Variable outcome of growth hormone administration in respiratory chain deficiency

Molecular Genetics and Metabolism

Volumn 93, Issue 2, 2008, Pages 195-199

  Romano, S ^a   Samara, D ^a   Crosnier, H ^a   Valayannopoulos, V ^a   Polak, M ^a   Chretien D ^a   Rotig A ^a   Munnich, A ^a   Brauner, R ^b   de Lonlay, P ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

^b UNIVERSITÉ PARIS DESCARTES   (France)

Author keywords

Growth hormone; Growth hormone treatment; Mitochondrial respiratory chain

Indexed keywords

GROWTH HORMONE; MITOCHONDRIAL DNA;

ANEMIA; ARTICLE; ATAXIA; CASE REPORT; CELL PROLIFERATION; CEREBELLAR ATAXIA; CLINICAL ASSESSMENT; CLINICAL EXAMINATION; DRUG WITHDRAWAL; FEMALE; GENERAL CONDITION DETERIORATION; GENETIC DISORDER; GROWTH HORMONE DEFICIENCY; GROWTH RATE; GROWTH RETARDATION; HUMAN; HYPERLACTATEMIA; MALE; MITOCHONDRIAL DNA DISORDER; MITOCHONDRIAL RESPIRATION; MITOSIS; MUSCLE HYPOTONIA; NEUROMUSCULAR DISEASE; NEUROTOXICITY; NUTRITIONAL STATUS; OUTCOME ASSESSMENT; OXIDATIVE PHOSPHORYLATION; PRESCHOOL CHILD; PRIORITY JOURNAL; PYRAMIDAL SIGN; RESPIRATORY CHAIN; SIDE EFFECT; SPEECH DISORDER; TREATMENT FAILURE; TREATMENT OUTCOME; TREATMENT RESPONSE; VISUAL ACUITY;

ADOLESCENT; CHILD; DNA, MITOCHONDRIAL; FEMALE; GROWTH DISORDERS; HUMAN GROWTH HORMONE; HUMANS; MALE; MITOCHONDRIAL DISEASES; MUTATION; RECOMBINANT PROTEINS; SAFETY;

EID: 38049056613     PISSN: 10967192     EISSN: 10967206     Source Type: Journal    
DOI: 10.1016/j.ymgme.2007.09.007     Document Type: Article

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