1. A Mild Form of Neurodegeneration with Brain Iron Accumulation attributed to Coenzyme A Synthase Mutation. Issue 2 (7th December 2022) Authors: Hashemi, Narges; Nejad Shahrokh Abadi, Reza; Alavi, Afagh; Tavasoli, Ali Reza; Rohani, Mohammad Journal: Movement disorders clinical practice Issue: Volume 10:Issue 2(2023) Page Start: 331 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Action Myoclonus and Seizure in Kufor‐Rakeb Syndrome. Issue 2 (28th December 2017) Authors: Rohani, Mohammad; Lang, Anthony E.; Sina, Farzad; Elahi, Elahe; Fasano, Alfonso; Hardy, John; Bras, Jose; Alavi, Afagh Journal: Movement disorders clinical practice Issue: Volume 5:Issue 2(2018) Page Start: 195 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. 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) ↗
4. Beta-propeller protein associated neurodegeneration (BPAN); the first report of three patients from Iran with de novo novel mutations. (April 2019) Authors: Rohani, Mohammad; Fasano, Alfonso; Akhoundi, Fahimeh Haji; Haeri, Ghazal; Lang, Anthony E.; Rahimi Bidgoli, Mohammad Masoud; Javanparast, Leila; Zamani, Babak; Shahidi, Gholamali; Alavi, Afagh Journal: Parkinsonism & related disorders Issue: Volume 61(2019) Page Start: 231 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. CAPN1 and hereditary spastic paraplegia: a novel variant in an Iranian family and overview of the genotype-phenotype correlation. (30th September 2021) Authors: Rahimi Bidgoli, Mohammad Masoud; Javanparast, Leila; Rohani, Mohammad; Najmabadi, Hossein; Zamani, Babak; Alavi, Afagh Journal: International journal of neuroscience Issue: Volume 131:Number 10(2021) Page Start: 962 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Clinical spectrum in multiple families with primary COQ10 deficiency. Issue 2 (20th November 2020) Authors: Hashemi, Seyyed S.; Zare‐Abdollahi, Davood; Bakhshandeh, Mohammad K.; Vafaee, Amirreza; Abolhasani, Sona; Inanloo Rahatloo, Kolsoum; DanaeeFard, Fardad; Farboodi, Niloofar; Rohani, Mohammad; Alavi, Afagh Journal: American journal of medical genetics Issue: Volume 185:Issue 2(2021) Page Start: 440 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Congenital Ichthyosis in a Case of Spinocerebellar Ataxia Type 34: A Novel Presentation for a Known Mutation. Issue 2 (11th January 2021) Authors: Haeri, Ghazal; Hajiakhoundi, Fahimeh; Alavi, Afagh; Ghiasi, Maryam; Munhoz, Renato P.; Rohani, Mohammad Journal: Movement disorders clinical practice Issue: Volume 8:Issue 2(2021) Page Start: 275 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. 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) ↗
9. 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) ↗
10. Description of combined ARHSP/JALS phenotype in some patients with SPG11 mutations. Issue 7 (8th May 2020) Authors: Khani, Marzieh; Shamshiri, Hosein; Fatehi, Farzad; Rohani, Mohammad; Haghi Ashtiani, Bahram; Akhoundi, Fahimeh Haji; Alavi, Afagh; Moazzeni, Hamidreza; Taheri, Hanieh; Ghani, Mina Tolou; Javanparast, Leila; Hashemi, Seyyed Saleh; Haji‐Seyed‐Javadi, Ramona; Heidari, Matineh; Nafissi, Shahriar; Ela... Journal: Molecular genetics & genomic medicine Issue: Volume 8:Issue 7(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗