Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Sedigheh Nikbakht"'
Autor:
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
Publikováno v:
Human Genomics, Vol 18, Iss 1, Pp 1-18 (2024)
Abstract Background To investigate the genetics of early-onset progressive cerebellar ataxia in Iran, we conducted a study at the Children’s Medical Center (CMC), the primary referral center for pediatric disorders in the country, over a three-year
Externí odkaz:
https://doaj.org/article/73901f9896264335a878fdd5b263980b
Autor:
Reyhaneh Kameli, Man Amanat, Zahra Rezaei, Sareh Hosseionpour, Sedigheh Nikbakht, Houman Alizadeh, Mahmoud Reza Ashrafi, Abdolmajid Omrani, Masoud Garshasbi, Ali Reza Tavasoli
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-7 (2019)
Abstract Background Ribonucleases (RNases) are crucial for degradation of ribosomal RNA (rRNA). RNASET2 as a subtype of RNASEs is a 256 amino acid protein, encoded by RNASET2 gene located on chromosome six. Defective RNASET2 leads to RNASET2-deficien
Externí odkaz:
https://doaj.org/article/da85c8a47676435d916fcf8992d52ec5
Autor:
Mozhgan Hashemieh, Mitra Radfar, Azita Azarkeivan, Seyed Mohammad Taghi Hosseini Tabatabaei, Sedigheh Nikbakht, Mehdi Yaseri, Kourosh Sheibani
Publikováno v:
International Journal of Hematology-Oncology and Stem Cell Research, Vol 11, Iss 2 (2017)
Background:In recent years, the success in management of thalassemic patients, has allowed for some previously unrecognized complications including renal abnormalities to emerge. This prospective study aimed to investigate kidney iron overload by mea
Externí odkaz:
https://doaj.org/article/d6c055241644444d80e466030fabecd0
Autor:
Gholam Reza Zamani, Sedigheh Nikbakht, Ali Reza Tavasoli, Mostafa Qorbani, Morteza Heidari, Zahra Rezaei, Reza Azizi Malamiri, Parastoo Rostami, Mojtaba Movahedinia, Mahmoud Mohammadi, Reza Shervin Badv, Mahmoud Reza Ashrafi, Man Amanat
Publikováno v:
Journal of Child Neurology. 33:255-259
Childhood leukodystrophies are a fast-growing field of pediatric neurology practice. Epidemiologic studies on the incidence of these disorders in children show different results. This is the first report of childhood leukodystrophies incidence from I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f17d8a5ac5efd90b23c0f24f25d317af
https://doi.org/10.1177/0883073817751804
https://doi.org/10.1177/0883073817751804
Autor:
Sareh Hosseionpour, Mahmoud Reza Ashrafi, Masoud Garshasbi, Man Amanat, Reyhaneh Kameli, Abdolmajid Omrani, Sedigheh Nikbakht, Houman Alizadeh, Ali Reza Tavasoli, Zahra Rezaei
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-7 (2019)
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-7 (2019)
Background Ribonucleases (RNases) are crucial for degradation of ribosomal RNA (rRNA). RNASET2 as a subtype of RNASEs is a 256 amino acid protein, encoded by RNASET2 gene located on chromosome six. Defective RNASET2 leads to RNASET2-deficient leukoen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7da80e125e25432197d0b9fe0f5860bf
http://europepmc.org/articles/PMC6660666
http://europepmc.org/articles/PMC6660666