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Alma Osmanovic

Showing results (21-30 of 48) with videos related to

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Journal of Neurology|April 9, 2020
Impact of comorbidities and co-medication on disease onset and progression in a large German ALS patient groupKristin Diekmann, Magdalena Kuzma-Kozakiewicz, Maria Piotrkiewicz, et al.
Brain Sciences|December 30, 2020
Cognitive Performance of Patients with Adult 5q-Spinal Muscular Atrophy and with Amyotrophic Lateral SclerosisAlma Osmanovic, Gary Wieselmann, Lucas Mix, et al.
Orphanet Journal of Rare Diseases|July 29, 2021
Increased chitotriosidase 1 concentration following nusinersen treatment in spinal muscular atrophyMaren Freigang, Petra Steinacker, Claudia Diana Wurster, et al.
Human Gene Therapy|August 9, 2022
Prevalence of Anti-Adeno-Associated Virus Serotype 9 Antibodies in Adult Patients with Spinal Muscular AtrophyBenjamin Stolte, Olivia Schreiber-Katz, René Günther, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 23, 2011
Homozygous THAP1 mutations as cause of early-onset generalized dystoniaSusanne A Schneider, Alfredo Ramirez, Kaveh Shafiee, et al.
Journal of Neuropathology and Experimental Neurology|July 29, 2024
Lipid and protein imbalances in muscle of a FAR1-patient with a heterozygous de novo variantAdela Della Marina, Andreas Hentschel, Martin Stenzel, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 16, 2011
Truncating mutations in THAP1 define the nuclear localization signalAlma Osmanovic, Andreas Dendorfer, Alev Erogullari, et al.
Frontiers in Neurology|July 30, 2019
Routine Cerebrospinal Fluid Cytology Reveals Unique Inclusions in Macrophages During Treatment With NusinersenStefan Gingele, Martin W Hümmert, Sascha Alvermann, et al.
Annals of Clinical and Translational Neurology|August 11, 2022
Glial fibrillary acidic protein in cerebrospinal fluid of patients with spinal muscular atrophyMaren Freigang, Petra Steinacker, Claudia D Wurster, et al.
Genes|January 21, 2022
Heterozygous <i>DHTKD1</i> Variants in Two European Cohorts of Amyotrophic Lateral Sclerosis PatientsAlma Osmanovic, Isabel Gogol, Helge Martens, et al.
Pageof 5

Showing results (21-30 of 48) with videos related to

Sort By:
Pageof 5
Journal of Neurology|April 9, 2020
Impact of comorbidities and co-medication on disease onset and progression in a large German ALS patient groupKristin Diekmann, Magdalena Kuzma-Kozakiewicz, Maria Piotrkiewicz, et al.
Brain Sciences|December 30, 2020
Cognitive Performance of Patients with Adult 5q-Spinal Muscular Atrophy and with Amyotrophic Lateral SclerosisAlma Osmanovic, Gary Wieselmann, Lucas Mix, et al.
Orphanet Journal of Rare Diseases|July 29, 2021
Increased chitotriosidase 1 concentration following nusinersen treatment in spinal muscular atrophyMaren Freigang, Petra Steinacker, Claudia Diana Wurster, et al.
Human Gene Therapy|August 9, 2022
Prevalence of Anti-Adeno-Associated Virus Serotype 9 Antibodies in Adult Patients with Spinal Muscular AtrophyBenjamin Stolte, Olivia Schreiber-Katz, René Günther, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 23, 2011
Homozygous THAP1 mutations as cause of early-onset generalized dystoniaSusanne A Schneider, Alfredo Ramirez, Kaveh Shafiee, et al.
Journal of Neuropathology and Experimental Neurology|July 29, 2024
Lipid and protein imbalances in muscle of a FAR1-patient with a heterozygous de novo variantAdela Della Marina, Andreas Hentschel, Martin Stenzel, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 16, 2011
Truncating mutations in THAP1 define the nuclear localization signalAlma Osmanovic, Andreas Dendorfer, Alev Erogullari, et al.
Frontiers in Neurology|July 30, 2019
Routine Cerebrospinal Fluid Cytology Reveals Unique Inclusions in Macrophages During Treatment With NusinersenStefan Gingele, Martin W Hümmert, Sascha Alvermann, et al.
Annals of Clinical and Translational Neurology|August 11, 2022
Glial fibrillary acidic protein in cerebrospinal fluid of patients with spinal muscular atrophyMaren Freigang, Petra Steinacker, Claudia D Wurster, et al.
Genes|January 21, 2022
Heterozygous <i>DHTKD1</i> Variants in Two European Cohorts of Amyotrophic Lateral Sclerosis PatientsAlma Osmanovic, Isabel Gogol, Helge Martens, et al.
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