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Katja Lohmann

Showing results (101-110 of 267) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|April 3, 2008
Childhood-onset restless legs syndrome: clinical and genetic features of 22 familiesHiltrud Muhle, Anja Neumann, Katja Lohmann-Hedrich, et al.
Journal of Neurology|February 3, 2009
MDR1 variants and risk of Parkinson disease. Association with pesticide exposure?Katja Zschiedrich, Inke R König, Norbert Brüggemann, et al.
Journal of Medical Genetics|November 5, 2014
EIF4G1 is neither a strong nor a common risk factor for Parkinson's disease: evidence from large European cohortsJohanna Huttenlocher, Rejko Krüger, Philipp Capetian, et al.
Stem Cell Research|November 10, 2019
Generation and characterization of human-derived iPSC lines from three pairs of monozygotic twins discordant for Parkinson's diseaseMarija Dulovic-Mahlow, Agnieszka Lukomska, Sokhna Haissatou Diaw, et al.
European Journal of Medical Genetics|April 29, 2023
Phenotypic specificity in patients with neurodevelopmental delay does not correlate with diagnostic yield of trio-exome sequencingNadja Baalmann, Malte Spielmann, Gabriele Gillessen-Kaesbach, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 29, 2011
An unusual neurological syndrome of crawling gait, dystonia, pyramidal signs, and limited speechBeenish Arif, Anne Grünewald, Amara Fatima, et al.
Frontiers in Cell and Developmental Biology|June 7, 2021
Reduced Expression of GABA <sub></sub> Receptor Alpha2 Subunit Is Associated With Disinhibition of DYT-THAP1 Dystonia Patient-Derived Striatal Medium Spiny NeuronsSelma Staege, Anna Kutschenko, Hauke Baumann, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 29, 2023
Shaking Up Ataxia: FGF14 and RFC1 Repeat Expansions in Affected and Unaffected Members of a Chilean FamilyPaula Saffie Awad, Katja Lohmann, Yasmin Hirmas, et al.
Journal of Medical Genetics|August 24, 2022
<i>MRM2</i> variants in families with complex dystonic syndromes: evidence for phenotypic heterogeneityAnum Shafique, Beenish Arif, Mary Lynn Chu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 14, 2022
Genotype-Phenotype Correlations for ATX-TBP (SCA17): MDSGene Systematic ReviewMalco Rossi, Moath Hamed, Jon Rodríguez-Antigüedad, et al.
Pageof 27

Showing results (101-110 of 267) with videos related to

Sort By:
Pageof 27
Movement Disorders : Official Journal of the Movement Disorder Society|April 3, 2008
Childhood-onset restless legs syndrome: clinical and genetic features of 22 familiesHiltrud Muhle, Anja Neumann, Katja Lohmann-Hedrich, et al.
Journal of Neurology|February 3, 2009
MDR1 variants and risk of Parkinson disease. Association with pesticide exposure?Katja Zschiedrich, Inke R König, Norbert Brüggemann, et al.
Journal of Medical Genetics|November 5, 2014
EIF4G1 is neither a strong nor a common risk factor for Parkinson's disease: evidence from large European cohortsJohanna Huttenlocher, Rejko Krüger, Philipp Capetian, et al.
Stem Cell Research|November 10, 2019
Generation and characterization of human-derived iPSC lines from three pairs of monozygotic twins discordant for Parkinson's diseaseMarija Dulovic-Mahlow, Agnieszka Lukomska, Sokhna Haissatou Diaw, et al.
European Journal of Medical Genetics|April 29, 2023
Phenotypic specificity in patients with neurodevelopmental delay does not correlate with diagnostic yield of trio-exome sequencingNadja Baalmann, Malte Spielmann, Gabriele Gillessen-Kaesbach, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 29, 2011
An unusual neurological syndrome of crawling gait, dystonia, pyramidal signs, and limited speechBeenish Arif, Anne Grünewald, Amara Fatima, et al.
Frontiers in Cell and Developmental Biology|June 7, 2021
Reduced Expression of GABA <sub></sub> Receptor Alpha2 Subunit Is Associated With Disinhibition of DYT-THAP1 Dystonia Patient-Derived Striatal Medium Spiny NeuronsSelma Staege, Anna Kutschenko, Hauke Baumann, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 29, 2023
Shaking Up Ataxia: FGF14 and RFC1 Repeat Expansions in Affected and Unaffected Members of a Chilean FamilyPaula Saffie Awad, Katja Lohmann, Yasmin Hirmas, et al.
Journal of Medical Genetics|August 24, 2022
<i>MRM2</i> variants in families with complex dystonic syndromes: evidence for phenotypic heterogeneityAnum Shafique, Beenish Arif, Mary Lynn Chu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 14, 2022
Genotype-Phenotype Correlations for ATX-TBP (SCA17): MDSGene Systematic ReviewMalco Rossi, Moath Hamed, Jon Rodríguez-Antigüedad, et al.
Pageof 27