Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Shima, Dehdahsi"'
Autor:
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
Publikováno v:
npj Genomic Medicine, Vol 9, Iss 1, Pp 1-11 (2024)
Abstract Next-generation sequencing (NGS) has been proven to be one of the most powerful diagnostic tools for rare Mendelian disorders. Several studies on the clinical application of NGS in unselected cohorts of Middle Eastern patients have reported
Externí odkaz:
https://doaj.org/article/d0de56f0485d43639ba3ed001723c22f
Autor:
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
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101510- (2024)
Externí odkaz:
https://doaj.org/article/2b6cd8a2516d4c7dba834e7f5dd8bf1b
Autor:
Parvaneh Karimzadeh, Hossein Najmabadi, Hanns Lochmuller, Marzieh Babaee, Shima Dehdahsi, Mohammad Miryounesi, Susan Amirsalari, Seyed Mansoor Rayegani, Seyed Hassan Tonekaboni
Publikováno v:
Neuromuscular Disorders. 32:806-810
Autor:
Niloofar BAZAZZADEGAN, Raheleh VAZEHAN, Mahsa FADAEE, Zohreh FATTAHI, Ayda ABOLHASSANI, Elham PARSIMEHR, Zahra KALHOR, Mehrshid FARAJI ZONOOZ, Fatemeh AHANGARI, Shima DEHDAHSI, Farshide SAMIEE, Payman JAMALI, Haleh HABIBI, Younes NOURIZADEH, Shokouh MAHDAVI, Maryam BEHESHTIAN, Ariana KARIMINEJAD, Richard JH SMITH, Hossein NAJMABADI
Publikováno v:
Iranian Journal of Public Health, Vol 48, Iss 10 (2019)
Background: Diagnosis of hereditary hearing loss (HHL) as a heterogeneous disorder is very important espe-cially in countries with high rates of consanguinity where the autosomal recessive pattern of inheritance is preva-lent. Techniques such as next
Externí odkaz:
https://doaj.org/article/2bb2e364df144354b6a117fcf7751f96
Autor:
Masoud, Edizadeh, Raheleh, Vazehan, Fatemeh, Javadi, Shima, Dehdahsi, Mahsa, Fadaee, Mehrshid, Faraji Zonooz, Elham, Parsimehr, Fatemeh, Ahangari, Ayda, Abolhassani, Zahra, Kalhor, Zohreh, Fattahi, Maryam, Beheshtian, Ariana, Kariminejad, Mohammad Reza, Akbari, Hossein, Najmabadi, Shahriar, Nafissi
Publikováno v:
Archives of Iranian medicine. 20(9)
The calcium channel, voltage-dependent, L-type, alpha 1S subunit (CACNA1S) gene encodes a skeletal Ca2+ channel which is involved in calcium-dependent processes such as muscle contraction and neurotransmitter release. Mutations in this gene have been
Autor:
Shima Dehdahsi, Ayda Abolhassani, Raheleh Vazehan, Mehrshid Faraji Zonooz, Zohreh Fattahi, Maryam Beheshtian, Shokouh Sadat Mahdavi, Hossein Najmabadi, Mahsa Fadaee, Payman Jamali, Elham Parsimehr, Richard J.H. Smith, Younes Nourizadeh, Ariana Kariminejad, Fatemeh Ahangari, Farshide Samiee, Zahra Kalhor, Niloofar Bazazzadegan, Haleh Habibi
Publikováno v:
Hossein Najmabadi
Iranian Journal of Public Health, Vol 48, Iss 10 (2019)
Iranian Journal of Public Health
Scopus-Elsevier
Iranian Journal of Public Health, Vol 48, Iss 10 (2019)
Iranian Journal of Public Health
Scopus-Elsevier
Background: Diagnosis of hereditary hearing loss (HHL) as a heterogeneous disorder is very important especially in countries with high rates of consanguinity where the autosomal recessive pattern of inheritance is prevalent. Techniques such as next-g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d0d9364e221ebcb0de68fe0cef60d59
https://europepmc.org/articles/PMC6908923
https://europepmc.org/articles/PMC6908923