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Safa Najmi

Showing results (1-10 of 10) with videos related to

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Archives of Iranian Medicine|March 3, 2011
Hemiparkinsonism-hemiatrophy syndromeHormoz Ayromlou, Safa Najmi, Mohammad Ali Arami
Iranian Journal of Neurology|November 20, 2013
Comparing the efficacy of botulinum toxin with tizanidine in upper limb post stroke spasticityMohammad Yazdchi, Zahra Ghasemi, Hanieh Moshayedi, et al.
Iranian Journal of Neurology|June 22, 2016
The efficacy of the ketogenic diet on motor functions in Parkinson's disease: A rat modelSheida Shaafi, Safa Najmi, Hamed Aliasgharpour, et al.
Neuromuscular Disorders : NMD|December 14, 2020
Sporadic late-onset nemaline myopathy with monoclonal gammopathy of undetermined significance: Report of four patientsAli Asghar Okhovat, Yalda Nilipour, Reza Boostani, et al.
Pediatric Neurology|November 24, 2017
Diffusion Tensor Imaging as a Biomarker to Differentiate Acute Disseminated Encephalomyelitis From Multiple Sclerosis at First DemyelinationWint Yan Aung, Parinaz Massoumzadeh, Safa Najmi, et al.
Neuroimage. Clinical|June 25, 2015
The effects of white matter hyperintensities and amyloid deposition on Alzheimer dementiaBrian A Gordon, Safa Najmi, Phillip Hsu, et al.
Letters in Applied Microbiology|January 27, 2026
Altered gut microbiota, SCFAs, and barrier integrity markers in Alzheimer's and Parkinson's disease patientsSomayeh Ahmadi, Alka Hasani, Mohammad Yasdchi, et al.
Annals of Clinical Psychiatry : Official Journal of the American Academy of Clinical Psychiatrists|December 1, 2016
Ideomotor limb apraxia as a staging tool in individuals with Alzheimer's disease (ILIAD)William D Soulsby, Nezar El-Ruwie, Shravan Gatla, et al.
Genetic Testing and Molecular Biomarkers|September 10, 2016
Genetic Analysis of the ZNF512B, SLC41A1, and ALDH2 Polymorphisms in Parkinson's Disease in the Iranian PopulationFaranak Madadi, Mahmoud Shekari Khaniani, Ehsan Esmaili Shandiz, et al.
Molecular Neurobiology|May 15, 2017
A Clinical and Molecular Genetic Study of 50 Families with Autosomal Recessive Parkinsonism Revealed Known and Novel Gene MutationsShaghayegh Taghavi, Rita Chaouni, Abbas Tafakhori, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Archives of Iranian Medicine|March 3, 2011
Hemiparkinsonism-hemiatrophy syndromeHormoz Ayromlou, Safa Najmi, Mohammad Ali Arami
Iranian Journal of Neurology|November 20, 2013
Comparing the efficacy of botulinum toxin with tizanidine in upper limb post stroke spasticityMohammad Yazdchi, Zahra Ghasemi, Hanieh Moshayedi, et al.
Iranian Journal of Neurology|June 22, 2016
The efficacy of the ketogenic diet on motor functions in Parkinson's disease: A rat modelSheida Shaafi, Safa Najmi, Hamed Aliasgharpour, et al.
Neuromuscular Disorders : NMD|December 14, 2020
Sporadic late-onset nemaline myopathy with monoclonal gammopathy of undetermined significance: Report of four patientsAli Asghar Okhovat, Yalda Nilipour, Reza Boostani, et al.
Pediatric Neurology|November 24, 2017
Diffusion Tensor Imaging as a Biomarker to Differentiate Acute Disseminated Encephalomyelitis From Multiple Sclerosis at First DemyelinationWint Yan Aung, Parinaz Massoumzadeh, Safa Najmi, et al.
Neuroimage. Clinical|June 25, 2015
The effects of white matter hyperintensities and amyloid deposition on Alzheimer dementiaBrian A Gordon, Safa Najmi, Phillip Hsu, et al.
Letters in Applied Microbiology|January 27, 2026
Altered gut microbiota, SCFAs, and barrier integrity markers in Alzheimer's and Parkinson's disease patientsSomayeh Ahmadi, Alka Hasani, Mohammad Yasdchi, et al.
Annals of Clinical Psychiatry : Official Journal of the American Academy of Clinical Psychiatrists|December 1, 2016
Ideomotor limb apraxia as a staging tool in individuals with Alzheimer's disease (ILIAD)William D Soulsby, Nezar El-Ruwie, Shravan Gatla, et al.
Genetic Testing and Molecular Biomarkers|September 10, 2016
Genetic Analysis of the ZNF512B, SLC41A1, and ALDH2 Polymorphisms in Parkinson's Disease in the Iranian PopulationFaranak Madadi, Mahmoud Shekari Khaniani, Ehsan Esmaili Shandiz, et al.
Molecular Neurobiology|May 15, 2017
A Clinical and Molecular Genetic Study of 50 Families with Autosomal Recessive Parkinsonism Revealed Known and Novel Gene MutationsShaghayegh Taghavi, Rita Chaouni, Abbas Tafakhori, et al.
Pageof 1