1. Amyotrophic lateral sclerosis progression: Iran-ALS clinical registry, a multicentre study. Issue 7 (27th November 2015) Authors: Shamshiri, Hosein; Fatehi, Farzad; Davoudi, Farnoush; Mir, Elham; Pourmirza, Behin; Abolfazli, Roya; Etemadifar, Masoud; Harirchian, Mohammad Hossein; Gharagozli, Koroush; Ayromlou, Hormoz; Basiri, Keivan; Zamani, Babak; Rohani, Mohammad; Sedighi, Behnaz; Roudbari, Ali; Delavar Kasmaei, Hossein; ... Journal: Amyotrophic lateral sclerosis and frontotemporal degeneration Issue: Volume 16:Issue 7/8(2015) Page Start: 506 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Anticipation Can Be More Common in Hereditary Spastic Paraplegia with SPAST Mutations Than It Appears. (6th September 2022) Authors: Hashemi, Seyyed-Saleh; Hajati, Reza; Davarzani, Atefeh; Rohani, Mohammad; DanaeeFard, Fardad; Rahimi Bidgoli, Mohammad Masoud; Fatehi, Farzad; Kariminejad, Ariana; Najmabadi, Hossein; Nafissi, Shahriar; Alavi, Afagh Journal: Canadian journal of neurological sciences Issue: Volume 49:Number 5(2022) Page Start: 651 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Application of muscle ultrasound for the evaluation of patients with amyotrophic lateral sclerosis: An observational cross‐sectional study. Issue 4 (14th August 2020) Authors: Rajabkhah, Sahebeh; Moradi, Kamyar; Okhovat, Ali A.; Van Alfen, Nens; Fathi, Davood; Aghaghazvini, Leila; Ashraf‐Ganjouei, Amir; Attarian, Shahram; Nafissi, Shahriar; Fatehi, Farzad Journal: Muscle & nerve Issue: Volume 62:Issue 4(2020) Page Start: 516 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
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) Authors: Elahi, Zohreh; Soveyzi, Mohamad; Nafissi, Shahriar; Nilipour, Yalda; Goleyjani Moghadam, Masoumeh; Keshavarz, Elham; Kariminejad, Ariana; Najmabadi, Hossein; Fattahi, Zohreh Journal: Molecular genetics & genomic medicine Issue: Volume 11:Issue 4(2023) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Blink Reflex May Help Discriminate Alzheimer Disease From Vascular Dementia. Issue 6 (December 2015) Authors: Mohammadian, Fatemeh; Noroozian, Maryam; Nafissi, Shahriar; Fatehi, Farzad Journal: Journal of clinical neurophysiology Issue: Volume 32:Issue 6(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Comparison of Clinical, Ultrasound, and Electrophysiologic Changes in Chronic Inflammatory Demyelinating Polyneuropathy: A Prospective Study. Issue 3 (6th March 2023) Authors: Okhovat, Ali Asghar; Nafissi, Shahriar; Moradi, Kamyar; Ziaadini, Bentolhoda; Panahi, Akram; Haghi Ashtiani, Bahram; Fatehi, Farzad Journal: Journal of clinical neurophysiology Issue: Volume 40:Issue 3(2023) Page Start: 250 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
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) Authors: Khani, Marzieh; Taheri, Hanieh; Shamshiri, Hosein; Houlden, Henry; Efthymiou, Stephanie; Alavi, Afagh; Nafissi, Shahriar; Elahi, Elahe Journal: American journal of medical genetics Issue: Volume 179:Issue 8(2019) Page Start: 1507 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. COVID-19-associated risks and effects in myasthenia gravis (CARE-MG). Issue 12 (December 2020) Authors: Muppidi, Srikanth; Guptill, Jeffrey T; Jacob, Saiju; Li, Yingkai; Farrugia, Maria E; Guidon, Amanda C; Tavee, Jinny O; Kaminski, Henry; Howard, James F; Cutter, Gary; Wiendl, Heinz; Maas, Matthew B; Illa, Isabel; Mantegazza, Renato; Murai, Hiroyuki; Utsugisawa, Kimiaki; Nowak, Richard J; Guidon, ... Journal: Lancet neurology Issue: Volume 19:Issue 12(2020) Page Start: 970 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Delayed‐onset inflammatory polyneuropathy without graft versus host disease after bone marrow transplantation. Issue 2 (25th March 2018) Authors: Sinaei, Farnaz; Khodabakhsh, Atena; Alimoghaddam, Kamran; Nafissi, Shahriar Journal: Muscle & nerve Issue: Volume 58:Issue 2(2018) Page Start: E11 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
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) Authors: Pashaei, Mahdieh; Davarzani, Atefeh; Hajati, Reza; Zamani, Babak; Nafissi, Shahriar; Larti, Farzaneh; Nilipour, Yalda; Rohani, Mohammad; Alavi, Afagh Journal: Journal of neurogenetics Issue: Volume 35:Number 2(2021) Page Start: 84 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗