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Congenital Brain Malformations : Clinical and Surgical Aspects
| Congenital Brain Malformations : Clinical and Surgical Aspects |
| Autore | AlAli Khaled Fares |
| Edizione | [1st ed.] |
| Pubbl/distr/stampa | Cham : , : Springer International Publishing AG, , 2024 |
| Descrizione fisica | 1 online resource (335 pages) |
| Altri autori (Persone) | HashimHashim Talib |
| ISBN | 3-031-58630-1 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Intro -- Preface -- Contents -- Contributors -- Chapter 1: General Introduction to the Congenital Brain Malformations -- 1.1 Introduction -- 1.2 Epidemiology -- 1.3 Diagnosis of These Malformations -- 1.4 The Management and the Prognosis -- 1.5 The Complications of Congenital Brain Malformations -- References -- Chapter 2: The Epidemiology of Congenital Brain Anomalies -- 2.1 Introduction -- 2.2 Anencephaly -- 2.3 Cephalocele -- 2.4 Chiari Malformations -- 2.5 Porencephaly -- 2.6 Septo-Optic Dysplasia -- 2.7 Pituitary Maldevelopement -- 2.8 Posterior Fossa Malformation -- 2.9 Microcephaly -- 2.10 Megalencephaly and Hemimegalencephaly -- 2.11 Neurocutaneous Syndromes -- 2.12 Schizencephaly -- 2.13 Lissencephaly -- 2.14 Heterotopia -- 2.15 Polymicrogyria -- 2.16 Encephalopathy Disorders -- References -- Chapter 3: Diagnosis of Congenital Brain Anomalies -- 3.1 Introduction -- 3.2 Prenatal Diagnosis: Limitations and Risks Associated with Each Method -- 3.2.1 Routine Ultrasounds Screening: Timings and Indications -- 3.2.2 Maternal Blood Tests for Risk Assessment -- 3.2.3 Fetal MRI: Benefits and Limitations -- 3.2.4 Amniocentesis and Genetic Testing -- 3.3 Postnatal Diagnosis -- 3.3.1 The Significance of Neonatal Examinations and Clinical Presentation -- 3.3.2 MRI and CT: Benefits and Limitations -- 3.3.3 Postnatal Genetic Testing -- 3.3.4 Electrophysiological Tests Electrocardiography (ECG) -- 3.4 Conclusion -- References -- Chapter 4: Anencephaly -- 4.1 Introduction -- 4.2 Pathophysiology -- 4.2.1 Nutritional Factors -- 4.2.2 Dietary Factors -- 4.3 Diagnosis -- 4.3.1 History and Physical Examination -- 4.3.2 Lab Studies -- 4.3.3 Imaging Studies -- 4.4 Management -- References -- Chapter 5: Encephalocele -- 5.1 Introduction -- 5.1.1 Classification -- 5.2 Etiology and Pathogenesis -- 5.2.1 Genetic Etiologies of Primary Encephalocele.
5.2.2 Environmental Etiologies of Primary Encephalocele -- 5.3 Clinical Presentation -- 5.3.1 Occipital Encephalocele -- 5.3.2 Sincipital Encephalocele -- 5.3.3 Basal Encephalocele -- 5.3.4 Associated Anomalies -- 5.4 Diagnosis -- 5.4.1 Neuroimaging -- Ultrasonography -- MRI -- CT Scan -- 5.4.2 Multimaterial 3D Printing Modeling -- 5.4.3 Genetic Studies and Counseling -- 5.5 Differential Diagnosis -- 5.6 Management -- 5.6.1 Occipital Encephalocele -- Sincipital Encephalocele -- Basal Encephalocele -- 5.7 Complications -- 5.8 Prognosis -- References -- Chapter 6: Chiari Malformation -- 6.1 Introduction -- 6.2 Anatomical Basis of the Disease -- 6.3 The Classification of Chiari Malformation -- 6.4 Chiari Type I -- 6.5 Chiari Type II -- 6.6 Chiari Malformation Type III -- 6.7 Diagnosis of Chiari Malformation -- 6.8 Management of Chiari Malformation -- References -- Chapter 7: Porencephaly -- 7.1 Introduction -- 7.2 Epidemiology -- 7.3 Etiology -- 7.4 Pathology -- 7.5 Clinical Manifestation -- 7.6 Diagnosis -- 7.7 Management -- 7.8 Differential Diagnosis -- 7.9 Prognosis -- References -- Chapter 8: Septo-Optic dysplasia -- 8.1 Introduction -- 8.2 Embryology -- 8.3 Etiology -- 8.4 Pathophysiology -- 8.4.1 Environmental Factors -- 8.4.2 Genetic Factors -- 8.5 Diagnosis -- 8.5.1 History -- 8.5.2 Examination -- 8.5.3 Investigations -- 8.6 Treatment -- References -- Chapter 9: Pituitary Maldevelopment -- 9.1 Embryology -- 9.1.1 Rathke Pouch -- 9.1.2 Signals Controlling Pituitary Development -- 9.1.3 Cells Differentiation -- 9.2 Anatomy and Physiology -- 9.2.1 Anatomy -- Adenohypophysis -- Neurohypophysis -- Vascularization -- Innervation -- 9.2.2 Physiology -- 9.3 Pituitary Developmental Factor Mutation -- 9.3.1 Prop1 -- 9.3.2 Pit1 -- 9.3.3 Shh-Gli2 -- 9.3.4 Hesx1 -- 9.3.5 Lhx 3/4 -- 9.3.6 Other Transcription Factor Deficiency -- References. Chapter 10: Posterior Fossa Malformation -- 10.1 Introduction -- 10.2 Malformations of the Posterior Fossa -- 10.2.1 Diseases with Cerebellar Agenesis, Aplasia or Hypoplasia -- 10.2.2 Rhombencephalosynapsis -- 10.2.3 Vermian-Cerebellar Hypoplasia -- 10.2.4 Lhermitte-Duclos Disease -- 10.2.5 Walker-Warburg Syndrome -- 10.2.6 Joubert Syndrome -- 10.2.7 Cystic Posterior Fossa Anomalies -- 10.2.8 Chiari Malformations -- References -- Chapter 11: Microcephaly -- 11.1 Introduction -- 11.2 Etiology and Pathogenesis -- 11.2.1 Genetic Etiologies of Primary Microcephaly -- 11.2.2 Environmental Etiologies of Primary Microcephaly -- 11.3 Diagnosis -- 11.3.1 History and Clinical Presentation -- 11.3.2 Physical Examination -- 11.3.3 Neuroimaging -- 11.3.4 Biochemical Tests and Virology -- 11.3.5 Genetic Studies -- 11.4 Management and Prevention -- 11.5 Complications -- 11.6 Prognosis -- References -- Chapter 12: Megalencephaly and Hemimegalencephaly -- 12.1 Introduction -- 12.2 Pathogenesis -- 12.2.1 Metabolic Megalencephaly -- 12.2.2 Anatomic Megalencephaly -- 12.3 Classifications -- 12.3.1 Megalencephaly -- 12.3.2 Benign Familial Megalencephaly (BFM) -- 12.3.3 Metabolic Megalencephaly -- 12.3.4 Defects of Organic Acids -- 12.3.5 Metabolic Leukoencephalopathies -- 12.3.6 Lysosomal Storage Diseases -- 12.3.7 Anatomical Megalencephaly -- 12.3.8 Megalencephaly with Dwarfism [23] -- 12.3.9 Megalencephaly with Gigantism [21] -- 12.3.10 Megalencephaly with Syndromes [22, 23] -- 12.3.11 Pretzel Syndrome [8, 24, 25] -- 12.4 Hemimegalencephaly -- 12.4.1 Isolated [28] -- 12.4.2 Syndromic [29-31] -- 12.4.3 Total Hemimegalencephaly [28] -- 12.5 Clinical Presentation -- 12.5.1 Clinically Significant Megalencephaly Are Characterized by 1 or More of the Following: [38] -- 12.6 Diagnosis -- 12.6.1 Megalencephaly [39, 40] -- 12.6.2 Hemimegaloencephaly. 12.7 Management and Prognosis -- References -- Chapter 13: Neurocutaneous Syndromes -- 13.1 Introduction -- 13.2 Etiology & -- Pathophysiology -- 13.3 Clinical Features -- 13.3.1 Neurofibromatosis Type 1 -- 13.3.2 Neurofibromatosis Type 2 -- 13.3.3 Tuberous Sclerosis -- Dermatological -- Other Dermatological Features Include -- Other Organs -- 13.3.4 Sturge-Weber Syndrome -- 13.3.5 Ataxia Telangiectasia -- 13.4 Diagnostic Evaluation -- 13.4.1 Neurofibromatosis Type 1 -- 13.4.2 Neurofibromatosis Type 2 -- 13.4.3 Tuberous Sclerosis -- 13.4.4 Sturge-Weber syndrome -- 13.4.5 Ataxia Telangiectasia -- 13.5 Treatment and Prognosis -- References -- Chapter 14: Schizencephaly -- 14.1 Introduction -- 14.2 Epidemiology -- 14.3 Clinical Presentations of Schizencephaly -- 14.4 Diagnosis -- 14.5 Management -- 14.6 Complications and Prognosis -- 14.7 Conclusion -- References -- Chapter 15: Lissencephaly -- 15.1 Introduction -- 15.2 Types of Lissencephaly -- 15.2.1 Lissencephaly Type I -- 15.2.2 Lissencephaly Type II -- 15.3 Epidemiology -- 15.3.1 Incidence -- 15.3.2 Prevalence -- 15.4 Etiology -- 15.4.1 Non-Genetic Factors -- 15.4.2 Genetic Factors -- X-Linked [3, 4] -- Chromosome 17-Linked [3, 4] -- Some of the Better-Studied Genetic Causes Are Listed Below -- LIS1 -- DCX (X-Linked Lissencephaly Type 1/XLIS 1 or LISX 1) -- ARX (X-Linked Lissencephaly Type 2/XLIS 2 or LISX 2) -- RELN -- 15.5 Signs and Symptoms -- 15.6 Diagnosis -- 15.7 Treatment -- 15.8 Prognosis -- References -- Chapter 16: Heterotopias -- 16.1 Introduction -- 16.2 Anatomy and Physiology of the Brain and Gray Matter -- 16.3 Overview of Gray Matter Heterotopias -- 16.4 Types of Gray Matter Heterotopias -- 16.4.1 Nodular or Focal Heterotopia -- Subependymal or Periventricular Heterotopia -- Focal Subcortical Heterotopia -- 16.4.2 Diffuse Heterotopia -- Band or Double Cortex Heterotopia. 16.5 Subcortical Band Heterotopia's Association with Lissencephaly -- 16.5.1 Type 1 Lissencephaly -- 16.5.2 Type 2 Lissencephaly -- 16.6 Treatment of Gray Matter Heterotopias -- References -- Chapter 17: Polymicrogyria -- 17.1 Introduction -- 17.2 Etiology and Molecular Basis -- 17.2.1 Genetics -- 17.2.2 Acquired Etiologies -- 17.3 Pathology -- 17.4 Clinical Features -- 17.4.1 Epileptic Seizures -- 17.4.2 Developmental Delay -- 17.4.3 Motor Affection -- 17.4.4 Head Changes -- 17.4.5 Other Neurological Changes -- 17.4.6 Psychiatric Manifestations -- 17.4.7 Other Clinical Manifestations -- 17.5 Diagnosis -- 17.5.1 Imaging Modalities for PMG -- 17.6 Management -- 17.6.1 Surgical Intervention -- 17.7 Differential Diagnosis -- References -- Chapter 18: Encephaloclastic Lesions of the Central Nervous System -- 18.1 Introduction -- 18.1.1 Overview -- 18.1.2 Historical Background -- 18.2 Epidemiology -- 18.3 Pathophysiology -- 18.4 Predisposing and Risk Factors -- 18.5 Classification of Encephaloclastic Disorders -- 18.6 MS Management -- 18.7 Clinical Presentation -- 18.8 Differential Diagnosis -- 18.9 Diagnostic Workup -- 18.10 Treatment Strategies -- 18.11 Prognosis and Outcomes -- 18.12 Future Directions and Research -- References -- Chapter 19: Cerebral Palsy -- 19.1 Introduction -- 19.2 Classification of Cerebral Palsy -- 19.2.1 According to Severity -- 19.2.2 Topographical Classification -- 19.2.3 Classification Based on Muscle Tone -- 19.2.4 Functional Classification -- 19.3 Risk Factors of Cerebral Palsy -- 19.4 Clinical Presentation of Cerebral Palsy -- 19.4.1 Spastic Cerebral Palsy -- 19.4.2 Ataxic Cerebral Palsy -- 19.4.3 Athetoid Cerebral Palsy -- 19.4.4 Hypotonic Cerebral Palsy -- 19.5 Diagnosis and Screening -- 19.5.1 Clinical Assessment -- Prechtl Qualitative Assessment of General Movements (GMs). Hammersmith Infant Neurological Examination (HINE). |
| Record Nr. | UNINA-9910864198503321 |
AlAli Khaled Fares
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| Cham : , : Springer International Publishing AG, , 2024 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Congenital Spine Malformations : Clinical and Surgical Aspects
| Congenital Spine Malformations : Clinical and Surgical Aspects |
| Autore | AlAli Khaled Fares |
| Edizione | [1st ed.] |
| Pubbl/distr/stampa | Cham : , : Springer International Publishing AG, , 2024 |
| Descrizione fisica | 1 online resource (229 pages) |
| Altri autori (Persone) | HashimHashim Talib |
| ISBN | 3-031-59031-7 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Intro -- Contents -- Contributors -- Chapter 1: General Introduction to Congenital Spine Malformations -- References -- Chapter 2: Epidemiology of Congenital Spine Malformation -- 2.1 Introduction -- 2.2 Spina Bifida -- 2.3 Klippel Feil Syndrome -- 2.4 Congenital Scoliosis -- 2.5 Congenital Kyphosis -- 2.6 Congenital Lordosis -- References -- Chapter 3: The Diagnosis of Congenital Spine Malformations -- 3.1 Introduction -- 3.2 Types of Congenital Spine Malformations -- 3.3 Clinical Manifestations -- 3.4 Prenatal Diagnosis -- 3.4.1 Laboratory Tests -- Triple Screen Blood Test -- Amniocentesis -- 3.4.2 Ultrasonography -- 3.4.3 Magnetic Resonance Imaging (MRI) -- 3.5 Postnatal Diagnosis -- 3.5.1 Clinical Examination -- 3.5.2 Plain Radiography -- 3.5.3 Ultrasonography -- 3.5.4 Magnetic Resonance Imaging (MRI) -- 3.6 Conclusion -- References -- Chapter 4: Kyphosis -- 4.1 Introduction -- 4.2 Scheuermann's Kyphosis -- 4.3 Clinical Evaluation of Scheuermann's Kyphosis -- 4.4 Clinical Presentation -- 4.5 Indications for Surgery -- 4.6 Indications for Surgical Treatment -- 4.7 Clinical Presentation/Complications -- 4.8 Diagnostic Investigations -- 4.9 Examination -- 4.10 Imaging -- 4.11 Other Tests -- 4.12 Treatment -- 4.13 Physical Therapy and Exercise -- 4.14 Medications -- 4.15 Surgery -- References -- Chapter 5: Lordosis -- 5.1 Introduction -- 5.2 Mechanism -- 5.3 Epidemiology -- 5.4 Etiology -- 5.5 Patient's Presentation -- 5.6 Work up -- 5.7 Complications -- 5.8 Associated Conditions -- 5.9 Treatment -- 5.9.1 Anterior Fusion -- 5.9.2 Corrective Surgery -- 5.10 Prognosis -- References -- Chapter 6: Scoliosis -- 6.1 Introduction -- 6.2 Clinical Presentation -- 6.3 History and Examination -- 6.4 Modalities of Diagnosis of Scoliosis -- 6.4.1 Diagnosis Depends on Clinical Evaluation and Imaging Techniques -- 6.4.2 X-Ray -- 6.4.3 CT Scan -- 6.4.4 MRI Scan.
6.5 Treatment of Scoliosis -- 6.5.1 Observation -- 6.5.2 Bracing -- 6.5.3 Surgery -- 6.6 Complication of Scoliosis -- 6.7 Prevention -- References -- Chapter 7: Spina Bifida -- 7.1 Introduction -- 7.2 Definition of Spina Bifida -- 7.3 Classification of Spina Bifida -- 7.3.1 Myelomeningocele -- 7.3.2 Meningocele -- 7.3.3 Spina Bifida Occuluta (SBO) -- 7.3.4 Lipomyeloschisis (Dorsal Spinal Dysraphism) -- 7.4 Causes and Risk Factors of Spina Bifida -- 7.4.1 Nutritional Factors -- 7.4.2 Environmental Factors -- 7.4.3 Genetic Factors -- 7.5 Clinical Presentation -- 7.5.1 Neurological Manifestations -- 7.5.2 Orthopedic Manifestations -- 7.5.3 Signs -- 7.6 Diagnosis -- 7.6.1 Prenatal Screening and Diagnosis -- Alpha-Fetoprotein (AFP) -- Ultrasonography -- Post-natal Diagnosis and Investigation -- 7.7 Prevention -- 7.8 Management -- 7.8.1 Pre-natal Management -- 7.8.2 Post-natal Management -- Steps of Lesion Management -- Surgical Technique of Myelomeningocele Repair -- 7.8.3 Post-operative Management -- References -- Chapter 8: Spinal Canal Stenosis -- 8.1 Lumbar Spinal Stenosis -- 8.2 Pathology of Lumbar Spine Stenosis -- 8.3 Typical Presentation of Lumbar Spinal Stenosis -- 8.4 Approach to the Patient with Lumbar Spinal Stenosis -- 8.5 Investigations and Tests for Lumbar Spinal Stenosis -- 8.6 Palin Radiographs -- 8.7 Magnetic Resonance Imaging -- 8.8 CT-Myelography -- 8.9 Complications of CT Myelography -- 8.10 Bicycle/Treadmill Tests -- 8.11 Electrodiagnostic Testing -- 8.12 EMG Limitations -- 8.12.1 Diagnosis of Lumbar Spinal Stenosis -- 8.13 Treatment -- 8.14 Surgical Techniques Used in Lumbar Spinal Stenosis -- 8.15 Central Laminectomy -- 8.16 Central Laminectomy -- 8.17 Laminectomy with Lateral Recess Decompression and Foraminotomy -- 8.18 Laminoplasty -- 8.19 Posterior Spinal Fusion -- 8.20 Interbody Fusion -- 8.21 Interspinous Devices. 8.22 Indications to Use Interspinous Devices -- References -- Chapter 9: Dorsal Enteric Fistula -- 9.1 Introduction -- 9.2 Classification -- 9.3 Embryogenesis and Pathophysiology -- 9.3.1 Formation of the Neurenteric Canal -- 9.3.2 Theories -- 9.4 Clinical Features -- 9.5 Types of Posterior Enteric Remnants -- 9.6 Presentation -- 9.7 Neuroimaging -- 9.8 Management -- References -- Chapter 10: Neuroenteric Cyst of the Spine -- 10.1 Introduction -- 10.2 Pathogenesis -- 10.3 The PNC Lumen Fails to Close -- 10.4 Clinical Presentation of Neuroenteric Cyst (NEC) of the Spine -- 10.5 Diagnosis of Neuroenteric Cyst (NEC) of the Spine -- 10.5.1 Diagnostic Imaging -- 10.5.2 Diagnostic Histopathology -- 10.6 Management of Neuroenteric Cysts (NECs) of the Spine -- 10.7 Prognosis and Clinical Outcomes -- 10.8 Conclusion -- References -- Chapter 11: Dermal Sinus -- 11.1 Introduction -- 11.2 Embryogenesis -- 11.3 Clinical Presentation -- 11.4 Diagnostic Studies -- 11.5 Management -- 11.6 Complications -- 11.7 Follow Up -- 11.8 Outcome -- References -- Chapter 12: Split Cord Malformations -- 12.1 Introduction -- 12.2 History -- 12.3 Embryology -- 12.4 Clinical Features -- 12.5 Diagnostic Aids -- 12.6 Management -- 12.7 Operative Technique for Type I SCM -- 12.8 Operative Technique for Type II SCM -- 12.8.1 Complications -- 12.9 Outcome -- References -- Chapter 13: Caudal Regression Syndrome -- 13.1 Introduction -- 13.2 Epidemiology -- 13.3 Etiology -- 13.4 Related Conditions -- 13.5 Types of CRS and Sirenomelia -- 13.6 Signs and Symptoms -- 13.7 Diagnosis -- 13.8 Treatment -- 13.9 Prevention -- References -- Chapter 14: Segmental Spinal Dysgenesis -- 14.1 Introduction -- 14.2 Embryogenesis of SSD -- 14.3 Pathogenesis of Classification -- 14.4 Clinical Features -- 14.5 Investigations -- 14.6 Management -- References -- Chapter 15: Intradural Lipoma -- 15.1 Embryology. 15.2 Classification -- 15.3 Location -- 15.4 Diagnosis -- 15.4.1 Imaging Modalities -- 15.4.2 Gross Picture -- 15.4.3 Microscopic Picture -- 15.5 Clinical Presentation -- 15.5.1 Time of Presentation -- 15.5.2 Signs and Symptoms -- 15.5.3 Tethered Cord Syndrome -- 15.6 Management -- 15.6.1 Different Management Plans -- 15.6.2 The Goal of Surgery and the Best Surgical Technique -- 15.6.3 When to Do the Surgery -- 15.6.4 Prognosis and Sequela after Surgery -- 15.6.5 Total Resection Dangers and Extent of Lipoma Debulking -- 15.7 Conclusion -- References -- Chapter 16: Filum Lipoma -- 16.1 Introduction -- 16.1.1 Embryology and Pathogenesis -- 16.2 Anatomy of Filum Terminate -- 16.3 Biochemistry -- 16.4 Histology and Histopathology -- 16.5 Clinical Features -- 16.6 Investigations -- 16.7 Classification and Grading -- 16.8 Management -- 16.9 Surgical Approach (Interlaminar Approach) -- 16.10 Prognosis -- References -- Chapter 17: Tight Filum Terminale -- 17.1 Introduction -- 17.2 Pathophysiology -- 17.3 Diagnosis -- 17.3.1 Clinical Presentation -- 17.3.2 Neuroimaging -- 17.4 Management -- 17.4.1 Preoperative Considerations -- 17.4.2 Intraoperative Management and Procedure -- 17.4.3 Postoperative Management -- 17.5 Complications -- 17.6 Prognosis and Outcomes -- References -- Chapter 18: Abnormally Elongated Spinal Cord -- 18.1 Overview -- 18.2 Types of Spina Bifida -- 18.3 Causes -- 18.4 Preventing Spina Bifida with Folic Acid -- References -- Chapter 19: Persistent Terminal Ventricle -- 19.1 Introduction -- 19.2 Pathogenesis and Pathophysiology -- 19.3 Clinical Presentation -- 19.4 Differential Diagnosis and Diagnosis -- 19.5 Investigations -- 19.5.1 Imaging -- 19.5.2 Sonography -- 19.6 Management -- 19.7 Conclusion -- References -- Chapter 20: Terminal Myelocystocele -- 20.1 Introduction -- 20.2 Etiology and Pathogenesis -- 20.3 Diagnosis. 20.3.1 History and Clinical Presentation -- 20.3.2 Physical Examination -- 20.3.3 Neuroimaging -- 20.3.4 Other Investigations -- 20.4 Management -- 20.4.1 Surgical Procedure -- 20.4.2 Pre- and Post-operative Observations -- 20.4.3 Prevention -- 20.5 Complications and Prognosis -- References -- Chapter 21: Cervical Myelocystocele -- 21.1 Introduction -- 21.2 Presentations -- 21.3 Diagnosis -- 21.4 Treatment -- 21.5 Complications and Follow Up -- References -- Chapter 22: Congenital Spine Malformation in the Arab World -- 22.1 Introduction -- 22.2 Epidemiology -- 22.3 Etiology and Pathogenesis -- 22.4 Prevention -- References -- Index. |
| Record Nr. | UNINA-9910864185803321 |
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AlAli Khaled Fares
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| Cham : , : Springer International Publishing AG, , 2024 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Heart transplantation / / Hashim Talib Hashim, Naseer Ahmed, Giuseppe Faggian, Martí Manyalich, Francesco Onorati, editors
| Heart transplantation / / Hashim Talib Hashim, Naseer Ahmed, Giuseppe Faggian, Martí Manyalich, Francesco Onorati, editors |
| Pubbl/distr/stampa | Cham, Switzerland : , : Springer International Publishing, , [2023] |
| Descrizione fisica | 1 online resource (314 pages) |
| Disciplina | 617.4120592 |
| Soggetto topico |
Heart - Transplantation
Heart - Transplantation - Complications Heart Transplantation Cardiac Surgical Procedures |
| ISBN | 3-031-17311-2 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Anatomy of the heart -- Physiology of the heart -- Embryology of the heart -- Pathology of the heart diseases -- Heart Transplantation Procedure -- Complications and Follow up -- Cardioimmunology and heart transplantation -- Organ Procurement -- Ethical issues of heart transplantation -- Religious aspects of heart transplantation -- Multiorgan Transplantation including heart -- Artificial heart -- Heart Failure outcomes -- General Principles in heart transplantation -- Outcomes and Impact on quality of life. |
| Record Nr. | UNINA-9910644259603321 |
| Cham, Switzerland : , : Springer International Publishing, , [2023] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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The psychology of anger / / Hashim Talib Hashim, Athanasios Alexiou, editors
| The psychology of anger / / Hashim Talib Hashim, Athanasios Alexiou, editors |
| Pubbl/distr/stampa | Singapore : , : Springer, , [2022] |
| Descrizione fisica | 1 online resource (181 pages) |
| Disciplina | 152.47 |
| Soggetto topico | Anger |
| ISBN | 3-031-16605-1 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910624309803321 |
| Singapore : , : Springer, , [2022] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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The psychology of consciousness : theory and practice / / Hashim Talib Hashim and Athanasios Alexiou, editors
| The psychology of consciousness : theory and practice / / Hashim Talib Hashim and Athanasios Alexiou, editors |
| Pubbl/distr/stampa | Cham, Switzerland : , : Springer International Publishing, , [2022] |
| Descrizione fisica | 1 online resource (151 pages) |
| Disciplina | 616.8 |
| Soggetto topico |
Neurosciences
Cognitive science - Research |
| ISBN | 3-030-90692-2 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910578684703321 |
| Cham, Switzerland : , : Springer International Publishing, , [2022] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||