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Heterogeneity of human bone marrow and blood natural killer cells defined by single-cell transcriptome

Nature communications, 2019-09, Vol.10 (1), p.3931-16, Article 3931

2019

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Rituximab and antimetabolite treatment of granulomatous and lymphocytic interstitial lung disease in common variable immunodeficiency

Journal of allergy and clinical immunology, 2021-02, Vol.147 (2), p.704-712.e17

2021

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Randomized, Double‐Blind, Placebo‐Controlled Trial of the Efficacy and Safety of Rilonacept in the Treatment of Systemic Juvenile Idiopathic Arthritis

Arthritis & rheumatology (Hoboken, N.J.), 2014-09, Vol.66 (9), p.2570-2579

2014

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CD25 deficiency causes an immune dysregulation, polyendocrinopathy, enteropathy, X-linked–like syndrome, and defective IL-10 expression from CD4 lymphocytes

Journal of allergy and clinical immunology, 2007-02, Vol.119 (2), p.482-487

2007

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When to Suspect Autoinflammatory/Recurrent Fever Syndromes

The Pediatric clinics of North America, 2017-02, Vol.64 (1), p.111

Verbsky, James W

2017

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Newborn Screening for Severe Combined Immunodeficiency; The Wisconsin Experience (2008–2011)

Journal of clinical immunology, 2012-02, Vol.32 (1), p.82-88

2012

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Hemophagocytic lymphohistiocytosis: Diagnosis, pathophysiology, treatment, and future perspectives

Annals of medicine (Helsinki), 2006-01, Vol.38 (1), p.20-31

2006

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A Practical Approach to Newborn Screening for Severe Combined Immunodeficiency Using the T Cell Receptor Excision Circle Assay

Frontiers in immunology, 2017-11, Vol.8, p.1470-1470

2017

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Gain of Function Mutations of PIK3CD as a Cause of Primary Sclerosing Cholangitis

Journal of clinical immunology, 2015-01, Vol.35 (1), p.11-14

2015

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Effective use of the recombinant interleukin 1 receptor antagonist anakinra in therapy resistant systemic onset juvenile rheumatoid arthritis

Journal of rheumatology, 2004-10, Vol.31 (10), p.2071

2004

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Immunodeficiency Presenting as an Undiagnosed Disease

The Pediatric clinics of North America, 2017-02, Vol.64 (1), p.27

2017

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Donor chimerism and immune reconstitution following haploidentical transplantation in sickle cell disease

Frontiers in immunology, 2022-12, Vol.13, p.1055497-1055497

2022

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Immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) and IPEX-related disorders: an evolving web of heritable autoimmune diseases

Current opinion in pediatrics, 2013-12, Vol.25 (6), p.708-714

2013

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Amicrobial pustolosis associated with autoimmune disease (APAD) responsive to mycophenolate and dapsone

Journal of allergy and clinical immunology, 2017-02, Vol.139 (2), p.AB215-AB215

2017

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Granulomatous and Lymphocytic Interstitial Lung Disease (GLILD) Associated with KMT2D Gene Mutation in Kabuki Syndrome

Journal of allergy and clinical immunology, 2016-02, Vol.137 (2), p.AB118-AB118

2016

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Defining the Percentage of T Helper 17 Cells in Patients with Eczema and Allergic Disease

Journal of allergy and clinical immunology, 2016-02, Vol.137 (2), p.AB26-AB26

2016

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Title: Hypersensitivity Pneumonitis in an Autosomal Recessive Chronic Granulomatous Disease Carrier

Journal of allergy and clinical immunology, 2016-02, Vol.137 (2), p.AB116-AB116

2016

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Efficient Precision Genome Editing in iPSCs via Genetic Co-targeting with Selection

Stem cell reports, 2017-03, Vol.8 (3), p.491-499

2017

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Practice parameter for the diagnosis and management of primary immunodeficiency

Journal of allergy and clinical immunology, 2015-11, Vol.136 (5), p.1186-1205.e78

2015

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Human T Regulatory Cells Can Use the Perforin Pathway to Cause Autologous Target Cell Death

Immunity (Cambridge, Mass.), 2004-10, Vol.21 (4), p.589-601

2004

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Sarcoidosis and common variable immunodeficiency: similarities and differences

Seminars in respiratory and critical care medicine, 2014-06, Vol.35 (3), p.330

2014

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Use of Combination Chemotherapy for Treatment of Granulomatous and Lymphocytic Interstitial Lung Disease (GLILD) in Patients with Common Variable Immunodeficiency (CVID)

Journal of clinical immunology, 2013-01, Vol.33 (1), p.30-39

2013

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Heterogeneity of human bone marrow and blood natural killer cells defined by single-cell transcriptome

Rituximab and antimetabolite treatment of granulomatous and lymphocytic interstitial lung disease in common variable immunodeficiency

Randomized, Double‐Blind, Placebo‐Controlled Trial of the Efficacy and Safety of Rilonacept in the Treatment of Systemic Juvenile Idiopathic Arthritis

Dominant gain-of-function STAT1 mutations in FOXP3 wild-type immune dysregulation–polyendocrinopathy–enteropathy–X-linked–like syndrome

CD25 deficiency causes an immune dysregulation, polyendocrinopathy, enteropathy, X-linked–like syndrome, and defective IL-10 expression from CD4 lymphocytes

When to Suspect Autoinflammatory/Recurrent Fever Syndromes

Newborn Screening for Severe Combined Immunodeficiency; The Wisconsin Experience (2008–2011)

Hemophagocytic lymphohistiocytosis: Diagnosis, pathophysiology, treatment, and future perspectives

A Practical Approach to Newborn Screening for Severe Combined Immunodeficiency Using the T Cell Receptor Excision Circle Assay

Gain of Function Mutations of PIK3CD as a Cause of Primary Sclerosing Cholangitis

Effective use of the recombinant interleukin 1 receptor antagonist anakinra in therapy resistant systemic onset juvenile rheumatoid arthritis

Immunodeficiency Presenting as an Undiagnosed Disease

Donor chimerism and immune reconstitution following haploidentical transplantation in sickle cell disease

Immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) and IPEX-related disorders: an evolving web of heritable autoimmune diseases

Amicrobial pustolosis associated with autoimmune disease (APAD) responsive to mycophenolate and dapsone

Granulomatous and Lymphocytic Interstitial Lung Disease (GLILD) Associated with KMT2D Gene Mutation in Kabuki Syndrome

Defining the Percentage of T Helper 17 Cells in Patients with Eczema and Allergic Disease

Title: Hypersensitivity Pneumonitis in an Autosomal Recessive Chronic Granulomatous Disease Carrier

Dominant-negative IKZF1 mutations cause a T, B, and myeloid cell combined immunodeficiency

Efficient Precision Genome Editing in iPSCs via Genetic Co-targeting with Selection

Practice parameter for the diagnosis and management of primary immunodeficiency

Making a definitive diagnosis: successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease

Human T Regulatory Cells Can Use the Perforin Pathway to Cause Autologous Target Cell Death

Sarcoidosis and common variable immunodeficiency: similarities and differences

Use of Combination Chemotherapy for Treatment of Granulomatous and Lymphocytic Interstitial Lung Disease (GLILD) in Patients with Common Variable Immunodeficiency (CVID)

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