Items where Author is "Rabbani, B."

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Number of items: 12.

Article

Mahdieh, N. and Rabbani, A. and Firouzi, A. and Zahedmehr, A. and Hoseinimoghaddam, M. and Saeidi, S. and Sanati, H. and Basiri, H. and Noohi, F. and Rabbani, B. and Maleki, M. (2018) Clopidogrel Pharmacogenetics in Iranian Patients Undergoing Percutaneous Coronary Intervention. Cardiovascular Toxicology. pp. 1-10.

Mahdieh, N. and Rabbani, A. and Firouzi, A. and Zahedmehr, A. and Hoseinimoghaddam, M. and Saedi, S. and Sanati, H. and Basiri, H. and Noohi, F. and Rabbani, B. and Maleki, M. (2018) Clopidogrel Pharmacogenetics in Iranian Patients Undergoing Percutaneous Coronary Intervention. Cardiovascular Toxicology, 18 (5). pp. 482-491.

Mahdieh, N. and Rabbani, A. and Firouzi, A. and Zahedmehr, A. and Hoseinimoghaddam, M. and Saedi, S. and Sanati, H. and Basiri, H. and Noohi, F. and Rabbani, B. and Maleki, M. (2018) Correction to: Clopidogrel Pharmacogenetics in Iranian Patients Undergoing Percutaneous Coronary Intervention (Cardiovascular Toxicology, (2018), 10.1007/s12012-018-9459-x). Cardiovascular Toxicology.

Mahdieh, N. and Mikaeeli, S. and Tavasoli, A.R. and Rezaei, Z. and Maleki, M. and Rabbani, B. (2018) Genotype, phenotype and in silico pathogenicity analysis of HEXB mutations: Panel based sequencing for differential diagnosis of gangliosidosis. Clinical Neurology and Neurosurgery, 167. pp. 43-53.

Mahdieh, N. and Mikaeeli, S. and Tavasoli, A.R. and Rezaei, Z. and Maleki, M. and Rabbani, B. (2018) Genotype, phenotype and in silico pathogenicity analysis of HEXB mutations: Panel based sequencing for differential diagnosis of gangliosidosis. Clinical Neurology and Neurosurgery, 167. pp. 43-53.

Mahdieh, N. and Hosseini Moghaddam, M. and Motavaf, M. and Rabbani, A. and Soveizi, M. and Maleki, M. and Rabbani, B. and Alizadeh-asl, A. (2018) Genotypic effect of a mutation of the MYBPC3 gene and two phenotypes with different patterns of inheritance. Journal of Clinical Laboratory Analysis, 32 (6).

Mahdieh, N. and Mikaeeli, S. and Badv, R.S. and Shirazi, A.G. and Maleki, M. and Rabbani, B. (2018) Pathogenic significance of SCN1A splicing variants causing Dravet syndrome: Improving diagnosis with targeted sequencing for variants by in silico analysis. Clinical Neurology and Neurosurgery, 166. pp. 80-90.

Mahdieh, N. and Mikaeeli, S. and Badv, R.S. and Shirazi, A.G. and Maleki, M. and Rabbani, B. (2018) Pathogenic significance of SCN1A splicing variants causing Dravet syndrome: Improving diagnosis with targeted sequencing for variants by in silico analysis. Clinical Neurology and Neurosurgery, 166. pp. 80-90.

Nejat, M. and Saedi, S. and Soveizi, M. and Rabbani, B. and Najafi, N. and Maleki, M. (2018) A novel PKP2 mutation and intrafamilial phenotypic variability in ARVC/D. Medical Journal of the Islamic Republic of Iran, 32 (1).

Nejat, M. and Saedi, S. and Soveizi, M. and Rabbani, B. and Najafi, N. and Maleki, M. (2018) A novel PKP2 mutation and intrafamilial phenotypic variability in ARVC/D. Medical Journal of the Islamic Republic of Iran, 32 (1).

Mahdieh, N. and Rabbani, B. (2016) Beta thalassemia in 31,734 cases with HBB gene mutations: Pathogenic and structural analysis of the common mutations; Iran as the crossroads of the Middle East. Blood Reviews, 30 (6). pp. 493-508.

Rabbani, B. and Nakaoka, H. and Akhondzadeh, S. and Tekin, M. and Mahdieh, N. (2016) Next generation sequencing: Implications in personalized medicine and pharmacogenomics. Molecular BioSystems, 12 (6). pp. 1818-1830.

This list was generated on Fri Sep 20 19:24:35 2019 +0430.