Oral Therapy in a Diabetic Patient With History of Infantile Hyperinsulinism

por Moravej, Hossein, Karamizadeh, Zohreh, Aryani, Omid
Publicado 2015

New Mutation of Pelizaeus­-Merzbacher-Like Disease; A Report from Iran

por Karimzadeh, Parvaneh, Ahmadabadi, Farzad, Aryani, Omid, Houshmand, Massoud, Khatami, Alireza
Publicado 2014

Investigation of the Mitochondrial ATPase 6/8 and tRNA(Lys) Genes Mutations in Autism

por Piryaei, Fahimeh, Houshmand, Massoud, Aryani, Omid, Dadgar, Sepideh, Soheili, Zahra-Soheila
Publicado 2012

Alexander Disease: Report of Two Unrelated Infantile Form Cases, Identified by GFAP Mutation Analysis and Review of Literature; The First Report from Iran

por Ashrafi, Mahmoud-Reza, Tavasoli, Alireza, Aryani, Omid, Alizadeh, Hooman, Houshmand, Massoud
Publicado 2013

A Novel Mutation in Aspartoacylase Gene; Canavan Disease

por ASHRAFI, Mahmoudreza, TAVASOLI, Alireza, KATIBEH, Pegah, ARYANI, Omid, VAFAEE-SHAHI, Mohammad
Publicado 2015

Repetitive Suicidal Behaviors in a Case With a New Mutation of Wolfram Syndrome: A Jump From the Gene to the Behavior

por Mirfazeli, Fatemeh Sadat, Mohebi, Fatemeh, Jahanbakhshi, Amin, Aryani, Omid, Almasi-Dooghaee, Mostafa
Publicado 2022

Measuring Serum Level of Ionized Magnesium in Patients with Migraine

por ASSARZADEGAN, Farhad, ASADOLLAHI, Mostafa, DERAKHSHANFAR, Hojjat, KASHEFIZADEH, Azam, ARYANI, Omid, KHORSHIDI, Mona
Publicado 2015

Oculopharyngeal muscular dystrophy misdiagnosed as myasthenia gravis: Case report and review of literature

por Aryani, Omid, Akbari, Mohammadreza, Aghsaei-Fard, Masoud, Mirmohammad-Sadeghi, Arash, Yadegari, Samira
Publicado 2017

Secondary headaches attributed to arterial hypertension

por Assarzadegan, Farhad, Asadollahi, Mostafa, Hesami, Omid, Aryani, Omid, Mansouri, Behnam, Beladi moghadam, Nahid
Publicado 2013

Clinical Feature and Genetics in Rett Syndrome: A Report on Iranian Patients

por KARIMZADEH, Parvaneh, KHEIROLLAHI, Majid, HOUSHMAND, Seyed Massoud, DADGAR, Sepideh, ARYANI, Omid, YAGHINI, Omid
Publicado 2019

Association of fibroblast growth factor (FGF-21) as a biomarker with primary mitochondrial disorders, but not with secondary mitochondrial disorders (Friedreich Ataxia)

por Salehi, Mohammad Hossein, Kamalidehghan, Behnam, Houshmand, Massoud, Aryani, Omid, Sadeghizadeh, Majid, Mossalaeie, Mir Majid
Publicado 2013

Identification of a new mutation in an Iranian family with hereditary multiple osteochondromas

por Akbaroghli, Susan, Balali, Maryam, Kamalidehghan, Behnam, Saber, Siamak, Aryani, Omid, Meng, Goh Yong, Houshmand, Massoud
Publicado 2016

Gene Expression Profiling of Mitochondrial Oxidative Phosphorylation (OXPHOS) Complex I in Friedreich Ataxia (FRDA) Patients

por Salehi, Mohammad Hossein, Kamalidehghan, Behnam, Houshmand, Massoud, Yong Meng, Goh, Sadeghizadeh, Majid, Aryani, Omid, Nafissi, Shahriar
Publicado 2014

A novel homozygous variation in the PANK2 gene in two Persian siblings with atypical pantothenate kinase associated neurodegeneration

por Habibi, Amir Hasan, Razmeh, Saeed, Aryani, Omid, Rohani, Mohammad, Taghavian, Laleh, Alizadeh, Elham, Kokhedan, Karim Moradian, Zaribafian, Maryam
Publicado 2019

Two Novel Tyrosinase (TYR) Gene Mutations with Pathogenic Impact on Oculocutaneous Albinism Type 1 (OCA1)

por Ghodsinejad Kalahroudi, Vadieh, Kamalidehghan, Behnam, Arasteh Kani, Ahoura, Aryani, Omid, Tondar, Mahdi, Ahmadipour, Fatemeh, Chung, Lip Yong, Houshmand, Massoud
Publicado 2014

Novel bi-allelic variants expand the SPTBN4-related genetic and phenotypic spectrum

por Buelow, Markus, Süßmuth, David, Smith, Laurie D., Aryani, Omid, Castiglioni, Claudia, Stenzel, Werner, Bertini, Enrico, Schuelke, Markus, Knierim, Ellen
Publicado 2021

Four novel ARSA gene mutations with pathogenic impacts on metachromatic leukodystrophy: a bioinformatics approach to predict pathogenic mutations

por Dehghan Manshadi, Masoumeh, Kamalidehghan, Behnam, Aryani, Omid, Khalili, Elham, Dadgar, Sepideh, Tondar, Mahdi, Ahmadipour, Fatemeh, Yong Meng, Goh, Houshmand, Massoud
Publicado 2017

Identification of novel mutations among Iranian NPC1 patients: a bioinformatics approach to predict pathogenic mutations

por Abtahi, Rezvan, Karimzadeh, Parvaneh, Aryani, Omid, Akbarzadeh, Diba, Salehpour, Shadab, Rezayi, Alireza, Tonekaboni, Seyed Hassan, Emameh, Reza Zolfaghari, Houshmand, Massoud
Publicado 2022

Association of human mtDNA mutations with autism in Iranian patients

por Mousavizadeh, Kazem, Askari, Mohammad, Arian, Hajar, Gourjipour, Fazel, Nikpour, Amin R., Tavafjadid, Maryam, Aryani, Omid, Kamalidehghan, Behnam, Maroof, Hamid R., Houshmand, Massoud
Publicado 2013

Four Novel p.N385K, p.V36A, c.1033–1034insT and c.1417–1418delCT Mutations in the Sphingomyelin Phosphodiesterase 1 (SMPD1) Gene in Patients with Types A and B Niemann-Pick Disease...

por Manshadi, Masoumeh Dehghan, Kamalidehghan, Behnam, Keshavarzi, Fatemeh, Aryani, Omid, Dadgar, Sepideh, Arastehkani, Ahoora, Tondar, Mahdi, Ahmadipour, Fatemeh, Meng, Goh Yong, Houshmand, Massoud
Publicado 2015