Yesim G. Parman
Istanbul, Turkey
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 86 publications
Significance of Phrenic Nerve Conduction Study in the Electrodiagnosis of Guillain Barré Syndrome.
Journal: Journal of the peripheral nervous system : JPNS
Published: February 01, 2026
Effect of CXCR5, PD-1 and ICOS on B-cell responses and relevance to myasthenia gravis.
Journal: Clinical & translational immunology
Published: November 14, 2025
Kyphoscoliosis peptidase deficiency-induced myofibrillar degeneration, focal depletion of mitochondria, and protein aggregation: A true myofibrillar myopathy?
Journal: Journal of neuromuscular diseases
Published: November 12, 2025
Charcot-Marie-Tooth-SORD: insights into pathology and pathophysiology from a human nerve biopsy series.
Journal: Brain : a journal of neurology
Published: September 17, 2025
Cytokine Profiles in Myasthenia Gravis Subgroups and the Lack of Any Effect of Immunosuppression.
Journal: Muscle & nerve
Published: August 30, 2025
Eplontersen for Hereditary Transthyretin Amyloidosis With Polyneuropathy: An Exploratory Analysis of Treatment Effect in Male and Female Patients.
Journal: Muscle & nerve
Published: August 07, 2025
Late-onset TK2 deficiency in adults: Long-term clinical outcomes of deoxynucleoside therapy.
Journal: Mitochondrion
Published: July 23, 2025
Subclinical Respiratory Muscle Weakness and Obstructive Sleep Apnea are Common in Glucosamine-UDP-N-acetyl-2-epimerase / N-acetylmannosamine kinase (GNE) Myopathy.
Journal: Annals of Indian Academy of Neurology
Published: July 22, 2025
The Effect of Aerobic Exercise Training on Patients with Type III Spinal Muscular Atrophy.
Journal: Journal of clinical medicine
Published: June 17, 2025
Disease Progression in Charcot-Marie-Tooth Disease Type 4B (CMT4B) Associated With Mutations in Myotubularin-Related Proteins 2 and 13.
Journal: European journal of neurology
Published: October 28, 2024
Delineating the genetic landscape of Charcot-Marie-tooth disease in Türkiye: Distinct distribution, rare phenotypes, and novel variants.
Journal: European journal of neurology
Published: July 16, 2024
Biallelic variants in ARHGAP19 cause a progressive inherited motor-predominant neuropathy.
Journal: The Journal of clinical investigation
Published: July 08, 2024
Last Updated: 09/26/2026