نتایج جستجو برای: severe combined

تعداد نتایج: 686486  

Journal: :Archives of disease in childhood 1997
C M Cale N J Klein V Novelli P Veys A M Jones G Morgan

Children presenting with disseminated viral infections should be carefully investigated because they almost invariably have an underlying immunodeficiency. A child is reported who had disseminated cytomegalovirus and a novel form of severe combined immunodeficiency with abnormal expression of the common leucocyte antigen, CD45.

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2000
P Bousso V Wahn I Douagi G Horneff C Pannetier F Le Deist F Zepp T Niehues P Kourilsky A Fischer G de Saint Basile

In this report, we have analyzed the human T cell repertoire derived in vivo from a single T cell precursor. A unique case of X-linked severe combined immunodeficiency in which a reverse mutation occurred in an early T cell precursor was analyzed to this end. It was determined that at least 1,000 T cell clones with unique T cell receptor-beta sequences were generated from this precursor. This d...

2017
Luiz Vicente Rizzo

aDirector of Research, Israelita Albert Einstein Hospital, São Paulo, SP, Brasil. Received on January 11, 2017. © 2017 Sociedade de Pediatria de São Paulo. Published by Zeppelini Publishers. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). EARLY DIAGNOSIS OF SEVERE COMBINED IMMUNODEFICIENCIES Diagnóstico precoce das imunodeficiências combinad...

Journal: :Medical Journal of Dr. D.Y. Patil Vidyapeeth 2021

Journal: :iranian journal of allergy, asthma and immunology 0
maryam nourizadeh immunology, asthma and allergy research institute, tehran university of medical sciences, tehran, iran. stephan borte division of clinical immunology, department of laboratory medicine, karolinska university hospital huddinge, stockholm, sweden and jeffrey modell diagnostic and research center for primary immunodeficiencies, municipal hospital st. georg, leipzig, germany. mohammadreza fazlollahi immunology, asthma and allergy research institute, tehran university of medical sciences, tehran, iran. lennart hammarström division of clinical immunology, department of laboratory medicine, karolinska university hospital huddinge, stockholm, sweden. zahra pourpak immunology, asthma and allergy research institute, tehran university of medical sciences, tehran, iran.

severe combined immunodeficiency (scid) represents a rare group of primary immunodeficiency disorders (pids), with known or unknown genetic alterations. here, we report a new interleukin 2 receptor, gamma chain (il-2rg) mutation in an iranian scid newborn.the patient was a 6-day old boy with a family history of pid. the child was screened using a molecular-based analysis for the assessment of t...

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...

Nateghian, Alireza, Bahrami, Ahmad , Parsania, Masoud , Soltani, Zahra ,

A five month-old girl was admitted in Ali Asghar Children’s Hospital with a history of three months of fever, cough and dyspnea that her symptoms have exacerbated since two weeks before admission. She was the first child of the family born to consanguineous parents. She was clinically healthy in the past and had gained weight normally and undergone vaccination program with no complication unti...

2009
Sylvestre Grizot Julianne Smith Fayza Daboussi Jesús Prieto Pilar Redondo Nekane Merino Maider Villate Séverine Thomas Laetitia Lemaire Guillermo Montoya Francisco J. Blanco Frédéric Pâques Philippe Duchateau

Sequence-specific endonucleases recognizing long target sequences are emerging as powerful tools for genome engineering. These endonucleases could be used to correct deleterious mutations or to inactivate viruses, in a new approach to molecular medicine. However, such applications are highly demanding in terms of safety. Mutations in the human RAG1 gene cause severe combined immunodeficiency (S...

Journal: :Cell 2016
Jonathan Hoggatt

Adenosine deaminase (ADA) deficiency results in the accumulation of toxic metabolites that destroy the immune system, causing severe combined immunodeficiency (ADA-SCID), often referred to as the "bubble boy" disease. Strimvelis is a European Medicines Agency approved gene therapy for ADA-SCID patients without a suitable bone marrow donor.

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