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Ebba Lohmann

Showing results (51-60 of 77) with videos related to

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Journal of Neuroimmunology|May 26, 2015
The interleukin 1 alpha, interleukin 1 beta, interleukin 6 and alpha-2-macroglobulin serum levels in patients with early or late onset Alzheimer's disease, mild cognitive impairment or Parkinson's diseaseErdinç Dursun, Duygu Gezen-Ak, Haşmet Hanağası, et al.
American Journal of Medical Genetics|July 13, 2002
Complex relationship between Parkin mutations and Parkinson diseaseAndrew West, Magali Periquet, Sarah Lincoln, et al.
Parkinsonism & Related Disorders|July 6, 2021
A new alpha-synuclein missense variant (Thr72Met) in two Turkish families with Parkinson's diseaseChristina Fevga, Yangshin Park, Ebba Lohmann, et al.
Human Molecular Genetics|July 10, 2015
The CACNA1B R1389H variant is not associated with myoclonus-dystonia in a large European multicentric cohortNiccolo E Mencacci, Léa R'bibo, Sara Bandres-Ciga, et al.
Brain : a Journal of Neurology|May 24, 2003
Parkin mutations are frequent in patients with isolated early-onset parkinsonismMagali Periquet, Morwena Latouche, Ebba Lohmann, et al.
Journal of Neurology|November 9, 2013
Recessive dystonia-ataxia syndrome in a Turkish family caused by a COX20 (FAM36A) mutationSarah Doss, Katja Lohmann, Philip Seibler, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 28, 2020
Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairmentThomas Roux, Mathieu Barbier, Mélanie Papin, et al.
Annals of Neurology|August 2, 2003
How much phenotypic variation can be attributed to parkin genotype?Ebba Lohmann, Magali Periquet, Vincenzo Bonifati, et al.
Archives of Neurology|March 14, 2007
LRRK2 exon 41 mutations in sporadic Parkinson disease in EuropeansSuzanne Lesage, Sabine Janin, Ebba Lohmann, et al.
Human Molecular Genetics|March 4, 2010
Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humansSuzanne Lesage, Etienne Patin, Christel Condroyer, et al.
Pageof 8

Showing results (51-60 of 77) with videos related to

Sort By:
Pageof 8
Journal of Neuroimmunology|May 26, 2015
The interleukin 1 alpha, interleukin 1 beta, interleukin 6 and alpha-2-macroglobulin serum levels in patients with early or late onset Alzheimer's disease, mild cognitive impairment or Parkinson's diseaseErdinç Dursun, Duygu Gezen-Ak, Haşmet Hanağası, et al.
American Journal of Medical Genetics|July 13, 2002
Complex relationship between Parkin mutations and Parkinson diseaseAndrew West, Magali Periquet, Sarah Lincoln, et al.
Parkinsonism & Related Disorders|July 6, 2021
A new alpha-synuclein missense variant (Thr72Met) in two Turkish families with Parkinson's diseaseChristina Fevga, Yangshin Park, Ebba Lohmann, et al.
Human Molecular Genetics|July 10, 2015
The CACNA1B R1389H variant is not associated with myoclonus-dystonia in a large European multicentric cohortNiccolo E Mencacci, Léa R'bibo, Sara Bandres-Ciga, et al.
Brain : a Journal of Neurology|May 24, 2003
Parkin mutations are frequent in patients with isolated early-onset parkinsonismMagali Periquet, Morwena Latouche, Ebba Lohmann, et al.
Journal of Neurology|November 9, 2013
Recessive dystonia-ataxia syndrome in a Turkish family caused by a COX20 (FAM36A) mutationSarah Doss, Katja Lohmann, Philip Seibler, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 28, 2020
Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairmentThomas Roux, Mathieu Barbier, Mélanie Papin, et al.
Annals of Neurology|August 2, 2003
How much phenotypic variation can be attributed to parkin genotype?Ebba Lohmann, Magali Periquet, Vincenzo Bonifati, et al.
Archives of Neurology|March 14, 2007
LRRK2 exon 41 mutations in sporadic Parkinson disease in EuropeansSuzanne Lesage, Sabine Janin, Ebba Lohmann, et al.
Human Molecular Genetics|March 4, 2010
Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humansSuzanne Lesage, Etienne Patin, Christel Condroyer, et al.
Pageof 8