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Andreas Puschmann

Showing results (31-40 of 90) with videos related to

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Molecular Genetics & Genomic Medicine|August 7, 2024
Maculopathy and adult-onset ataxia in patients with biallelic MFSD8 variantsSigurd Dobloug, Ulrika Kjellström, Glenn Anderson, et al.
Parkinsonism & Related Disorders|November 8, 2024
GBA1 T369M and Parkinson's disease - Further evidence of a lack of association in the Swedish populationKajsa Atterling Brolin, David Bäckström, Joel Wallenius, et al.
Parkinsonism & Related Disorders|May 24, 2011
An African-American family with dystoniaAndreas Puschmann, Jianfeng Xiao, Robert W Bastian, et al.
Medrxiv : the Preprint Server for Health Sciences|April 1, 2024
Is <i>GBA1</i> T369M not a risk factor for Parkinson's disease in the Swedish population?Kajsa Atterling Brolin, David Bäckström, Joel Wallenius, et al.
Brain : a Journal of Neurology|July 1, 2016
18F-AV-1451 tau PET imaging correlates strongly with tau neuropathology in MAPT mutation carriersRuben Smith, Andreas Puschmann, Michael Schöll, et al.
Journal of Parkinson'S Disease|November 15, 2021
Insights on Genetic and Environmental Factors in Parkinson's Disease from a Regional Swedish Case-Control CohortKajsa Brolin, Sara Bandres-Ciga, Cornelis Blauwendraat, et al.
Lakartidningen|September 26, 2018
Gösta Eggertsen, Andreas Puschmann, Sara Hall, et al.
Parkinsonism & Related Disorders|May 3, 2014
Autosomal dominant cerebellar ataxia with slow ocular saccades, neuropathy and orthostatism: a novel entity?Klas Wictorin, Björn Brådvik, Karin Nilsson, et al.
European Journal of Human Genetics : EJHG|October 17, 2022
Updated Stroke Gene Panels: Rapid evolution of knowledge on monogenic causes of strokeAndreea Ilinca, Andreas Puschmann, Jukka Putaala, et al.
Neurology. Genetics|March 17, 2021
<i>MAP3K6</i> Mutations in a Neurovascular Disease Causing Stroke, Cognitive Impairment, and TremorAndreea Ilinca, Elisabet Englund, Sofie Samuelsson, et al.
Pageof 9

Showing results (31-40 of 90) with videos related to

Sort By:
Pageof 9
Molecular Genetics & Genomic Medicine|August 7, 2024
Maculopathy and adult-onset ataxia in patients with biallelic MFSD8 variantsSigurd Dobloug, Ulrika Kjellström, Glenn Anderson, et al.
Parkinsonism & Related Disorders|November 8, 2024
GBA1 T369M and Parkinson's disease - Further evidence of a lack of association in the Swedish populationKajsa Atterling Brolin, David Bäckström, Joel Wallenius, et al.
Parkinsonism & Related Disorders|May 24, 2011
An African-American family with dystoniaAndreas Puschmann, Jianfeng Xiao, Robert W Bastian, et al.
Medrxiv : the Preprint Server for Health Sciences|April 1, 2024
Is <i>GBA1</i> T369M not a risk factor for Parkinson's disease in the Swedish population?Kajsa Atterling Brolin, David Bäckström, Joel Wallenius, et al.
Brain : a Journal of Neurology|July 1, 2016
18F-AV-1451 tau PET imaging correlates strongly with tau neuropathology in MAPT mutation carriersRuben Smith, Andreas Puschmann, Michael Schöll, et al.
Journal of Parkinson'S Disease|November 15, 2021
Insights on Genetic and Environmental Factors in Parkinson's Disease from a Regional Swedish Case-Control CohortKajsa Brolin, Sara Bandres-Ciga, Cornelis Blauwendraat, et al.
Lakartidningen|September 26, 2018
Gösta Eggertsen, Andreas Puschmann, Sara Hall, et al.
Parkinsonism & Related Disorders|May 3, 2014
Autosomal dominant cerebellar ataxia with slow ocular saccades, neuropathy and orthostatism: a novel entity?Klas Wictorin, Björn Brådvik, Karin Nilsson, et al.
European Journal of Human Genetics : EJHG|October 17, 2022
Updated Stroke Gene Panels: Rapid evolution of knowledge on monogenic causes of strokeAndreea Ilinca, Andreas Puschmann, Jukka Putaala, et al.
Neurology. Genetics|March 17, 2021
<i>MAP3K6</i> Mutations in a Neurovascular Disease Causing Stroke, Cognitive Impairment, and TremorAndreea Ilinca, Elisabet Englund, Sofie Samuelsson, et al.
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