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I Giurgea

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 4, 2005
[Congenital hyperinsulinism in newborn and infant]I Giurgea, M-J Ribeiro, N Boddaert, et al.
Journal of Inherited Metabolic Disease|May 4, 2005
Dominantly inherited hyperinsulinaemic hypoglycaemiaP de Lonlay, I Giurgea, C Sempoux, et al.
Journal of Medical Genetics|May 13, 2006
Prenatal diagnosis of myopathy, encephalopathy, lactic acidosis, and stroke-like syndrome: contribution to understanding mitochondrial DNA segregation during human embryofetal developmentC Bouchet, J Steffann, J Corcos, et al.
Human Pathology|February 17, 2007
Neonatal hyperinsulinism: clinicopathologic correlationP Delonlay, A Simon, L Galmiche-Rolland, et al.
Molecular Psychiatry|April 19, 2021
Wnt/β-catenin pathway and cell adhesion deregulation in CSDE1-related intellectual disability and autism spectrum disordersE El Khouri, J Ghoumid, D Haye, et al.
La Revue De Medecine Interne|July 23, 2022
Neutrophilic dermatosesJ Delaleu, C Lepelletier, A Calugareanu, et al.
European Journal of Medical Genetics|February 4, 2014
SALL4 and NFATC2: two major actors of interstitial 20q13.2 duplicationA Briand-Suleau, J Martinovic, L Tosca, et al.
Journal of Medical Genetics|July 22, 2005
Congenital hyperinsulinism and mosaic abnormalities of the ploidyI Giurgea, D Sanlaville, J-C Fournet, et al.
American Journal of Medical Genetics. Part A|April 23, 2015
Clinical spectrum of eye malformations in four patients with Mowat-Wilson syndromeA Bourchany, I Giurgea, J Thevenon, et al.
Neurogenetics|March 8, 2018
MED13L-related intellectual disability: involvement of missense variants and delineation of the phenotypeT Smol, F Petit, A Piton, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 4, 2005
[Congenital hyperinsulinism in newborn and infant]I Giurgea, M-J Ribeiro, N Boddaert, et al.
Journal of Inherited Metabolic Disease|May 4, 2005
Dominantly inherited hyperinsulinaemic hypoglycaemiaP de Lonlay, I Giurgea, C Sempoux, et al.
Journal of Medical Genetics|May 13, 2006
Prenatal diagnosis of myopathy, encephalopathy, lactic acidosis, and stroke-like syndrome: contribution to understanding mitochondrial DNA segregation during human embryofetal developmentC Bouchet, J Steffann, J Corcos, et al.
Human Pathology|February 17, 2007
Neonatal hyperinsulinism: clinicopathologic correlationP Delonlay, A Simon, L Galmiche-Rolland, et al.
Molecular Psychiatry|April 19, 2021
Wnt/β-catenin pathway and cell adhesion deregulation in CSDE1-related intellectual disability and autism spectrum disordersE El Khouri, J Ghoumid, D Haye, et al.
La Revue De Medecine Interne|July 23, 2022
Neutrophilic dermatosesJ Delaleu, C Lepelletier, A Calugareanu, et al.
European Journal of Medical Genetics|February 4, 2014
SALL4 and NFATC2: two major actors of interstitial 20q13.2 duplicationA Briand-Suleau, J Martinovic, L Tosca, et al.
Journal of Medical Genetics|July 22, 2005
Congenital hyperinsulinism and mosaic abnormalities of the ploidyI Giurgea, D Sanlaville, J-C Fournet, et al.
American Journal of Medical Genetics. Part A|April 23, 2015
Clinical spectrum of eye malformations in four patients with Mowat-Wilson syndromeA Bourchany, I Giurgea, J Thevenon, et al.
Neurogenetics|March 8, 2018
MED13L-related intellectual disability: involvement of missense variants and delineation of the phenotypeT Smol, F Petit, A Piton, et al.
Pageof 2