about
Loss-of-function mutation in GATA4 causes anomalies of human testicular developmentAetiological diagnosis of male sex ambiguity: a collaborative studyLong-term surgical results and patient satisfaction with male pseudohermaphroditism or true hermaphroditism: a cohort of 63 patients[Radiological innovations in the screening and diagnosis of the inborn errors of metabolism].Mutation analysis of NR5A1 encoding steroidogenic factor 1 in 77 patients with 46, XY disorders of sex development (DSD) including hypospadiasHeterogeneity of persistent hyperinsulinaemic hypoglycaemia. A series of 175 cases.Omphalocele: beyond the size issue.Glucose metabolism in 105 children and adolescents after pancreatectomy for congenital hyperinsulinism.Inflammatory myofibroblastic tumor in children: clinical review with anaplastic lymphoma kinase, Epstein-Barr virus, and human herpesvirus 8 detection analysis.Molecular mechanisms of neonatal hyperinsulinism.Pitfalls in the diagnosis and management of obstructive uterovaginal duplication: a series of 32 cases.In vitro insulin secretion by pancreatic tissue from infants with diazoxide-resistant congenital hyperinsulinism deviates from model predictions.Congenital hyperinsulinism: pancreatic [18F]fluoro-L-dihydroxyphenylalanine (DOPA) positron emission tomography and immunohistochemistry study of DOPA decarboxylase and insulin secretion.BPDZ 154 activates adenosine 5'-triphosphate-sensitive potassium channels: in vitro studies using rodent insulin-secreting cells and islets isolated from patients with hyperinsulinism.Value of 18F-fluoro-L-dopa PET in the preoperative localization of focal lesions in congenital hyperinsulinism.Outcome of suprarenal localized masses diagnosed during the perinatal period: a retrospective multicenter study.Facial appearance in persistent hyperinsulinemic hypoglycemia.Acute insulin responses to calcium and tolbutamide do not differentiate focal from diffuse congenital hyperinsulinism.[Hermaphroditism pathology].Characterization of hyperinsulinism in infancy assessed with PET and 18F-fluoro-L-DOPA.Functional imaging of the pancreas: the role of [18F]fluoro-L-DOPA PET in the diagnosis of hyperinsulinism of infancy.The Isabel Forshall Lecture. Surgical management of the intersex patient: an overview in 2003.Genetic mutations and somatic anomalies in association with 46,XY gonadal dysgenesis.Fetal intestinal obstruction induces alteration of enteric nervous system development in human intestinal atresia.Aniridia, male pseudohermaphroditism, gonadoblastoma, mental retardation, and del 11p13.New clinical and therapeutic perspectives in Currarino syndrome (study of 29 cases)Exclusion ofWNT4 as a major gene in Rokitansky-Küster-Hauser anomalyThe added value of [18F]fluoro-L-DOPA PET in the diagnosis of hyperinsulinism of infancy: a retrospective study involving 49 childrenThe Knudson’s Two-Hit Model and Timing of Somatic Mutation May Account for the Phenotypic Diversity of Focal Congenital Hyperinsulinism
P50
Q24336463-1DD4C352-11B5-4C2C-847A-A449CCF0FD55Q28216466-6408B15A-C73D-46CE-984E-57ED878CB684Q28306189-35E10F8D-8A7A-4F65-AF4D-DB358427E3F0Q31016379-4079696D-C647-4F4A-96FD-BCF2EE74D129Q34058239-9D7006A3-515F-4AA6-B750-29A2244ED4C9Q34504717-6995207A-C12A-409F-A9CC-C738F4C478E4Q34961616-19B47A96-C31C-45C5-861D-1C188A6B0853Q35688376-A6C5C452-D6C5-4131-8A8E-591BA8CBD080Q36287401-63C4BD5E-6225-4CD0-832E-6AABDA204939Q36604826-266B4FFF-0829-4A86-BA49-8DE0FD7169DBQ37282100-3667A608-1AE2-4F6E-B442-A424F30DC5BFQ38732653-A515E609-77F5-45DE-8C58-2917C04004C1Q40332110-A0294508-1A70-4248-A749-9921B568825EQ40692591-15A5AA28-B072-46D3-83A5-542AB09E1004Q43285358-A4B279F0-AC24-438A-A7A0-C174C26A24D7Q43996950-53ED2A40-6FA3-4B5C-BB61-664F138AA883Q44124704-D677C268-E9B8-401F-8E82-AF0696D3A7ABQ44757187-D3DBB623-A783-415A-AAAE-D7DEB2D46C93Q46399194-122ADCE6-18ED-4A6B-B2A1-FED9F4682946Q46421494-FBC13F8F-8625-44B5-9DE5-0507CC13EBCFQ46960337-58F40991-7DF9-4DE4-BC33-D32727993902Q48567831-E9146145-0D26-459B-AF20-9758DCF23C90Q50575275-2946A1C4-6618-4864-94BC-87BE26A50776Q52086508-A23F7D29-C54D-4F0B-AAD0-A5E4B0E823CCQ52101607-DE558C4F-E5D9-4E10-B59E-FB5B005E0893Q57199410-9B63F405-251E-4A1F-A2B9-70075CCF150DQ57199418-51D94173-F1BE-484D-AE5C-B8F6501AA4ADQ57199759-5988FB5C-B60A-4766-8230-F8EE7DCDBB54Q57199763-1B49878F-AFCE-4E7C-8AF9-08D237F890FA
P50
description
Chirurgien, Universitaire
@fr
name
Claire Nihoul-Fékété
@ast
Claire Nihoul-Fékété
@de
Claire Nihoul-Fékété
@en
Claire Nihoul-Fékété
@es
Claire Nihoul-Fékété
@fr
Claire Nihoul-Fékété
@it
type
label
Claire Nihoul-Fékété
@ast
Claire Nihoul-Fékété
@de
Claire Nihoul-Fékété
@en
Claire Nihoul-Fékété
@es
Claire Nihoul-Fékété
@fr
Claire Nihoul-Fékété
@it
prefLabel
Claire Nihoul-Fékété
@ast
Claire Nihoul-Fékété
@de
Claire Nihoul-Fékété
@en
Claire Nihoul-Fékété
@es
Claire Nihoul-Fékété
@fr
Claire Nihoul-Fékété
@it
P21
P31
P4124
claire-nihoul-fekete_35389
P569
1939-01-01T00:00:00Z
P735
P7578
claire-nihoul-fekete