Zobrazeno 1 - 10
of 15
pro vyhledávání: '"zahra kalhor"'
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
Publikováno v:
حکمت سینوی, Vol 24, Iss 63, Pp 71-88 (2020)
The issues of Avicenna's philosophy begin with the topicality of being qua being; in the works of Avicenna, the human mind can draw the actualized external existence away into two distinct concepts of existence and whatness. Later this basic question
Externí odkaz:
https://doaj.org/article/69f3fce080334c80953adf2feb8a8925
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
Publikováno v:
Animals, Vol 14, Iss 18, p 2701 (2024)
This study investigates the efficacy of hormone-induced artificial reproduction in goldfish (Carassius auratus) under controlled temperatures. Ovaprim injections significantly enhanced ovulation and sperm production compared to controls. Medium tempe
Externí odkaz:
https://doaj.org/article/9e5011a5979d46c59a86443f0efc6815
Autor:
Raheleh Vazehan, Hans-Hilger Ropers, Elham Parsimehr, Zahra Kalhor, Seyedeh Sedighe Abedini, Mahboubeh Kamgar, Faezeh Mojahedi, K. Kahrizi, Ariana Kariminejad, Farahnaz Sabbagh Kermani, Mahsa Fadaee, Zohreh Fattahi, Vera M. Kalscheuer, Mehrshid Faraji Zonooz, Maryam Beheshtian, Sanaz Arzhangi, Shokouh Sadat Mahdavi, Payman Jamali, Hossein Najmabadi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fff711e3ecf3e7c1323f891e04ae0d9f
https://doi.org/10.1111/cge.13549/v2/response1
https://doi.org/10.1111/cge.13549/v2/response1
Autor:
Shokouh Sadat Mahdavi, Ariana Kariminejad, Hossein Najmabadi, Raheleh Vazehan, Kimia Kahrizi, Payman Jamali, Seyedeh Sedigheh Abedini, Faezeh Mojahedi, Mehrshid Faraji Zonooz, Hans-Hilger Ropers, Vera M. Kalscheuer, Sanaz Arzhangi, Mahsa Fadaee, Zohreh Fattahi, Maryam Beheshtian, Zahra Kalhor, Mahboubeh Kamgar, Farahnaz Sabbagh Kermani, Elham Parsimehr
Publikováno v:
Clinical genetics. 95(6)
Neurodevelopmental delay and intellectual disability (ID) can arise from numerous genetic defects. To date, variants in the EXOSC gene family have been associated with such disorders. Using next-generation sequencing (NGS), known and novel variants i
Autor:
Mahsa Fadaee, Gholamreza Zamani, Hossein Najmabadi, Elham Parsimehr, Ayda Abolhassani, Mohammad R. Akbari, Kimia Kahrizi, Zahra Kalhor, Ariana Kariminejad, Shahriar Nafissi, Zohreh Fattahi, Maryam Beheshtian, Raheleh Vazehan, Yalda Nilipour
Publikováno v:
Clinical Genetics. 91:386-402
Neuromuscular diseases (NMDs) include a broad range of disorders affecting muscles, nerves and neuromuscular junctions. Their overlapping phenotypes and heterogeneous genetic nature have created challenges in diagnosis which calls for the implementat
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:
Zohreh Fattahi, Zahra Kalhor, Mehrshid Faraji Zonooz, Hossein Najmabadi, Ariana Kariminejad, Hilda Yazdan, Mahmoud Reza Ashrafi, Elham Rahimian
Publikováno v:
European journal of medical genetics. 62(9)
The seizure threshold 2 (SZT2) gene has been shown to confer a low seizure threshold and may enhance epileptogenesis in mice. However, its biological function is still not known. Mutations in SZT2 have been reported in very few patients and features