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Neurology. Genetics

Showing results (341-350 of 1,012) with videos related to

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Neurology. Genetics|August 18, 2020
Hydrocephalus and diffuse choroid plexus hyperplasia in primary ciliary dyskinesia-related MCIDAS mutationEvie Alexandra Robson, Luke Dixon, Liam Causon, et al.
Neurology. Genetics|August 18, 2020
D-DEMØ, a distinct phenotype caused by <i>ATP1A3</i> mutationsLyndsey Prange, Milton Pratt, Kristin Herman, et al.
Neurology. Genetics|July 9, 2020
Brainstem ischemic syndrome in juvenile NF2John W Henson, Tara Benkers, Connor McCormick
Neurology. Genetics|July 9, 2020
Synonymous variants associated with Alzheimer disease in multiplex familiesMin Tang, Maria Eugenia Alaniz, Daniel Felsky, et al.
Neurology. Genetics|July 9, 2020
Novel truncating mutations of <i>MYO18B</i> causing congenital myopathy in a Swiss patientVioleta Mihaylova, Fabian Chablais, Yvan Herenger, et al.
Neurology. Genetics|August 6, 2020
<i>APOE ϵ</i>4 modifies the relationship between infectious burden and poor cognitionChen Zhao, Kevin Strobino, Yeseon Park Moon, et al.
Neurology. Genetics|August 6, 2020
Disease-modifying effects of an <i>SCAF4</i> structural variant in a predominantly <i>SOD1</i> ALS cohortJulia Pytte, Loren L Flynn, Ryan S Anderton, et al.
Neurology. Genetics|April 23, 2021
<i>Neurology: Genetics</i> Year in ReviewStefan Pulst, Massimo Pandolfo, Raymond Roos, et al.
Neurology. Genetics|April 26, 2021
Clonal Evolution of a High-Grade Pediatric Glioma With Distant Metastatic SpreadEliana Marinari, Valerie Dutoit, Sergey Nikolaev, et al.
Neurology. Genetics|April 26, 2021
<i>PRPS1</i> Gene Mutation Causes Complex X-Linked Adult-Onset Cerebellar Ataxia in WomenFlávio M Rezende Filho, Mariana M Palma, José Luiz Pedroso, et al.
Pageof 102

Showing results (341-350 of 1,012) with videos related to

Sort By:
Pageof 102
Neurology. Genetics|August 18, 2020
Hydrocephalus and diffuse choroid plexus hyperplasia in primary ciliary dyskinesia-related MCIDAS mutationEvie Alexandra Robson, Luke Dixon, Liam Causon, et al.
Neurology. Genetics|August 18, 2020
D-DEMØ, a distinct phenotype caused by <i>ATP1A3</i> mutationsLyndsey Prange, Milton Pratt, Kristin Herman, et al.
Neurology. Genetics|July 9, 2020
Brainstem ischemic syndrome in juvenile NF2John W Henson, Tara Benkers, Connor McCormick
Neurology. Genetics|July 9, 2020
Synonymous variants associated with Alzheimer disease in multiplex familiesMin Tang, Maria Eugenia Alaniz, Daniel Felsky, et al.
Neurology. Genetics|July 9, 2020
Novel truncating mutations of <i>MYO18B</i> causing congenital myopathy in a Swiss patientVioleta Mihaylova, Fabian Chablais, Yvan Herenger, et al.
Neurology. Genetics|August 6, 2020
<i>APOE ϵ</i>4 modifies the relationship between infectious burden and poor cognitionChen Zhao, Kevin Strobino, Yeseon Park Moon, et al.
Neurology. Genetics|August 6, 2020
Disease-modifying effects of an <i>SCAF4</i> structural variant in a predominantly <i>SOD1</i> ALS cohortJulia Pytte, Loren L Flynn, Ryan S Anderton, et al.
Neurology. Genetics|April 23, 2021
<i>Neurology: Genetics</i> Year in ReviewStefan Pulst, Massimo Pandolfo, Raymond Roos, et al.
Neurology. Genetics|April 26, 2021
Clonal Evolution of a High-Grade Pediatric Glioma With Distant Metastatic SpreadEliana Marinari, Valerie Dutoit, Sergey Nikolaev, et al.
Neurology. Genetics|April 26, 2021
<i>PRPS1</i> Gene Mutation Causes Complex X-Linked Adult-Onset Cerebellar Ataxia in WomenFlávio M Rezende Filho, Mariana M Palma, José Luiz Pedroso, et al.
Pageof 102