Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Asghar Ramyar"'
Publikováno v:
Acta Medica Iranica, Vol 55, Iss 1 (2017)
Hemophagocytic lymphohistiocytosis (HLH) is a syndrome of pathologic immune activation, occurring as either a familial disorder or a sporadic condition, in association with a variety of triggers. This article will introduce a neonate with HLH in Iran
Externí odkaz:
https://doaj.org/article/5060f803d51847c18ce2ca755173399a
Autor:
Asghar Ramyar, Asghar Aghamohammadi, Hossein Mozdarani, Majid Mahmoodi, Cyrus Azimi, Zahra Safari, Hassan-Ali Nedaei, Fareedeh Farzanfar, Nima Rezaei, Majid Asadi-Shekaari, Mahbod Esfahani, Seyed Kazem Hosseini, Mahdi Yazdani, Hassan Abolhassani, Fatemeh Khalesi, Mohamad Ali Mohagheghi
Publikováno v:
Basic & Clinical Cancer Research, Vol 3, Iss 2 (2016)
Background: Acute lymphoblastic leukemia (ALL) constitutes a heterogeneous group of diseases characterized by abnormal proliferation and accumulation of immature lymphoblasts arrested at various differentiation stages. Increasing evidence suggests th
Externí odkaz:
https://doaj.org/article/b9d4418205374c38a1cc864c328e5415
Autor:
Azim Mehrvar, Mohammad Saeid Rahiminejad, Amir Abbas Hedayati Asl, Maryam Tashvighi, Mohammad Faranoush, Mardawig Alebouyeh, Leili Kuchakzadeh, Asghar Ramyar, Javad Sabery nejad, Narjes Mehrvar
Publikováno v:
Acta Medica Iranica, Vol 53, Iss 12 (2015)
Acute Myeloblastic Leukemia is one of the important malignancies in children. For better managing the prognosis of this disease, there should be enough information about common features of this malignancy. The aim of this study was to evaluate these
Externí odkaz:
https://doaj.org/article/ca77cf6243584a15b79f96ce6be72ab0
Autor:
Behdad Gharib, Mina Almasi, Sara Esmaeili, Soheila Sotoudeh, Maryam Monajemzadeh, Asghar Ramyar, Hossein Farshadmoghadam, Farah Sabouni
Publikováno v:
Acta Medica Iranica, Vol 52, Iss 4 (2014)
We presents an infant with several indurated plaques and nodules scattered on her body. She was brought to the hospital because of fever, runny nose and cough from one month ago. During the examination and investigation the plaques and nodules grabbe
Externí odkaz:
https://doaj.org/article/4219b447332449968a47223019047ecc
Autor:
Nima Rezaei, Abolhassan Farhoudi, Zahra Pourpak, Asghar Aghamohammadi, Asghar Ramyar, Mostafa Moin, Mohammad Gharagozlou, Masoud Movahedi, Behzad Mohammadpour, Bahram MirSaeid Ghazi, Mina Izadyar, Maryam Mahmoudi
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 3, Iss 1 (2004)
Cyclic neutropenia is a rare immunodeficiency syndrome, characterized by regular periodic oscillations in the circulating neutrophil count from normal to neutropenic levels through 3 weeks period, and lasting for 3-6 days. In order to determine the c
Externí odkaz:
https://doaj.org/article/fef6777621714811895eab0f9a2cbbf0
Autor:
Gholamreza Azizi, Mohammad Ali Mohagheghi, Rasoul Nasiri Kalmarzi, Asghar Aghamohammadi, Hosein Rafiemanesh, Nima Rezaei, Kouros Divsalar, Hossein Mozdarani, Asghar Ramyar, Hassan Abolhassani, Farideh Farzanfar, Majid Mahmoodi, Reza Yazdani
Publikováno v:
Central-European Journal of Immunology
Common variable immunodeficiency (CVID) is one of the predominant antibody deficiency disorders, some evidence of which indicates that chromosome instability is present in these patients. An increased risk of cancer in patients with CVID has been doc
Publikováno v:
International Archives of Allergy and Immunology. 147:255-259
Severe congenital neutropenia (SCN) and CD40 ligand deficiency (CD40LD) are two primary immunodeficiency diseases caused by different underlying genetic defects. In this report, we present a case who clinically presented as a SCN patient, but subsequ
Autor:
Zahra Pourpak, Mostafa Moin, Maryam Mahmoudi, Magda Grudzien, Marshall S. Horwitz, Roya Sherkat, Fatemeh Mahjoub, Asghar Aghamohammadi, Manuela Germeshausen, Mina Izadyar, Mehdi Yeganeh, Abolhassan Farhoudi, Zahra Chavoshzadeh, Christoph Klein, Asghar Ramyar, Nima Rezaei
Publikováno v:
Journal of Clinical Immunology. 27:525-533
Severe congenital neutropenia (SCN) is a rareE primary immunodeficiency disorder characterized by early onset recurrent infections in association with persistent severe agranulocytosis. To identify the clinical, immunohematological, and molecular cha
Publikováno v:
European Journal of Inflammation, Vol 5 (2007)
Severe congenital neutropenia (SCN), often referred to as Kostmann syndrome, is a rare immune deficiency syndrome diagnosed at or soon after birth, characterized by maturation arrest of myeloid cells at the promyelocyte stage of hematopoiesis. In sev
Autor:
Mostafa Moin, Asghar Ramyar, Mohammad Gharagozlou, Kiara Rezaei-Kalantari, Nima Rezaei, Asghar Aghamohammadi, Fatemeh Mahjoub
Publikováno v:
Pediatric Hematology and Oncology. 24:337-342
Common variable immunodeficiency (CVID) is a heterogeneous group of disorders, characterized by decreased serum immunoglobulin levels, and increased susceptibility to recurrent bacterial infections, malignancies, and autoimmune disorders. In this rep