Prader-Labhart-Willi syndrome with central precocious puberty and empty sella syndrome

Acta Paediatrica, International Journal of Paediatrics

Volumn 88, Issue 11, 1999, Pages 1295-1297

  Linnemann, K ^a   Schroder C ^a   Mix, M ^b   Kruger G ^b   Fusch, C ^a  

^a UNIVERSITY OF GREIFSWALD   (Germany)

^b UNIVERSITY OF ROSTOCK   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CORTICOTROPIN[4-10]; FOLLITROPIN; LUTEINIZING HORMONE;

ANDROGEN BLOOD LEVEL; ARTICLE; BONE AGE; CASE REPORT; CHROMOSOME 15Q; EMPTY SELLA SYNDROME; HUMAN; HUMAN CELL; HUMAN TISSUE; MALE; NEWBORN; PRADER WILLI SYNDROME; PRECOCIOUS PUBERTY; PRIORITY JOURNAL;

EMPTY SELLA SYNDROME; FOLLOW-UP STUDIES; HUMANS; INFANT, NEWBORN; MAGNETIC RESONANCE IMAGING; MALE; PRADER-WILLI SYNDROME; PUBERTY, PRECOCIOUS;

EID: 0032704136     PISSN: 08035253     EISSN: None     Source Type: Journal    
DOI: 10.1080/080352599750030482     Document Type: Article

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