Case seminar: A young female with acute hyponatremia and a sellar mass

Endocrine

Volumn 40, Issue 3, 2011, Pages 325-331

  Pekic, Sandra ^a,b   Doknic, Mirjana ^a,b   Miljic, Dragana ^a   Saveanu, Alexandru ^c,d   Reynaud, Rachel ^c   Barlier, Anne ^c,d   Brue, Thierry ^c   Popovic, Vera ^a,b  

^a CLINICAL CENTER OF SERBIA   (Serbia)

^b UNIVERSITY OF BELGRADE   (Serbia)

^c TIMONE HOSPITAL   (France)

^d HÔPITAL DE LA CONCEPTION   (France)

Author keywords

Hypocorticism; Hyponatremia; Hypopituitarism; PROP1 mutation; Sellar mass

Indexed keywords

CORTICOTROPIN; GROWTH HORMONE; HYDROCORTISONE; LEVOTHYROXINE; RECOMBINANT GROWTH HORMONE; SODIUM; SODIUM CHLORIDE; THYROTROPIN; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR PROP1; UNCLASSIFIED DRUG; CORTICOSTEROID; HOMEODOMAIN PROTEIN; PROPHET OF PIT 1 PROTEIN; PROPHET OF PIT-1 PROTEIN;

ADOLESCENT; ADULT; CASE REPORT; CHILD; COMA; COMPUTER ASSISTED TOMOGRAPHY; CONFERENCE PAPER; CORTICOTROPIN DEFICIENCY; CRANIOPHARYNGIOMA; DIFFERENTIAL DIAGNOSIS; EMERGENCY WARD; EMPTY SELLA SYNDROME; EOSINOPHIL; FEMALE; GENE MUTATION; GENETIC ANALYSIS; GROWTH HORMONE DEFICIENCY; HISTOPATHOLOGY; HOMOZYGOSITY; HUMAN; HYPONATREMIA; HYPOPITUITARISM; HYPOTHYROIDISM; INCIDENTAL FINDING; INTENSIVE CARE UNIT; PLASMA OSMOLALITY; PRIORITY JOURNAL; PROP1 GENE; RATHKE CLEFT CYST; RESPIRATORY ARREST; SCHOOL CHILD; SELLA TURCICA TUMOR; SIBLING; TRANSSPHENOIDAL HYPOPHYSECTOMY; ACUTE DISEASE; ARTICLE; BLOOD; CONGENITAL MALFORMATION; GENE DELETION; GENETICS; HYPOPHYSIS; PATHOLOGY; SELLA TURCICA; TREATMENT OUTCOME;

ACUTE DISEASE; ADOLESCENT; ADRENAL CORTEX HORMONES; ADRENOCORTICOTROPIC HORMONE; CHILD; FEMALE; HOMEODOMAIN PROTEINS; HUMANS; HYDROCORTISONE; HYPONATREMIA; HYPOPITUITARISM; PITUITARY GLAND; SELLA TURCICA; SEQUENCE DELETION; TREATMENT OUTCOME; YOUNG ADULT;

EID: 84858769712     PISSN: 1355008X     EISSN: 15590100     Source Type: Journal    
DOI: 10.1007/s12020-011-9516-8     Document Type: Conference Paper

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