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Health Expectations : an International Journal of Public Participation in Health Care and Health Policy
|
November 7, 2023
Parents' experiences of parenting a child with profound intellectual and multiple disabilities in France: A qualitative study
Marie-Anastasie Aim, Marie-Christine Rousseau, Ilyes Hamouda, et al.
American Journal of Medical Genetics. Part A
|
June 9, 2012
Recurrent mutations in the CDKL5 gene: genotype-phenotype relationships
Nadia Bahi-Buisson, Nathalie Villeneuve, Emilie Caietta, et al.
American Journal of Medical Genetics. Part A
|
May 13, 2014
Intragenic rearrangements in X-linked intellectual deficiency: results of a-CGH in a series of 54 patients and identification of TRPC5 and KLHL15 as potential XLID genes
Cécile Mignon-Ravix, Pierre Cacciagli, Nancy Choucair, et al.
American Journal of Medical Genetics. Part A
|
May 12, 2015
Variable clinical expression in patients with mosaicism for KCNQ2 mutations
Mathieu Milh, Caroline Lacoste, Pierre Cacciagli, et al.
Cerebral Cortex (New York, N.Y. : 1991)
|
October 9, 2018
Diadenosine-Polyphosphate Analogue AppCH2ppA Suppresses Seizures by Enhancing Adenosine Signaling in the Cortex
Alexandre Pons-Bennaceur, Vera Tsintsadze, Thi-Thien Bui, et al.
Epilepsia
|
May 5, 2018
Everolimus dosing recommendations for tuberous sclerosis complex-associated refractory seizures
David N Franz, John A Lawson, Zuhal Yapici, et al.
Epilepsia
|
July 21, 2011
Epileptic and nonepileptic features in patients with early onset epileptic encephalopathy and STXBP1 mutations
Mathieu Milh, Nathalie Villeneuve, Mondher Chouchane, et al.
Brain : a Journal of Neurology
|
August 15, 2018
Interictal stereotactic-EEG functional connectivity in refractory focal epilepsies
Stanislas Lagarde, Nicolas Roehri, Isabelle Lambert, et al.
Epilepsia
|
January 28, 2025
Stereoelectroencephalographic exploration and surgical outcome in Lennox-Gastaut syndrome
Soomi Cho, Julia Makhalova, Samuel Medina Villalon, et al.
Epilepsia
|
June 18, 2025
GABRA2-related encephalopathy: Identification of two phenotypes with distinctive electroclinical features
Marie Adamo-Croux, Chloé Angelini, Jérôme Aupy, et al.
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Search research articles
Search
Showing results (61-70 of 138) with videos related to
Sort By:
Page
of 14
Health Expectations : an International Journal of Public Participation in Health Care and Health Policy
|
November 7, 2023
Parents' experiences of parenting a child with profound intellectual and multiple disabilities in France: A qualitative study
Marie-Anastasie Aim, Marie-Christine Rousseau, Ilyes Hamouda, et al.
American Journal of Medical Genetics. Part A
|
June 9, 2012
Recurrent mutations in the CDKL5 gene: genotype-phenotype relationships
Nadia Bahi-Buisson, Nathalie Villeneuve, Emilie Caietta, et al.
American Journal of Medical Genetics. Part A
|
May 13, 2014
Intragenic rearrangements in X-linked intellectual deficiency: results of a-CGH in a series of 54 patients and identification of TRPC5 and KLHL15 as potential XLID genes
Cécile Mignon-Ravix, Pierre Cacciagli, Nancy Choucair, et al.
American Journal of Medical Genetics. Part A
|
May 12, 2015
Variable clinical expression in patients with mosaicism for KCNQ2 mutations
Mathieu Milh, Caroline Lacoste, Pierre Cacciagli, et al.
Cerebral Cortex (New York, N.Y. : 1991)
|
October 9, 2018
Diadenosine-Polyphosphate Analogue AppCH2ppA Suppresses Seizures by Enhancing Adenosine Signaling in the Cortex
Alexandre Pons-Bennaceur, Vera Tsintsadze, Thi-Thien Bui, et al.
Epilepsia
|
May 5, 2018
Everolimus dosing recommendations for tuberous sclerosis complex-associated refractory seizures
David N Franz, John A Lawson, Zuhal Yapici, et al.
Epilepsia
|
July 21, 2011
Epileptic and nonepileptic features in patients with early onset epileptic encephalopathy and STXBP1 mutations
Mathieu Milh, Nathalie Villeneuve, Mondher Chouchane, et al.
Brain : a Journal of Neurology
|
August 15, 2018
Interictal stereotactic-EEG functional connectivity in refractory focal epilepsies
Stanislas Lagarde, Nicolas Roehri, Isabelle Lambert, et al.
Epilepsia
|
January 28, 2025
Stereoelectroencephalographic exploration and surgical outcome in Lennox-Gastaut syndrome
Soomi Cho, Julia Makhalova, Samuel Medina Villalon, et al.
Epilepsia
|
June 18, 2025
GABRA2-related encephalopathy: Identification of two phenotypes with distinctive electroclinical features
Marie Adamo-Croux, Chloé Angelini, Jérôme Aupy, et al.
Page
of 14