Chronic granulomatous disease: Clinical, functional, molecular, and genetic studies. The Israeli experience with 84 patients

Baruch Wolach; Ronit Gavrieli; Martin de Boer; Karin van Leeuwen; Sivan Berger-Achituv; Tal Stauber; Josef Ben Ari; Menachem Rottem; Yechiel Schlesinger; Galia Grisaru-Soen; Omar Abuzaitoun; Nufar Marcus; Ben Zion Garty; Arnon Broides; Jakov Levy; Polina Stepansky; Amos Etzioni; Raz Somech; Dirk Roos

doi:10.1002/ajh.24573

Chronic granulomatous disease: Clinical, functional, molecular, and genetic studies. The Israeli experience with 84 patients

American Journal of Hematology ◽

10.1002/ajh.24573 ◽

2016 ◽

Vol 92 (1) ◽

pp. 28-36 ◽

Cited By ~ 51

Author(s):

Baruch Wolach ◽

Ronit Gavrieli ◽

Martin de Boer ◽

Karin van Leeuwen ◽

Sivan Berger-Achituv ◽

...

Keyword(s):

Chronic Granulomatous Disease ◽

Granulomatous Disease ◽

Genetic Studies ◽

Israeli Experience

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Faculty Opinions recommendation of Chronic granulomatous disease: Clinical, functional, molecular, and genetic studies. The Israeli experience with 84 patients.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.726820730.793535121 ◽

2017 ◽

Author(s):

Andrew Gennery

Keyword(s):

Chronic Granulomatous Disease ◽

Granulomatous Disease ◽

Genetic Studies ◽

Israeli Experience

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Genetic studies of three Japanese patients with p22-phox-deficient chronic granulomatous disease: detection of a possible common mutant CYBA allele in Japan and a genotype-phenotype correlation in these patients

British Journal of Haematology ◽

10.1046/j.1365-2141.2000.01857.x ◽

2000 ◽

Vol 108 (3) ◽

pp. 511-517 ◽

Cited By ~ 18

Author(s):

Masafumi Yamada ◽

Tadashi Ariga ◽

Nobuaki Kawamura ◽

Makoto Ohtsu ◽

Shinobu Imajoh-Ohmi ◽

...

Keyword(s):

Chronic Granulomatous Disease ◽

Japanese Patients ◽

Disease Detection ◽

Granulomatous Disease ◽

Phenotype Correlation ◽

Genetic Studies ◽

Genotype Phenotype Correlation ◽

P22 Phox

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Molecular genetic studies of two families with X-linked chronic granulomatous disease: Mutation analysis and definitive determination of carrier status in patients' sisters

European Journal Of Haematology ◽

10.1111/j.1600-0609.1994.tb01293.x ◽

2009 ◽

Vol 52 (2) ◽

pp. 99-102 ◽

Cited By ~ 13

Author(s):

Tadashi Ariga ◽

Yukio Sakiyama ◽

Hirofumi Furuta ◽

Shuzo Matsumoto

Keyword(s):

Chronic Granulomatous Disease ◽

Mutation Analysis ◽

Molecular Genetic ◽

Carrier Status ◽

Granulomatous Disease ◽

Genetic Studies ◽

Disease Mutation

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CORTICOSTEROID THERAPY FOR MULTIPLE LIVER ABSCESSES IN A CASE OF CHRONIC GRANULOMATOUS DISEASE

10.26226/morressier.57bc1756d462b80290b4da31 ◽

2016 ◽

Author(s):

Mihaela Bataneant

Keyword(s):

Chronic Granulomatous Disease ◽

Corticosteroid Therapy ◽

Granulomatous Disease ◽

Liver Abscesses

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AUTOSOMAL RECESSIVE CHRONIC GRANULOMATOUS DISEASE, HYPERINFLAMMATORY STATE AND HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS; CASE REPORT

10.26226/morressier.57bc1755d462b80290b4d812 ◽

2016 ◽

Author(s):

Nesrin Gulez

Keyword(s):

Case Report ◽

Chronic Granulomatous Disease ◽

Hemophagocytic Lymphohistiocytosis ◽

Autosomal Recessive ◽

Granulomatous Disease

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CORRELATION BETWEEN THE NUMBER OF B-MEMORY CELLS AND FOLLICULAR T-HELPERS IN PATIENTS WITH X-LINKED CHRONIC GRANULOMATOUS DISEASE (CGD)

10.26226/morressier.57bc1757d462b80290b4dbe0 ◽

2016 ◽

Author(s):

Inga Sakovich

Keyword(s):

Chronic Granulomatous Disease ◽

Granulomatous Disease ◽

Memory Cells ◽

T Helpers

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CHRONIC GRANULOMATOUS DISEASE, THE MCLEOD NEUROACANTHOCYTOSIS SYNDROME AND THE CONTIGUOUS GENE DELETION SYNDROME. CASE REPORT

10.26226/morressier.57bc1758d462b80290b4d387 ◽

2016 ◽

Author(s):

Jose Antonio Galian Megias

Keyword(s):

Case Report ◽

Chronic Granulomatous Disease ◽

Gene Deletion ◽

Deletion Syndrome ◽

Granulomatous Disease ◽

Contiguous Gene ◽

Contiguous Gene Deletion Syndrome

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NADPH Oxidase 2 Derived Reactive Oxygen Species Promote CD8+ T cell Effector Function in Murine Model of Chronic Granulomatous Disease

10.26226/morressier.594a7d45d462b8028d8932ce ◽

2017 ◽

Author(s):

Jennifer Leiding

Keyword(s):

Reactive Oxygen Species ◽

T Cell ◽

Nadph Oxidase ◽

Chronic Granulomatous Disease ◽

Murine Model ◽

Cd8 T Cell ◽

Oxygen Species ◽

Granulomatous Disease ◽

Cell Effector Function ◽

Cell Effector

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Dysregulated cytokine production in monocytes from patients with chronic granulomatous disease

10.26226/morressier.594a7d46d462b8028d8934f6 ◽

2017 ◽

Author(s):

Kyung-Sue Shin

Keyword(s):

Chronic Granulomatous Disease ◽

Cytokine Production ◽

Granulomatous Disease

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Faculty Opinions recommendation of Correction of X-linked chronic granulomatous disease by gene therapy, augmented by insertional activation of MDS1-EVI1, PRDM16 or SETBP1.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.1014387.371927 ◽

2006 ◽

Author(s):

Mary Dinauer

Keyword(s):

Gene Therapy ◽

Chronic Granulomatous Disease ◽

Granulomatous Disease

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