Rezultati pretrage - Mahsa Fadaee

DOK7 congenital myasthenic syndrome: case series and review of literature od Bentolhoda Ziaadini, Bardyia Ghaderi Yazdi, Elham Dirandeh, Reza Boostani, Narges Karimi, Akram Panahi, Ariana Kariminejad, Mahsa Fadaee, Fatemeh Ahangari, Shahriar Nafissi

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P604: Diagnostic utility of NGS testing in a highly consanguineous population: Findings from 1400+ Iranian patients with Mendelian disorders od Ayda Abolhassani, Zohreh Fattahi, Maryam Beheshtian, Mahsa Fadaee, Raheleh Vazehan, Fatemeh Ahangari, Shima Dehdahsi, Mehrshid Faraji Zonooz, Elham Parsimehr, Zahra Kalhor, Fatemeh Peymani, Maryam Mozaffarpour Nouri, Mojgan Babanejad, Khadijeh Noudehi, Fatemeh Fatehi, Shima Zamanian Najafabadi, Fariba Afroozan, Hilda Yazdan, Bita Bozorgmehr, Azita Azarkeivan, Shokouh Sadat Mahdavi, Pooneh Nikuei, Farzad Fatehi, Payman Jamali, Mahmoud Reza Ashrafi, Parvaneh Karimzadeh, Haleh Habibi, Kimia Kahrizi, Shahriar Nafissi, Ariana Kariminejad, Hossein Najmabadi

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Clinical application of next generation sequencing for Mendelian disease diagnosis in the Iranian population od Ayda Abolhassani, Zohreh Fattahi, Maryam Beheshtian, Mahsa Fadaee, Raheleh Vazehan, Fatemeh Ahangari, Shima Dehdahsi, Mehrshid Faraji Zonooz, Elham Parsimehr, Zahra Kalhor, Fatemeh Peymani, Maryam Mozaffarpour Nouri, Mojgan Babanejad, Khadijeh Noudehi, Fatemeh Fatehi, Shima Zamanian Najafabadi, Fariba Afroozan, Hilda Yazdan, Bita Bozorgmehr, Azita Azarkeivan, Shokouh Sadat Mahdavi, Pooneh Nikuei, Farzad Fatehi, Payman Jamali, Mahmoud Reza Ashrafi, Parvaneh Karimzadeh, Haleh Habibi, Kimia Kahrizi, Shahriar Nafissi, Ariana Kariminejad, Hossein Najmabadi

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P251: New insights into the genetic landscape of DMD gene mutations in Iran and the applicability of exon skipping therapies od Ali Khanbazi, Farzane Zare Ashrafi, Masoumeh Akbari Kelishomi, Raziye Rezvani Rezvandeh, Maryam Azad, Fatemeh Ahangari, Mahsa Fadaee, Shima Dehdahsi, Mina Makvand, Banafsheh Salmani, Zohreh Vahidi, Mahdieh Kooshki, Elmira Shiuokhi, Armita Ghaderi, Mahsa Tahmasebivand, Fariba Afroozan, Khadijeh Noudehi, Fatemeh Fatehi, Shima Zamanian Najafabadi, Shahriar Nafissi, Haleh Habibi, Maryam Taghdiri, Bahram Haghi Ashtiani, Gholamreza Zamani, Fatemeh Mohsenifar, Farzad Fatehi, MohammadKazem Bakhshandeh, Payman Jamali, Kimia Kahrizi, Ariana Kariminejad, Hossein Najmabadi

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P279: Application of next-generation sequencing in the diagnosis of inherited metabolic disorders in Iran: An 11-year overview od Parnian Alagha, Negar Molaei, Maryam Beheshtian, Fatemeh Ahangari, Mahsa Fadaee, Mehri Ashki, Zohreh Elahi, Raheleh Vazehan, Shima Dehdahsi, Elham Parsimehr, Maryam Mozaffarpour Nouri, Parishad Saei, Khadijeh Noudehi, Fatemeh Fatehi, Shima Zamanian Najafabadi, Hilda Yazdan, Fariba Afroozan, Banafsheh Salmani, Mahdieh Kooshki, Armita Ghaderi, Zohreh Vahidi, Mina Makvand, Atiyeh Ahmadpour, Mahsa Tahmasebivand, Elmira Shiuokhi, Saeed Talebi, Babak Zamani, Farhad Mahvelati Shamsabadi, Bahram Haghi Ashtiani, Payam Sarraf, Haleh Habibi, Afshin Fayyazi, Ali Asghar Okhovat, Mahmoud Reza Ashrafi, Farzad Fatehi, Parvaneh Karimzadeh, Shahriar Nafissi, Kimia Kahrizi, Ariana Kariminejad, Hossein Najmabadi

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Genetic spectrum among 2009 Iranian individuals with neuromuscular disorders using next generation sequencing and multiple ligation dependent probe amplification methods od Negar Molaei, Parnian Alagha, Ali Khanbazi, Maryam Beheshtian, Fatemeh Ahangari, Shima Dehdahsi, Mahsa Fadaee, Mehri Ashki, Zhila Ghaderi, Zohreh Elahi, Raheleh Vazehan, Elham Parsimehr, Maryam Mozaffarpour Nouri, Parishad Saei, Khadijeh Noudehi, Fatemeh Fatehi, Shima Zamanian Najafabadi, Ayda Abolhassani, Fariba Afroozan, Hilda Yazdan, Masoumeh Akbari Kelishomi, Maryam Azad, Farshid Parvini, Seyed Mehrdad Kassaee, Mahtab Ramezani, Fariba Zemorshidi, Houman Salimipour, Siamak Abdi, MohammadKazem Bakhshandeh, Afshin Fayyazi, Gholamreza Zamani, Mahmoud Reza Ashrafi, Payman Jamali, Payam Sarraf, Ali Asghar Okhovat, Bahram Haghi Ashtiani, Farzad Fatehi, Parvaneh Karimzadeh, Shahriar Nafissi, Kimia Kahrizi, Ariana Kariminejad, Hossein Najmabadi

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P159: Gene and mutation spectrum among Iranian individuals with neuromuscular disorders: An 11-year consolidated overview* od Negar Molaei, Parnian Alagha, Ali Khanbazi, Maryam Beheshtian, Fatemeh Ahangari, Mahsa Fadaee, Mehri Ashki, Zohreh Elahi, Raheleh Vazehan, Shima Dehdahsi, Elham Parsimehr, Maryam Mozaffarpour Nouri, Parishad Saei, Khadijeh Noudehi, Fatemeh Fatehi, Shima Zamanian Najafabadi, Fariba Afroozan, Hilda Yazdan, Fariba Afroozan, Masoumeh Akbari Kelishomi, Maryam Azad, Seyed Mehrdad Kassaee, Mahtab Ramezani, Fariba Zemorshidi, Houman Salimipour, Siamak Abdi, MohammadKazem Bakhshandeh, Afshin Fayyazi, Gholamreza Zamani, Mahmoud Reza Ashrafi, Parvaneh Karimzadeh, Payman Jamali, Payam Sarraf, Ali Asghar Okhovat, Bahram Haghi Ashtiani, Farzad Fatehi, Shahriar Nafissi, Kimia Kahrizi, Ariana Kariminejad, Hossein Najmabadi

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