Prolonged jaundice and hypothyroidism as the presenting symptoms in a neonate with a novel Prop1 gene mutation (Q83X)

European Journal of Endocrinology

Volumn 150, Issue 3, 2004, Pages 257-264

  Voutetakis, Antonis ^a   Maniati Christidi, Maria ^a   Kanaka Gantenbein, Christina ^a   Dracopoulou, Maria ^a   Argyropoulou, Maria ^a   Livadas, Sarantis ^a   Dacou Voutetakis, Catherine ^a   Sertedaki, Amalia ^a  

^a UNIVERSITY OF ATHENS MEDICAL SCHOOL   (Greece)

Author keywords

[No Author keywords available]

Indexed keywords

GLUCAGON; GONADORELIN; GROWTH HORMONE; HYDROCORTISONE; LEVOTHYROXINE; PROLACTIN; PROTIRELIN; THYROID HORMONE; THYROTROPIN; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR PROP1; UNCLASSIFIED DRUG;

ARTICLE; CASE REPORT; CHEMOLUMINESCENCE; CONTRAST ENHANCEMENT; DIFFUSION WEIGHTED IMAGING; EARLY DIAGNOSIS; GENE MUTATION; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC COUNSELING; GENETIC DISORDER; HORMONE DEFICIENCY; HORMONE DETERMINATION; HUMAN; HYPOPHYSIS; HYPOPHYSIS FUNCTION; HYPOTHYROIDISM; INFANT; JAUNDICE; MALE; MORPHOLOGY; NEWBORN; NEWBORN DISEASE; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; RADIOIMMUNOASSAY; SYMPTOMATOLOGY;

CODON, NONSENSE; HOMEODOMAIN PROTEINS; HUMAN GROWTH HORMONE; HUMANS; HYPOTHYROIDISM; INFANT; JAUNDICE; MALE; PEDIGREE; THYROTROPIN; THYROXINE; TRIIODOTHYRONINE;

EID: 1842579537     PISSN: 08044643     EISSN: None     Source Type: Journal    
DOI: 10.1530/eje.0.1500257     Document Type: Article

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