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David S Lynch

Showing results (21-30 of 53) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|June 3, 2017
Truncating mutations in <i>SPAST</i> patients are associated with a high rate of psychiatric comorbidities in hereditary spastic paraplegiaViorica Chelban, Arianna Tucci, David S Lynch, et al.
Practical Neurology|May 22, 2020
How to diagnose difficult white matter disordersThomas Williams, Henry Houlden, Elaine Murphy, et al.
Neurology. Genetics|September 29, 2017
Nonsyndromic Parkinson disease in a family with autosomal dominant optic atrophy due to <i>OPA1</i> mutationsDavid S Lynch, Samantha H Y Loh, Jasmine Harley, et al.
Practical Neurology|September 17, 2024
Genetic testing in dementiaAntoinette O'Connor, Natalie S Ryan, Christopher R S Belder, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 21, 2023
Leukoencephalopathy caused by a 17p13.3 microdeletionCharles Wade, Thomas Williams, Robyn Labrum, et al.
Neurology. Genetics|July 14, 2017
Brainstem phenotype of cathepsin A-related arteriopathy with strokes and leukoencephalopathyYun Tae Hwang, Rahul Lakshmanan, Indran Davagnanam, et al.
Neurology. Genetics|July 14, 2017
Homozygous mutation in <i>HSPB1</i> causing distal vacuolar myopathy and motor neuropathyEnrico Bugiardini, Alexander M Rossor, David S Lynch, et al.
Neurology. Genetics|March 1, 2017
Redefining the phenotype of ALSP and <i>AARS2</i> mutation-related leukodystrophyRahul Lakshmanan, Matthew E Adams, David S Lynch, et al.
Plos One|November 19, 2010
Angiogenin levels and ANG genotypes: dysregulation in amyotrophic lateral sclerosisRussell Lewis McLaughlin, Julie Phukan, William McCormack, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 10, 2022
Extreme Clinical Variability Among Carriers of Pathogenic Variant in SSBP1Eduardo Sousa de Melo, Anderson Rodrigues Brandão de Paiva, Antônio Duarte de Amorim, et al.
Pageof 6

Showing results (21-30 of 53) with videos related to

Sort By:
Pageof 6
Journal of Neurology, Neurosurgery, and Psychiatry|June 3, 2017
Truncating mutations in <i>SPAST</i> patients are associated with a high rate of psychiatric comorbidities in hereditary spastic paraplegiaViorica Chelban, Arianna Tucci, David S Lynch, et al.
Practical Neurology|May 22, 2020
How to diagnose difficult white matter disordersThomas Williams, Henry Houlden, Elaine Murphy, et al.
Neurology. Genetics|September 29, 2017
Nonsyndromic Parkinson disease in a family with autosomal dominant optic atrophy due to <i>OPA1</i> mutationsDavid S Lynch, Samantha H Y Loh, Jasmine Harley, et al.
Practical Neurology|September 17, 2024
Genetic testing in dementiaAntoinette O'Connor, Natalie S Ryan, Christopher R S Belder, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 21, 2023
Leukoencephalopathy caused by a 17p13.3 microdeletionCharles Wade, Thomas Williams, Robyn Labrum, et al.
Neurology. Genetics|July 14, 2017
Brainstem phenotype of cathepsin A-related arteriopathy with strokes and leukoencephalopathyYun Tae Hwang, Rahul Lakshmanan, Indran Davagnanam, et al.
Neurology. Genetics|July 14, 2017
Homozygous mutation in <i>HSPB1</i> causing distal vacuolar myopathy and motor neuropathyEnrico Bugiardini, Alexander M Rossor, David S Lynch, et al.
Neurology. Genetics|March 1, 2017
Redefining the phenotype of ALSP and <i>AARS2</i> mutation-related leukodystrophyRahul Lakshmanan, Matthew E Adams, David S Lynch, et al.
Plos One|November 19, 2010
Angiogenin levels and ANG genotypes: dysregulation in amyotrophic lateral sclerosisRussell Lewis McLaughlin, Julie Phukan, William McCormack, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 10, 2022
Extreme Clinical Variability Among Carriers of Pathogenic Variant in SSBP1Eduardo Sousa de Melo, Anderson Rodrigues Brandão de Paiva, Antônio Duarte de Amorim, et al.
Pageof 6