Publications by authors named "Joie Davis"

47Publications

West Nile virus encephalitis in GATA2 deficiency.

Allergy Asthma Clin Immunol 2019 24;15. Epub 2019 Jan 24.

1Division of Allergy, Immunology, and Rheumatology, Department of Pediatrics, Stanford University School of Medicine, 269 Campus Drive, CCSR 3215, MC 5366, Stanford, CA 94305 USA.

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January 2019

Comprehensive RNAi-based screening of human and mouse TLR pathways identifies species-specific preferences in signaling protein use.

Sci Signal 2016 Jan 5;9(409):ra3. Epub 2016 Jan 5.

Signaling Systems Unit, Laboratory of Systems Biology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.

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January 2016

Natural history of autoimmune lymphoproliferative syndrome associated with FAS gene mutations.

Blood 2014 Mar 7;123(13):1989-99. Epub 2014 Jan 7.

Molecular Development Section, Laboratory of Immunology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD;

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March 2014

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

J Allergy Clin Immunol 2013 Jun 25;131(6):1586-93. Epub 2013 Apr 25.

Laboratory of Clinical Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Md., USA.

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June 2013

Lung parenchyma surgery in autosomal dominant hyper-IgE syndrome.

J Clin Immunol 2013 Jul 13;33(5):896-902. Epub 2013 Apr 13.

Laboratory of Clinical Infectious Diseases, NIAID, NIH, NIH Building 10 Room 11 N234, 9000 Rockville Pike, Bethesda, MD 20892, USA.

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July 2013

A rapid ex vivo clinical diagnostic assay for fas receptor-induced T lymphocyte apoptosis.

J Clin Immunol 2013 Feb 11;33(2):479-88. Epub 2012 Oct 11.

Laboratory of Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.

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February 2013

Autoimmune lymphoproliferative syndrome due to FAS mutations outside the signal-transducing death domain: molecular mechanisms and clinical penetrance.

Genet Med 2012 Jan 7;14(1):81-9. Epub 2011 Oct 7.

Laboratory of Clinical Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.

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January 2012

Cutaneous manifestations of DOCK8 deficiency syndrome.

Arch Dermatol 2012 Jan 19;148(1):79-84. Epub 2011 Sep 19.

Dermatology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland, USA.

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January 2012

A Markov model to analyze cost-effectiveness of screening for severe combined immunodeficiency (SCID).

Mol Genet Metab 2011 Nov 12;104(3):383-9. Epub 2011 Jul 12.

Department of Health Sciences, College of Health and Rehabilitation Sciences: Sargent College, Boston University, Boston, MA 02215, USA.

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November 2011

Coronary artery abnormalities in Hyper-IgE syndrome.

J Clin Immunol 2011 Jun 15;31(3):338-45. Epub 2011 Apr 15.

Immunopathogenesis Section, Laboratory of Clinical Infectious Diseases, National Institute of Allergy and Infectious Diseases (NIAID), 10 Center Drive, Bethesda, MD 20892-1899, USA.

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June 2011

FAS haploinsufficiency is a common disease mechanism in the human autoimmune lymphoproliferative syndrome.

J Immunol 2011 May 13;186(10):6035-43. Epub 2011 Apr 13.

Department of Laboratory Medicine, Clinical Center, National Institutes of Health, Bethesda, MD 20814, USA.

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May 2011

Paucity of genotype-phenotype correlations in STAT3 mutation positive Hyper IgE Syndrome (HIES).

Clin Immunol 2011 Apr 14;139(1):75-84. Epub 2011 Jan 14.

Laboratory of Clinical Infectious Diseases, Immunopathogenesis Section, National Institute of Allergy and Infectious Disease/NIH, Bethesda, MD 20892, USA.

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April 2011

Somatic FAS mutations are common in patients with genetically undefined autoimmune lymphoproliferative syndrome.

Blood 2010 Jun 1;115(25):5164-9. Epub 2010 Apr 1.

Laboratory of Clinical Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892-1888, USA.

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June 2010

Combined immunodeficiency associated with DOCK8 mutations.

N Engl J Med 2009 Nov 23;361(21):2046-55. Epub 2009 Sep 23.

Laboratory of Host Defenses, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.

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November 2009

The spectrum of parkinsonian manifestations associated with glucocerebrosidase mutations.

Arch Neurol 2008 Oct;65(10):1353-7

Section on Molecular Neurogenetics, National Human Genome Research Institute, National Institutes of Health, 35 Convent Dr, MSC 3708, Bldg 35, Room 1A213, Bethesda, MD 20892-3708, USA.

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October 2008

Brain abnormalities in patients with hyperimmunoglobulin E syndrome.

Pediatrics 2007 May 16;119(5):e1121-5. Epub 2007 Apr 16.

National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.

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May 2007

Gene therapy improves immune function in preadolescents with X-linked severe combined immunodeficiency.

Blood 2007 Jul 16;110(1):67-73. Epub 2007 Mar 16.

Genetics and Molecular Biology Branch, National Human Genome Research Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, MD 20892-1456, USA.

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July 2007

Causes of death in hyper-IgE syndrome.

J Allergy Clin Immunol 2007 May 1;119(5):1234-40. Epub 2007 Mar 1.

National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892-1684, USA.

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May 2007

Pneumocystis jiroveci infection in patients with hyper-immunoglobulin E syndrome.

Pediatrics 2006 Oct 28;118(4):e1271-5. Epub 2006 Aug 28.

National Institute of Allergy and Infectious Disease, National Institutes of Health, 9000 Rockville Pike, Bethesda, MD 20892, USA.

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October 2006

HLA B44 is associated with decreased severity of autoimmune lymphoproliferative syndrome in patients with CD95 defects (ALPS type Ia).

Clin Immunol 2006 Jan 27;118(1):59-65. Epub 2005 Oct 27.

Genetics and Molecular Biology Branch, National Human Genome Research Institute, National Institutes of Health, 49 Convent Drive, Building 49, Room 4A14, Bethesda, MD 20892, USA.

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January 2006

Stickler syndrome: clinical characteristics and diagnostic criteria.

Am J Med Genet A 2005 Oct;138A(3):199-207

Warren Magnuson Grant Clinical Center, National Institutes of Health, Bethesda, Maryland, USA.

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October 2005

Use of mycophenolate mofetil for chronic, refractory immune cytopenias in children with autoimmune lymphoproliferative syndrome.

Br J Haematol 2005 May;129(4):534-8

Laboratory of Clinical Infectious Diseases, National Institute of Allergy and Infectious Diseases/NIH, 10 Center Drive, Bethesda, MD 20892, USA.

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May 2005

Dermatitis and the newborn rash of hyper-IgE syndrome.

Arch Dermatol 2004 Sep;140(9):1119-25

Dermatology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD 20892-1908, USA.

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September 2004

Familial immunodeficiency with cutaneous vasculitis, myoclonus, and cognitive impairment.

Am J Med Genet A 2004 Mar;125A(2):145-51

National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.

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March 2004

Autosomal recessive hyperimmunoglobulin E syndrome: a distinct disease entity.

J Pediatr 2004 Jan;144(1):93-9

Department of Infectious Diseases and Clinical Immunology, University Children's Hospital, Dr v. Haunersches Kinderspital, Munich, Germany.

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January 2004

The role of the nurse in cancer genetics.

Cancer Nurs 2002 Jun;25(3):196-206

Urology Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Md. 20892-1873, USA.

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June 2002