Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Atefeh, Valaei"'
Autor:
Atefeh Valaei, Sobhan Bamdad, Arsalan Golfam, Golnoosh Golmohammadi, Hayat Ameri, Mohammad Reza Raoufy
Publikováno v:
Frontiers in Human Neuroscience, Vol 18 (2024)
IntroductionStuttering is a speech disorder characterized by impaired connections between brain regions involved in speech production. This study aimed to investigate functional connectivity and frequency power during rest in adults who stutter (AWS)
Externí odkaz:
https://doaj.org/article/ea37b2a6b81546c2bd615e2b6b591ce3
Publikováno v:
Iranian Biomedical Journal
Alpha-thalassemia (α-thal) is probably the most prevalent monogenic condition in the world. Deletions are the most common types of mutations in α-thal, followed by point mutations and small insertion/deletion. In the context of national screening p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::81c8eede50218d3dba4dabf1b6632603
https://pubmed.ncbi.nlm.nih.gov/29115104
https://pubmed.ncbi.nlm.nih.gov/29115104
Autor:
Azam Amirian, Atefeh Valaei, Fereshteh Maryami, Sirous Zeinali, Morteza Karimipoor, Alireza Kordafshari
Publikováno v:
Hemoglobin. 40(1)
δ-Thalassemia (δ-thal) (OMIM #142000) resulting from mutations on the HBD gene usually has no clinical consequences. However, it may cause the misdiagnosis of β-thalassemia (β-thal) carriers by lowering the Hb A2 level to the normal range. Theref
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03c41d05b2ec4dddc5750e6a3e30ab53
https://pubmed.ncbi.nlm.nih.gov/26754299
https://pubmed.ncbi.nlm.nih.gov/26754299
Publikováno v:
Hemoglobin. 33:417-421
beta-Thalassemia (beta-thal) is a major health problem in Iran and the incidence of carriers is around 3-4%. The disease is caused by heterogeneous mutations in the beta-globin gene and is characterized by hypochromic microcytic anemia. The human bet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6249843ba77630329cc4937147dea4a6
https://doi.org/10.3109/03630260903327817
https://doi.org/10.3109/03630260903327817
Autor:
Zahra, Kainimoghaddam, Atefeh, Valaei, Fatemeh, Bayat, Maryam, Taghavi Basmanj, Fatemeh, Navabmoghaddam, Marjanalsadat, Mortezazadeh, Ladan, Teimoori-Toolabi, Setareh, Ahmadi, Shaghayegh, Sadegh, Alireza, Kordafshari, Morteza, Karimipoor, Sirous, Zeinali
Publikováno v:
Archives of Iranian medicine. 16(10)
Prenatal diagnosis of β-thalassemia carrier couples has helped to prevent bearing affected children. Among 177 couples referred to our laboratory for prenatal diagnosis, 14 mothers had twin pregnancies. By using direct and indirect methods, we deter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9077ead539cf8d970b64796f2d855608
https://pubmed.ncbi.nlm.nih.gov/24093136
https://pubmed.ncbi.nlm.nih.gov/24093136
Publikováno v:
Clinical Biochemistry. 44:S293
C677TpolymorphismofMTHFRgenewere77, 22 and1% inpreeclamptic women and 73, 19.5 and 7.5% in controls and significantly were not different(P=0.06). But the frequency of TT genotype was significantly higher in controls. OR=8.5 (95% CI 1.1–71, P=.018).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce9aaa49e1741316b8361d59fca32731
https://doi.org/10.1016/j.clinbiochem.2011.08.736
https://doi.org/10.1016/j.clinbiochem.2011.08.736
Autor:
Sirous Zeinali, Alireza Kordafshari, Atefeh Valaei, Farnaz Eghbalpour, Morteza Karimipour, Zahra Kainimoghaddam, Fatemeh Navabmoghaddam
Publikováno v:
Clinical Biochemistry. 44:S292
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2541bae237c6822844858fc2cd50773
https://doi.org/10.1016/j.clinbiochem.2011.08.734
https://doi.org/10.1016/j.clinbiochem.2011.08.734
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Akademický článek
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