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Neurology. Genetics

Showing results (61-70 of 1,011) with videos related to

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Neurology. Genetics|February 24, 2018
AP4 deficiency: A novel form of neurodegeneration with brain iron accumulation?Agathe Roubertie, Nelson Hieu, Charles-Joris Roux, et al.
Neurology. Genetics|March 20, 2018
2017 Year in Review and Message from the Editors to Our ReviewersStefan M Pulst, Nicholas Elwood Johnson, Massimo Pandolfo, et al.
Neurology. Genetics|January 26, 2023
Expanding the Allelic Heterogeneity of <i>ANO10</i>-Associated Autosomal Recessive Cerebellar AtaxiaSean Massey, Yiran Guo, Lisa G Riley, et al.
Neurology. Genetics|October 22, 2016
Epidermolysis bullosa simplex with muscular dystrophy associated with <i>PLEC</i> deletion mutationValeria Carolina Alvarez, Sini Tellervo Penttilä, Valeria Luján Salutto, et al.
Neurology. Genetics|October 21, 2016
Reassessing carrier status for dystrophinopathiesTara M Newcomb, Kevin M Flanigan
Neurology. Genetics|December 14, 2016
A novel <i>WDR45</i> mutation in a patient with β-propeller protein-associated neurodegenerationDonRaphael P Wynn, Stefan M Pulst
Neurology. Genetics|November 24, 2016
Mitochondrial cytopathy with common MELAS mutation presenting as multiple system atrophy mimicAnne-Katrin Pröbstel, André Schaller, Johanna Lieb, et al.
Neurology. Genetics|January 19, 2017
Everolimus does not prevent Lafora body formation in murine Lafora diseaseNavin Mishra, Peixiang Wang, Danielle Goldsmith, et al.
Neurology. Genetics|January 19, 2017
Centrally involved X-linked Charcot-Marie-Tooth disease presenting as a stroke-mimicPatrick D Nicholson, Stefan M Pulst
Neurology. Genetics|January 21, 2017
<i>MAPT</i> association with REM sleep behavior disorderRubén Fernández-Santiago, Alex Iranzo, Carles Gaig, et al.
Pageof 102

Showing results (61-70 of 1,011) with videos related to

Sort By:
Pageof 102
Neurology. Genetics|February 24, 2018
AP4 deficiency: A novel form of neurodegeneration with brain iron accumulation?Agathe Roubertie, Nelson Hieu, Charles-Joris Roux, et al.
Neurology. Genetics|March 20, 2018
2017 Year in Review and Message from the Editors to Our ReviewersStefan M Pulst, Nicholas Elwood Johnson, Massimo Pandolfo, et al.
Neurology. Genetics|January 26, 2023
Expanding the Allelic Heterogeneity of <i>ANO10</i>-Associated Autosomal Recessive Cerebellar AtaxiaSean Massey, Yiran Guo, Lisa G Riley, et al.
Neurology. Genetics|October 22, 2016
Epidermolysis bullosa simplex with muscular dystrophy associated with <i>PLEC</i> deletion mutationValeria Carolina Alvarez, Sini Tellervo Penttilä, Valeria Luján Salutto, et al.
Neurology. Genetics|October 21, 2016
Reassessing carrier status for dystrophinopathiesTara M Newcomb, Kevin M Flanigan
Neurology. Genetics|December 14, 2016
A novel <i>WDR45</i> mutation in a patient with β-propeller protein-associated neurodegenerationDonRaphael P Wynn, Stefan M Pulst
Neurology. Genetics|November 24, 2016
Mitochondrial cytopathy with common MELAS mutation presenting as multiple system atrophy mimicAnne-Katrin Pröbstel, André Schaller, Johanna Lieb, et al.
Neurology. Genetics|January 19, 2017
Everolimus does not prevent Lafora body formation in murine Lafora diseaseNavin Mishra, Peixiang Wang, Danielle Goldsmith, et al.
Neurology. Genetics|January 19, 2017
Centrally involved X-linked Charcot-Marie-Tooth disease presenting as a stroke-mimicPatrick D Nicholson, Stefan M Pulst
Neurology. Genetics|January 21, 2017
<i>MAPT</i> association with REM sleep behavior disorderRubén Fernández-Santiago, Alex Iranzo, Carles Gaig, et al.
Pageof 102