Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ehsan Jaripour"'
Autor:
Mohammad Ehsan Jaripour, Kourosh Hayatigolkhatmi, Vahid Iranmanesh, Farhad Khadivi Zand, Zahra Badiei, Hamid Farhangi, Ali Ghasemi, Abdollah Banihashem, Reza Jafarzadeh Esfehani, Ariane Sadr-Nabavi
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 10, Iss 1, Pp e2018042-e2018042 (2018)
Background and objective: ß-thalassemia results from a diverse range of mutations inside the hemoglobin subunit β (HBB) gene. In a study of β-thalassemia carriers and some of their at-risk fetuses in the Khorasan province of Iran we aimed to recog
Externí odkaz:
https://doaj.org/article/d9e9d272f7464e4b9808e56afd273a8c
Autor:
Mohammad Pourafshar, Ariane Sadr-Nabavi, Somayyeh Hashemian, Narjes Forouzanfar, Samaneh Vojdani, Mohammadreza Mirinezhad, Mohammad Ehsan Jaripour, Reza Jafarzadeh-Esfehani, Selma Zargari
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 33:355-359
Background Phenylketonuria (PKU) is a common metabolic disorder with great burden if left untreated or undiagnosed. Genetic variations in the phenylalanine hydroxylase (PAH) gene may be widely varied across different regions of a country. By knowing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1daf9beacba5e7d0ba3895c7457390a
https://doi.org/10.1515/jpem-2019-0351
https://doi.org/10.1515/jpem-2019-0351
Autor:
Reza Jafarzadeh Esfehani, Masood Zahmatkesh, Reza Goldozian, Javad Farkhonde, Ehsan Jaripour, Asghar Hatami, Hamid Reza Bidkhori, Seyyed Khosro Shamsian, Seyyed AliAkbar Shamsian, Faezeh Mojahedi
Publikováno v:
Clinical and Experimental Vaccine Research. 12:25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d61a95a87c2bd5e5e2558ba2487b78da
https://doi.org/10.7774/cevr.2023.12.1.25
https://doi.org/10.7774/cevr.2023.12.1.25
Autor:
Arash Salmaninejad, Ariane Sadr-Nabavi, Hassan Darabi, Mahmoud Reza Azarpazhooh, Mohamad Ehsan Jaripour, Majid Mojarrad
Publikováno v:
Journal of Cellular Physiology. 234:3874-3886
Stroke is one of the most common type of cerebrovascular disease threatening human health and life with high mortality, disability, and morbidity. Ischemic stroke (IS) is determined to be a complex disease containing a group of heterogeneous disorder
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9bba30d5390e5eac216cdf5a4e413bf
https://doi.org/10.1002/jcp.27159
https://doi.org/10.1002/jcp.27159
Autor:
Samaneh, Vojdani, Reza, Jafarzadeh Esfehani, Vahid, Iranmanesh, Hafezeh, Davari, Nafiseh, Amini, Mohammad Ehsan, Jaripour, Peyman, Zargari, Mahtab, Dastpak, Ariane, Sadrnabavi
Publikováno v:
Iranian Journal of Otorhinolaryngology
Introduction: Hearing impairment is a complex medical disorder which has genetic and non-genetic causes. Gap Junction Protein Beta 2 (GJB2) gene variant is a well-known disease-causing gene among patients with hearing impairment. The frequencies of g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e2795b647450838102c499925f5b76ea
https://pubmed.ncbi.nlm.nih.gov/30989077
https://pubmed.ncbi.nlm.nih.gov/30989077
Molecular Evaluation of Children with Clinical Russell-Silver Phenotypes: The First Report From Iran
Autor:
Mohammad Ehsan Jaripour, Reza Jafarzadeh Esfehani, Rahim Vakili, Ariane Sadr-Nabavi, Somayyeh Hashemian
Publikováno v:
Iranian Journal of Pediatrics.
Background: Russell-Silver syndrome is a rare heterogeneous genetic disorder that is mostly known because of its prenatal and postnatal growth retardation. Patients with Russell-Silver syndrome have syndromic facial appearance, as well as some other
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32361470e5eb6ceda7fe03fb7230dd05
https://doi.org/10.5812/ijp.81388
https://doi.org/10.5812/ijp.81388
Autor:
Kourosh Hayatigolkhatmi, Ali Ghasemi, Zahra Badiei, Mohammad Ehsan Jaripour, Abdollah Banihashem, Hamid Farhangi, Vahid Iranmanesh, Reza Jafarzadeh Esfehani, Farhad Khadivi zand, Ariane Sadr-Nabavi
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 10, Iss 1, Pp e2018042-e2018042 (2018)
Mediterranean Journal of Hematology and Infectious Diseases
Mediterranean Journal of Hematology and Infectious Diseases
Background and objective: ß-thalassemia results from a diverse range of mutations inside the hemoglobin subunit β (HBB) gene. In a study of β-thalassemia carriers and some of their at-risk fetuses in the Khorasan province of Iran we aimed to recog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c742e22a907c274195ad29fcb7188eb
https://doi.org/10.4084/mjhid.2018.042
https://doi.org/10.4084/mjhid.2018.042