Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Seyed Mohammad-Kazem Nourbakhsh"'
Autor:
Samira Norzaee, Masud Yunesian, Arsalan Ghorbanian, Mahdi Farzadkia, Roshanak Rezaei Kalantary, Majid Kermani, Seyed Mohammad-Kazem Nourbakhsh, Aziz Eghbali
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-11 (2024)
Abstract We conducted a hospital-based case–control study to explore the association between proximity to various land use types and childhood leukemia and lymphoma. This research involved 428 cases of childhood leukemia and lymphoma (2016–2021),
Externí odkaz:
https://doaj.org/article/822a3d81e770401db4c4cb4cea240f42
Autor:
Abolfazl Khoshdel, Hajar Noormohammadi, Soleiman Kheiri, Roya Reisi, Seyed Mohammad-Kazem Nourbakhsh, Gholam Reza Panahandeh, Esfandiar Heidarian
Publikováno v:
Oman Medical Journal, Vol 31, Iss 5, Pp 332-335 (2016)
Objectives: Perinatal asphyxia (PA) is very significant in perinatal medicine due to the involvement of the central nervous system. This study was conducted to investigate the biochemical, clinical, and paraclinical changes associated with phenobarbi
Externí odkaz:
https://doaj.org/article/ea55047636fb4a43ba7c29781732fc41
Autor:
Behnaz Esmaeili, Behnaz Bayat, Mohamad Reza Fazlollahi, Leila Moradi, Arash Kalantari, Seyed Mohammad Kazem Nourbakhsh, Zahra Pourpak
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 20, Iss 6 (2021)
Autoimmune neutropenia is a type of immune-mediated neutropenia, caused by antibody-induced neutrophil destruction. Here we report two cases (3-year-old boy and 9-year-old girl) with suspected autoimmune neutropenia. The presence of neutrophil antibo
Externí odkaz:
https://doaj.org/article/1942f8e55e9c406e808e3c25de5516e6
Autor:
Arash Alghasi, Zohreh Hassanpour, Mohammad Bahadoram, Somayeh Ashrafi, Seyed Mohammad Kazem Nourbakhsh
Publikováno v:
Journal of Preventive Epidemiology, Vol 5, Iss 1, Pp e13-e13 (2020)
Introduction: Sickle cell disease (SCD) is a genetic disorder that can be diagnosed by early onset screening tests. In embryos and newborns with sickle cell syndrome, the anatomic development and brain circulation is less than the normal people, and
Externí odkaz:
https://doaj.org/article/c345b6f83d9d46439e2209ca7d68d9f4
Autor:
Mohammadreza Salehi, Seyed Mohammad Kazem Nourbakhsh, Mohammad Vahedian Ardakani, Alireza Abdollahi, Pegah Afarinesh Khaki, Amir Aliramezani
Publikováno v:
International journal of surgery case reports. 95
Introduction and importance Nontyphoidal Salmonella infection can lead to gastroenteritis, enteric fever, and bacteremia. However, joint infections due to this bacterium are rare, and usually associated with immunosuppressive disorders. Case presenta
Autor:
Rostampour, Noushin1,2, Seyed Mohammad Kazem Nourbakhsh3 dr.nourbakhsh2010@gmail.com, Navabfar, Narges4, Bahadoram, Mohammad5
Publikováno v:
Journal of Parathyroid Disease. 2019, Vol. 7 Issue 1, p7-12. 6p.
Autor:
Roya Reisi, Hajar Noormohammadi, Soleiman Kheiri, Abolfazl Khoshdel, Gholam Reza Panahandeh, Esfandiar Heidarian, Seyed Mohammad-Kazem Nourbakhsh
Publikováno v:
Oman Medical Journal, Vol 31, Iss 5, Pp 332-335 (2016)
Objectives: Perinatal asphyxia (PA) is very significant in perinatal medicine due to the involvement of the central nervous system. This study was conducted to investigate the biochemical, clinical, and paraclinical changes associated with phenobarbi
Autor:
Elham Hashemi Dehkordi, Seyed Mohammad Kazem Nourbakhsh, Noushin Rostampour, Fateme Alizadeh Boroujeni
Publikováno v:
International Journal of Preventive Medicine
International Journal of Preventive Medicine, Vol 5, Iss 10, Pp 1269-1273 (2014)
International Journal of Preventive Medicine, Vol 5, Iss 10, Pp 1269-1273 (2014)
Background: Understanding the possible role of visfatin in the pathogenesis of beta-thalassemia major (BTM) and its relationship with markers of endothelial function could help us to provide more effective therapeutic approaches for treatment of pati
Autor:
Seyed Mohammad Kazem Nourbakhsh, Mohammad Bahadoram, Ali Rashidi‐Nezhad, Laleh Habibi, Fatemeh Mansouri, Esma'il Akade
Publikováno v:
Clinical Case Reports, Vol 11, Iss 12, Pp n/a-n/a (2023)
Key Clinical Message Purpura fulminans is a severe coagulation disorder that often leads to death in neonates. Mutations in the protein C (PROC) gene can cause protein C deficiency, leading to this disorder. This study aimed to investigate a family w
Externí odkaz:
https://doaj.org/article/195fcb6dc14243d8948528e29ffc39a8