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Journal of Magnetic Resonance Imaging : JMRI
|
August 23, 2012
Assessment of myelination in hypomyelinating disorders by quantitative MRI
Steffi F Dreha-Kulaczewski, Knut Brockmann, Marco Henneke, et al.
Cephalalgia : an International Journal of Headache
|
October 8, 2013
Clinical spectrum in three families with familial hemiplegic migraine type 2 including a novel mutation in the ATP1A2 gene
Christian Roth, Tobias Freilinger, Georgi Kirovski, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 5, 2005
Levodopa-responsive infantile parkinsonism due to a novel mutation in the tyrosine hydroxylase gene and exacerbation by viral infections
Katharina Diepold, Barbara Schütz, Kevin Rostasy, et al.
Frontiers in Cell and Developmental Biology
|
January 2, 2023
A new model for fatty acid hydroxylase-associated neurodegeneration reveals mitochondrial and autophagy abnormalities
Frida Mandik, Yuliia Kanana, Jost Rody, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 1, 2018
Effect of rescue medication on seizure duration in non-institutionalized children with epilepsy
Federico Vigevano, Fenella J Kirkham, Bernd Wilken, et al.
Klinische Padiatrie
|
January 30, 2018
[Intrathecal Nursinersen Therapy in Children with Spinal Muscular Atrophy and Spinal Deformities]
Heiko M Lorenz, Ingrid Kühnle, Jan Edler, et al.
American Journal of Medical Genetics. Part A
|
April 14, 2007
Partial trisomy of distal 19q detected by quantitative real-time PCR and FISH in a girl with mild facial dysmorphism, hypotonia and developmental delay
S M Sauter, Detlef Böhm, Iris Bartels, et al.
Epilepsy & Behavior : E&B
|
November 17, 2019
Health-related quality of life and the burden of prolonged seizures in noninstitutionalized children with epilepsy
Fenella J Kirkham, Federico Vigevano, Miquel Raspall-Chaure, et al.
Molecular Syndromology
|
April 8, 2020
A Novel Mutation in <i>PIGA</i> Associated with Multiple Congenital Anomalies-Hypotonia-Seizure Syndrome 2 (MCAHS2) in a Boy with a Combination of Severe Epilepsy and Gingival Hyperplasia
Christiane M Neuhofer, Rudolf Funke, Bernd Wilken, et al.
Zeitschrift Fur Orthopadie Und Unfallchirurgie
|
April 10, 2018
[S2-Guideline: Pediatric Flat Foot]
Anna K Hell, Leo Döderlein, Oliver Eberhardt, et al.
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Search research articles
Search
Showing results (11-20 of 40) with videos related to
Sort By:
Page
of 4
Journal of Magnetic Resonance Imaging : JMRI
|
August 23, 2012
Assessment of myelination in hypomyelinating disorders by quantitative MRI
Steffi F Dreha-Kulaczewski, Knut Brockmann, Marco Henneke, et al.
Cephalalgia : an International Journal of Headache
|
October 8, 2013
Clinical spectrum in three families with familial hemiplegic migraine type 2 including a novel mutation in the ATP1A2 gene
Christian Roth, Tobias Freilinger, Georgi Kirovski, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 5, 2005
Levodopa-responsive infantile parkinsonism due to a novel mutation in the tyrosine hydroxylase gene and exacerbation by viral infections
Katharina Diepold, Barbara Schütz, Kevin Rostasy, et al.
Frontiers in Cell and Developmental Biology
|
January 2, 2023
A new model for fatty acid hydroxylase-associated neurodegeneration reveals mitochondrial and autophagy abnormalities
Frida Mandik, Yuliia Kanana, Jost Rody, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 1, 2018
Effect of rescue medication on seizure duration in non-institutionalized children with epilepsy
Federico Vigevano, Fenella J Kirkham, Bernd Wilken, et al.
Klinische Padiatrie
|
January 30, 2018
[Intrathecal Nursinersen Therapy in Children with Spinal Muscular Atrophy and Spinal Deformities]
Heiko M Lorenz, Ingrid Kühnle, Jan Edler, et al.
American Journal of Medical Genetics. Part A
|
April 14, 2007
Partial trisomy of distal 19q detected by quantitative real-time PCR and FISH in a girl with mild facial dysmorphism, hypotonia and developmental delay
S M Sauter, Detlef Böhm, Iris Bartels, et al.
Epilepsy & Behavior : E&B
|
November 17, 2019
Health-related quality of life and the burden of prolonged seizures in noninstitutionalized children with epilepsy
Fenella J Kirkham, Federico Vigevano, Miquel Raspall-Chaure, et al.
Molecular Syndromology
|
April 8, 2020
A Novel Mutation in <i>PIGA</i> Associated with Multiple Congenital Anomalies-Hypotonia-Seizure Syndrome 2 (MCAHS2) in a Boy with a Combination of Severe Epilepsy and Gingival Hyperplasia
Christiane M Neuhofer, Rudolf Funke, Bernd Wilken, et al.
Zeitschrift Fur Orthopadie Und Unfallchirurgie
|
April 10, 2018
[S2-Guideline: Pediatric Flat Foot]
Anna K Hell, Leo Döderlein, Oliver Eberhardt, et al.
Page
of 4