نتایج جستجو برای: Severe Combined Immunodeficiency (SCID)

تعداد نتایج: 787021  

2003
Rebecca H. Buckley Daniel A. Ozaki Shui Cao Scott Langdon Marcella Sarzotti Dhavalkumar D. Patel Xiaojing Li Roberta E. Parrott Katherine Coyne

Abbasi S Honaramooz A

Background: The aim of the present study was to examine factors that may affect the outcome of testis tissue xenografting. Recipient factors were examined by grafting small fragments of testis tissue from newborn piglets under the back skin of immunodeficient mice of different strains [severe combined immunodeficiency (SCID) vs. nude), sex (male vs. female) and gonadal status (intact vs. gonade...

Farhad Abolnezhadian, Maryam Khoshkhui Soheyla Alyasin

Major histocompatibility complex (MHC) class II deficiency is a primary immunodeficiency disease characterized by abnormality of MHC class II molecules surface expression on peripheral blood lymphocytes and monocytes. Clinical manifestations include extreme susceptibility to viral, bacterial, and fungal infections but the immunodeficiency is not as severe as SCID (severe combined immunodeficien...

قرگزلو, محمد, مردانی حموله, مرجان, نژادسروری, نسرین, کدیور, ملیحه,

Severe combined immunodeficiency (SCID) is an inherited primary immunodeficiency syndrome characterized by a profound deficiency in T-lymphocytes and variable defects in the B-lymphocyte number. The present study aimed to evaluate the ethical aspects of the clinical management of children with SCID. This report is based on the case of a 6-month-old male infant with SCID diagnosis presented duri...

Severe Combined Immunodeficiency (SCID), characterized by a profound decrease in both the number and function of T cells, is related to more than 20 different mutations. Recombination-activating gene (RAG) 1 and 2 seem to be two of the most common forms presenting with various manifestations, including typical SCID, Omenn syndrome (OS), atypical SCID (AS), or delayed onset combined immunodefici...

Journal: :iranian journal of immunology 0
soheyla alyasin clinical immunology and allergy, allergy research center farhad abolnezhadian department of pediatrics, division of immunology and allergy, namazi hospital, shiraz university of medical sciences, shiraz maryam khoshkhui department of clinical immunology and allergy, mashhad university of medical science , mashhad, iran

major histocompatibility complex (mhc) class ii deficiency is a primary immunodeficiency disease characterized by abnormality of mhc class ii molecules surface expression on peripheral blood lymphocytes and monocytes. clinical manifestations include extreme susceptibility to viral, bacterial, and fungal infections but the immunodeficiency is not as severe as scid (severe combined immunodeficien...

Bahrami, Ahmad , Rezaei, Nima , Smaeelnezhad, Hamideh , Vafapour, Maryam ,

Severe combined immunodeficiency is a rare, fatal syndrome of diverse genetic cause in which there is combined absence of T-lymphocyte and B-lymphocyte function (and in many cases also natural killer, or NK lymphocyte function). These defects lead to extreme susceptibility to serious infections. Without intervention, the T and B-cell dysfunction usually results in severe infection and death in ...

Journal: :iranian journal of allergy, asthma and immunology 0
sepideh safaei immunology, asthma & allergy research institute , children’s medical center, tehran university of medical sciences, tehran, iran zahra pourpak immunology, asthma & allergy research institute , children’s medical center, tehran university of medical sciences, tehran, iran mostafa moin immunology, asthma & allergy research institute , children’s medical center, tehran university of medical sciences, tehran, iran massoud houshmand national institute for genetic engineering and biotechnology, tehran, iran

scid disorder is major failure of the immune system, usually genetic. the aim of this study was on mutations detection of rag1, rag2, and il7rg genes in scid cases. mutation detection was performed by pcr sequencing. our results  indicated  that 13  mutations  were found  through  cases which  include 4 mutations in il7r gene (t661i, i138v, t56a, c57w), 7 mutations in rag1 (w896x, w204r, m324v,...

Journal: :archives of pediatric infectious diseases 0
abdollah karimi pediatric infections research center, mofid children’s hospital, shahid beheshti university of medical sciences, tehran, ir iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) sedigheh rafiei tabatabaei pediatric infections research center, mofid children’s hospital, shahid beheshti university of medical sciences, tehran, ir iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) ali amanati pediatric infections research center, mofid children’s hospital, shahid beheshti university of medical sciences, tehran, ir iran; pediatric infections research center, department of pediatric infectious diseases, mofid children’s hospital, shahid beheshti university of medical sciences, tehran, ir iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) javad ghoroubi mofid children’s hospital, shahid beheshti university of medical sciences, tehran, ir iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) mohsen karami mofid children’s hospital, shahid beheshti university of medical sciences, tehran, ir iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences)

introduction bacillus calmette-guérin (bcg) vaccine, a live attenuated mycobacterium bovis strain, is administrated to all newborn infants in endemic regions according to the current world health organization (who) recommendation. case presentation we report a 10-month-boy who was a known case of severe combined immunodeficiency (scid) admitted with multi-focal fusiform painful swelling in his ...

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