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Disease severity and response to treatment in Iranian patients with myasthenia gravis.
Published in:
Neurological Sciences, 2022, v. 43, n. 2, p. 1233, doi. 10.1007/s10072-021-05382-0
By:
- Sinaei, Farnaz;
- Fatehi, Farzad;
- Oveis Gharan, Shahram;
- Ehsan, Soroush;
- Kamali, Koorosh;
- Nafissi, Shahriar
Publication type:
Article
Association between trinucleotide CAG repeats of the DNA polymerase gene (POLG) with age of onset of Iranian Friedreich's ataxia patients.
Published in:
2008
By:
- Heidari MM;
- Houshmand M;
- Hosseinkhani S;
- Nafissi S;
- Scheiber-Mojdehkar B;
- Khatami M;
- Heidari, Mohammad Mehdi;
- Houshmand, Massoud;
- Hosseinkhani, Saman;
- Nafissi, Shahriar;
- Scheiber-Mojdehkar, Barbara;
- Khatami, Mehri
Publication type:
journal article
Association between trinucleotide CAG repeats of the DNA polymerase gene (POLG) with age of onset of Iranian Friedreich’s ataxia patients.
Published in:
Neurological Sciences, 2008, v. 29, n. 6, p. 489, doi. 10.1007/s10072-008-1026-y
By:
- Heidari, Mohammad Mehdi;
- Houshmand, Massoud;
- Hosseinkhani, Saman;
- Nafissi, Shahriar;
- Scheiber-Mojdehkar, Barbara;
- Khatami, Mehri
Publication type:
Article
An Iranian familial amyotrophic lateral sclerosis pedigree with p.Val48Phe causing mutation in SOD1: a genetic and clinical report.
Published in:
Iranian Journal of Basic Medical Sciences, 2014, v. 17, n. 10, p. 735
By:
- Alavi, Afagh;
- Khani, Marzieh;
- Nafissi, Shahriar;
- Shamshiri, Hosein;
- Elahi, Elahe
Publication type:
Article
Clinical and genetic spectrum of a large cohort of patients with δ-sarcoglycan muscular dystrophy.
Published in:
2022
By:
- Alonso-Pérez, Jorge;
- González-Quereda, Lidia;
- Bruno, Claudio;
- Panicucci, Chiara;
- Alavi, Afagh;
- Nafissi, Shahriar;
- Nilipour, Yalda;
- Zanoteli, Edmar;
- Isihi, Lucas Michielon de Augusto;
- Melegh, Béla;
- Hadzsiev, Kinga;
- Muelas, Nuria;
- Vílchez, Juan J;
- Dourado, Mario Emilio;
- Kadem, Naz;
- Kutluk, Gultekin;
- Umair, Muhammad;
- Younus, Muhammad;
- Pegorano, Elena;
- Bello, Luca
Publication type:
journal article
Evaluation of point mutations in dystrophin gene in Iranian Duchenne and Becker muscular dystrophy patients: introducing three novel variants.
Published in:
Journal of Genetics, 2016, v. 95, n. 2, p. 325, doi. 10.1007/s12041-016-0641-2
By:
- HAGHSHENAS, MARYAM;
- AKBARI, MOHAMMAD;
- KARIZI, SHOHREH;
- DEILAMANI, FARAVAREH;
- NAFISSI, SHAHRIAR;
- SALEHI, ZIVAR
Publication type:
Article
Bi‐allelic loss of function variant in the NRCAM gene is associated with motor‐predominant axonal polyneuropathy; the second report.
Published in:
Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 4, p. 1, doi. 10.1002/mgg3.2131
By:
- Elahi, Zohreh;
- Soveyzi, Mohamad;
- Nafissi, Shahriar;
- Nilipour, Yalda;
- Goleyjani Moghadam, Masoumeh;
- Keshavarz, Elham;
- Kariminejad, Ariana;
- Najmabadi, Hossein;
- Fattahi, Zohreh
Publication type:
Article
Description of combined ARHSP/JALS phenotype in some patients with SPG11 mutations.
Published in:
Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 7, p. 1, doi. 10.1002/mgg3.1240
By:
- 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;
- Elahi, Elahe
Publication type:
Article
Four novel C20orf54 mutations identified in Brown-Vialetto-Van Laere syndrome patients.
Published in:
Journal of Human Genetics, 2012, v. 57, n. 9, p. 613, doi. 10.1038/jhg.2012.70
By:
- Dezfouli, Mitra Ansari;
- Yadegari, Samira;
- Nafissi, Shahriar;
- Elahi, Elahe
Publication type:
Article
Adverse drug reactions of Rituximab in patients suffering from autoimmune neurological diseases.
Published in:
DARU: Journal of Pharmaceutical Sciences, 2022, v. 30, n. 2, p. 323, doi. 10.1007/s40199-022-00452-w
By:
- Mohebbi, Niayesh;
- Taghizadeh-Ghehi, Maryam;
- Savar, Seyed Mehrdad;
- Abdi, Siamak;
- Kouhsari, Romina;
- Gholami, Kheirollah;
- Nafissi, Shahriar
Publication type:
Article
Continuum of phenotypes in hereditary motor and sensory neuropathy with proximal predominance and Charcot–Marie–Tooth patients with TFG mutation.
Published in:
American Journal of Medical Genetics. Part A, 2019, v. 179, n. 8, p. 1507, doi. 10.1002/ajmg.a.61184
By:
- Khani, Marzieh;
- Taheri, Hanieh;
- Shamshiri, Hosein;
- Houlden, Henry;
- Efthymiou, Stephanie;
- Alavi, Afagh;
- Nafissi, Shahriar;
- Elahi, Elahe
Publication type:
Article
Intellectual disability, muscle weakness and characteristic face in three siblings: A newly described recessive syndrome mapping to 3p24.3-p25.3.
Published in:
American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 11, p. 2508, doi. 10.1002/ajmg.a.37248
By:
- Kariminejad, Ariana;
- Nafissi, Shahriar;
- Nilipoor, Yalda;
- Tavasoli, Alireza;
- Van Veldhoven, Paul P.;
- Bonnard, Carine;
- Ng, Yeng Ting;
- Majoie, Charles B.;
- Reversade, Bruno;
- Hennekam, Raoul C.
Publication type:
Article
Novel Mutations of the TYMP Gene in Mitochondrial Neurogastrointestinal Encephalomyopathy: Case Series and Literature Review.
Published in:
Journal of Molecular Neuroscience, 2021, v. 71, n. 12, p. 2526, doi. 10.1007/s12031-021-01822-w
By:
- Mojtabavi, Helia;
- Fatehi, Farzad;
- Shahkarami, Sepideh;
- Rezaei, Nima;
- Nafissi, Shahriar
Publication type:
Article
Impact of Vitamin A Supplementation on RAR Gene Expression in Multiple Sclerosis Patients.
Published in:
Journal of Molecular Neuroscience, 2013, v. 51, n. 2, p. 478, doi. 10.1007/s12031-013-0090-9
By:
- Bitarafan, Sama;
- Harirchian, Mohammad;
- Sahraian, Mohammad;
- Keramatipour, Mohammad;
- Beladi Moghadam, Nahid;
- Togha, Mansoureh;
- Nafissi, Shahriar;
- Siassi, Fereydoun;
- Eshraghian, Mohammad;
- Mohammadzadeh Honarvar, Niyaz;
- Ansar, Hasti;
- Talebi, Saeed;
- Saboor-Yarghi, Ali
Publication type:
Article
Recommendations for Infantile-Onset and Late-Onset Pompe Disease: An Iranian Consensus.
Published in:
Frontiers in Neurology, 2021, v. 12, p. 1, doi. 10.3389/fneur.2021.739931
By:
- Fatehi, Farzad;
- Ashrafi, Mahmoud Reza;
- Babaee, Marzieh;
- Ansari, Behnaz;
- Beiraghi Toosi, Mehran;
- Boostani, Reza;
- Eshraghi, Peyman;
- Fakharian, Atefeh;
- Hadipour, Zahra;
- Haghi Ashtiani, Bahram;
- Moravej, Hossein;
- Nilipour, Yalda;
- Sarraf, Payam;
- Sayadpour Zanjani, Keyhan;
- Nafissi, Shahriar
Publication type:
Article
Zytux in Refractory Myasthenia Gravis: A Multicenter, Open-Labeled, Clinical Trial Study of Effectiveness and Safety of a Rituximab Biosimilar.
Published in:
Frontiers in Neurology, 2021, v. 12, p. 1, doi. 10.3389/fneur.2021.682622
By:
- Fatehi, Farzad;
- Moradi, Kamyar;
- Okhovat, Ali Asghar;
- Shojatalab, Ghazaleh;
- Sedighi, Behnaz;
- Boostani, Reza;
- Sarraf, Payam;
- Haghi Ashtiani, Bahram;
- Ghasemi, Majid;
- Moussavi, Soussan;
- Anjidani, Nassim;
- Nafissi, Shahriar
Publication type:
Article
Detection of variants in dystroglycanopathy-associated genes through the application of targeted whole-exome sequencing analysis to a large cohort of patients with unexplained limb-girdle muscle weakness.
Published in:
Skeletal Muscle, 2018, v. 8, n. 1, p. N.PAG, doi. 10.1186/s13395-018-0170-1
By:
- Johnson, Katherine;
- Bertoli, Marta;
- Phillips, Lauren;
- Töpf, Ana;
- Van den Bergh, Peter;
- Vissing, John;
- Witting, Nanna;
- Nafissi, Shahriar;
- Jamal-Omidi, Shirin;
- Łusakowska, Anna;
- Kostera-Pruszczyk, Anna;
- Potulska-Chromik, Anna;
- Deconinck, Nicolas;
- Wallgren-Pettersson, Carina;
- Strang-Karlsson, Sonja;
- Colomer, Jaume;
- Claeys, Kristl G.;
- De Ridder, Willem;
- Baets, Jonathan;
- von der Hagen, Maja
Publication type:
Article
Gene Expression Profiling of Mitochondrial Oxidative Phosphorylation (OXPHOS) Complex I in Friedreich Ataxia (FRDA) Patients.
Published in:
PLoS ONE, 2014, v. 9, n. 4, p. 1, doi. 10.1371/journal.pone.0094069
By:
- Salehi, Mohammad Hossein;
- Kamalidehghan, Behnam;
- Houshmand, Massoud;
- Yong Meng, Goh;
- Sadeghizadeh, Majid;
- Aryani, Omid;
- Nafissi, Shahriar
Publication type:
Article
The value of MUNIX as an objective electrophysiological biomarker of disease progression in chronic inflammatory demyelinating polyneuropathy.
Published in:
Muscle & Nerve, 2022, v. 65, n. 4, p. 433, doi. 10.1002/mus.27498
By:
- Okhovat, Ali Asghar;
- Advani, Soroor;
- Ziaadini, Bentolhoda;
- Panahi, Akram;
- Salehizadeh, Saeideh;
- Nafissi, Shahriar;
- Haghi Ashtiani, Bahram;
- Rajabally, Yusuf A.;
- Fatehi, Farzad
Publication type:
Article
Investigating the possible association between NLRP3 gene polymorphisms and myasthenia gravis.
Published in:
2021
By:
- Agah, Elmira;
- Nafissi, Shahriar;
- Saleh, Fatemeh;
- Sarraf, Payam;
- Tafakhori, Abbas;
- Mousavi, Seyed Vahid;
- Saghazadeh, Amene;
- Sadr, Maryam;
- Sinaei, Farnaz;
- Mohebbi, Bahareh;
- Mahmoudi, Mahdi;
- Shadi, Hamideh;
- Rezaei, Nima
Publication type:
journal article
Application of muscle ultrasound for the evaluation of patients with amyotrophic lateral sclerosis: An observational cross-sectional study.
Published in:
2020
By:
- Rajabkhah, Sahebeh;
- Moradi, Kamyar;
- Okhovat, Ali A.;
- Van Alfen, Nens;
- Fathi, Davood;
- Aghaghazvini, Leila;
- Ashraf‐Ganjouei, Amir;
- Attarian, Shahram;
- Nafissi, Shahriar;
- Fatehi, Farzad;
- Ashraf-Ganjouei, Amir
Publication type:
journal article
Delayed-onset inflammatory polyneuropathy without graft versus host disease after bone marrow transplantation.
Published in:
2018
By:
- Sinaei, Farnaz;
- Khodabakhsh, Atena;
- Alimoghaddam, Kamran;
- Nafissi, Shahriar
Publication type:
journal article
Late-onset pompe disease in Iran: A clinical and genetic report.
Published in:
2017
By:
- Nazari, Ferdos;
- Sinaei, Farnaz;
- Nilipour, Yalda;
- Fatehi, Farzad;
- Streubel, Berthold;
- Ashrafi, Mahmoud Reza;
- Aryani, Omid;
- Nafissi, Shahriar
Publication type:
journal article
Validation of the 15-item myasthenia gravis quality of life questionnaire (MG-QOL15) Persian version.
Published in:
2016
By:
- Ostovan, Vahid Reza;
- Fatehi, Farzad;
- Davoudi, Farnoush;
- Nafissi, Shahriar
Publication type:
journal article
Iranian consensus on use of vitamin D in patients with multiple sclerosis.
Published in:
2016
By:
- Jahromi, Soodeh Razeghi;
- Sahraian, Mohammad Ali;
- Togha, Mansoureh;
- Sedighi, Behnaz;
- Shayegannejad, Vahid;
- Nickseresht, Alireza;
- Nafissi, Shahriar;
- Mohebbi, Niayesh;
- Majdinasab, Nastran;
- Foroughipour, Mohsen;
- Etemadifar, Masoud;
- Moghadam, Nahid Beladi;
- Ayramlou, Hormoz;
- Ashtari, Fereshteh;
- Alaie, Shekoofe
Publication type:
journal article
Diagnosis and treatment of late-onset Pompe disease in the Middle East and North Africa region: consensus recommendations from an expert group.
Published in:
2015
By:
- Al Jasmi, Fatma;
- Al Jumah, Mohammed;
- Alqarni, Fatimah;
- Al-Sanna'a, Nouriya;
- Al-Sharif, Fawziah;
- Bohlega, Saeed;
- Cupler, Edward J.;
- Fathalla, Waseem;
- Hamdan, Mohamed A.;
- Makhseed, Nawal;
- Nafissi, Shahriar;
- Nilipour, Yalda;
- Selim, Laila;
- Shembesh, Nuri;
- Sunbul, Rawda;
- Hassan Tonekaboni, Seyed;
- MENA Pompe Working Group;
- Tonekaboni, Seyed Hassan
Publication type:
journal article
Islamic fasting and multiple sclerosis.
Published in:
BMC Neurology, 2014, v. 14, n. 1, p. 1, doi. 10.1186/1471-2377-14-56
By:
- Jahromi, Soodeh Razeghi;
- Ali Sahraian, Mohammad;
- Ashtari, Fereshteh;
- Ayromlou, Hormoz;
- Etemadifar, Massoud;
- Ghaffarpour, Majid;
- Mohammadianinejad, Ehsan;
- Nafissi, Shahriar;
- Nickseresht, Alireza;
- Shaygannejad, Vahid;
- Togha, Mansoreh;
- Torabi, Hamid Reza;
- Ziaie, Shadi
Publication type:
Article
Islamic fasting and multiple sclerosis.
Published in:
2014
By:
- Jahromi, Soodeh Razeghi;
- Sahraian, Mohammad Ali;
- Ashtari, Fereshteh;
- Ayromlou, Hormoz;
- Etemadifar, Massoud;
- Ghaffarpour, Majid;
- Mohammadianinejad, Ehsan;
- Nafissi, Shahriar;
- Nickseresht, Alireza;
- Shaygannejad, Vahid;
- Togha, Mansoreh;
- Torabi, Hamid Reza;
- Ziaie, Shadi
Publication type:
journal article
Celiac Disease in Patients with Neuropathy.
Published in:
Iranian Journal of Gastroenterology & Hepatology (GOVARESH), 2018, v. 23, n. 1, p. 41
By:
- Shahbazkhani, Bijan;
- Abdehagh, Mohammad;
- Nafissi, Shahriar
Publication type:
Article
Prevalence of HLA-associated Celiac Disease in Patients Referred as idiopathic Neuropathy.
Published in:
Iranian Journal of Gastroenterology & Hepatology (GOVARESH), 2017, v. 22, n. 3, p. 43
By:
- Bijan, Shahbazkhani;
- Masoume, Mansouri;
- Mohammad, Abdehagh;
- Shahriar, Nafissi;
- Mehdi, Mahdavi;
- Golnaz, Ekhlasi
Publication type:
Article
Expanding the Molecular Spectrum of HK1-Related Charcot-Marie-Tooth Disease, Type 4G; the First Report in Iran.
Published in:
Archives of Iranian Medicine (AIM), 2023, v. 26, n. 5, p. 279, doi. 10.34172/aim.2023.43
By:
- Moghadam, Masoumeh Goleyjani;
- Elahi, Zohreh;
- Soveyzi, Mohamad;
- Arzhangi, Sanaz;
- Nafissi, Shahriar;
- Najmabadi, Hossein;
- Kahrizi, Kimia;
- Fattahi, Zohreh
Publication type:
Article
Iranian Consensus Recommendations for Treatment of Myasthenia Gravis.
Published in:
Archives of Iranian Medicine (AIM), 2022, v. 25, n. 1, p. 37, doi. 10.34172/aim.2022.07
By:
- Nafissi, Shahriar;
- Okhovat, Ali Asghar;
- Sinaei, Farnaz;
- Ansari, Behnaz;
- Ayramloo, Hormoz;
- Basiri, Keyvan;
- Boostani, Reza;
- Ashtiani, Bahram Haghi;
- Sarraf, Payam;
- Fatehi, Farzad
Publication type:
Article
COLQ-Congenital myasthenic syndrome in an Iranian cohort: the clinical and genetics spectrum.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03116-x
By:
- Hesami, Omid;
- Ramezani, Mahtab;
- Ghasemi, Aida;
- Fatehi, Farzad;
- Okhovat, Ali Asghar;
- Ziaadini, Bentolhoda;
- Kariminejad, Ariana;
- Nafissi, Shahriar
Publication type:
Article
DOK7 congenital myasthenic syndrome: case series and review of literature.
Published in:
BMC Neurology, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12883-024-03713-0
By:
- Ziaadini, Bentolhoda;
- Ghaderi Yazdi, Bardyia;
- Dirandeh, Elham;
- Boostani, Reza;
- Karimi, Narges;
- Panahi, Akram;
- Kariminejad, Ariana;
- Fadaee, Mahsa;
- Ahangari, Fatemeh;
- Nafissi, Shahriar
Publication type:
Article
Association of amyotrophic lateral sclerosis and Behcet's disease: is there a relationship? A multi-national case series.
Published in:
Clinical Rheumatology, 2012, v. 31, n. 4, p. 733, doi. 10.1007/s10067-011-1923-y
By:
- Mrabet, Hela;
- Borhani-Haghighi, Afshin;
- Koseoglu, Emel;
- Mutlu, Melike;
- Baydemir, Recep;
- Nafissi, Shahriar;
- Eschebbi, Slim;
- Delibas, Emel;
- Samangooie, Shahdokht;
- Yetkin, Fatih;
- Mrabet, Amel;
- Parman, Yesim;
- Heydari, Seyed;
- Akman-Demir, Gulsen
Publication type:
Article
High Frequency of Tc22 and Th22 Cells in Myasthenia Gravis Patients and Their Significant Reduction after Thymectomy.
Published in:
Neuroimmunomodulation, 2018, v. 25, n. 2, p. 80, doi. 10.1159/000490855
By:
- Robat-Jazi, Behrouz;
- Hosseini, Mina;
- Shaygannejad, Vahid;
- Nafissi, Shahriar;
- Rezaei, Abbas;
- Mansourain, Marjan;
- Mirmosayyeb, Omid;
- Esmaeil, Nafiseh
Publication type:
Article
Long-term subclinical severe hyperCKemia associated with a rare VPS13A gene mutation in an Iranian patient: Case report.
Published in:
Current Journal of Neurology, 2024, v. 23, n. 1, p. 86, doi. 10.18502/cjn.v23i1.16439
By:
- Hadei, Seyed Jalaleddin;
- Ghaderi-Yazdi, Bardiya;
- Nafissi, Shahriar
Publication type:
Article
Validation of myasthenia gravis activity of daily living questionnaire: Persian version.
Published in:
Current Journal of Neurology, 2022, v. 21, n. 1, p. 35, doi. 10.18502/cjn.v21i1.9360
By:
- Faghani, Shahriar;
- Okhvat, Ali Asghar;
- Karimi, Narges;
- Moassefi, Mana;
- Maroufi, Seyed Farzad;
- Nafissi, Shahriar;
- Fatehi, Farzad
Publication type:
Article
A retrospective study of the safety and efficacy of rituximab in Iranian patients with myasthenia gravis: A single-center experience.
Published in:
Current Journal of Neurology, 2022, v. 21, n. 2, p. 91, doi. 10.18502/cjn.v21i2.10492
By:
- Ziaadini, Bentolhoda;
- Karimi, Narges;
- Panahi, Akram;
- Okhovat, Ali Asghar;
- Fatehi, Farzad;
- Nafissi, Shahriar
Publication type:
Article
Electrophysiological studies in patients with seropositive/seronegative myasthenia gravis.
Published in:
Current Journal of Neurology, 2021, v. 20, n. 3, p. 120
By:
- Vahabi, Zahra;
- Nazari, Ferdos;
- Fatehi, Farzad;
- Bayegi, Valiolah;
- Saffarian, Zahra;
- Saffarian, Fatemeh;
- Nafissi, Shahriar
Publication type:
Article
Evaluation of quality of life and mood disorders in caregivers of patients with amyotrophic lateral sclerosis: A single-center cross-sectional study.
Published in:
Current Journal of Neurology, 2020, v. 19, n. 4, p. 190
By:
- Okhovat, Ali Asghar;
- Fatehi, Farzad;
- Rafiemehr, Melika;
- Moradi, Kamyar;
- Kiani-Mehr, Gilda;
- Nafissi, Shahriar
Publication type:
Article
Guillain-Barre syndrome in patients with coronavirus disease-2019: Report of six cases and review of literature.
Published in:
Current Journal of Neurology, 2020, v. 19, n. 3, p. 122
By:
- Okhovat, Ali Asghar;
- Ansari, Behnaz;
- Hemasian, Helia;
- Haghi-Ashtiani, Bahram;
- Advani, Soroor;
- Ziaadini, Bentolhoda;
- Abdi, Siamak;
- Sikaroudi, Hajir;
- Nafissi, Shahriar;
- Fatehi, Farzad
Publication type:
Article
Validation of Persian Individualized Neuromuscular Quality of Life in patients with muscular dystrophies.
Published in:
Current Journal of Neurology, 2020, v. 19, n. 1, p. 13
By:
- Moradi, Kamyar;
- Jamal-Omidi, Shirin;
- Masoudi, Maryam;
- Bagheri, Sayna;
- Nafissi, Shahriar;
- Fatehi, Farzad
Publication type:
Article
A New Case of Granulomatosis with Polyangiitis Presented with Tolosa–Hunt Syndrome Manifestations.
Published in:
2024
By:
- Mohebbi, Maryam;
- Nafissi, Shahriar;
- Alikhani, Majid
Publication type:
Case Study
Mitochondrial Copy Number and D-Loop Variants in Pompe Patients.
Published in:
Cell Journal (Yakhteh), 2016, v. 18, n. 3, p. 405
By:
- Bahreini, Fatemeh;
- Houshmand, Massoud;
- Modaresi, Mohammad Hossein;
- Tonekaboni, Hassan;
- Nafissi, Shahriar;
- Nazari, Ferdoss;
- Akrami, Seyed Mohammad
Publication type:
Article
The First Report of Iranian Registry of Patients with Spinal Muscular Atrophy.
Published in:
Journal of Neuromuscular Diseases, 2023, v. 10, n. 2, p. 211, doi. 10.3233/JND-221614
By:
- Mansouri, Vahid;
- Heidari, Morteza;
- Bemanalizadeh, Maryam;
- Azizimalamiri, Reza;
- Nafissi, Shahriar;
- Akbari, Masood Ghahvechi;
- Barzegar, Mohammad;
- Moayedi, Ali Reza;
- Badv, Reza Shervin;
- Mohamadi, Mahmood;
- Tavasoli, Ali Reza;
- Amirsalari, Susan;
- Khajeh, Ali;
- Inaloo, Soroor;
- Fatehi, Farzad;
- Hosseinpour, Sareh;
- Babaei, Meisam;
- Hosseini, Seyed Ahmad;
- Mahdi Hosseiny, Seyyed Mohammad;
- Fayyazi, Afshin
Publication type:
Article
Association of HLA Class II Alleles with Disease Severity and Treatment Response in Iranian Patients with Myasthenia Gravis.
Published in:
Journal of Neuromuscular Diseases, 2021, v. 8, n. 5, p. 827, doi. 10.3233/JND-210700
By:
- Sinaei, Farnaz;
- Fatehi, Farzad;
- Gharan, Shahram Oveis;
- Ehsan, Soroush;
- Kamali, Koorosh;
- Amirzargar, Aliakbar;
- Mahmoudi, Mahdi;
- Vaghefifar, Alaleh;
- Nafissi, Shahriar
Publication type:
Article
Thigh and Leg Muscle MRI Findings in GNE Myopathy.
Published in:
Journal of Neuromuscular Diseases, 2021, v. 8, n. 4, p. 735, doi. 10.3233/JND-210629
By:
- Fatehi, Farzad;
- Advani, Soroor;
- Okhovat, Ali Asghar;
- Ziaadini, Bentolhoda;
- Shamshiri, Hosein;
- Nafissi, Shahriar
Publication type:
Article
Identification of a mutation in TNRC18 in a patient with clinical features of Fazio‐Londe disease.
Published in:
2024
By:
- Khani, Marzieh;
- Shamshiri, Hosein;
- Nafissi, Shahriar;
- Salehi, Najmeh;
- Moazzeni, Hamidreza;
- Taheri, Hanieh;
- Elahi, Elahe
Publication type:
Case Study
Electrophysiologic studies in patients with Leukodystrophy.
Published in:
Iranian Journal of Child Neurology, 2014, v. 8, n. 4, p. 8
By:
- NAFISSI, Shahriar
Publication type:
Article

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