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Diagnosis and management of mitochondrial diseases

Author
GILLIS, Lynette1 2 ; KAYE, Edward1
[1] Section of Biochemical Genetics, Department of Human Genetics and Molecular Biology, University of Pennsylvania School of Medicine, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States
[2] Division of Gastroenterology and Nutrition, University of Pennsylvania School of Medicine, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States
Issue title
Pediatric gastroenterology and nutrition
Author (monograph)
MASCARENHAS, Maria R (Editor)1 ; PICCOLI, David A (Editor)2
[1] Department of Pediatrics, University of Pennsylvania School of Medicine, The Children's Hospital of Philadelphia, Philadelphia, PA, United States
[2] Division of Gastroenterology and Nutrition, University of Pennsylvania School of Medicine, The Children's Hospital of Philadelphia, Philadelphia, PA, United States
Source

The Pediatric clinics of North America. 2002, Vol 49, Num 1, pp vii-viii, 18 p ; ref : 82 ref

CODEN
PCNAA8
ISSN
0031-3955
Scientific domain
Pediatrics
Publisher
Elsevier, Philadelphia, PA
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Anémie sidéroblastique Chaîne respiratoire Chimiothérapie Cytopathie mitochondriale Diagnostic Encéphalomyélopathie Enfant Phosphorylation oxydative Symptomatologie Traitement Syndrome Pearson Encéphale pathologie Enzymopathie Homme Hémopathie Maladie héréditaire Myélodysplasique syndrome Métabolisme pathologie Système nerveux central pathologie Système nerveux pathologie
Keyword (en)
Sideroblastic anemia Respiratory chain Chemotherapy Mitochondrial disorder Diagnosis Encephalomyelopathy Child Oxidative phosphorylation Symptomatology Treatment Pearson syndrome Cerebral disorder Enzymopathy Human Hemopathy Genetic disease Myelodysplastic syndrome Metabolic diseases Central nervous system disease Nervous system diseases
Keyword (es)
Anemia sideroblástica Cadena respiratoria Quimioterapia Citopatía mitocondrial Diagnóstico Encefalomielopatía Niño Fosforilación oxidativa Sintomatología Tratamiento Encéfalo patología Enzimopatía Hombre Hemopatía Enfermedad hereditaria Mielodisplastico síndrome Metabolismo patología Sistema nervosio central patología Sistema nervioso patología
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B22 Metabolic diseases / 002B22D Errors of metabolism / 002B22D03 Carbohydrates (enzymatic deficiencies). Glycogenosis

Discipline
Metabolic diseases
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
13479378

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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