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Developmental Medicine and Child Neurology
|
June 28, 2003
Brainstem dysgenesis: report of five patients with congenital hypotonia, multiple cranial nerve involvement, and ocular motor apraxia
Manuel Roig, Margarida Gratacòs, Elida Vazquez, et al.
Plos One
|
February 26, 2013
Chiari malformation type I: a case-control association study of 58 developmental genes
Aintzane Urbizu, Claudio Toma, Maria A Poca, et al.
Journal of Neurosurgery
|
May 7, 2016
Cephalometric oropharynx and oral cavity analysis in Chiari malformation Type I: a retrospective case-control study
Aintzane Urbizu, Alex Ferré, Maria-Antonia Poca, et al.
Seizure
|
September 14, 2021
Early-onset eyelid stereotypies are a frequent and distinctive feature in Dravet syndrome
Júlia Sala-Coromina, Miquel Raspall-Chaure, Anna Marcé-Grau, et al.
Revista De Neurologia
|
November 23, 2012
[Reversible encephalopathy caused by valproic acid in an adolescent with idiopathic generalised epilepsy]
Miquel Raspall-Chaure, Elena Lainez, Manuel Toledo, et al.
Plos One
|
August 4, 2012
Cortical thickness and behavior abnormalities in children born preterm
Leire Zubiaurre-Elorza, Sara Soria-Pastor, Carme Junque, et al.
Pflugers Archiv : European Journal of Physiology
|
February 4, 2009
The hemiplegic migraine-associated Y1245C mutation in CACNA1A results in a gain of channel function due to its effect on the voltage sensor and G-protein-mediated inhibition
Selma A Serra, Noèlia Fernàndez-Castillo, Alfons Macaya, et al.
Neuropediatrics
|
March 21, 2018
Diagnosis and Treatment of Tuberous Sclerosis Manifestations in Children: A Multicenter Study
Marina Flotats-Bastardas, Daniel Ebrahimi-Fakhari, Ludwig Gortner, et al.
Neurogenetics
|
January 21, 2009
Familial hemiplegic migraine: linkage to chromosome 14q32 in a Spanish kindred
Ester Cuenca-León, Roser Corominas, Magda Montfort, et al.
Headache
|
November 16, 2011
Acute striatal necrosis in hemiplegic migraine with de novo CACNA1A mutation
Oriel Carreño, María Teresa García-Silva, Óscar García-Campos, et al.
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of 14
Search research articles
Search
Showing results (21-30 of 137) with videos related to
Sort By:
Page
of 14
Developmental Medicine and Child Neurology
|
June 28, 2003
Brainstem dysgenesis: report of five patients with congenital hypotonia, multiple cranial nerve involvement, and ocular motor apraxia
Manuel Roig, Margarida Gratacòs, Elida Vazquez, et al.
Plos One
|
February 26, 2013
Chiari malformation type I: a case-control association study of 58 developmental genes
Aintzane Urbizu, Claudio Toma, Maria A Poca, et al.
Journal of Neurosurgery
|
May 7, 2016
Cephalometric oropharynx and oral cavity analysis in Chiari malformation Type I: a retrospective case-control study
Aintzane Urbizu, Alex Ferré, Maria-Antonia Poca, et al.
Seizure
|
September 14, 2021
Early-onset eyelid stereotypies are a frequent and distinctive feature in Dravet syndrome
Júlia Sala-Coromina, Miquel Raspall-Chaure, Anna Marcé-Grau, et al.
Revista De Neurologia
|
November 23, 2012
[Reversible encephalopathy caused by valproic acid in an adolescent with idiopathic generalised epilepsy]
Miquel Raspall-Chaure, Elena Lainez, Manuel Toledo, et al.
Plos One
|
August 4, 2012
Cortical thickness and behavior abnormalities in children born preterm
Leire Zubiaurre-Elorza, Sara Soria-Pastor, Carme Junque, et al.
Pflugers Archiv : European Journal of Physiology
|
February 4, 2009
The hemiplegic migraine-associated Y1245C mutation in CACNA1A results in a gain of channel function due to its effect on the voltage sensor and G-protein-mediated inhibition
Selma A Serra, Noèlia Fernàndez-Castillo, Alfons Macaya, et al.
Neuropediatrics
|
March 21, 2018
Diagnosis and Treatment of Tuberous Sclerosis Manifestations in Children: A Multicenter Study
Marina Flotats-Bastardas, Daniel Ebrahimi-Fakhari, Ludwig Gortner, et al.
Neurogenetics
|
January 21, 2009
Familial hemiplegic migraine: linkage to chromosome 14q32 in a Spanish kindred
Ester Cuenca-León, Roser Corominas, Magda Montfort, et al.
Headache
|
November 16, 2011
Acute striatal necrosis in hemiplegic migraine with de novo CACNA1A mutation
Oriel Carreño, María Teresa García-Silva, Óscar García-Campos, et al.
Page
of 14