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Journal of Molecular Neuroscience : MN
|
March 17, 2017
In-depth Characterization of the Homodimerization Domain of the Transcription Factor THAP1 and Dystonia-Causing Mutations Therein
Alev Richter, Ronja Hollstein, Eva Hebert, et al.
Journal of Neurology
|
May 3, 2022
A SUMO4 initiator codon variant in amyotrophic lateral sclerosis reduces SUMO4 expression and alters stress granule dynamics
Alma Osmanovic, Alisa Förster, Maylin Widjaja, et al.
European Journal of Human Genetics : EJHG
|
January 5, 2017
FIG4 variants in central European patients with amyotrophic lateral sclerosis: a whole-exome and targeted sequencing study
Alma Osmanovic, Isolde Rangnau, Anne Kosfeld, et al.
Journal of Tissue Engineering and Regenerative Medicine
|
February 28, 2019
Analysis of the therapeutic potential of different administration routes and frequencies of human mesenchymal stromal cells in the SOD1<sup>G93A</sup> mouse model of amyotrophic lateral sclerosis
Franziska Bursch, Klaus Jan Rath, Anastasia Sarikidi, et al.
International Journal of Molecular Sciences
|
December 17, 2016
Fingolimod Associated Bilateral Cystoid Macular Edema-Wait and See?
Refik Pul, Alma Osmanovic, Holger Schmalstieg, et al.
Journal of Neurology
|
May 4, 2020
Treatment expectations and patient-reported outcomes of nusinersen therapy in adult spinal muscular atrophy
Alma Osmanovic, Gresa Ranxha, Mareike Kumpe, et al.
Clinical Case Reports
|
July 23, 2021
An unusual presentation of Huntington's disease
Martin Schulze Westhoff, Alma Osmanovic, Catharina Meissner, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
March 29, 2023
Cranial nerve involvement in patients with immune-mediated neuropathy: An observational blink reflex study
Sonja Körner, Markus Maximilian Koch, Lars Hendrik Müschen, et al.
Orphanet Journal of Rare Diseases
|
January 7, 2021
Executive function is inversely correlated with physical function: the cognitive profile of adult Spinal Muscular Atrophy (SMA)
Lucas Mix, Olivia Schreiber-Katz, Claudia D Wurster, et al.
Journal of Neurology
|
May 25, 2020
SPG7 mutations in amyotrophic lateral sclerosis: a genetic link to hereditary spastic paraplegia
Alma Osmanovic, Maylin Widjaja, Alisa Förster, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 48) with videos related to
Sort By:
Page
of 5
Journal of Molecular Neuroscience : MN
|
March 17, 2017
In-depth Characterization of the Homodimerization Domain of the Transcription Factor THAP1 and Dystonia-Causing Mutations Therein
Alev Richter, Ronja Hollstein, Eva Hebert, et al.
Journal of Neurology
|
May 3, 2022
A SUMO4 initiator codon variant in amyotrophic lateral sclerosis reduces SUMO4 expression and alters stress granule dynamics
Alma Osmanovic, Alisa Förster, Maylin Widjaja, et al.
European Journal of Human Genetics : EJHG
|
January 5, 2017
FIG4 variants in central European patients with amyotrophic lateral sclerosis: a whole-exome and targeted sequencing study
Alma Osmanovic, Isolde Rangnau, Anne Kosfeld, et al.
Journal of Tissue Engineering and Regenerative Medicine
|
February 28, 2019
Analysis of the therapeutic potential of different administration routes and frequencies of human mesenchymal stromal cells in the SOD1<sup>G93A</sup> mouse model of amyotrophic lateral sclerosis
Franziska Bursch, Klaus Jan Rath, Anastasia Sarikidi, et al.
International Journal of Molecular Sciences
|
December 17, 2016
Fingolimod Associated Bilateral Cystoid Macular Edema-Wait and See?
Refik Pul, Alma Osmanovic, Holger Schmalstieg, et al.
Journal of Neurology
|
May 4, 2020
Treatment expectations and patient-reported outcomes of nusinersen therapy in adult spinal muscular atrophy
Alma Osmanovic, Gresa Ranxha, Mareike Kumpe, et al.
Clinical Case Reports
|
July 23, 2021
An unusual presentation of Huntington's disease
Martin Schulze Westhoff, Alma Osmanovic, Catharina Meissner, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
March 29, 2023
Cranial nerve involvement in patients with immune-mediated neuropathy: An observational blink reflex study
Sonja Körner, Markus Maximilian Koch, Lars Hendrik Müschen, et al.
Orphanet Journal of Rare Diseases
|
January 7, 2021
Executive function is inversely correlated with physical function: the cognitive profile of adult Spinal Muscular Atrophy (SMA)
Lucas Mix, Olivia Schreiber-Katz, Claudia D Wurster, et al.
Journal of Neurology
|
May 25, 2020
SPG7 mutations in amyotrophic lateral sclerosis: a genetic link to hereditary spastic paraplegia
Alma Osmanovic, Maylin Widjaja, Alisa Förster, et al.
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of 5