Familial focal congenital hyperinsulinism

Journal of Clinical Endocrinology and Metabolism

Volumn 96, Issue 1, 2011, Pages 24-28

  Ismail, Dunia ^a   Smith, Virpi V ^a   De Lonlay, Pascale ^b   Ribeiro, Maria Joao ^b   Rahier, Jacques ^c   Blankenstein, Oliver ^d   Flanagan, Sarah E ^e   Bellanné Chantelot, Christine ^f   Verkarre, Virginie ^b   Aigrain, Yves ^b   Pierro, Agostino ^a   Ellard, Sian ^e   Hussain, Khalid ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b HÔPITAL NECKER ENFANTS MALADES   (France)

^c CLINIQUES UNIVERSITAIRES SAINT LUC   (Belgium)

^d HUMBOLDT UNIVERSITY   (Germany)

^e UNIVERSITY OF EXETER   (United Kingdom)

^f PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

DIAZOXIDE; LEVO DIHYDROXYPHENYLALANINE F 18; OCTREOTIDE; RADIOPHARMACEUTICAL AGENT; UNCLASSIFIED DRUG;

CASE REPORT; CHILD; CONFERENCE PAPER; DRUG TREATMENT FAILURE; FAMILIAL FOCAL CONGENITAL HYPERINSULINISM; GENE MUTATION; GENE SEQUENCE; GENETIC COUNSELING; HETEROZYGOTE; HUMAN; HUMAN TISSUE; NUCLEOTIDE SEQUENCE; PANCREAS; PANCREATICOJEJUNOSTOMY; PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY; POLYMERASE CHAIN REACTION; POSITRON EMISSION TOMOGRAPHY; PRIORITY JOURNAL; RISK; SCHOOL CHILD; SIBLING; TERM BIRTH; THYROID GLAND; TREATMENT RESPONSE;

EID: 78650854017     PISSN: 0021972X     EISSN: 0021972X     Source Type: Journal    
DOI: 10.1210/jc.2010-1524     Document Type: Conference Paper

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