03702 am 2200865 n 450 99102149255033212017082210000242302-8218-9487-2(CKB)3710000001633508(FrMaCLE)OB-ksp-3904(oapen)https://directory.doabooks.org/handle/20.500.12854/54456(PPN)204524512(EXLCZ)99371000000163350820170823j|||||||| ||| 0geruu||||||m||||txtrdacontentcrdamediacrrdacarrierNeues Erbe Aspekte, Perspektiven und Konsequenzen der digitalen Überlieferung /Caroline Y. Robertson-von Trotha, Robert HauserKarlsruhe KIT Scientific Publishing20171 online resource (326 p.) Kulturelle Überlieferung - Digital3-86644-737-X Die zunehmende Digitalisierung von Informationen und ihre ausschließliche Produktion in digitalen Formen führen zu einer sehr hohen Technikabhängigkeit. Das dokumentarische Erbe, das wir zukünftigen Generationen überliefern, wird primär ein digitales Erbe sein, dessen Erhaltung und Überlieferung heutige Gesellschaften vor große und bisher weitestgehend ungelöste Probleme stellt. Der erste Band der Reihe »Kulturelle Überlieferung - digital« diskutiert unter Beteiligung namhafter Experten aus Wissenschaft und Praxis zentrale Aspekte, Probleme und Konsequenzen, die im Zusammenhang mit Digitalisierung und Bewahrung des digitalen kulturellen Erbes stehen. Damit leistet er disziplinübergreifend eine erste Annäherung an das große Themenfeld der digitalen kulturellen Überlieferung.Library, Information & Communication sciencesSociology & Anthropologydigitale ÜberlieferungKulturTechnikdigitale Langzeiterhaltungdigitales ArchivKulturTechnikdigitale Überlieferungdigitale Langzeiterhaltungdigitales ArchivLibrary, Information & Communication sciencesSociology & Anthropologydigitale ÜberlieferungKulturTechnikdigitale Langzeiterhaltungdigitales ArchivBähr Hans-Peter1317219Brandtner Andreas1317220Dreier Thomas1317221Enge Jürgen1317222Friedewald Michael592632Hauser Robert229134Heesen Jessica1317223Holz Verena1289805Kleinmanns Joachim1317224Kraemer Harald1317225Leimbach Timo1317226Lipp Thorolf1317227Lurk Tabea1280010Muñoz Morcillo Jesús1317228Robertson-von Trotha Caroline Y801736Robertson-von Trotha Caroline Y1289814Schneider Svenia1317229Schumann Natascha1317230Serexhe Bernhard1317231von Bülow Ulrich1317232Weissenberger-Eibl Marion A1317233Werner Kramski Heinz1317234Ziegaus Sebastian1317235Robertson-von Trotha Caroline Y801736Hauser Robert229134FR-FrMaCLEBOOK9910214925503321Neues Erbe3032913UNINA03598nam 22006735 450 991068647180332120251008153512.09783031258138(electronic bk.)978303125812110.1007/978-3-031-25813-8(MiAaPQ)EBC7234911(Au-PeEL)EBL7234911(OCoLC)1375293738(DE-He213)978-3-031-25813-8(PPN)269660399(CKB)26396538600041(EXLCZ)992639653860004120230405d2023 u| 0engurcnu||||||||txtrdacontentcrdamediacrrdacarrierThe Pendock Barry Porcelain Service A Forensic Evaluation /by Rachel L. Denyer, Morgan C. T. Denyer, Howell G. M. Edwards1st ed. 2023.Cham :Springer International Publishing :Imprint: Springer,2023.1 online resource (144 pages)Print version: Denyer, Rachel L. The Pendock Barry Porcelain Service Cham : Springer International Publishing AG,c2023 9783031258121 1. Origins of Heraldic Porcelain -- 2. Eighteenth Century Gentry and Heraldic Device Display -- 3. Development of Armorial Ceramics market in the UK -- 4. Pendock Neale Barry (1757 - 1833) and the resurrection of the Barry arms by Royal -- 5. Case Study: The Making of the Service and the Derby Attribution -- 6. Case Study: The Decoration of the Plate and the Billingsley Attribution -- 7. Summary and Conclusions.Heraldic devices first appeared on ceramics in Western Europe from the sixteenth century onwards; however, it was not until the 1760s that British ceramic manufactories began executing commissions for services displaying heraldic devices for the gentry. This book explores the rise of the new gentry class and the market for armorial services through the case study of the Pendock Barry service. The case study is presented from three angles. It looks at Pendock Neale Barry (1757–1833) who commissioned the service, then considers the evidence for attributing the service to the Derby factory during the period 1805–1810, and finally looks at the evidence supporting an attribution of the decoration to Billingsley. The case study sets out a novel approach to understanding heraldic devices on ceramics by bringing together the disciplines of detailed genealogical research, cultural knowledge, and chemical analytical compositional data. This multidisciplinary approach enables the armorial services to be considered and understood through the lens of heritage, culture, and science.Cultural propertyEthnologyGreat BritainCultureAnalytical chemistryCeramic materialsCultural HeritageBritish CultureAnalytical ChemistryCeramicsCultural property.EthnologyCulture.Analytical chemistry.Ceramic materials.Cultural Heritage.British Culture.Analytical Chemistry.Ceramics.738.380941738.380941Denyer Rachel L.1351108Denyer Morgan C. T.Edwards Howell G. M.1943-MiAaPQMiAaPQMiAaPQ9910686471803321The Pendock Barry porcelain service3418785UNINA04946nam 22006135 450 991030016240332120251116135200.03-319-17819-910.1007/978-3-319-17819-6(CKB)3710000000452108(EBL)3567879(SSID)ssj0001534584(PQKBManifestationID)11867004(PQKBTitleCode)TC0001534584(PQKBWorkID)11498107(PQKB)11225354(DE-He213)978-3-319-17819-6(MiAaPQ)EBC3567879(PPN)187684847(EXLCZ)99371000000045210820150722d2015 u| 0engur|n|---|||||txtccrAcrodermatitis Enteropathica A Clinician's Guide /by Pooya Khan Mohammad Beigi, Emanual Maverakis1st ed. 2015.Cham :Springer International Publishing :Imprint: Springer,2015.1 online resource (165 p.)Description based upon print version of record.3-319-17818-0 Includes bibliographical references and index.1. History of Acrodermatitis Enteropathica -- 2. Epidemiology and Etiology -- 2.1. Epidemiology -- 2.2. Etiology -- 2.2.1. Molecular Etiology of AE -- 2.2.2. Hypothetical Etiology 1: the Alteration of Zinc Bioavailability -- 2.2.3. Hypothetical Etiology 2: a Defective Zinc Transporter -- 2.2.4. Alternative Forms of AE-like Zinc Deficiencies -- 3. Analysis of Disorder -- 3.1. Clinical Forms of AE -- 3.2. Nomenclature of Zinc Deficiencies -- 3.3. Acquired Non-hereditary Zinc Deficiency -- 3.3.1. Zinc Deficient Maternal Breast Milk -- 3.3.2. Zinc Deficient Caused by Metabolism Disorders -- 4. Clinical Symptoms -- 5. Diagnosis -- 5.1. Laboratory Diagnosis of Zinc Deficiency -- 5.2. Histopathology -- 5.3. Biological Diagnosis of AE -- 5.4. Clinical Diagnosis -- 5.5. Molecular Diagnosis -- 5.6. Differential Diagnosis -- 6. Disease Course and Treatment -- 6.1. Treatment -- 7. The Role of Zinc in Different Body Systems -- 7.1. Biochemistry of Zinc Metabolism -- 7.2. Skin and Hair Physiology -- 7.3. Gastrointestinal System and Other Organs -- 7.4. Neurological Development, Growth, and Mental Status -- 7.5. Enzymes -- 7.6. Endocrine System -- 7.7. Metabolism of Nucleic Acids -- 7.8. Mitosis and Meiosis Cycles -- 7.9. Cell Membranes -- 7.10. Synthesis of Proteins and Collagen -- 7.11. Immune System -- 8. History of AE in Adults -- 9. Iranian Hospital Cases in Literature -- 9.1. Patient One -- 9.2. Patient Two -- 9.3. Patient Three -- 9.4. Patient Four -- 9.5. Zinc Deficiency Similarities to AE in Infants (Fifth Patient) -- 10. Clinical Research -- 10.1. Abstract -- 10.2. Synopsis of Study -- 10.3. Purpose of Study -- 10.4. The Considered Hypotheses -- 10.5. Introduction -- 10.5. Methods -- 10.6. Ethical Considerations -- 10.7. Results -- 10.8. Discussion -- 11. Evaluation of Symptoms in Razi Dermatology Hospital -- 12. Case Photos.Written by and for dermatologists, pediatric and obstetrics specialists. This book presents the groundbreaking work of Dr. Pooya Khan Mohammad Beigi M.D., whose clinical research study on Acrodermatitis Enteropathica (AE) is the largest ever conducted on this rare disorder. The only book of its kind to offer insights into AE, it not only includes dozens of high quality photographs, illustrations, and clinical tables, but also covers everything from the history of AE to categories of the disorder, molecular analysis, epidemiology, disorder signs and symptoms, diagnosis, treatment, and more. Acrodermatitis Enteropathica is a rare disorder of zinc metabolism that occurs in one of two forms: inborn and acquired. If untreated, this disease is fatal and affected individuals may die within just a few years. Therefore, it is critical that physicians are aware of the signs and symptoms related to AE and the appropriate treatments available for patients.DermatologyPediatricsObstetricsDermatologyhttps://scigraph.springernature.com/ontologies/product-market-codes/H1900XPediatricshttps://scigraph.springernature.com/ontologies/product-market-codes/H49006Obstetrics/Perinatology/Midwiferyhttps://scigraph.springernature.com/ontologies/product-market-codes/H26014Dermatology.Pediatrics.Obstetrics.Dermatology.Pediatrics.Obstetrics/Perinatology/Midwifery.610Khan Mohammad Beigi Pooyaauthttp://id.loc.gov/vocabulary/relators/aut909074Maverakis Emanualauthttp://id.loc.gov/vocabulary/relators/autBOOK9910300162403321Acrodermatitis Enteropathica2521524UNINA