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Chronic granulomatous disease: Clinical, functional, molecular, and genetic studies. The Israeli experience with 84 patients.
- Published in:
- American Journal of Hematology, 2017, v. 92, n. 1, p. 28, doi. 10.1002/ajh.24573
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- Article
Complications after mandibular third molar extraction.
- Published in:
- Quintessence International, 1995, v. 26, n. 11, p. 779
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- Publication type:
- Article
A novel mutation in NCF1 in an adult CGD patient with a liver abscess as first presentation.
- Published in:
- Journal of Human Genetics, 2009, v. 54, n. 6, p. 313, doi. 10.1038/jhg.2009.24
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- Article
Functional and genetic characterization of two extremely rare cases of Williams-Beuren Syndrome associated with chronic granulomatous disease.
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- European Journal of Human Genetics, 2013, v. 21, n. 10, p. 1079, doi. 10.1038/ejhg.2012.310
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- Article
A new exon created by intronic insertion of a rearranged LINE-1 element as the cause of chronic granulomatous disease.
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- European Journal of Human Genetics, 2000, v. 8, n. 9, p. 697, doi. 10.1038/sj.ejhg.5200523
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- Article
Complementation in monocyte hybrids revealing genetic heterogeneity in chronic granulomatous disease.
- Published in:
- Nature, 1984, v. 307, n. 5951, p. 553, doi. 10.1038/307553a0
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- Publication type:
- Article
Clinical and Immunological Characteristics of 63 Patients with Chronic Granulomatous Disease: Hacettepe Experience.
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- Journal of Clinical Immunology, 2021, v. 41, n. 5, p. 992, doi. 10.1007/s10875-021-01002-w
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- Article
Approach to Molecular Diagnosis of Chronic Granulomatous Disease (CGD): an Experience from a Large Cohort of 90 Indian Patients.
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- Journal of Clinical Immunology, 2018, v. 38, n. 8, p. 898, doi. 10.1007/s10875-018-0567-y
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- Article
p47<sup>phox-/-</sup> Chronic Granulomatous Disease Patient with Incomplete Kawasaki Disease.
- Published in:
- 2018
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- Publication type:
- Case Study
Analysis of Chronic Granulomatous Disease in the Kavkazi Population in Israel Reveals Phenotypic Heterogeneity in Patients with the Same NCF1 mutation (c.579G>A).
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- Journal of Clinical Immunology, 2018, v. 38, n. 2, p. 193, doi. 10.1007/s10875-018-0475-1
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- Article
Diagnosis of Interstitial Lung Disease Caused by Possible Hypersensitivity Pneumonitis in a Child: Think CGD.
- Published in:
- 2017
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- Publication type:
- Letter
Molecular Basis of Autosomal Recessive Chronic Granulomatous Disease in Iran.
- Published in:
- Journal of Clinical Immunology, 2010, v. 30, n. 4, p. 587, doi. 10.1007/s10875-010-9421-6
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- Publication type:
- Article
Genetic Characteristics, Infectious, and Noninfectious Manifestations of 32 Patients with Chronic Granulomatous Disease.
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- International Archives of Allergy & Immunology, 2020, v. 181, n. 7, p. 540, doi. 10.1159/000507366
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- Publication type:
- Article
Prenatal diagnosis in two families with autosomal, p47(phox)-deficient chronic granulomatous disease due to a novel point mutation in NCF1.
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- 2002
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- Publication type:
- journal article
Prenatal diagnosis in a family with X-linked chronic granulomatous disease with the use of the polymerase chain reaction.
- Published in:
- 1992
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- Publication type:
- journal article
Genetic variation of human neutrophil Fcγ receptors and SIRPα in antibody‐dependent cellular cytotoxicity towards cancer cells.
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- European Journal of Immunology, 2018, v. 48, n. 2, p. 344, doi. 10.1002/eji.201747215
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- Publication type:
- Article
Extensive Variation in Gene Copy Number at the Killer Immunoglobulin-Like Receptor Locus in Humans.
- Published in:
- PLoS ONE, 2013, v. 8, n. 6, p. 1, doi. 10.1371/journal.pone.0067619
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- Article
Inherited p40phox deficiency differs from classic chronic granulomatous disease.
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- 2018
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- Publication type:
- journal article
Factor h-related (Fhr)-1 and Fhr-2 Form homo- and heterodimers, while Fhr-5 circulates Only as homodimer in human Plasma.
- Published in:
- Frontiers in Immunology, 2017, p. 1, doi. 10.3389/fimmu.2017.01328
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- Publication type:
- Article
Chronic granulomatous disease - haematopoietic stem cell transplantation versus conventional treatment.
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- Acta Paediatrica, 2013, v. 102, n. 11, p. 1087, doi. 10.1111/apa.12384
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- Publication type:
- Article
Alu-repeat-induced deletions within the NCF2 gene causing p67- phox-deficient chronic granulomatous disease (CGD).
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- Human Mutation, 2010, v. 31, n. 2, p. 151, doi. 10.1002/humu.21156
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- Publication type:
- Article
Copy number variation at the FCGR locus includes FCGR3A, FCGR2C and FCGR3B but not FCGR2A and FCGR2B.
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- Human Mutation, 2009, v. 30, n. 5, p. E640, doi. 10.1002/humu.20997
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- Publication type:
- Article
Chronic granulomatous disease caused by mutations other than the common GT deletion in NCF1, the gene encoding the p47<sup>phox</sup> component of the phagocyte NADPH oxidase.
- Published in:
- Human Mutation, 2006, v. 27, n. 12, p. 1218, doi. 10.1002/humu.20413
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- Publication type:
- Article
Prenatal Diagnosis of Chronic Granulomatous Disease in a Male Fetus.
- Published in:
- Iranian Journal of Allergy, Asthma & Immunology, 2009, v. 8, n. 1, p. 57
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- Publication type:
- Article
Activation of cryptic splice sites in three patients with chronic granulomatous disease.
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- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 9, p. N.PAG, doi. 10.1002/mgg3.854
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- Publication type:
- Article