نتایج جستجو برای: cgd

تعداد نتایج: 685  

Journal: :Blood 2002
Joachim Roesler Sebastian Brenner Anatoly A Bukovsky Narda Whiting-Theobald Thomas Dull Michael Kelly Curt I Civin Harry L Malech

HIV-1-derived lentivectors are promising for gene transfer into hematopoietic stem cells but require preclinical in vivo evaluation relevant to specific human diseases. Nonobese diabetic/severe combined immunodeficient (NOD/SCID) mice accept human hematopoietic stem cell grafts, providing a unique opportunity for in vivo evaluation of therapies targeting human hematopoietic diseases. We demonst...

2002
Harry L Malech Joachim Roesler Sebastian Brenner Anatoly A Bukovsky Narda Whiting-Theobald Thomas Dull Anatoly A. Bukovsky Michael Kelly Curt I. Civin Harry L. Malech

HIV-1 derived lentivectors are promising for gene transfer into hematopoietic stem cells, but require pre-clinical in vivo evaluation relevant to specific human diseases. Non-obese diabetic/severe combined immunodeficient (NOD/SCID) mice accept human hematopoietic stem cell grafts providing a unique opportunity for in vivo evaluation of therapies targeting human hematopoietic diseases. We demon...

Journal: :European Physical Journal C 2022

In the present paper, we discuss role of gravitational decoupling to isotropize anisotropic solution Einstein's field equations in context complete geometric deformation (CGD) approach and its influence on complexity factor introduced by L. Herrera (Phys. Rev. D 97, 044010 (2018)) static self-gravitating system. Moreover, also proposed a simple effective technique generate new solutions for obj...

Journal: :iranian journal of allergy, asthma and immunology 0
alborzi abdolvahab professor alborzi clinical microbiology research center, shiraz university of medical sciences, shir mostafavi nasser isfahan university of medical sciences, isfahan, iran pouladfar gholam reza professor alborzi clinical microbiology research center, shiraz university of medical sciences, shir

in chronic granulomatous disease (cgd) patients, esophageal stricture is a rare complication and the treatment of choice is still controversial. there are few reports of successful therapy with antibiotics, corticosteroids, multiple balloon dilatations or their combination. we report a 3-three-year-old iranian boy with recurrent esophageal obstruction due to cgd. the patient transiently respond...

ژورنال: ابن سینا 2007
امیری, مجید, بنی اقبال, بهزاد, طبرسی, پیام, منصوری, داوود, میرسعیدی, مهدی, کریمی, شیرین,

یک نقص ایمنی اولیه ی نادر است که ابتدا در کودکان شرح داده شد . این بیماری عمدتاً در CGD کودکان دیده می شود ولی مواردی از بیماری در بزرگسالان نیز گزارش شده است. در این گزارش که به همراه با برونشیولیت لنفوسیتیک در یک فرد بالغ بوده CGD به اولین مورد بررسی پرداخته شده است . بیماری 40 ساله که با سرفه و خلط چرکی و تنگی نفس و کاهش وزن مراجعه اسکن، بیوپسی باز ریه CT نموده است، دو دوره تحت درمان ضد س...

Journal: Current Medical Mycology 2016

Background and Purpose: Chronic granulomatous disease (CGD) is an inherited disorder of the nicotinamide adenine dinucleotide phosphate (NADPH) oxidase complex. This disorder results in recurrent life-threatening bacterial and fungal infections. Aspergillus species are the most common fungal infections in these patients. Case Report: Herein, we present a case of fungal infection in a girl wi...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1988
J M Sechler H L Malech C J White J I Gallin

Monocytes from 19 of 30 patients with the classic phenotype of chronic granulomatous disease of childhood (CGD) responded to 3 days of treatment in culture with recombinant human interferon-gamma (rHuIFN-gamma) at 100 units/ml by producing superoxide after stimulation with phorbol 12-myristate 13-acetate. Cells from 15 of 16 patients with cytochrome b-positive CGD (15 with autosomal and 1 with ...

2016
E. Liana Falcone Loreto Abusleme Muthulekha Swamydas Michail S. Lionakis Li Ding Amy P. Hsu Adrian M. Zelazny Niki M. Moutsopoulos Douglas B. Kuhns Clay Deming Mariam Quiñones Julia A. Segre Clare E. Bryant Steven M. Holland

Background: Chronic granulomatous disease (CGD) is caused by defects in nicotinamide adenine dinucleotide phosphate oxidase 2 (NOX2) complex subunits (gp91 (a.k.a. Nox2), p47, p67, p22, p40) leading to reduced phagocyte-derived reactive oxygen species production. Almost half of patients with CGD develop inflammatory bowel disease, and the involvement of the intestinal microbiome in relation to ...

Journal: :Hepatology 2007
Nadeem Hussain Jordan J Feld David E Kleiner Jay H Hoofnagle Reyes Garcia-Eulate Sushil Ahlawat Deloris E Koziel Victoria Anderson Dianne Hilligoss Peter Choyke John I Gallin T Jake Liang Harry L Malech Steven M Holland Theo Heller

UNLABELLED Chronic granulomatous disease (CGD) is a rare congenital disorder characterized by repeated bacterial and fungal infections. Aside from a high incidence of liver abscess, little is known about hepatic involvement in CGD. The aim of this study was to describe the spectrum of liver abnormalities seen in CGD. The charts of 194 patients with CGD followed at the NIH were reviewed, with a ...

Journal: :Blood 1997
W M Weil G F Linton N Whiting-Theobald S J Vowells S P Rafferty F Li H L Malech

Chronic granulomatous disease (CGD) can result from any of four single gene defects involving the components of the superoxide (O-2) generating phagocyte nicotinamide adenine dinucleotide phosphate (NADPH) oxidase. We show that transduction of peripheral blood CD34+ hematopoietic progenitors from a p67phox deficient CGD patient with replication defective amphotropic retrovirus encoding p67phox ...

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