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Neurological Research and Practice
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February 1, 2022
Heterozygous POLG variant Ser1181Asn co-segregating in a family with autosomal dominant axonal neuropathy, proximal muscle fatigability, ptosis, and ragged red fibers
Maike F Dohrn, Corina Heller, Diana Zengeler, et al.
Journal of Neurology
|
May 19, 2017
Screening for lipoprotein receptor-related protein 4-, agrin-, and titin-antibodies and exploring the autoimmune spectrum in myasthenia gravis
Isabell Cordts, Nicolas Bodart, Kathi Hartmann, et al.
Orphanet Journal of Rare Diseases
|
January 15, 2020
The Latin American experience with a next generation sequencing genetic panel for recessive limb-girdle muscular weakness and Pompe disease
Jorge A Bevilacqua, Maria Del Rosario Guecaimburu Ehuletche, Abayuba Perna, et al.
Brain Communications
|
May 12, 2021
Intracerebroventricular delivery of vascular endothelial growth factor in patients with amyotrophic lateral sclerosis, a phase I study
Philip Van Damme, Petra Tilkin, Katarina Jansson Mercer, et al.
Annals of Clinical and Translational Neurology
|
April 14, 2025
ADAPT NXT: Fixed Cycles or Every-Other-Week IV Efgartigimod in Generalized Myasthenia Gravis
Ali A Habib, Kristl G Claeys, Vera Bril, et al.
Journal of Autoimmunity
|
January 12, 2023
Identification of new telomere- and telomerase-associated autoantigens in systemic sclerosis
Jean-Baptiste Vulsteke, Vanessa Smith, Carolien Bonroy, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 15, 2019
Maternal copy-number variations in the DMD gene as secondary findings in noninvasive prenatal screening
Nathalie Brison, Jazz Storms, Darine Villela, et al.
European Journal of Neurology
|
June 13, 2025
What Are the Normal Serum Creatine Kinase Values for Skeletal Muscle? A Worldwide Systematic Review
Katina Aleksovska, Theodoros Kyriakides, Corrado Angelini, et al.
European Journal of Neurology
|
January 31, 2026
EAN 2024 Guideline on the Diagnostic Approach to Oligo/Asymptomatic HyperCKemia
T Kyriakides, K Aleksovska, C Angelini, et al.
Orphanet Journal of Rare Diseases
|
April 7, 2020
Late-onset Pompe disease (LOPD) in Belgium: clinical characteristics and outcome measures
P Vanherpe, S Fieuws, A D'Hondt, et al.
Page
of 24
Search research articles
Search
Showing results (171-180 of 239) with videos related to
Sort By:
Page
of 24
Neurological Research and Practice
|
February 1, 2022
Heterozygous POLG variant Ser1181Asn co-segregating in a family with autosomal dominant axonal neuropathy, proximal muscle fatigability, ptosis, and ragged red fibers
Maike F Dohrn, Corina Heller, Diana Zengeler, et al.
Journal of Neurology
|
May 19, 2017
Screening for lipoprotein receptor-related protein 4-, agrin-, and titin-antibodies and exploring the autoimmune spectrum in myasthenia gravis
Isabell Cordts, Nicolas Bodart, Kathi Hartmann, et al.
Orphanet Journal of Rare Diseases
|
January 15, 2020
The Latin American experience with a next generation sequencing genetic panel for recessive limb-girdle muscular weakness and Pompe disease
Jorge A Bevilacqua, Maria Del Rosario Guecaimburu Ehuletche, Abayuba Perna, et al.
Brain Communications
|
May 12, 2021
Intracerebroventricular delivery of vascular endothelial growth factor in patients with amyotrophic lateral sclerosis, a phase I study
Philip Van Damme, Petra Tilkin, Katarina Jansson Mercer, et al.
Annals of Clinical and Translational Neurology
|
April 14, 2025
ADAPT NXT: Fixed Cycles or Every-Other-Week IV Efgartigimod in Generalized Myasthenia Gravis
Ali A Habib, Kristl G Claeys, Vera Bril, et al.
Journal of Autoimmunity
|
January 12, 2023
Identification of new telomere- and telomerase-associated autoantigens in systemic sclerosis
Jean-Baptiste Vulsteke, Vanessa Smith, Carolien Bonroy, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 15, 2019
Maternal copy-number variations in the DMD gene as secondary findings in noninvasive prenatal screening
Nathalie Brison, Jazz Storms, Darine Villela, et al.
European Journal of Neurology
|
June 13, 2025
What Are the Normal Serum Creatine Kinase Values for Skeletal Muscle? A Worldwide Systematic Review
Katina Aleksovska, Theodoros Kyriakides, Corrado Angelini, et al.
European Journal of Neurology
|
January 31, 2026
EAN 2024 Guideline on the Diagnostic Approach to Oligo/Asymptomatic HyperCKemia
T Kyriakides, K Aleksovska, C Angelini, et al.
Orphanet Journal of Rare Diseases
|
April 7, 2020
Late-onset Pompe disease (LOPD) in Belgium: clinical characteristics and outcome measures
P Vanherpe, S Fieuws, A D'Hondt, et al.
Page
of 24