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Fabien Guimiot

Showing results (41-50 of 92) with videos related to

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Endocrinology|November 6, 2013
Somatostatin receptors type 2 and 5 expression and localization during human pituitary developmentStéphane Peineau, Fabien Guimiot, Zsolt Csaba, et al.
Prenatal Diagnosis|October 28, 2014
Biochemical analysis of ascites fluid as an aid to etiological diagnosis: a series of 100 cases of nonimmune fetal ascitesSophie Dreux, Laurent J Salomon, Jonathan Rosenblatt, et al.
Pediatric Research|August 15, 2013
Specific biochemical amniotic fluid pattern of fetal isolated esophageal atresiaCécile Muller, Isabelle Czerkiewicz, Fabien Guimiot, et al.
Prenatal Diagnosis|April 18, 2013
Fetal serum α-1 microglobulin for renal function assessment: comparison with β2-microglobulin and cystatin CClaire Nguyen, Sophie Dreux, Laurence Heidet, et al.
Gene Expression Patterns : GEP|May 24, 2005
Molecular cloning and expression pattern of the Fkbp25 gene during cerebral cortical neurogenesisChristophe Mas, Ismahane Guimiot-Maloum, Fabien Guimiot, et al.
Acta Neuropathologica Communications|December 18, 2025
Biallelic null RAB3GAP1 variants impair cortical development and autophagy in Warburg Micro syndrome: evidence from fetal brain tissue and patient fibroblastsEmma Noël, Fabien Guimiot, Yline Capri, et al.
Fetal and Pediatric Pathology|January 15, 2019
TRAP Sequence in Monochorionic/Monoamniotic (MC/MA) Discordant Twins: Two Cases Treated with Fetoscopic Laser SurgeryGabriele Tonni, Gianpaolo Grisolia, Paolo Zampriolo, et al.
American Journal of Medical Genetics. Part A|August 7, 2013
COL2A1 gene disruption by a balanced translocation t(12;15)(q13;q22.2) in familial Stickler syndromeCéline Dupont, Clarisse Baumann, Nathalie Le Du, et al.
Brain : a Journal of Neurology|October 7, 2023
Homozygous MFN2 variants causing severe antenatal encephalopathy with clumped mitochondriaArnaud Chevrollier, Adeline Alice Bonnard, Lyse Ruaud, et al.
Elife|January 17, 2017
Phenotypic outcomes in Mouse and Human <i>Foxc1</i> dependent Dandy-Walker cerebellar malformation suggest shared mechanismsParthiv Haldipur, Derek Dang, Kimberly A Aldinger, et al.
Pageof 10

Showing results (41-50 of 92) with videos related to

Sort By:
Pageof 10
Endocrinology|November 6, 2013
Somatostatin receptors type 2 and 5 expression and localization during human pituitary developmentStéphane Peineau, Fabien Guimiot, Zsolt Csaba, et al.
Prenatal Diagnosis|October 28, 2014
Biochemical analysis of ascites fluid as an aid to etiological diagnosis: a series of 100 cases of nonimmune fetal ascitesSophie Dreux, Laurent J Salomon, Jonathan Rosenblatt, et al.
Pediatric Research|August 15, 2013
Specific biochemical amniotic fluid pattern of fetal isolated esophageal atresiaCécile Muller, Isabelle Czerkiewicz, Fabien Guimiot, et al.
Prenatal Diagnosis|April 18, 2013
Fetal serum α-1 microglobulin for renal function assessment: comparison with β2-microglobulin and cystatin CClaire Nguyen, Sophie Dreux, Laurence Heidet, et al.
Gene Expression Patterns : GEP|May 24, 2005
Molecular cloning and expression pattern of the Fkbp25 gene during cerebral cortical neurogenesisChristophe Mas, Ismahane Guimiot-Maloum, Fabien Guimiot, et al.
Acta Neuropathologica Communications|December 18, 2025
Biallelic null RAB3GAP1 variants impair cortical development and autophagy in Warburg Micro syndrome: evidence from fetal brain tissue and patient fibroblastsEmma Noël, Fabien Guimiot, Yline Capri, et al.
Fetal and Pediatric Pathology|January 15, 2019
TRAP Sequence in Monochorionic/Monoamniotic (MC/MA) Discordant Twins: Two Cases Treated with Fetoscopic Laser SurgeryGabriele Tonni, Gianpaolo Grisolia, Paolo Zampriolo, et al.
American Journal of Medical Genetics. Part A|August 7, 2013
COL2A1 gene disruption by a balanced translocation t(12;15)(q13;q22.2) in familial Stickler syndromeCéline Dupont, Clarisse Baumann, Nathalie Le Du, et al.
Brain : a Journal of Neurology|October 7, 2023
Homozygous MFN2 variants causing severe antenatal encephalopathy with clumped mitochondriaArnaud Chevrollier, Adeline Alice Bonnard, Lyse Ruaud, et al.
Elife|January 17, 2017
Phenotypic outcomes in Mouse and Human <i>Foxc1</i> dependent Dandy-Walker cerebellar malformation suggest shared mechanismsParthiv Haldipur, Derek Dang, Kimberly A Aldinger, et al.
Pageof 10