Primary ovarian insufficiency in classic galactosemia: Role of FSH dysfunction and timing of the lesion

Journal of Inherited Metabolic Disease

Volumn 36, Issue 1, 2013, Pages 29-34

  Gubbels, Cynthia S ^a   Land, Jolande A ^b   Evers, Johannes L H ^a   Bierau, Jörgen ^a   Menheere, Paul P C A ^a   Robben, Simon G F ^a   Rubio Gozalbo, M Estela ^a  

^a MAASTRICHT UNIVERSITY MEDICAL CENTER   (Netherlands)

^b UNIVERSITY MEDICAL CENTER GRONINGEN   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ESTRADIOL; FOLLITROPIN; GALACTOSE 1 PHOSPHATE URIDYLYLTRANSFERASE; GONADOTROPIN; HUMAN MENOPAUSAL GONADOTROPIN; LUTEINIZING HORMONE; MUELLERIAN INHIBITING FACTOR; RECOMBINANT FOLLITROPIN; RECOMBINANT LUTEINIZING HORMONE;

ADOLESCENT; ADULT; ARTICLE; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE ASSOCIATION; ENDOCRINE DISEASE; FEMALE; GALACTOSEMIA; GALT GENE; GENE; GENE MUTATION; HORMONE ACTION; HORMONE DETERMINATION; HORMONE RESPONSE; HUMAN; LIMIT OF DETECTION; NUCLEAR MAGNETIC RESONANCE IMAGING; ORGAN SIZE; OVARIAN RESERVE; OVULATION INDUCTION; POSTMENOPAUSE; PREMATURE OVARIAN FAILURE; PREPUBERTY; PRESCHOOL CHILD; SCHOOL CHILD; WOMEN'S HEALTH;

ADOLESCENT; ADULT; ANTI-MULLERIAN HORMONE; CHILD; FEMALE; FOLLICLE STIMULATING HORMONE; GALACTOSEMIAS; GONADOTROPINS; HUMANS; OVARY; PRIMARY OVARIAN INSUFFICIENCY; YOUNG ADULT;

EID: 84872615426     PISSN: 01418955     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/s10545-012-9497-7     Document Type: Article

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