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Human Mutation
|
December 28, 2006
Truncation of NHEJ1 in a patient with polymicrogyria
Vincent Cantagrel, Anne-Marie Lossi, Steven Lisgo, et al.
Brain : a Journal of Neurology
|
April 2, 2009
Pilocytic astrocytoma of the optic pathway: a tumour deriving from radial glia cells with a specific gene signature
Aurélie Tchoghandjian, Carla Fernandez, Carole Colin, et al.
Current Topics in Medicinal Chemistry
|
September 18, 2012
Search for distinctive markers in DNT and cortical grade II glioma in children: same clinicopathological and molecular entities?
Laetitia Padovani, Carole Colin, Carla Fernandez, et al.
Genes
|
June 26, 2025
<i>MPDZ</i> Pathogenic Variants Cause Obstructive Ventriculomegaly Related to Diencephalosynapsis and Third Ventricle Atresia
Sara Cabet, Jean-François Ghersi-Egea, Suonavy Khung-Savatovsky, et al.
European Journal of Heart Failure
|
September 27, 2017
Characteristics, treatments and 1-year prognosis of hospitalized and ambulatory heart failure patients with chronic obstructive pulmonary disease in the European Society of Cardiology Heart Failure Long-Term Registry
Marco Canepa, Ewa Straburzynska-Migaj, Jaroslaw Drozdz, et al.
Journal of Medical Genetics
|
September 1, 2010
BBS10 mutations are common in 'Meckel'-type cystic kidneys
Audrey Putoux, Soumaya Mougou-Zerelli, Sophie Thomas, et al.
Human Molecular Genetics
|
June 20, 2013
Dysregulation of 4q35- and muscle-specific genes in fetuses with a short D4Z4 array linked to facio-scapulo-humeral dystrophy
Natacha Broucqsault, Julia Morere, Marie-Cécile Gaillard, et al.
Human Mutation
|
October 15, 2008
Analysis of the DYSF mutational spectrum in a large cohort of patients
Martin Krahn, Christophe Béroud, Véronique Labelle, et al.
Acta Neuropathologica
|
July 4, 2013
Neuropathological review of 138 cases genetically tested for X-linked hydrocephalus: evidence for closely related clinical entities of unknown molecular bases
Homa Adle-Biassette, Pascale Saugier-Veber, Catherine Fallet-Bianco, et al.
BMJ Open
|
December 11, 2021
Impact of the first wave of the SARS-CoV-2 pandemic on the outcome of neurosurgical patients: a nationwide study in Spain
Igor Paredes, Ana Maria Castaño Leon, Alfonso Lagares, et al.
Page
of 7
Search research articles
Search
Showing results (61-70 of 70) with videos related to
Sort By:
Page
of 7
You have reached the last page of results.
This site can display upto 70 results.
Human Mutation
|
December 28, 2006
Truncation of NHEJ1 in a patient with polymicrogyria
Vincent Cantagrel, Anne-Marie Lossi, Steven Lisgo, et al.
Brain : a Journal of Neurology
|
April 2, 2009
Pilocytic astrocytoma of the optic pathway: a tumour deriving from radial glia cells with a specific gene signature
Aurélie Tchoghandjian, Carla Fernandez, Carole Colin, et al.
Current Topics in Medicinal Chemistry
|
September 18, 2012
Search for distinctive markers in DNT and cortical grade II glioma in children: same clinicopathological and molecular entities?
Laetitia Padovani, Carole Colin, Carla Fernandez, et al.
Genes
|
June 26, 2025
<i>MPDZ</i> Pathogenic Variants Cause Obstructive Ventriculomegaly Related to Diencephalosynapsis and Third Ventricle Atresia
Sara Cabet, Jean-François Ghersi-Egea, Suonavy Khung-Savatovsky, et al.
European Journal of Heart Failure
|
September 27, 2017
Characteristics, treatments and 1-year prognosis of hospitalized and ambulatory heart failure patients with chronic obstructive pulmonary disease in the European Society of Cardiology Heart Failure Long-Term Registry
Marco Canepa, Ewa Straburzynska-Migaj, Jaroslaw Drozdz, et al.
Journal of Medical Genetics
|
September 1, 2010
BBS10 mutations are common in 'Meckel'-type cystic kidneys
Audrey Putoux, Soumaya Mougou-Zerelli, Sophie Thomas, et al.
Human Molecular Genetics
|
June 20, 2013
Dysregulation of 4q35- and muscle-specific genes in fetuses with a short D4Z4 array linked to facio-scapulo-humeral dystrophy
Natacha Broucqsault, Julia Morere, Marie-Cécile Gaillard, et al.
Human Mutation
|
October 15, 2008
Analysis of the DYSF mutational spectrum in a large cohort of patients
Martin Krahn, Christophe Béroud, Véronique Labelle, et al.
Acta Neuropathologica
|
July 4, 2013
Neuropathological review of 138 cases genetically tested for X-linked hydrocephalus: evidence for closely related clinical entities of unknown molecular bases
Homa Adle-Biassette, Pascale Saugier-Veber, Catherine Fallet-Bianco, et al.
BMJ Open
|
December 11, 2021
Impact of the first wave of the SARS-CoV-2 pandemic on the outcome of neurosurgical patients: a nationwide study in Spain
Igor Paredes, Ana Maria Castaño Leon, Alfonso Lagares, et al.
Page
of 7