönlein Purpora: Gastrointestinal Features -- Henoch–Schönlein Purpura: Dermatological Features -- Pseudoxanthoma Elasticum: Gastrointestinal Features -- Pseudoxanthoma Elasticum: Dermatological Features -- Ehlers–Danlos Syndrome Type IV (Vascular): Gastrointestinal Features -- Ehlers–Danlos Syndrome Type IV (Vascular): Dermatological Features -- Gastric Cancer: Gastrointestinal Features -- Malignant Acanthosis Nigricans, Sign of Leser–Trélat, and Tripe Palms -- Hereditary Hemorrhagic Telangiectasia: Gastrointestinal Features -- Hereditary Hemorrhagic Telangiectasia: Dermatological Features -- Peutz-Jeghers Syndrome: Gastrointestinal Features -- Peutz–Jeghers Syndrome: Dermatological Features -- Cowden’s Syndrome: Gastrointestinal Features -- Cowden’s Syndrome: Dermatological Features -- Behçet’s Syndrome: Gastrointestinal Features -- Behçet’s Syndrome: Dermatological Features -- Gardner Syndrome: Gastrointestinal Features -- Gardner Syndrome: Dermatological Features -- Klippel–Trenaunay–Weber Syndrome: Gastrointestinal Features -- Klippel–Trenaunay–Weber Syndrome: Dermatological Features -- Tuberous Sclerosis: Gastrointestinal Features -- Tuberous Sclerosis: Dermatological Features -- Churg-Strauss Syndrome: Gastrointestinal Features -- Churg-Strauss Syndrome: Dermatological Features -- Ulcerative Colitis: Gastrointestinal Features -- Pyoderma Gangrenosum -- Hereditary Nonpolyposis Colorectal Cancer or Lynch Syndrome: Gastrointestinal Features -- Muir–Torre Syndrome: Dermatological Features -- Hereditary Angioedema: Gastrointestinal Features -- Hereditary Angioedema: Dermatological Features -- Glucagonoma: Gastrointestinal Features -- Necrolytic Migratory Erythema -- Typhoid Fever: Gastrointestinal Features -- Rose Spots -- Cronkhite–Canada Syndrome: Gastrointestinal Features -- Cronkhite-Canada Syndrome: Dermatological Features -- Von Hippel-Lindau Syndrome: Gastrointestinal Features -- Von Hippel–Lindau Syndrome: Dermatological Features -- Hepatitis C Virus: Gastrointestinal Features -- Hepatitis C Virus: Dermatological Features -- Primary Biliary Cirrhosis: Gastrointestinal Features -- Primary Biliary Cirrhosis: Dermatological Features -- Cirrhosis: Gastrointestinal Features -- Cirrhosis: Dermatological Features -- Wilson’s Disease: Gastrointestinal Features -- Wilson’s Disease (Hepatolenticular Degeneration): Dermatological Features -- Hereditary hemochromatosis: Gastrointestinal Features -- Hemochromatosis: Dermatological Features.
Record Nr. UNINA-9910438127603321
New York, NY : , : Springer New York : , : Imprint : Springer, , 2013
Materiale a stampa
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Atlas of Differential Diagnosis in Breast Pathology [[electronic resource] /] / by Puay Hoon Tan, Aysegul A. Sahin
Atlas of Differential Diagnosis in Breast Pathology [[electronic resource] /] / by Puay Hoon Tan, Aysegul A. Sahin
Autore Tan Puay Hoon
Edizione [1st ed. 2017.]
Pubbl/distr/stampa New York, NY : , : Springer New York : , : Imprint : Springer, , 2017
Descrizione fisica 1 online resource (XX, 625 p. 1012 illus., 998 illus. in color.)
Disciplina 616.07
Collana Atlas of Anatomic Pathology
Soggetto topico Pathology
Oncology  
Oncology
Soggetto genere / forma Atlases.
Scientific atlases.
ISBN 1-4939-6697-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Normal Breast and Physiological Changes -- Developmental, Reactive, and Inflammatory Conditions -- Fibroepithelial Lesions -- Papillary Lesions -- Benign Sclerosing Lesions -- Mucinous Lesions -- Apocrine Lesions -- Vascular Lesions -- Intraductal Proliferative Lesions -- Lobular Lesions (Lobular Neoplasia, Invasive Lobular Carcinoma) -- Spindle Cell Lesions -- Invasive Carcinoma -- Nipple Lesions -- Male Breast Lesions -- Treatment-Related Changes.
Record Nr. UNINA-9910254477303321
Tan Puay Hoon  
New York, NY : , : Springer New York : , : Imprint : Springer, , 2017
Materiale a stampa
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Atlas of Emergency Medicine Procedures [[electronic resource] /] / edited by Latha Ganti
Atlas of Emergency Medicine Procedures [[electronic resource] /] / edited by Latha Ganti
Edizione [1st ed. 2016.]
Pubbl/distr/stampa New York, NY : , : Springer New York : , : Imprint : Springer, , 2016
Descrizione fisica 1 online resource (718 p.)
Disciplina 616.025
Soggetto topico Emergency medicine
Emergency Medicine
ISBN 1-78684-653-5
1-4939-2507-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Arterial Cannulation (Radial and Femoral) -- Ultrasound-Guided Peripheral Intravenous Access -- Central Venous Line Placement: Internal Jugular Vein, Subclavian Vein, and Femoral Vein -- Pulmonary Artery Catheter -- Noninvasive Cardiac Monitoring: The Edwards Vigileo System -- Peripheral Venous Cutdown -- Bag-Valve-Mask Ventilation -- Awake Orotracheal Intubation -- Rapid-Sequence Intubation -- Direct Laryngoscopy -- Laryngeal Mask Airway -- Combitube -- Assessment of the Difficult Airway -- GlideScope -- Endotracheal Tube Introducer (Bougie) -- Lighted Stylet Intubation -- Fiberoptic Stylet Intubation (Rigid and Semirigid) -- Storz Video Laryngoscope -- Cricothyroidotomy -- Tracheostomy Tube Malfunction -- Percutaneous Transtracheal Jet Ventilation -- Needle Thoracostomy -- Chest Tube Thoracostomy -- Thoracentesis -- Open Chest Wounds and Flail Chest -- Emergent Resuscitative Thoracotomy, Open Cardiac Massage, and Aortic Occlusion -- Lung Ultrasonography -- Repair of Cardiac Injuries -- Synchronized Electrical Cardioversion -- Unsynchronized Cardioversion (Defibrillation) -- Transcutaneous Pacing -- Transvenous Cardiac Pacing -- Pericardiocentesis (Optional: Ultrasound Guidance) -- Ultrasound Evaluation of Pulmonary Embolism and Heart Strain -- Pacemaker Evaluation in the Emergency Department -- Cervical Collar Placement -- Cervical Spine Clearance -- Log Roll -- Burr Hole Craniotomy -- External Ventricular Drain Placement -- Lumbar Puncture in Adults -- Reflex Eye Movements (Doll’s Eyes and Caloric Testing) -- Dix-Hallpike Maneuver -- Epley Maneuver for Vertigo (Particle Repositioning or Canalith Repositioning Procedure) -- Clinical Brain Death Examination in Adults -- Slit Lamp Examination -- Eye Irrigation -- Corneal Foreign Body Removal -- Ultrasound Evaluation of Retinal Detachment -- Ultrasonography in the Evaluation of Intraocular Pathology -- Tonometry -- Lateral Canthotomy -- Epistaxis Control -- Treatment of Septal Hematoma -- Nasal Foreign Body Removal -- Cerumen Removal -- Ear Foreign Body Removal -- Treatment of Auricular Hematoma -- Incision and Drainage of Peritonsillar Abscess -- Incision and Drainage of Sublingual Abscess -- Incision and Drainage of Parotid Duct Abscess.-  Techniques of Mandibular Anesthesia -- Reduction of Dislocated Temporomandibular Joint -- Dry Socket (Alveolar Osteitis, Fibrinolytic Osteitis) -- Postextraction Hemorrhage -- Fractured Tooth -- Dental Avulsion Management -- Excision of Thrombosed External Hemorrhoid -- Diagnostic Peritoneal Lavage -- Manual Reduction of Abdominal Hernia -- Extended Focused Assessment With Sonography for Trauma -- Nasogastric Tube Placement -- Esophageal Foreign Body Removal -- Activated Charcoal -- Gastric Lavage -- Whole Bowel Irrigation -- Sengstaken-Blakemore Tube -- Gastrostomy Tube Placement -- Paracentesis -- Anal Fissure Management -- Bladder Catheterization -- Pelvic Examination and Wet Preparation -- Bartholin Gland Abscess/Cysts Drainage -- Sexual Assault Forensic Examination -- Treatment of Priapism -- Reduction of Phimosis/Paraphimosis -- Manual Testicular Detorsion.-  Local Anesthesia -- Regional Anesthesia (Nerve Blocks) -- Burn Care -- Wound Closure -- Wound Closure With Tissue Adhesive -- Fishhook Removal -- Tick Removal -- Subungal Hematoma Drainage -- Incision and Drainage of Abscess -- Splinting -- Ulnar Gutter Splint -- Shoulder Dislocation Reduction Techniques -- Elbow Dislocation Reduction -- Distal Interphalangeal Joint Reduction -- Hip Dislocation Reduction -- Knee Dislocation Reduction -- Ankle Dislocation Reduction -- Arthrocentesis -- Intra-articular Injection -- Sugar-Tong Splint -- Fetal Heart Rate Monitoring -- Ultrasonography for Ectopic Pregnancy -- Ultrasonography for Hydatidiform Mole -- Ultrasonography for Blighted Ovum (Anembryonic Gestation) -- Ultrasonography for Threatened, Incomplete, or Compete Abortion -- Ultrasonography for Placenta Previa -- Vaginal Delivery -- Shoulder Dystocia Management -- Breech Delivery in the Emergency Department -- Management of Primary Postpartum Hemorrhage -- Perimortem Cesarean Section -- Peripheral Venous Catheterization -- Umbilical Venous Catheters (Insertion and Removal) -- Intraosseous Access -- Lumbar Puncture in Pediatrics -- Suprapubic Bladder Aspiration -- Removal of Hair/Thread Tourniquet -- Use of the Broselow Tape -- Nursemaid’s Elbow.
Record Nr. UNINA-9910254502503321
New York, NY : , : Springer New York : , : Imprint : Springer, , 2016
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Atlas of Endocrine Pathology [[electronic resource] /] / by Lori A. Erickson
Atlas of Endocrine Pathology [[electronic resource] /] / by Lori A. Erickson
Autore Erickson Lori A
Edizione [1st ed. 2014.]
Pubbl/distr/stampa New York, NY : , : Springer New York : , : Imprint : Springer, , 2014
Descrizione fisica 1 online resource (208 p.)
Disciplina 612.4
616.4
Collana Atlas of Anatomic Pathology
Soggetto topico Pathology
Endocrinology 
Endocrinology
Soggetto genere / forma Atlases.
ISBN 1-4939-0443-4
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Thyroid Histology -- Thyroiditis -- Graves Disease (Diffuse Hyperplasia) -- Thyroid Goiter -- Papillary Thyroid Carcinoma -- Hyalinizing Trabecular Tumor -- Follicular Thyroid Neoplasms -- Hurthle Cell Thyroid Neoplasms -- Poorly Differentiated Thyroid Carcinoma -- Anaplastic Thyroid Carcinoma -- Tumors of C Cells -- Unusual Thyroid Tumors -- Metastases to Thyroid -- Parathyroid Histology -- Parathyroid Hyperplasia -- Parathyroid Adenoma -- Parathyroid Carcinoma -- Parathyromatosis -- Metastases to Parathyroid -- Adrenal Gland Histology -- Adrenal Cysts -- Adrenal Cortical Hyperplasia -- Adrenal Cortical Adenoma -- Adrenal Cortical Carcinoma -- Adrenal Myelolipoma -- Pheochromocytoma and Adrenal Medullary Hyperplasia -- Ganglioneuroma and Neuroblastoma -- Unusual Adrenal Tumors -- Metastases to the Adrenal Gland.
Record Nr. UNINA-9910300081403321
Erickson Lori A  
New York, NY : , : Springer New York : , : Imprint : Springer, , 2014
Materiale a stampa
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Atlas of Esophageal Disease and Intervention [[electronic resource] ] : A Multidisciplinary Approach / / edited by Shanda H. Blackmon, Min P. Kim, Karen J. Dickinson
Atlas of Esophageal Disease and Intervention [[electronic resource] ] : A Multidisciplinary Approach / / edited by Shanda H. Blackmon, Min P. Kim, Karen J. Dickinson
Edizione [1st ed. 2015.]
Pubbl/distr/stampa New York, NY : , : Springer New York : , : Imprint : Springer, , 2015
Descrizione fisica 1 online resource (240 p.)
Disciplina 610
Soggetto topico Gastroenterology 
Surgery
Surgical oncology
Gastroenterology
General Surgery
Surgical Oncology
Soggetto genere / forma Atlases
ISBN 1-4939-3088-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Gross Anatomy -- Histologic Anatomy -- Esophageal Anatomy As Seen During Endoscopy and Basic Endoscopic Orientation -- Radiographic Anatomy -- Mapping Esophageal Disease With Endoscopic Ultrasound -- Endoluminal Interventions -- Surgical Techniques -- Management of Esophageal Leaks and Fistulas -- Esophagostomy Management -- Esophageal Reconstruction.
Record Nr. UNINA-9910300178203321
New York, NY : , : Springer New York : , : Imprint : Springer, , 2015
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Atlas of Esophagus and Stomach Pathology [[electronic resource] /] / by Scott R. Owens, Henry D. Appelman
Atlas of Esophagus and Stomach Pathology [[electronic resource] /] / by Scott R. Owens, Henry D. Appelman
Autore Owens Scott R
Edizione [1st ed. 2014.]
Pubbl/distr/stampa New York, NY : , : Springer New York : , : Imprint : Springer, , 2014
Descrizione fisica 1 online resource (191 p.)
Disciplina 616.307
Collana Atlas of Anatomic Pathology
Soggetto topico Pathology
ISBN 1-4614-8084-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Normal Histologic Anatomy and Common Variations -- General Microscopic Changes -- Noninfectious Inflammatory Conditions -- Infectious Esophagitis and Organisms -- Benign Squamous Proliferations -- Squamous Intraepithelial Neoplasia -- Invasive Squamous Cell Carcinoma -- Unusual Carcinomas, Including Squamous Variants -- Nonneoplastic Barrett's Mucosa -- Dysplasia and Dysplasia Mimics in Barrett's Mucosa -- Invasive Adenocarcinoma in Barrett's Mucosa -- Mesenchymal and Melanocytic Proliferations -- Esophageal Odds and Ends -- Gastric Cardiac Mucosa -- Normal Biopsy Anatomy/Histology and General Changes -- General Microscopic Changes and Findings to Ignore -- Structural Abnormalities/Heterotopias -- Vascular Abnormalities -- Toxic and Medication-Induced Conditions -- Noninfectious Inflammatory and Systemic Diseases Affecting the Stomach -- Infectious Diseases and Organisms -- Hyperplastic/Metaplastic Conditions -- Benign Tumors and Polyps -- Epithelial Dysplasia and Adenomas -- Carcinoma of the Stomach -- Carcinoid Tumor of the Stomach -- Mesenchymal Neoplasms -- Hematolymphoid Neoplasms -- Gastric Metastases.
Record Nr. UNINA-9910300080403321
Owens Scott R  
New York, NY : , : Springer New York : , : Imprint : Springer, , 2014
Materiale a stampa
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Atlas of genetic diagnosis and counseling / / Harold Chen
Atlas of genetic diagnosis and counseling / / Harold Chen
Autore Chen Harold
Pubbl/distr/stampa New York : , : Springer New York : , : Imprint : Springer, , 2020
Descrizione fisica 1 online resource (LX, 2224 p. 2472 illus., 2018 illus. in color.)
Disciplina 611.01816
599.935
Soggetto topico Genetic counseling
Genetic disorders - Diagnosis
Scientific atlases
ISBN 1-4614-6430-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Acardia -- Achondrogenesis -- Achondroplasia -- Adams-Oliver syndrome -- Agnathia -- Aicardi syndrome -- Alagille syndrome -- Albinism -- Alpha thalassemia-mental retardation (ATR-X) syndrome -- Ambiguous genitalia -- Amniotic deformity, adhesions, mutilations (ADAM) syndrome -- Androgen insensitivity syndrome -- Angelman syndrome -- Apert syndrome -- Aplasia cutis congenita -- Arthrogryposis multiplex congenita -- Asphyxiating thoracic dystrophy -- Ataxia telangiectasia -- Atelosteogenesis -- Autism -- Bannayan-Riley-Ruvalcaba syndrome -- Beckwith-Wiedemann syndrome -- Behcet disease -- Biotinidase deficiency -- Bladder exstrophy -- Blepharophimosis, ptosis, and epicanthus inversus syndrome (BPES) -- Body stalk anomaly -- Brachydactyly -- Branchial cleft cyst -- Calcinosis cutis -- Campomelic dysplasia -- Carpenter syndrome -- Cat-eye syndrome -- Celiac disease -- Cerebral palsy -- Cerebro-costo-mandibular syndrome -- Charcot-Marie-Tooth disease -- CHARGE association -- Cherubism -- Chiari malformation -- Chondrodysplasia punctata -- Chromosome abnormalities in pediatric solid tumors -- Cleft lip/palate -- Cleidocranial dysplasia -- Cloacal exstrophy -- Clubfoot (talipes equinovarus) -- Collodion baby -- Congenital adrenal hyperplasia -- Congenital cutis laxa -- Congenital cytomegalovirus infection -- Congenital generalized lipodystrophy -- Congenital hemihyperplasia (congenital hemihypertrophy) -- Congenital hydrocephalus -- Congenital hypothyroidism -- Congenital muscular dystrophy -- Congenital toxoplasmosis -- Conjoined twins -- Corpus-callosum agenesis/dysgenesis -- Craniometaphyseal dysplasia -- Cri-du-chat syndrome -- Crouzon syndrome -- Cutis marmorata telangiectatica congenita -- Cystic fibrosis -- Dandy-Walker malformation -- De Lange syndrome -- Del(18p) syndrome -- Del(22q11.2) syndrome -- Del(Yq) syndrome -- Diabetic embryopathy -- Down syndrome -- Duncan syndrome (X-linked lymphoproliferative disease) -- Dyschondrosteosis/Langer mesomelic dysplasia -- Dysmelia (limb deficiency/reduction) -- Dysplasia epiphysealis hemimelica -- Dystonia -- Dystrophinopathies -- EEC syndrome -- Ehlers-Danlos syndrome -- Ellis-van Creveld syndrome -- Enchondromatosis -- Epidermolysis bullosa -- Epidermolytic palmoplantar keratoderma -- Faciogenital (Aarskog) syndrome -- Facioscapulohumeral muscular dystrophy (FSH) -- Familial adenomatous polyposis syndrome -- Familial hyperlysinemia -- Familial Mediterranean fever -- Fanconi anemia -- Femoral hypoplasia-unusual facies syndrome -- Fetal akinesia syndrome -- Fetal alcohol syndrome -- Fetal hydantoin syndrome -- Fibrodysplasia ossificans progressiva -- Finlay-Marks syndrome -- Floppy infant -- Fragile X syndrome -- Fraser syndrome -- Freeman-Sheldon (whistling face) syndrome -- Friedreich ataxia -- Frontonasal dysplasia -- Galactosemia -- Gastroschisis -- Gaucher disease -- Generalized arterial calcification -- Genitopatellar syndrome -- Giant congenital melanocytic nevi (giant congenital nevi) -- Glucose-6-phosphate dehydrogenase deficiency -- Glycogen storage disease, type II (Pompe) -- Goldenhar syndrome -- Gorlin (nevoid basal cell carcinoma) syndrome -- Greig cephalopolysyndactyly syndrome -- Hallermann-Streiff syndrome -- Harlequin fetus -- Hemophilia A -- Hereditary hearing loss -- Hereditary hemochromatosis -- Hereditary multiple exostosis -- Herlyn-Werner-Wunderlich syndrome -- Holoprosencephaly -- Holt-Oram syndrome -- Huntington disease -- Hydrolethalus syndrome -- Hydrops fetalis -- Hyper-IgE syndrome -- Hypochondroplasia -- Hypoglossia-hypodactyly (oromandibular limb hypogenesis) syndrome -- Hypohidrotic ectodermal dysplasia -- Hypomelanosis of Ito -- Hypophosphatasia -- Hypopituitarism -- I(1p),I(1q) syndrome -- Isodic(Yq) syndrome -- Incontinentia pigmenti -- Infantile myofibromatosis -- Ivemark syndrome -- Jarcho-Levin syndrome -- Joubert syndrome -- Kabuki syndrome -- Kassback-Merritt syndrome -- KID syndrome -- Klinefelter syndrome -- Klippel-Feil syndrome -- Klippel-Trenaunay syndrome -- Kniest dysplasia -- Larsen syndrome -- LEOPARD syndrome -- Lesch-Nyhan syndrome -- Lethal multiple pterygium syndrome -- Loeys-Dietz syndrome -- Lowe syndrome -- Marfan syndrome -- McCune-Albright syndrome -- Meckel-Gruber syndrome -- Megalencephalic leukoencephalopathy with subcortical cysts (van der Knaap disease) -- Menkes disease -- Metachromatic leukodystrophy -- Miller-Dieker syndrome -- Mitochondrial Leber hereditary optic neuropathy -- Mobius syndrome -- Mowat-Wilson Disease -- Mucolipidosis II (I-cell disease) -- Mucolipidosis III (pseudo-Hurler Polydystrophy) -- MPS I (Hurler syndrome) -- MPS II (Hunter syndrome) -- MPS III (Sanfilippo syndrome) -- MPS IV (Morquio syndrome) -- MPS VI (Maroteaux-Lamy syndrome) -- Multiple endocrine neoplasia Syndrome -- Multiple epiphyseal dysplasia -- Multiple pterygium syndrome -- Myotonic dystrophy -- Nail-Patella Syndrome (hereditary Osteo-onychodysplasia) -- Neonatal Herpes simplex infection -- Nephrogenic diabetes insipidus -- Netherton syndrome -- Neu-Laxova syndrome -- Neural tube defects -- Neurofibromatosis 1 -- Neurofibromatosis 2 -- Noonan syndrome -- Oblique facial cleft syndrome -- Oligohydramnios sequence -- Omphalocele -- Oro-Facial-Digital Syndrome -- Osteogenesis imperfecta -- Osteopetrosis -- Osteopoikilosis -- Otopalatodigital spectrum disorders -- Pachyonychia congenita -- Pallister-Killian syndrome -- Phenylketonuria (PKU) -- Pierre Robin sequence -- Polycystic kidney disease, AD form -- Polycystic kidney disease, AR form -- Popliteal pterygium syndrome -- Prader-Willi syndrome -- Progeria -- Prune belly syndrome -- Pseudoachondroplasia -- R(18) syndrome -- Retinoid embryopathy -- Rett syndrome -- Rickets -- Rigid spine syndrome -- Roberts syndrome -- Robinow syndrome -- Rubinstein-Taybi syndrome -- Saethre-Chotzen syndrome -- Sagittal synostosis associated with chromosome abnormalities -- Schizencephaly -- Schmid metaphyseal chondrodystrophy -- Seckel syndrome -- Severe combined immune deficiency -- Short rib polydactyly syndromes (SRPS) -- Sickle cell disease -- Silver-Russell syndrome -- Sirenomelia -- Smith-Lemli-Optiz syndrome -- Smith-Magenis syndrome -- Sotos syndrome -- Spinal muscular atrophy -- Spondyloepiphyseal dysplasia -- Stickler syndrome -- Sturge-Weber syndrome -- Tay-Sachs disease -- Tetrasomy 9p syndrome -- Thalassemia -- Thanatophoric dysplasia -- Thrombocytopenia-absent radius (TAR) syndrome -- Treacher-Collins syndrome -- Trimethylaminuria -- Triploidy -- Trismus pseudocamptodactyly (Hecht syndrome) -- Trisomy 8 mosaicism (Warkany) syndrome -- Trisomy 13 syndrome -- Trisomy 18 syndrome -- Tuberous sclerosis -- Turner syndrome -- Twin-twin transfusion syndrome -- Ulnar-mammary syndrome -- Urofacial (Ochoa) Syndrome -- VATER (VACTERL) association -- Von Hippel-Lindau disease -- Waardenburg syndrome -- Weill-Marchesani syndrome -- Williams syndrome -- Wolf-Hirschhorn syndrome -- X-linked agammaglobulinemia (Bruton type) -- X-linked ichthyosis -- XX Male -- XXX syndrome -- XXXXX syndrome -- XXXXY syndrome -- XY female.-XYY syndrome.
Record Nr. UNINA-9910349295903321
Chen Harold  
New York : , : Springer New York : , : Imprint : Springer, , 2020
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Atlas of Genetic Diagnosis and Counseling [[electronic resource] /] / by Harold Chen
Atlas of Genetic Diagnosis and Counseling [[electronic resource] /] / by Harold Chen
Autore Chen Harold
Edizione [3rd ed. 2017.]
Pubbl/distr/stampa New York, NY : , : Springer New York : , : Imprint : Springer, , 2017
Descrizione fisica 1 online resource (1242 illus., 1050 illus. in color. eReference.)
Disciplina 616.042
Soggetto topico Pathology
Pediatrics
Neurology 
Neurology
ISBN 1-4939-2401-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Acardia -- Achondrogenesis -- Achondroplasia -- Adams-Oliver Syndrome -- Agnathia -- Aicardi Syndrome -- Alagille Syndrome -- Albinism -- Alpha-Thalassemia X-linked Mental Retardation Syndrome -- Ambiguous Genitalia -- Amniotic Deformity, Adhesions, Mutilations (ADAM) Complex -- Androgen Insensitivity Syndrome -- Angelman Syndrome -- Apert Syndrome -- Aplasia Cutis Congenita -- Arthrogryposis Multiplex Congenita -- Asphyxiating Thoracic Dystrophy -- Ataxia-Telangiectasia -- Atelosteogenesis -- Autism -- Bannayan-Riley-Ruvalcaba Syndrome -- Beckwith-Wiedemann Syndrome -- Behcet Disease -- Biotinidase Deficiency -- Bladder Exstrophy -- Blepharophimosis, Ptosis, and Epicanthus Inversus Syndrome -- Body Stalk Anomaly -- Brachydactyly -- Branchial Cleft Anomalies -- Calcinosis Cutis -- Campomelic Dysplasia -- Carpenter Syndrome -- Cat Eye Syndrome -- Celiac Disease -- Cerebral Palsy -- Cerebro-Costo-Mandibular Syndrome -- Charcot-Marie-Tooth Disease -- CHARGE Syndrome -- Cherubism -- Chiari Malformation -- Chondrodysplasia Punctata -- Chromosome Abnormalities in Pediatric Solid Tumors -- Cleft Lip and/or Cleft Palate -- Cleidocranial Dysplasia -- Cloacal Exstrophy -- Clubfoot -- Collodion Baby -- Congenital Adrenal Hyperplasia -- Congenital Cutis Laxa -- Congenital Cytomegalovirus Infection -- Congenital Generalized Lipodystrophy -- Congenital Hemihyperplasia -- Congenital Hydrocephalus -- Congenital Hypothyroidism -- Congenital Muscular Dystrophy -- Congenital Toxoplasmosis -- Conjoined Twins -- Corpus Callosum Agenesis/Dysgenesis -- Craniometaphyseal Dysplasia -- Cri-Du-Chat Syndrome -- Crouzon Syndrome -- Cutaneous Vasculitis -- Cutis Marmorata Telangiectatica Congenita -- Cystic Fibrosis -- Dandy-Walker Malformation -- De Lange Syndrome -- Del(18p) Syndrome -- Del(22q11.2) Syndrome -- Del(Yq) Syndrome -- Diabetic Embryopathy -- Down Syndrome -- Duncan Syndrome -- Dyschondrosteosis -- Dysmelia -- Dysplasia Epiphysealis Hemimelica -- Dystonia -- Dystrophinopathies -- Ectrodactyly-Ectodermal Dysplasia-Clefting (EEC) Syndrome -- Ehlers-Danlos Syndrome -- Ellis-van Creveld Syndrome -- Enchondromatosis -- Epidermolysis Bullosa -- Epidermolytic Palmoplantar Keratoderma -- Faciogenital (Faciodigitogenital) Dysplasia -- Facioscapulohumeral Muscular Dystrophy -- Familial Adenomatous Polyposis -- Familial Hyperlysinemia -- Familial Mediterranean Fever -- Familial Patella Instability -- Familial Spastic Paraplegia -- Fanconi Anemia -- Feingold Syndrome -- Femoral Hypoplasia - Unusual Facies Syndrome -- Fetal Akinesia Deformation Sequence -- Fetal Alcohol Spectrum Disorders -- Fetal Hydantoin Syndrome -- Fibrodysplasia Ossificans Progressiva -- Fibular Hemimelia -- Finlay-Marks Syndrome -- Floppy Infant -- Fragile X Syndrome -- Fraser Syndrome -- Freeman-Sheldon Syndrome -- Friedreich Ataxia -- Frontonasal Dysplasia -- Galactosemia -- Gastroschisis -- Gaucher Disease -- Generalized Arterial Calcification of Infancy -- Genitopatellar Syndrome -- Giant Congenital Melanocytic Nevi -- Gilbert Syndrome -- Glucose-6-Phosphate Dehydrogenase Deficiency -- Glycogen Storage Disease, Type 2 -- Goldenhar Syndrome -- Gorlin Syndrome -- Greig Cephalopolysyndactyly Syndrome -- Growth Hormone Deficiency -- Hallermann-Streiff Syndrome -- Harlequin Ichthyosis -- Hemangiomas of Infancy -- Hemophilia A -- Hereditary Hearing Loss -- Hereditary -- Hemochromatosis -- Hereditary Multiple Exostoses -- Hereditary Sensory and Autonomic Neuropathies -- Herlyn-Werner-Wunderlich Syndrome -- Holoprosencephaly -- Holt-Oram Syndrome -- Huntington Disease -- Hydranencephaly -- Hydrolethalus Syndrome -- Hydrops Fetalis -- Hyper-IgE Syndrome -- Hypertrophic Cardiomyopathy (HCM) -- Hypochondroplasia -- Hypoglossia-Hypodactylia Syndrome -- Hypohidrotic Ectodermal Dysplasia -- Hypomelanosis of Ito -- Hypophosphatasia -- Hypopituitarism -- I(1p), I(1q) Syndrome -- Idic(Yq) Syndrome -- Incontinentia Pigmenti -- Infantile Myofibromatosis -- Ivemark Syndrome -- Jarcho-Levin Syndrome -- Joubert Syndrome -- Kabuki Syndrome -- Kasabach-Merritt Syndrome -- KID Syndrome -- Klinefelter Syndrome -- Klippel-Feil Syndrome -- Klippel-Trenaunay Syndrome -- Kniest Dysplasia -- Larsen Syndrome -- LEOPARD Syndrome -- Lesch-Nyhan Syndrome -- Lethal Multiple Pterygium Syndrome -- Loeys-Dietz Syndrome -- Lowe Syndrome -- Lymphangiomas and Lymphangiomatosis -- M#xf6;bius Syndrome -- Macrodactyly -- Marfan Syndrome -- McCune-Albright Syndrome -- Meckel-Gruber Syndrome -- Megalencephalic Leukoencephalopathy with Subcortical Cysts -- Menkes Disease -- Metachromatic Leukodystrophy -- Miller-Dieker Syndrome -- Mitochondrial Leber Hereditary Optic Neuropathy -- Mitochondrial Myopathy -- Mowat-Wilson Syndrome -- Mucolipidosis 2 -- Mucolipidosis 3 -- Mucopolysaccharidosis 1 (MPS 1) -- Mucopolysaccharidosis 2 -- Mucopolysaccharidosis 3 -- Mucopolysaccharidosis 4 -- Mucopolysaccharidosis 6 -- Multiple Endocrine Neoplasia Syndromes -- Multiple Epiphyseal Dysplasia -- Multiple Pterygium Syndrome -- Myotonic Dystrophy Type 1 -- Nager Acrofacial Dysostosis -- Nail-Patella Syndrome -- Nasal Obstruction in Neonates and Children -- Neonatal Herpes Simplex Infection -- Nephrogenic Diabetes Insipidus -- Netherton Syndrome -- Neu-Laxova Syndrome -- Neural Tube Defects -- Neurofibromatosis 1 -- Neurofibromatosis 2 -- Niemann-Pick Disease -- Noonan Syndrome -- Oblique Facial Cleft Syndrome -- Oligohydramnios Sequence -- Omphalocele -- Opitz Trigonocephaly (C) Syndrome -- Oral-Facial-Digital Syndrome -- Osteogenesis Imperfecta -- Osteogenesis Imperfecta Ehlers-Danlos Overlap Syndrome -- Osteopetrosis -- Osteopoikilosis -- Otopalatodigital Spectrum Disorders -- Pachyonychia Congenita -- Pallister-Killian Syndrome -- Peutz-Jeghers Syndrome -- Phenylketonuria -- Pierre Robin Sequence -- Polycystic Kidney Disease, Autosomal Dominant Type -- Polycystic Kidney Disease: Autosomal Recessive Type -- Popliteal Pterygium Syndrome -- Prader-Willi Syndrome -- Primary Microcephaly -- Progeria -- Prune Belly Syndrome -- Pseudoachondroplasia -- R(18) Syndrome -- Radioulnar Synostosis -- Retinoid Embryopathy -- Rett Syndrome -- Rickets -- Rigid Spine Syndrome -- Roberts Syndrome -- Robinow Syndrome -- Rubinstein-Taybi Syndrome -- Saethre-Chotzen Syndrome -- Sagittal Craniosynostosis Associated with Chromosome Abnormalities with a Brief Review on Craniosynostosis -- Schizencephaly Schmid Metaphyseal Chondrodysplasia -- Seckel Syndrome -- Severe Combined Immune Deficiency -- Short Rib-Polydactyly Syndromes -- Sickle Cell Disease -- Silver-Russell Syndrome -- Sirenomelia -- Smith-Lemli-Opitz Syndrome -- Smith-Magenis Syndrome -- Sotos Syndrome -- Spinal Muscular Atrophy -- Spondyloepiphyseal Dysplasia -- Stickler Syndrome -- Sturge-Webber Syndrome -- Symphalangism -- Tay-Sachs Disease -- Tetrasomy 9p Syndrome -- Thalassemia -- Thanatophoric Dysplasia -- Thrombocytopenia-Absent Radius Syndrome -- Treacher-Collins Syndrome -- Trimethylaminuria -- Triploidy -- Trismus-Pseudocamptodactyly Syndrome -- Trisomy 13 Syndrome -- Trisomy 18 Syndrome -- Trisomy 8 Mosaicism Syndrome -- Tuberous Sclerosis -- Turner Syndrome -- Twin-Twin Transfusion Syndrome -- Tyrosinemia -- Ulnar-Mammary Syndrome -- Urofacial Syndrome -- VATER (VACTERL) Association -- Von Hippel-Lindau Disease -- Waardenburg Syndrome -- Weill-Marchesani Syndrome -- Williams Syndrome -- Winchester syndrome -- Wolf-Hirschhorn Syndrome -- X-Linked Agammaglobulinemia -- X-Linked Ichthyosis -- XX Male -- XXX Syndrome -- XXXXX Syndrome -- XXXXY Syndrome -- XY Female -- XYY Syndrome.
Record Nr. UNINA-9910254482103321
Chen Harold  
New York, NY : , : Springer New York : , : Imprint : Springer, , 2017
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Atlas of Genetic Diagnosis and Counseling [[electronic resource] /] / by Harold Chen
Atlas of Genetic Diagnosis and Counseling [[electronic resource] /] / by Harold Chen
Autore Chen Harold
Edizione [2nd ed. 2012.]
Pubbl/distr/stampa New York, NY : , : Springer New York : , : Imprint : Springer, , 2012
Descrizione fisica 1 online resource (2472 illus., 2018 illus. in color. eReference.)
Disciplina 616/.042
Soggetto topico Human genetics
Cytogenetics
Molecular biology
Pathology
Human Genetics
Molecular Medicine
ISBN 1-4614-1037-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Acardia -- Achondrogenesis -- Achondroplasia -- Adams-Oliver syndrome -- Agnathia -- Aicardi syndrome -- Alagille syndrome -- Albinism -- Alpha thalassemia-mental retardation (ATR-X) syndrome -- Ambiguous genitalia -- Amniotic deformity, adhesions, mutilations (ADAM) syndrome -- Androgen insensitivity syndrome -- Angelman syndrome -- Apert syndrome -- Aplasia cutis congenita -- Arthrogryposis multiplex congenita -- Asphyxiating thoracic dystrophy -- Ataxia telangiectasia -- Atelosteogenesis -- Autism -- Bannayan-Riley-Ruvalcaba syndrome -- Beckwith-Wiedemann syndrome -- Behcet disease -- Biotinidase deficiency -- Bladder exstrophy -- Blepharophimosis, ptosis, and epicanthus inversus syndrome (BPES) -- Body stalk anomaly -- Brachydactyly -- Branchial cleft cyst -- Calcinosis cutis -- Campomelic dysplasia -- Carpenter syndrome -- Cat-eye syndrome -- Celiac disease -- Cerebral palsy -- Cerebro-costo-mandibular syndrome -- Charcot-Marie-Tooth disease -- CHARGE association -- Cherubism -- Chiari malformation -- Chondrodysplasia punctata -- Chromosome abnormalities in pediatric solid tumors -- Cleft lip/palate -- Cleidocranial dysplasia -- Cloacal exstrophy -- Clubfoot (talipes equinovarus) -- Collodion baby -- Congenital adrenal hyperplasia -- Congenital cutis laxa -- Congenital cytomegalovirus infection -- Congenital generalized lipodystrophy -- Congenital hemihyperplasia (congenital hemihypertrophy) -- Congenital hydrocephalus -- Congenital hypothyroidism -- Congenital muscular dystrophy -- Congenital toxoplasmosis -- Conjoined twins -- Corpus-callosum agenesis/dysgenesis -- Craniometaphyseal dysplasia -- Cri-du-chat syndrome -- Crouzon syndrome -- Cutis marmorata telangiectatica congenita -- Cystic fibrosis -- Dandy-Walker malformation -- De Lange syndrome -- Del(18p) syndrome -- Del(22q11.2) syndrome -- Del(Yq) syndrome -- Diabetic embryopathy -- Down syndrome -- Duncan syndrome (X-linked lymphoproliferative disease) -- Dyschondrosteosis/Langer mesomelic dysplasia -- Dysmelia (limb deficiency/reduction) -- Dysplasia epiphysealis hemimelica -- Dystonia -- Dystrophinopathies -- EEC syndrome -- Ehlers-Danlos syndrome -- Ellis-van Creveld syndrome -- Enchondromatosis -- Epidermolysis bullosa -- Epidermolytic palmoplantar keratoderma -- Faciogenital (Aarskog) syndrome -- Facioscapulohumeral muscular dystrophy (FSH) -- Familial adenomatous polyposis syndrome -- Familial hyperlysinemia -- Familial Mediterranean fever -- Fanconi anemia -- Femoral hypoplasia-unusual facies syndrome -- Fetal akinesia syndrome -- Fetal alcohol syndrome -- Fetal hydantoin syndrome -- Fibrodysplasia ossificans progressiva -- Finlay-Marks syndrome -- Floppy infant -- Fragile X syndrome -- Fraser syndrome -- Freeman-Sheldon (whistling face) syndrome -- Friedreich ataxia -- Frontonasal dysplasia -- Galactosemia -- Gastroschisis -- Gaucher disease -- Generalized arterial calcification -- Genitopatellar syndrome -- Giant congenital melanocytic nevi (giant congenital nevi) -- Glucose-6-phosphate dehydrogenase deficiency -- Glycogen storage disease, type II (Pompe) -- Goldenhar syndrome -- Gorlin (nevoid basal cell carcinoma) syndrome -- Greig cephalopolysyndactyly syndrome -- Hallermann-Streiff syndrome -- Harlequin fetus -- Hemophilia A -- Hereditary hearing loss -- Hereditary hemochromatosis -- Hereditary multiple exostosis -- Herlyn-Werner-Wunderlich syndrome -- Holoprosencephaly -- Holt-Oram syndrome -- Huntington disease -- Hydrolethalus syndrome -- Hydrops fetalis -- Hyper-IgE syndrome -- Hypochondroplasia -- Hypoglossia-hypodactyly (oromandibular limb hypogenesis) syndrome -- Hypohidrotic ectodermal dysplasia -- Hypomelanosis of Ito -- Hypophosphatasia -- Hypopituitarism -- I(1p),I(1q) syndrome -- Isodic(Yq) syndrome -- Incontinentia pigmenti -- Infantile myofibromatosis -- Ivemark syndrome -- Jarcho-Levin syndrome -- Joubert syndrome -- Kabuki syndrome -- Kassback-Merritt syndrome -- KID syndrome -- Klinefelter syndrome -- Klippel-Feil syndrome -- Klippel-Trenaunay syndrome -- Kniest dysplasia -- Larsen syndrome -- LEOPARD syndrome -- Lesch-Nyhan syndrome -- Lethal multiple pterygium syndrome -- Loeys-Dietz syndrome -- Lowe syndrome -- Marfan syndrome -- McCune-Albright syndrome -- Meckel-Gruber syndrome -- Megalencephalic leukoencephalopathy with subcortical cysts (van der Knaap disease) -- Menkes disease -- Metachromatic leukodystrophy -- Miller-Dieker syndrome -- Mitochondrial Leber hereditary optic neuropathy -- Mobius syndrome -- Mowat-Wilson Disease -- Mucolipidosis II (I-cell disease) -- Mucolipidosis III (pseudo-Hurler Polydystrophy) -- MPS I (Hurler syndrome) -- MPS II (Hunter syndrome) -- MPS III (Sanfilippo syndrome) -- MPS IV (Morquio syndrome) -- MPS VI (Maroteaux-Lamy syndrome) -- Multiple endocrine neoplasia Syndrome -- Multiple epiphyseal dysplasia -- Multiple pterygium syndrome -- Myotonic dystrophy -- Nail-Patella Syndrome (hereditary Osteo-onychodysplasia) -- Neonatal Herpes simplex infection -- Nephrogenic diabetes insipidus -- Netherton syndrome -- Neu-Laxova syndrome -- Neural tube defects -- Neurofibromatosis 1 -- Neurofibromatosis 2 -- Noonan syndrome -- Oblique facial cleft syndrome -- Oligohydramnios sequence -- Omphalocele -- Oro-Facial-Digital Syndrome -- Osteogenesis imperfecta -- Osteopetrosis -- Osteopoikilosis -- Otopalatodigital spectrum disorders -- Pachyonychia congenita -- Pallister-Killian syndrome -- Phenylketonuria (PKU) -- Pierre Robin sequence -- Polycystic kidney disease, AD form -- Polycystic kidney disease, AR form -- Popliteal pterygium syndrome -- Prader-Willi syndrome -- Progeria -- Prune belly syndrome -- Pseudoachondroplasia -- R(18) syndrome -- Retinoid embryopathy -- Rett syndrome -- Rickets -- Rigid spine syndrome -- Roberts syndrome -- Robinow syndrome -- Rubinstein-Taybi syndrome -- Saethre-Chotzen syndrome -- Sagittal synostosis associated with chromosome abnormalities -- Schizencephaly -- Schmid metaphyseal chondrodystrophy -- Seckel syndrome -- Severe combined immune deficiency -- Short rib polydactyly syndromes (SRPS) -- Sickle cell disease -- Silver-Russell syndrome -- Sirenomelia -- Smith-Lemli-Optiz syndrome -- Smith-Magenis syndrome -- Sotos syndrome -- Spinal muscular atrophy -- Spondyloepiphyseal dysplasia -- Stickler syndrome -- Sturge-Weber syndrome -- Tay-Sachs disease -- Tetrasomy 9p syndrome -- Thalassemia -- Thanatophoric dysplasia -- Thrombocytopenia-absent radius (TAR) syndrome -- Treacher-Collins syndrome -- Trimethylaminuria -- Triploidy -- Trismus pseudocamptodactyly (Hecht syndrome) -- Trisomy 8 mosaicism (Warkany) syndrome -- Trisomy 13 syndrome -- Trisomy 18 syndrome -- Tuberous sclerosis -- Turner syndrome -- Twin-twin transfusion syndrome -- Ulnar-mammary syndrome -- Urofacial (Ochoa) Syndrome -- VATER (VACTERL) association -- Von Hippel-Lindau disease -- Waardenburg syndrome -- Weill-Marchesani syndrome -- Williams syndrome -- Wolf-Hirschhorn syndrome -- X-linked agammaglobulinemia (Bruton type) -- X-linked ichthyosis -- XX Male -- XXX syndrome -- XXXXX syndrome -- XXXXY syndrome -- XY female.-XYY syndrome.
Record Nr. UNINA-9910483792303321
Chen Harold  
New York, NY : , : Springer New York : , : Imprint : Springer, , 2012
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui