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Mitochondrion
|
July 30, 2013
Practice patterns of mitochondrial disease physicians in North America. Part 1: diagnostic and clinical challenges
Sumit Parikh, Amy Goldstein, Mary Kay Koenig, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 1, 2010
Definition and classification of hyperkinetic movements in childhood
Terence D Sanger, Daofen Chen, Darcy L Fehlings, et al.
Plos One
|
September 1, 2015
Correction: Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry
Louis Viollet, Gustavo Glusman, Kelley J Murphy, et al.
Plos One
|
May 22, 2015
Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry
Louis Viollet, Gustavo Glusman, Kelley J Murphy, et al.
Nature Communications
|
May 8, 2021
Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder
Sukhleen Kour, Deepa S Rajan, Tyler R Fortuna, et al.
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of 4
Search research articles
Search
Showing results (31-40 of 35) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 35 results.
Mitochondrion
|
July 30, 2013
Practice patterns of mitochondrial disease physicians in North America. Part 1: diagnostic and clinical challenges
Sumit Parikh, Amy Goldstein, Mary Kay Koenig, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 1, 2010
Definition and classification of hyperkinetic movements in childhood
Terence D Sanger, Daofen Chen, Darcy L Fehlings, et al.
Plos One
|
September 1, 2015
Correction: Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry
Louis Viollet, Gustavo Glusman, Kelley J Murphy, et al.
Plos One
|
May 22, 2015
Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry
Louis Viollet, Gustavo Glusman, Kelley J Murphy, et al.
Nature Communications
|
May 8, 2021
Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder
Sukhleen Kour, Deepa S Rajan, Tyler R Fortuna, et al.
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of 4