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The Changing Paradigm of Management of Liver Abscesses in Chronic Granulomatous Disease

Clinical infectious diseases, 2018-04, Vol.66 (9), p.1427-1434

2018

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Principles and Practice of Clinical Research

Fourth edition, 2017

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Principles and Practice of Clinical Research

3rd ed., 2012

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Principles and Practice of Clinical Research

2nd Edition, 2007

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The Use of Radiolabelled 18-F-2-Deoxy-2-Fluro-Glucose (18-FDG) in Combined Positron Emission Tomography-Computed Tomography (PET-CT) to Evaluate Infection: Lessons Learned from a Case Series of 23 Patients with Chronic Granulomatous Disease (CGD)

Journal of allergy and clinical immunology, 2015-02, Vol.135 (2), p.AB98-AB98

2015

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Spectrum of LYST mutations in Chediak-Higashi syndrome: a report of novel variants and a comprehensive review of the literature

Journal of medical genetics, 2024-03, Vol.61 (3), p.212-223

2024

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Gastrointestinal Computed Tomography Findings in Chronic Granulomatous Disease with Subgroup Clinicopathologic Analysis

Digestive diseases and sciences, 2022-05, Vol.67 (5), p.1831-1842

2022

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Michael M. Frank: February 28, 1937–August 1, 2019

Journal of allergy and clinical immunology, 2019-12, Vol.144 (6), p.1507-1508

2019

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Principles and Practice of Clinical Research

Gallin, John I

1, 2002

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Introduction of Anthony S. Fauci, MD

The Journal of clinical investigation, 2007-10, Vol.117 (10), p.3131-3135

Gallin, John I

2007

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Thioglycollate peritonitis in mice lacking C5, 5-lipoxygenase, or p47phox: complement, leukotrienes, and reactive oxidants in acute inflammation

Journal of leukocyte biology, 2002-03, Vol.71 (3), p.410-416

2002

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Neutrophils in Human Diseases

The New England journal of medicine, 1987-09, Vol.317 (11), p.687-694

1987

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Fibrinogen Induces IL-8 Synthesis in Human Neutrophils Stimulated with Formyl-Methionyl-Leucyl-Phenylalanine or Leukotriene B4

The Journal of immunology (1950), 2001-09, Vol.167 (5), p.2869-2878

2001

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Genotype, Phenotype, and Clinical Course in Five Patients With PAPA Syndrome (Pyogenic Sterile Arthritis, Pyoderma Gangrenosum, and Acne)

Arthritis and rheumatism, 2012-06, Vol.64 (6), p.2022-2027

2012

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New infrastructure to support clinical translational research at the US National Institutes of Health: role of the NIH Clinical Center

Journal of translational medicine, 2012-10, Vol.10 (S2), p.A2-A2, Article A2

Gallin, John I

2012

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Su1927 GASTROINTESTINAL IMAGING IN CHRONIC GRANULOMATOUS DISEASE: CT FINDINGS IN 141 PATIENTS WITH CLINICOPATHOLOGIC CORRELATION

Gastroenterology (New York, N.Y. 1943), 2020-05, Vol.158 (6), p.S-705-S-706

2020

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Granulibacter bethesdensis, a Pathogen from Patients with Chronic Granulomatous Disease, Produces a Penta-Acylated Hypostimulatory Glycero-D-talo-oct-2-ulosonic Acid–Lipid A Glycolipid (Ko-Lipid A)

International journal of molecular sciences, 2021-03, Vol.22 (7)

2021

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Emerging Infections

1, 1998

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Residual NADPH Oxidase and Survival in Chronic Granulomatous Disease

The New England journal of medicine, 2010-12, Vol.363 (27), p.2600-2610

2010

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Persistence of the bacterial pathogen Granulibacter bethesdensis in Chronic Granulomatous Disease monocytes and macrophages lacking a functional NADPH oxidase1

The Journal of immunology (1950), 2013-08, Vol.191 (6), p.3297-3307

2013

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Inherited p40^sup phox^ deficiency differs from classic chronic granulomatous disease

The Journal of clinical investigation, 2018-09, Vol.128 (9), p.3957-3975

2018

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Phagocyte Function and Dysfunction: From Descriptive Biology to Molecular Defects and Cytokine Therapy

Infectious diseases in clinical practice (Baltimore, Md.), 2001-03, Vol.10 (3), p.129-132

Gallin, John I

2001

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Principles and Practice of Clinical Research:Principles and Practice of Clinical Research

Clinical infectious diseases, 2003-03, Vol.36 (5), p.677-677

2003

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Aspergillus nidulans Infection in Chronic Granulomatous Disease

Medicine (Baltimore), 1998-09, Vol.77 (5), p.345-354

1998

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Intermediate phenotypes in patients with autosomal dominant hyper-lgE syndrome caused by somatic mosaicism

Journal of allergy and clinical immunology, 2013, Vol.131 (6), p.1586-1593

2013

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The Changing Paradigm of Management of Liver Abscesses in Chronic Granulomatous Disease

Principles and Practice of Clinical Research

Principles and Practice of Clinical Research

Principles and Practice of Clinical Research

The Use of Radiolabelled 18-F-2-Deoxy-2-Fluro-Glucose (18-FDG) in Combined Positron Emission Tomography-Computed Tomography (PET-CT) to Evaluate Infection: Lessons Learned from a Case Series of 23 Patients with Chronic Granulomatous Disease (CGD)

Spectrum of LYST mutations in Chediak-Higashi syndrome: a report of novel variants and a comprehensive review of the literature

Gastrointestinal Computed Tomography Findings in Chronic Granulomatous Disease with Subgroup Clinicopathologic Analysis

Michael M. Frank: February 28, 1937–August 1, 2019

Principles and Practice of Clinical Research

Introduction of Anthony S. Fauci, MD

Thioglycollate peritonitis in mice lacking C5, 5-lipoxygenase, or p47phox: complement, leukotrienes, and reactive oxidants in acute inflammation

Neutrophils in Human Diseases

Fibrinogen Induces IL-8 Synthesis in Human Neutrophils Stimulated with Formyl-Methionyl-Leucyl-Phenylalanine or Leukotriene B4

Genotype, Phenotype, and Clinical Course in Five Patients With PAPA Syndrome (Pyogenic Sterile Arthritis, Pyoderma Gangrenosum, and Acne)

New infrastructure to support clinical translational research at the US National Institutes of Health: role of the NIH Clinical Center

Su1927 GASTROINTESTINAL IMAGING IN CHRONIC GRANULOMATOUS DISEASE: CT FINDINGS IN 141 PATIENTS WITH CLINICOPATHOLOGIC CORRELATION

Granulibacter bethesdensis, a Pathogen from Patients with Chronic Granulomatous Disease, Produces a Penta-Acylated Hypostimulatory Glycero-D-talo-oct-2-ulosonic Acid–Lipid A Glycolipid (Ko-Lipid A)

Emerging Infections

Residual NADPH Oxidase and Survival in Chronic Granulomatous Disease

Persistence of the bacterial pathogen Granulibacter bethesdensis in Chronic Granulomatous Disease monocytes and macrophages lacking a functional NADPH oxidase1

Inherited p40^sup phox^ deficiency differs from classic chronic granulomatous disease

Phagocyte Function and Dysfunction: From Descriptive Biology to Molecular Defects and Cytokine Therapy

Principles and Practice of Clinical Research:Principles and Practice of Clinical Research

Aspergillus nidulans Infection in Chronic Granulomatous Disease

Intermediate phenotypes in patients with autosomal dominant hyper-lgE syndrome caused by somatic mosaicism

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