Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Yesim Parman

Showing results (21-30 of 61) with videos related to

Pageof 7
Sort By:
Neuromuscular Disorders : NMD|October 1, 2013
Prepubertal anti-Musk positive myasthenia gravis with long remissionOzlem Gungor-Tuncer, Elif Kocasoy Orhan, Vuslat Yilmaz, et al.
European Neurology|January 13, 2006
fasciculations, autonomic symptoms and limbic encephalitis: a thymoma-associated Morvan's-like syndromeFeza Deymeer, Sukriye Akca, Gulsen Kocaman, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 2, 2021
Episodic psychosis, ataxia, motor neuropathy with pyramidal signs (PAMP syndrome) caused by a novel mutation in ADPRHL2 (AHR3)Hacer Durmus, Elif Mertoğlu, Heinrich Sticht, et al.
Journal of Neuroimmunology|June 17, 2023
Thymoma patients with or without myasthenia gravis have increased Th17 cells, IL-17 production and ICOS expressionMerve Cebi, Arman Cakar, Eren Erdogdu, et al.
Neuromuscular Disorders : NMD|June 30, 2006
Clinical spectrum of CMT4C disease in patients homozygous for the p.Arg1109X mutation in SH3TC2Jaume Colomer, Rebecca Gooding, Dora Angelicheva, et al.
Neuromuscular Disorders : NMD|February 4, 2018
Congenital myasthenic syndromes in Turkey: Clinical clues and prognosis with long term follow-upHacer Durmus, Xin-Ming Shen, Piraye Serdaroglu-Oflazer, et al.
Neuromuscular Disorders : NMD|October 7, 2018
Corrigendum to "Congenital myasthenic syndromes in Turkey: Clinical clues and prognosis with long term follow-up" [Neuromuscular Disorders 28/4 (2018) 315-322]Hacer Durmus, Xin-Ming Shen, Piraye Serdaroglu-Oflazer, et al.
Brain : a Journal of Neurology|November 8, 2025
Charcot-Marie-Tooth-SORD: insights into pathology and pathophysiology from a human nerve biopsy seriesMaike F Dohrn, Davide Pareyson, Chiara Pisciotta, et al.
Journal of Clinical Medicine|September 13, 2025
The Effect of Aerobic Exercise Training on Patients with Type III Spinal Muscular AtrophySezan Mergen Kilic, Fatma Mutluay, Arman Cakar, et al.
Journal of Neuromuscular Diseases|November 12, 2025
Kyphoscoliosis peptidase deficiency-induced myofibrillar degeneration, focal depletion of mitochondria, and protein aggregation: A true myofibrillar myopathy?Hacer Durmuş, Christoph S Clemen, Evren Önay Uçar, et al.
Pageof 7

Showing results (21-30 of 61) with videos related to

Sort By:
Pageof 7
Neuromuscular Disorders : NMD|October 1, 2013
Prepubertal anti-Musk positive myasthenia gravis with long remissionOzlem Gungor-Tuncer, Elif Kocasoy Orhan, Vuslat Yilmaz, et al.
European Neurology|January 13, 2006
fasciculations, autonomic symptoms and limbic encephalitis: a thymoma-associated Morvan's-like syndromeFeza Deymeer, Sukriye Akca, Gulsen Kocaman, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 2, 2021
Episodic psychosis, ataxia, motor neuropathy with pyramidal signs (PAMP syndrome) caused by a novel mutation in ADPRHL2 (AHR3)Hacer Durmus, Elif Mertoğlu, Heinrich Sticht, et al.
Journal of Neuroimmunology|June 17, 2023
Thymoma patients with or without myasthenia gravis have increased Th17 cells, IL-17 production and ICOS expressionMerve Cebi, Arman Cakar, Eren Erdogdu, et al.
Neuromuscular Disorders : NMD|June 30, 2006
Clinical spectrum of CMT4C disease in patients homozygous for the p.Arg1109X mutation in SH3TC2Jaume Colomer, Rebecca Gooding, Dora Angelicheva, et al.
Neuromuscular Disorders : NMD|February 4, 2018
Congenital myasthenic syndromes in Turkey: Clinical clues and prognosis with long term follow-upHacer Durmus, Xin-Ming Shen, Piraye Serdaroglu-Oflazer, et al.
Neuromuscular Disorders : NMD|October 7, 2018
Corrigendum to "Congenital myasthenic syndromes in Turkey: Clinical clues and prognosis with long term follow-up" [Neuromuscular Disorders 28/4 (2018) 315-322]Hacer Durmus, Xin-Ming Shen, Piraye Serdaroglu-Oflazer, et al.
Brain : a Journal of Neurology|November 8, 2025
Charcot-Marie-Tooth-SORD: insights into pathology and pathophysiology from a human nerve biopsy seriesMaike F Dohrn, Davide Pareyson, Chiara Pisciotta, et al.
Journal of Clinical Medicine|September 13, 2025
The Effect of Aerobic Exercise Training on Patients with Type III Spinal Muscular AtrophySezan Mergen Kilic, Fatma Mutluay, Arman Cakar, et al.
Journal of Neuromuscular Diseases|November 12, 2025
Kyphoscoliosis peptidase deficiency-induced myofibrillar degeneration, focal depletion of mitochondria, and protein aggregation: A true myofibrillar myopathy?Hacer Durmuş, Christoph S Clemen, Evren Önay Uçar, et al.
Pageof 7