Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Sepideh Shahkarami"'
Autor:
Elham Rayzan, Mona Sadeghalvad, Sepideh Shahkarami, Samaneh Zoghi, Zahra Aryan, Seyed Alireza Mahdaviani, Kaan Boztug, Nima Rezaei
Publikováno v:
Journal of Medical Case Reports, Vol 17, Iss 1, Pp 1-7 (2023)
Abstract Background X-linked severe combined immunodeficiency is caused by IL2RG gene mutation. Several variations have been identified in the IL2RG gene, which potentially can prevent the production of nonfunctional proteins. Herein, a novel X-linke
Externí odkaz:
https://doaj.org/article/3a4da6bb995544f2a6a77cdc0364ef17
Autor:
Sepideh Shahkarami, Samareh Younesian, Shahrbano Rostami, Farzad Kompani, Davood Bashash, Seyed Mousavi, Seyed Ghaffari
Publikováno v:
Cell Journal, Vol 25, Iss 2, Pp 85-91 (2023)
Objective: Minimal residual disease (MRD) is considered the greatest prognostic factor in acute lymphoblastic leukemia(ALL). MRD is a valuable tool for anticipating impending relapse and treatment response assessment. The objective ofthe present stud
Externí odkaz:
https://doaj.org/article/405207f106af4f929872eed85a2a5988
Autor:
Fatemeh Sodeifian, Noosha Samieefar, Sepideh Shahkarami, Elham Rayzan, Simin Seyedpour, Meino Rohlfs, Christoph Klein, Delara Babaie, Nima Rezaei
Publikováno v:
Case Reports in Medicine, Vol 2023 (2023)
Background. Primary ciliary dyskinesia (PCD), also known as the immotile-cilia syndrome, is a clinically and genetically heterogeneous syndrome. Improper function of the cilia causes impaired mucociliary clearance. Neonatal respiratory distress, rhin
Externí odkaz:
https://doaj.org/article/c73f774e21704c209edc96daffcd871f
Autor:
Sara Momtazmanesh, Elham Rayzan, Sepideh Shahkarami, Meino Rohlfs, Christoph Klein, Nima Rezaei
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-6 (2020)
Abstract Background Cohen syndrome, an autosomal recessive syndrome, is a rare syndrome with diverse clinical manifestations including failure to thrive, hypotonia, hypermobile joints, microcephaly, intellectual disabilities, craniofacial and limb an
Externí odkaz:
https://doaj.org/article/2ac1c58069254cbf8a4995ca13ea5bd2
Autor:
Zahra Hamidi Esfahani, Reza Yazdani, Sepideh Shahkarami, Fateme Babaha, Hassan Abolhassani, Maryam Sadr, Ali Akbar Pourfathollah, Asghar Aghamohammadi
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 20, Iss 6 (2021)
Common variable immunodeficiency (CVID) is the most prevalent form of symptomatic primary humoral immunodeficiencies characterized by failure in the final differentiation of B lymphocytes. The majority of CVID cases have no identified genetic defect,
Externí odkaz:
https://doaj.org/article/6cfbbfef2b4a4197a7ba1405fef2397f
Autor:
Sepideh Shahkarami, Nima Rezaei
Publikováno v:
Acta Medica Iranica, Vol 51, Iss 1 (2013)
No Abstract
Externí odkaz:
https://doaj.org/article/f7347772951547c5ae7f4d7baadcbc4a
Autor:
Sepideh Shahkarami, Nima Rezaei
Publikováno v:
Acta Medica Iranica, Vol 50, Iss 10 (2012)
No Abstract
Externí odkaz:
https://doaj.org/article/3c34d602d5414040956c32f54b81fb53
Autor:
Nima Rezaei, Sepideh Shahkarami
Publikováno v:
Acta Medica Iranica, Vol 50, Iss 10, Pp 721-722 (2012)
Externí odkaz:
https://doaj.org/article/dab3dc854308475f9344f7a665824c7f
Autor:
Nima Rezaei, Hossein Esmaeilzadeh, Arya Aminorroaya, Elham Rayzan, Sepideh Shahkarami, Simin Seyedpour, Samaneh Zoghi, Zahra Aryan, Ido Somekh, Meino Rohlfs, Christoph Klein
Publikováno v:
Endocrine, Metabolic & Immune Disorders - Drug Targets. 23:410-415
Background: Immunodeficiency, centromeric instability, and facial anomalies (ICF) syndrome is a rare autosomal recessive disorder. ICF1 is caused by bi-allelic mutations in the gene encoding deoxyribonucleic acid methyltransferase-3B (DNMT3B). Herein
Autor:
Nima Rezaei, Khashayar Danandeh, Parnian Jabbari, Elham Rayzan, Samaneh Zoghi, Sepideh Shahkarami, Raul Jimenez Heredia, Ana Krolo, Bibi Shahin Shamsian, Kaan Boztug
Publikováno v:
Endocrine, Metabolic & Immune Disorders - Drug Targets. 22:1040-1046
Background: Lymphoproliferative disorders include a heterogeneous list of conditions that commonly involve dysregulation of lymphocyte proliferation resulting in lymphadenopathy and bone marrow infiltration. These disorders have various presentations