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Peter Bauer

Showing results (331-340 of 585) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|July 30, 2010
Spinocerebellar ataxia type 11 (SCA11) is an uncommon cause of dominant ataxia among French and German kindredsPeter Bauer, Giovanni Stevanin, Christian Beetz, et al.
Journal of Neurology|July 3, 2021
COVID-19 and Parkinson's disease: a casual association or a possible second hit in neurodegeneration?Francesco Cavallieri, Valentina Fioravanti, Giulia Toschi, et al.
Frontiers in Medicine|April 14, 2022
Identification of 27 Novel Variants in Genes <i>COL4A3, COL4A4</i>, and <i>COL4A5</i> in Lithuanian Families With Alport SyndromeAgne Cerkauskaite, Judy Savige, Karolina Janonyte, et al.
Dementia and Geriatric Cognitive Disorders|May 1, 2008
Risk factors for Alzheimer dementia in a community-based birth cohort at the age of 75 yearsPeter Fischer, Sonja Zehetmayer, Susanne Jungwirth, et al.
European Journal of Human Genetics : EJHG|February 18, 2011
De novo MECP2 duplication in two females with random X-inactivation and moderate mental retardationUte Grasshoff, Michael Bonin, Ina Goehring, et al.
Environmental Pollution (Barking, Essex : 1987)|March 29, 2023
Gene-environment interaction in the association of residential greenness and 25(OH) vitamin DElisabeth Thiering, Iana Markevych, Sara Kress, et al.
Journal of the American Society of Nephrology : JASN|October 6, 2020
Biallelic Pathogenic <i>GFRA1</i> Variants Cause Autosomal Recessive Bilateral Renal AgenesisVeronica Arora, Suliman Khan, Ayman W El-Hattab, et al.
Human Molecular Genetics|September 7, 2010
Dissecting the role of the mitochondrial chaperone mortalin in Parkinson's disease: functional impact of disease-related variants on mitochondrial homeostasisLena F Burbulla, Carina Schelling, Hiroki Kato, et al.
Neurology. Genetics|April 5, 2017
<i>CNTNAP1</i> mutations cause CNS hypomyelination and neuropathy with or without arthrogryposisHolger Hengel, Alex Magee, Muhammad Mahanjah, et al.
Cerebral Cortex (New York, N.Y. : 1991)|December 30, 2009
The effects of COMT (Val108/158Met) and DRD4 (SNP -521) dopamine genotypes on brain activations related to valence and magnitude of rewardsEstela Camara, Ulrike M Krämer, Toni Cunillera, et al.
Pageof 59

Showing results (331-340 of 585) with videos related to

Sort By:
Pageof 59
Journal of Neurology, Neurosurgery, and Psychiatry|July 30, 2010
Spinocerebellar ataxia type 11 (SCA11) is an uncommon cause of dominant ataxia among French and German kindredsPeter Bauer, Giovanni Stevanin, Christian Beetz, et al.
Journal of Neurology|July 3, 2021
COVID-19 and Parkinson's disease: a casual association or a possible second hit in neurodegeneration?Francesco Cavallieri, Valentina Fioravanti, Giulia Toschi, et al.
Frontiers in Medicine|April 14, 2022
Identification of 27 Novel Variants in Genes <i>COL4A3, COL4A4</i>, and <i>COL4A5</i> in Lithuanian Families With Alport SyndromeAgne Cerkauskaite, Judy Savige, Karolina Janonyte, et al.
Dementia and Geriatric Cognitive Disorders|May 1, 2008
Risk factors for Alzheimer dementia in a community-based birth cohort at the age of 75 yearsPeter Fischer, Sonja Zehetmayer, Susanne Jungwirth, et al.
European Journal of Human Genetics : EJHG|February 18, 2011
De novo MECP2 duplication in two females with random X-inactivation and moderate mental retardationUte Grasshoff, Michael Bonin, Ina Goehring, et al.
Environmental Pollution (Barking, Essex : 1987)|March 29, 2023
Gene-environment interaction in the association of residential greenness and 25(OH) vitamin DElisabeth Thiering, Iana Markevych, Sara Kress, et al.
Journal of the American Society of Nephrology : JASN|October 6, 2020
Biallelic Pathogenic <i>GFRA1</i> Variants Cause Autosomal Recessive Bilateral Renal AgenesisVeronica Arora, Suliman Khan, Ayman W El-Hattab, et al.
Human Molecular Genetics|September 7, 2010
Dissecting the role of the mitochondrial chaperone mortalin in Parkinson's disease: functional impact of disease-related variants on mitochondrial homeostasisLena F Burbulla, Carina Schelling, Hiroki Kato, et al.
Neurology. Genetics|April 5, 2017
<i>CNTNAP1</i> mutations cause CNS hypomyelination and neuropathy with or without arthrogryposisHolger Hengel, Alex Magee, Muhammad Mahanjah, et al.
Cerebral Cortex (New York, N.Y. : 1991)|December 30, 2009
The effects of COMT (Val108/158Met) and DRD4 (SNP -521) dopamine genotypes on brain activations related to valence and magnitude of rewardsEstela Camara, Ulrike M Krämer, Toni Cunillera, et al.
Pageof 59