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1. Amyotrophic lateral sclerosis progression: Iran-ALS clinical registry, a multicentre study. Issue 7 (27th November 2015)

2. Anticipation Can Be More Common in Hereditary Spastic Paraplegia with SPAST Mutations Than It Appears. (6th September 2022)

3. Application of muscle ultrasound for the evaluation of patients with amyotrophic lateral sclerosis: An observational cross‐sectional study. Issue 4 (14th August 2020)

4. Bi‐allelic loss of function variant in the NRCAM gene is associated with motor‐predominant axonal polyneuropathy; the second report. Issue 4 (6th January 2023)

6. Comparison of Clinical, Ultrasound, and Electrophysiologic Changes in Chronic Inflammatory Demyelinating Polyneuropathy: A Prospective Study. Issue 3 (6th March 2023)

7. Continuum of phenotypes in hereditary motor and sensory neuropathy with proximal predominance and Charcot–Marie–Tooth patients with TFG mutation. Issue 8 (20th May 2019)

8. COVID-19-associated risks and effects in myasthenia gravis (CARE-MG). Issue 12 (December 2020)

10. Description of clinical features and genetic analysis of one ultra-rare (SPG64) and two common forms (SPG5A and SPG15) of hereditary spastic paraplegia families. (3rd April 2021)