Granulomatous disease
Nocardia farcinica Pneumonia in Chronic Granulomatous Disease
... A 15-year-old white male with X-linked CGD was admitted to the hospital with a 5-day history of fever to 40°C, intermittent chills, and malaise, and a 2-day history of nonproductive cough and right shoulder pain with ...
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Corticosteroids in the Management of Cystitis Secondary to Chronic Granulomatous Disease
... Gastric outlet obstruction in chronic granulomatous disease of childhood. Kontras SB, Bodenbander JG, McClave CR, et al[r] ...
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X linked Inheritance in Females with Chronic Granulomatous Disease
... Chronic granulomatous disease in males is familial and its transmission is is usually clearly ...this disease is associated with an absence of the respiratory burst generated in stimulated phagocytes ...
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NADPH oxidase deficiency in X linked chronic granulomatous disease
... deficiency of myeloperoxidase, and 7 patients with X-linked chronic granulomatous disease (CGD). When measured under optimal conditions (at pH 5.5 and in the presence of 0.5 mM Mn++), NADPH oxidase activity ...
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Citation classics in chronic granulomatous disease: a bibliometric analysis
... Abstract: The number of times a scientific article has been cited reflects its impact on a specific field. Highly cited articles are known as citation classics. Here, we aim to characterize the most frequently cited ...
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Continuous Antibiotic Therapy in Chronic Granulomatous Disease: Preliminary Communication
... Continuous Antibiotic Therapy in Chronic Granulomatous Disease: Preliminary. Services[r] ...
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CHRONIC GRANULOMATOUS DISEASE: CORRELATION BETWEEN PATHOGENESIS AND CLINICAL FINDINGS
... drogen peroxide antibacterial system. : Quantita- tive nitroblue tetrazoliiiii, test in chronic granuloniatous disease. A.: Chronic granulomatous disease in females: A deficiency of leuk[r] ...
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Recent Advances in Gene Therapy and Modeling of Chronic Granulomatous Disease
... Chronic granulomatous disease (CGD) is a primary immunodeficiency that characterized by mutations in phagocyte nicotinamide adenine dinucleotide phosphate (NADPH) oxidase, resulting in deficient ...
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Recombinant interferon gamma augments phagocyte superoxide production and X chronic granulomatous disease gene expression in X linked variant chronic granulomatous disease
... chronic granulomatous disease (CGD) by studying its effects on CGD phagocyte superoxide generation, NADPH oxidase kinetics, cytochrome b559 content, and expression of X-CGD (the gene for the X-linked ...
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Chronic Granulomatous Disease Presenting as Hemophagocytic Lymphohistiocytosis: A Case Report
... Chronic granulomatous disease (CGD) is a primary immunode fi ciency characterized by recurrent infections and a dysregulated in fl ammatory response. Infection-triggered hemophagocytic lymphohistiocytosis ...
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Gastrointestinal Involvement in Chronic Granulomatous Disease
... Conclusion. GI involvement is a common and recur- ring problem in CGD, especially in those with X-linked inheritance. Currently, there is no clear evidence for an infectious cause. The frequency of GI involvement is ...
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Cytochrome b deficiency in an autosomal form of chronic granulomatous disease A third form of chronic granulomatous disease recognized by monocyte hybridization
... autosomal because the granulocytes of both parents (first cousins) and a nonaffected sister of the patients expressed 70-80% of the normal cytochrome b signal, showed low-normal or subnormal oxidative reactions during ...
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Inherited p40phox deficiency differs from classic chronic granulomatous disease
... Chronic granulomatous disease (CGD) is a recessive primary immunodeficiency (PID) caused by loss-of-function (LOF) muta- tions of autosomal or X-linked genes encoding 5 components of the phagocyte-reduced ...
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Leukocyte degranulation and vacuole formation in patients with chronic granulomatous disease of childhood
... granulomatous disease. Two additional patients with chronic granulomatous disease have also been found to have apparently adequate degranulation ...
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The pattern of genetic transmission of the leukocyte defect in fatal granulomatous disease of childhood
... The leukocyte-phagocytic function test which was found to be abnormal in boys with fatal granulomatous disease of childhood has been found to be abnormal to an intermediate extent in their mothers. Nine of ...
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Correction of metabolic deficiencies in the leukocytes of patients with chronic granulomatous disease
... Polymorphonuclear leukocytes from patients with chronic granulomatous disease (CGD) exhibit metabolic and bactericidal deficiencies that may be the result of inadequate production of H 2 O 2 . A hydrogen ...
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Disseminated BCG in Twin Boys with Presumed Chronic Granulomatous Disease of Childhood
... Disseminated BCG in Twin Boys with Presumed Chronic Granulomatous Disease of. http://pediatrics.aappublications.org/content/48/1/141[r] ...
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Degranulation of leukocytes in chronic granulomatous disease
... Quantitative chemical analyses of the subcellular distribution patterns for acid and alkaline phosphatase, beta glucuronidase and peroxidase were obtained for human peripheral blood leukocytes of four patients with ...
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Sarcoidosis in Chronic Granulomatous Disease
... In addition to increased susceptibility to infections in patients with chronic granulomatous disease (CGD), a higher incidence of sterile inflammatory disorders in these patients has been noted. However, ...
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Chronic Recurrent Multifocal Osteomyelitis and Thalidomide in Chronic Granulomatous Disease
... Chronic granulomatous disease (CGD) is a primary immunodeficiency that leads to severe recurrent infection and inflammatory complications that are usually difficult to diagnose and ...
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