Zobrazeno 1 - 10
of 70
pro vyhledávání: '"Gholamreza, Shariati"'
Autor:
Farhad Abolnezhadian, Sara Iranparast, Mojtaba Shohan, Zahra Shokati Eshkiki, Mahtab Hamed, Maryam Seyedtabib, Roohangiz Nashibi, Mohammad-Ali Assarehzadegan, Seyed Ali Mard, Ali Akbar Shayesteh, Niloofar Neisi, Manoochehr Makvandi, Seyed Mohammad Alavi, Gholamreza Shariati
Publikováno v:
Heliyon, Vol 10, Iss 7, Pp e28528- (2024)
Background: Severe acute respiratory syndrome coronavirus 2 was first reported in December 2019 and it has spread globally ever since. The HLA system is crucial in directing anti-viral immunity and recent studies are investigating the possible involv
Externí odkaz:
https://doaj.org/article/afa25566f62e44e9a5a19d1cb16e2263
Autor:
Rezvan Zabihi, Mina Zamani, Majid Aminzadeh, Niloofar Chamanrou, Fatemeh Zahra Kiani, Tahere Seifi, Jawaher Zeighami, Tahere Yadegari, Alireza Sedaghat, Alihossein Saberi, Mohammad Hamid, Gholamreza Shariati, Hamid Galehdari
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Introduction: Mucopolysaccharidoses are a group of lysosomal storage disorders that include seven types that are classified based on the enzymes that are disrupted. Malfunction of these enzymes leads to the accumulation of glycosaminoglycans (GAGs) i
Externí odkaz:
https://doaj.org/article/10be7dec0c684c42be05458add309a27
Autor:
Rauan Kaiyrzhanov, Maha S. Zaki, Tracy Lau, Sambuddha Sen, Reza Azizimalamiri, Mina Zamani, Gözde Yeşil Sayin, Taru Hilander, Stephanie Efthymiou, Viorica Chelban, Ruth Brown, Kyle Thompson, Maria Irene Scarano, Jaya Ganesh, Kairgali Koneev, Ismail Musab Gülaçar, Richard Person, Dinara Sadykova, Yerdan Maidyrov, Tahereh Seifi, Aizhan Zadagali, Geneviève Bernard, Katrina Allis, Houda Zghal Elloumi, Amanda Lindy, Ehsan Taghiabadi, Sumit Verma, Rachel Logan, Brian Kirmse, Renkui Bai, Shaimaa M. Khalaf, Mohamed S. Abdel‐Hamid, Alireza Sedaghat, Gholamreza Shariati, Mahmoud Issa, Jawaher Zeighami, Hasnaa M. Elbendary, Garry Brown, Robert W. Taylor, Hamid Galehdari, Joseph J. Gleeson, Christopher J. Carroll, James A. Cowan, Andres Moreno‐De‐Luca, Henry Houlden, Reza Maroofian
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 9, Iss 12, Pp 2025-2035 (2022)
Abstract Bi‐allelic variants in Iron–Sulfur Cluster Scaffold (NFU1) have previously been associated with multiple mitochondrial dysfunctions syndrome 1 (MMDS1) characterized by early‐onset rapidly fatal leukoencephalopathy. We report 19 affecte
Externí odkaz:
https://doaj.org/article/711cfaa4bbdd40c88cf90df5e876adc6
Autor:
Mohammad Hamid, Bijan keikhaei, Hamid Galehdari, Alihossein Saberi, Alireza Sedaghat, Gholamreza Shariati, Marziye Mohammadi-Anaei
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-7 (2022)
Abstract We studied the alpha-globin gene genotypes, hematologic values, and transfusion-dependence of patients with Hb H disease. Molecular characterization of alpha-thalassemia was performed. We identified 120 patients with Hb H disease. Of these p
Externí odkaz:
https://doaj.org/article/705c41e1ec984ca0873e9ba140e7c232
Autor:
Atefe Papi, Mina Zamani, Gholamreza Shariati, Alireza Sedaghat, Tahere Seifi, Samira Negahdari, Sahar Sadat Sedighzadeh, Jawaher Zeighami, Alihossein Saberi, Mohammad Hamid, Hamid Galehdari
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 2, Pp n/a-n/a (2023)
Abstract Background Congenital disorder of glycosylation (CDG) and Glycogen storage diseases (GSDs) are inborn metabolic disorders caused by defects in some metabolic pathways. These disorders are a heterogeneous group of diseases caused by impaired
Externí odkaz:
https://doaj.org/article/e7160f880c5e4592936d54159ff4662d
Autor:
Mohammad Hamid, Bijan keikhaei, Hamid Galehdari, Alihossein Saberi, Alireza Sedaghat, Gholamreza Shariati, Marziye Mohammadi‐Anaei
Publikováno v:
eJHaem, Vol 2, Iss 3, Pp 366-374 (2021)
Abstract The genotype and phenotype correlation between coinheritance of heterozygous beta‐thalassemia with the alpha‐globin triplication is unclear. In this study we have investigated and reviewed alpha triplication frequency in beta‐thalassem
Externí odkaz:
https://doaj.org/article/d6c6b109f1b7465fb91a3bb7d6af75af
Autor:
Mina Zamani, Tahereh Seifi, Jawaher Zeighami, Neda Mazaheri, Emad Jahangirnezhad, Minoo Gholamzadeh, Alireza Sedaghat, Gholamreza Shariati, Hamid Galehdari
Publikováno v:
Basic and Clinical Neuroscience, Vol 11, Iss 4, Pp 549-556 (2020)
Introduction: Whole Exome Sequencing (WES) has been increasingly utilized in genetic determinants of various inherited diseases. Methods: We applied WES for a patient presenting 3-Methylglutaconic Aciduria (MEG), Deafness (D), Encephalopathy (E), and
Externí odkaz:
https://doaj.org/article/dcfa234a49af4b1187b40b154d1921c0
Publikováno v:
Jornal de Pediatria (Versão em Português), Vol 96, Iss 1, Pp 60-65 (2020)
Objective: Permanent hypoparathyroidism can be presented as part of genetic disorders such as Sanjad–Sakati syndrome (also known as hypoparathyroidism—intellectual disability‐dysmorphism), which is a rare autosomal recessive disorder. Our aim w
Externí odkaz:
https://doaj.org/article/2f3fa6b3819841979a2fe60ad262b4bf
Autor:
Negar Noorbakhsh, Mina Zamani, Alireza Sedaghat, Jawaher Zeighami, Farangis Foroughi, Sahere Parvas, Alihossein Saberi, Mohammad Hamid, Roya Ghanavati, Gholamreza Shariati, Hamid Galehdari
Publikováno v:
OBM Genetics. :1-16
Familial Mediterranean Fever (FMF) is classified as an autoinflammatory genetic disease inherited by mutations in MEFV. These mutations can affect the dysregulation of inflammatory processes in the human body and lead to fever and pain in the chest a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c6b21ebcdf1f27d42446676d8a70933
https://doi.org/10.21926/obm.genet.2302181
https://doi.org/10.21926/obm.genet.2302181
Autor:
Farhad Abolnezhadian, Manoochehr Makvandi, Seyed Mohammad Alavi, Azarakhsh Azaran, Shahram Jalilian, Mohammad Rashno, Gholam Abbas Kaydani, Maniya Arshadi, Seyed Mehdi Hosseinizadeh, Hatam Boostani, Seyed Saeed Seyedian, Sasan Moogahi, Shokrolah Salmanzadeh, Mehran Varnaseri, Niloofar Neisi, Hooman Keifarrokhi, Gholamreza Shariati, Homayoun Amiri, Mehdi Parsanahad, Roohangiz Nashibi, Farid Yousefi, Fatemeh Ahmadi, Kambiz AhmadiAngali
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 19, Iss 5 (2020)
The emergence of a highly pathogenic virus named severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) accounts for severe pneumonia throughout the world. More than 7 million world population have been infected with SARS-CoV-2, and the number
Externí odkaz:
https://doaj.org/article/0c1d311d58b1410a9ad5a4e5dd0d196c