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Neurology. Genetics

Showing results (311-320 of 1,012) with videos related to

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Neurology. Genetics|November 20, 2019
Digital necrosis in an infant with severe spinal muscular atrophyDiana Carrasco, Pilar Magoulas, Jennifer C Scull, et al.
Neurology. Genetics|July 8, 2021
Erratum: KCNQ2 Encephalopathy Manifesting With Rett-like Features: A Follow-up Into Adulthood
Neurology. Genetics|December 9, 2020
Herpes simplex virus 2 encephalitis in a patient heterozygous for a TLR3 mutationTimo Hautala, Jie Chen, Laura Tervonen, et al.
Neurology. Genetics|October 5, 2018
Protein network analysis reveals selectively vulnerable regions and biological processes in FTDLuke W Bonham, Natasha Z R Steele, Celeste M Karch, et al.
Neurology. Genetics|October 5, 2018
Homozygosity for <i>SCN4A</i> Arg1142Gln causes congenital myopathy with variable disease expressionChristine K Sloth, Federico Denti, Nicole Schmitt, et al.
Neurology. Genetics|August 16, 2018
De novo <i>DNM1L</i> mutation associated with mitochondrial epilepsy syndrome with fever sensitivityEmma Ladds, Andrea Whitney, Eszter Dombi, et al.
Neurology. Genetics|May 31, 2018
Brain copper storage after genetic long-term correction in a mouse model of Wilson diseaseRicarda Uerlings, Daniel Moreno, Oihana Murillo, et al.
Neurology. Genetics|May 25, 2019
Lithium chloride corrects weakness and myopathology in a preclinical model of LGMD1DAndrew R Findlay, Rocio Bengoechea, Sara K Pittman, et al.
Neurology. Genetics|May 2, 2019
Clinical, genetic, and pathologic characterization of <i>FKRP</i> Mexican founder mutation c.1387A>GAngela J Lee, Karra A Jones, Russell J Butterfield, et al.
Neurology. Genetics|May 2, 2019
Somatic expansion of the <i>C9orf72</i> hexanucleotide repeat does not occur in ALS spinal cord tissuesJay P Ross, Claire S Leblond, Hélène Catoire, et al.
Pageof 102

Showing results (311-320 of 1,012) with videos related to

Sort By:
Pageof 102
Neurology. Genetics|November 20, 2019
Digital necrosis in an infant with severe spinal muscular atrophyDiana Carrasco, Pilar Magoulas, Jennifer C Scull, et al.
Neurology. Genetics|July 8, 2021
Erratum: KCNQ2 Encephalopathy Manifesting With Rett-like Features: A Follow-up Into Adulthood
Neurology. Genetics|December 9, 2020
Herpes simplex virus 2 encephalitis in a patient heterozygous for a TLR3 mutationTimo Hautala, Jie Chen, Laura Tervonen, et al.
Neurology. Genetics|October 5, 2018
Protein network analysis reveals selectively vulnerable regions and biological processes in FTDLuke W Bonham, Natasha Z R Steele, Celeste M Karch, et al.
Neurology. Genetics|October 5, 2018
Homozygosity for <i>SCN4A</i> Arg1142Gln causes congenital myopathy with variable disease expressionChristine K Sloth, Federico Denti, Nicole Schmitt, et al.
Neurology. Genetics|August 16, 2018
De novo <i>DNM1L</i> mutation associated with mitochondrial epilepsy syndrome with fever sensitivityEmma Ladds, Andrea Whitney, Eszter Dombi, et al.
Neurology. Genetics|May 31, 2018
Brain copper storage after genetic long-term correction in a mouse model of Wilson diseaseRicarda Uerlings, Daniel Moreno, Oihana Murillo, et al.
Neurology. Genetics|May 25, 2019
Lithium chloride corrects weakness and myopathology in a preclinical model of LGMD1DAndrew R Findlay, Rocio Bengoechea, Sara K Pittman, et al.
Neurology. Genetics|May 2, 2019
Clinical, genetic, and pathologic characterization of <i>FKRP</i> Mexican founder mutation c.1387A>GAngela J Lee, Karra A Jones, Russell J Butterfield, et al.
Neurology. Genetics|May 2, 2019
Somatic expansion of the <i>C9orf72</i> hexanucleotide repeat does not occur in ALS spinal cord tissuesJay P Ross, Claire S Leblond, Hélène Catoire, et al.
Pageof 102