Showing 1 - 7 results of 7 for search 'Nejat Mahdieh', query time: 0.03s
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TCAP gene is not a common cause of cardiomyopathy in Iranian patients by Zahra Alaei, Nasrin Zamani, Bahareh Rabbani, Nejat Mahdieh
Published 2023-09-01
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A novel stop-gain pathogenic variant in the KCNQ1 gene causing long QT syndrome 1 by Samira Kalayinia, Mohammad Dalili, Maryam Pourirahim, Majid Maleki, Nejat Mahdieh
Published 2023-01-01
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A Mutational Hotspot in The LAMP2 Gene: Unravelling Intrafamilial Phenotypic Variation and Global Distribution of The c.877C>T Variant: A Descriptive Study by Saeideh Kavousi, Mohammad Dalili, Bahareh Rabbani, Mehrdad Behmanesh, Mehrdad Noruzinia, Nejat Mahdieh
Published 2024-01-01
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Neurofibromatosis-Noonan syndrome and growth deficiency in an Iranian girl due to a pathogenic variant in NF1 gene by Setila Dalili, Seyyedeh Azade Hoseini Nouri, Reza Bayat, Shahin Koohmanaee, Manijeh Tabrizi, Marjaneh Zarkesh, Alireza Tarang, Nejat Mahdieh
Published 2023-02-01
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Expanding the genetic spectrum of giant axonal neuropathy: Two novel variants in Iranian families by Mahmoud Reza Ashrafi, Ali Zare Dehnavi, Ali Reza Tavasoli, Morteza Heidari, Masoud Ghahvechi Akbari, Ali Reza Ronagh, Mohammad Ghafouri, Nejat Mahdieh, Pouria Mohammadi, Zahra Rezaei
Published 2023-06-01
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The genetic basis of early-onset hereditary ataxia in Iran: results of a national registry of a heterogeneous population by Nejat Mahdieh, Morteza Heidari, Zahra Rezaei, Ali Reza Tavasoli, Sareh Hosseinpour, Maryam Rasulinejad, Ali Zare Dehnavi, Masoud Ghahvechi Akbari, Reza Shervin Badv, Elahe Vafaei, Ali Mohebbi, Pouria Mohammadi, Seyyed Mohammad Mahdi Hosseiny, Reza Azizimalamiri, Ali Nikkhah, Elham Pourbakhtyaran, Mohammad Rohani, Narges Khanbanha, Sedigheh Nikbakht, Mojtaba Movahedinia, Parviz Karimi, Homa Ghabeli, Seyed Ahmad Hosseini, Fatemeh Sadat Rashidi, Masoud Garshasbi, Morteza Rezvani Kashani, Noor M. Ghiasvand, Stephan Zuchner, Matthis Synofzik, Mahmoud Reza Ashrafi
Published 2024-04-01
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