Absence of mutation in the follicle-stimulating hormone receptor gene in severe primary hypothyroidism associated with gonadal hyperstimulation

Journal of Pediatric Endocrinology and Metabolism

Volumn 20, Issue 8, 2007, Pages 923-931

  Suarez, Elizabeth A ^a   d'Alvas, Catarina B ^b   Campbell, Andrew ^a   Millet Horn, Jill ^a   Dever, Maureen ^a   Faerber, Eric ^a   Medonca, Berenice B ^b   Latronico, Ana Claudia ^b   De Luca, Francesco ^a  

^a DREXEL UNIVERSITY COLLEGE OF MEDICINE   (United States)

^b UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

Follicle stimulating hormone receptor; Gonadal hyperstimulation; Primary hypothyroidism

Indexed keywords

DNA; ESTRADIOL; FOLLITROPIN RECEPTOR; LEVOTHYROXINE; PROLACTIN; THYROTROPIN; THYROXINE;

ADOLESCENT; ARTICLE; CASE REPORT; CLINICAL FEATURE; DISEASE ASSOCIATION; DISEASE SEVERITY; DNA EXTRACTION; DNA POLYMORPHISM; DRUG DOSE INCREASE; DRUG RESPONSE; FEMALE; GALACTORRHEA; GENE MUTATION; GENE SEQUENCE; GONADAL DISEASE; HORMONE BLOOD LEVEL; HUMAN; HYPOPHYSIS DISEASE; HYPOTHYROIDISM; IN VITRO STUDY; LOW DRUG DOSE; MALE; MUTATIONAL ANALYSIS; NUCLEAR MAGNETIC RESONANCE IMAGING; PHYSICAL EXAMINATION; PRECOCIOUS PUBERTY; SCHOOL CHILD; SEQUENCE ANALYSIS; TREATMENT DURATION;

ADOLESCENT; CHILD; FEMALE; GONADAL DISORDERS; HUMANS; HYPOTHYROIDISM; MALE; MUTATION; PITUITARY GLAND; PUBERTY, PRECOCIOUS; RECEPTORS, FSH; SEVERITY OF ILLNESS INDEX; THYROTROPIN;

EID: 34648813617     PISSN: 0334018X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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