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Experimental Neurology
|
October 14, 2003
Synemin expression in developing normal and pathological human retina and lens
Marcel Tawk, Matthias Titeux, Catherine Fallet, et al.
Pediatric Radiology
|
November 27, 2004
MRI of the fetal posterior fossa
Catherine Adamsbaum, Marie Laure Moutard, Christine André, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society
|
April 6, 2022
Prenatal Diagnosis of <i>COL4A1</i> Mutations in Eight Cases: Further Delineation of the Neurohistopathological Phenotype
Francesca Gubana, Christo Christov, Thibault Coste, et al.
Acta Neuropathologica
|
June 27, 2007
Acrocallosal syndrome in fetus: focus on additional brain abnormalities
Carla Fernandez, Marie Soulier, Béma Coulibaly, et al.
European Journal of Medical Genetics
|
February 20, 2008
Inherited 18q23 duplication in a fetus with multiple congenital anomalies
Bertrand Isidor, Norbert Winer, Madeleine Joubert, et al.
BMC Neurology
|
September 3, 2020
A case report of severe tuberous sclerosis complex detected in utero and linked to a novel duplication in the TSC2 gene
Valérie Mongrain, Nicolaas H van Doesburg, Françoise Rypens, et al.
Brain : a Journal of Neurology
|
August 2, 2008
Neuropathological phenotype of a distinct form of lissencephaly associated with mutations in TUBA1A
Catherine Fallet-Bianco, Laurence Loeuillet, Karine Poirier, et al.
The European Journal of Neuroscience
|
March 8, 2006
Human disorders of cortical development: from past to present
Fiona Francis, Gundela Meyer, Catherine Fallet-Bianco, et al.
Archives of Virology
|
January 19, 2024
Zika virus infection during pregnancy and vertical transmission: case reports and peptide-specific cell-mediated immune responses
Stéphanie Hindle, Agnès Depatureaux, Samuel Fortin-Dion, et al.
Neuropediatrics
|
August 15, 2016
Epileptic Phenotype of Two Siblings with Asparagine Synthesis Deficiency Mimics Neonatal Pyridoxine-Dependent Epilepsy
Svetlana Gataullina, Julia Lauer-Zillhardt, Anna Kaminska, et al.
Page
of 7
Search research articles
Search
Showing results (21-30 of 64) with videos related to
Sort By:
Page
of 7
Experimental Neurology
|
October 14, 2003
Synemin expression in developing normal and pathological human retina and lens
Marcel Tawk, Matthias Titeux, Catherine Fallet, et al.
Pediatric Radiology
|
November 27, 2004
MRI of the fetal posterior fossa
Catherine Adamsbaum, Marie Laure Moutard, Christine André, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society
|
April 6, 2022
Prenatal Diagnosis of <i>COL4A1</i> Mutations in Eight Cases: Further Delineation of the Neurohistopathological Phenotype
Francesca Gubana, Christo Christov, Thibault Coste, et al.
Acta Neuropathologica
|
June 27, 2007
Acrocallosal syndrome in fetus: focus on additional brain abnormalities
Carla Fernandez, Marie Soulier, Béma Coulibaly, et al.
European Journal of Medical Genetics
|
February 20, 2008
Inherited 18q23 duplication in a fetus with multiple congenital anomalies
Bertrand Isidor, Norbert Winer, Madeleine Joubert, et al.
BMC Neurology
|
September 3, 2020
A case report of severe tuberous sclerosis complex detected in utero and linked to a novel duplication in the TSC2 gene
Valérie Mongrain, Nicolaas H van Doesburg, Françoise Rypens, et al.
Brain : a Journal of Neurology
|
August 2, 2008
Neuropathological phenotype of a distinct form of lissencephaly associated with mutations in TUBA1A
Catherine Fallet-Bianco, Laurence Loeuillet, Karine Poirier, et al.
The European Journal of Neuroscience
|
March 8, 2006
Human disorders of cortical development: from past to present
Fiona Francis, Gundela Meyer, Catherine Fallet-Bianco, et al.
Archives of Virology
|
January 19, 2024
Zika virus infection during pregnancy and vertical transmission: case reports and peptide-specific cell-mediated immune responses
Stéphanie Hindle, Agnès Depatureaux, Samuel Fortin-Dion, et al.
Neuropediatrics
|
August 15, 2016
Epileptic Phenotype of Two Siblings with Asparagine Synthesis Deficiency Mimics Neonatal Pyridoxine-Dependent Epilepsy
Svetlana Gataullina, Julia Lauer-Zillhardt, Anna Kaminska, et al.
Page
of 7