The spectrum of hypopituitarism caused by PROP1 mutations

Best Practice and Research: Clinical Endocrinology and Metabolism

Volumn 16, Issue 3, 2002, Pages 421-431

  Mody, Sushil ^a   Brown, Milton R ^b   Parks, John S ^b  

^a JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Combined pituitary hormone deficiency (CPHD); Corticotrophin (ACTH); Deletion; Follicle stimulating hormone (FSH); Growth hormone (GH); Hypopituitarism; Luteinizing hormone (LH); Macroadenoma; Multiple pituitary hormone deficiency (MPHD); Mutation; Pituitary; Prolactin (Prl); PROP1 gene; Thyroid stimulating hormone (TSH)

Indexed keywords

ARGININE; CORTICOTROPIN; FOLLITROPIN; GONADORELIN; GONADOTROPIN; GROWTH HORMONE; HUMAN GROWTH HORMONE; HYDROCORTISONE; INSULIN; LEVODOPA; LUTEINIZING HORMONE; PROLACTIN; PROTEIN PROP1; SEX HORMONE; THYROID HORMONE; THYROTROPIN; THYROXINE; TRANSCRIPTION FACTOR PIT 1; UNCLASSIFIED DRUG; HYPOPHYSIS HORMONE;

ADENOHYPOPHYSIS; ADENOHYPOPHYSIS DISEASE; CHILDHOOD; CLINICAL FEATURE; COMPARATIVE STUDY; CORTICOTROPIN DEFICIENCY; DISEASE COURSE; GENE MUTATION; GENETIC TRANSCRIPTION; GROWTH DISORDER; GROWTH HORMONE DEFICIENCY; HORMONE DEFICIENCY; HORMONE RESPONSE; HORMONE SUBSTITUTION; HORMONE SYNTHESIS; HUMAN; HYPOPITUITARISM; HYPOTHYROIDISM; IMAGE ANALYSIS; MEDICAL RESEARCH; MOLECULAR GENETICS; MORPHOLOGY; NONHUMAN; PHENOTYPE; PUBERTY DISORDERS; REVIEW; DIAGNOSTIC IMAGING; HYPOGLYCEMIA; PUBERTY;

EID: 0036423939     PISSN: 1521690X     EISSN: None     Source Type: Journal    
DOI: 10.1053/beem.2002.0218     Document Type: Article

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