S. McGhee

发表

Defects along the T(H)17 differentiation pathway underlie genetically distinct forms of the hyper IgE syndrome.

T. Chatila, M. Yılmaz, A. Somer, 2009, The Journal of allergy and clinical immunology.

Immune deficiencies , infection , and systemic immune disorders Defects along the TH 17 differentiation pathway underlie genetically distinct forms of the hyper IgE syndrome

T. Chatila, M. Yılmaz, A. Somer, 2009 .

Genetic and mechanistic diversity in pediatric hemophagocytic lymphohistiocytosis.

Ivan K. Chinn, J. Lupski, R. Gibbs, 2018, Blood.

Immunoglobulin replacement therapy in children.

T. Chatila, M. Garcia-Lloret, S. Mcghee, 2008, Immunology and allergy clinics of North America.

Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome.

T. Chatila, S. Holland, C. Klein, 2009, The Journal of allergy and clinical immunology.

Primary Immune Deficiency Treatment Consortium (PIDTC) report.

M. van der Burg, L. Notarangelo, H. Bobby Gaspar, 2014, The Journal of allergy and clinical immunology.

Newborn screening for severe combined immunodeficiency and T-cell lymphopenia in California: results of the first 2 years.

J. Puck, J. Church, D. Lewis, 2013, The Journal of allergy and clinical immunology.

Infant Allergy Testing and Food Allergy Diagnoses Before and After Guidelines for Early Peanut Introduction.

Maya B. Mathur, G. Shaw, A. Schroeder, 2020, The journal of allergy and clinical immunology. In practice.

Vehicular exhaust particles promote allergic airway inflammation through an aryl hydrocarbon receptor-notch signaling cascade.

T. Chatila, C. Sioutas, M. Garcia-Lloret, 2015, The Journal of allergy and clinical immunology.

Use and interpretation of diagnostic vaccination in primary immunodeficiency: a working group report of the Basic and Clinical Immunology Interest Section of the American Academy of Allergy, Asthma & Immunology.

J. Orange, M. T. de la Morena, R. Scherzer, 2012, The Journal of allergy and clinical immunology.

Subtyping of Eosinophilic Esophagitis Based on Disease Presentation in a pediatric Cohort

A. Goyal, Yiwen Wang, D. Bass, 2020, Journal of pediatric gastroenterology and nutrition.

Long-term results of bone marrow transplantation in complete DiGeorge syndrome.

Karin Chen, P. N. Rao, J. Gorski, 2007, The Journal of allergy and clinical immunology.

International consensus guidelines for the diagnosis and management of food protein–induced enterocolitis syndrome: Executive summary—Workgroup Report of the Adverse Reactions to Foods Committee, American Academy of Allergy, Asthma & Immunology

A. Muraro, H. Sampson, G. Konstantinou, 2017, The Journal of allergy and clinical immunology.

Allergic Diseases and Immune-Mediated Food Disorders in Pediatric Acute-Onset Neuropsychiatric Syndrome.

J. Frankovich, D. Lewis, Talia Mahony, 2018, Pediatric allergy, immunology, and pulmonology.

Newborn screening for severe combined immunodeficiency in 11 screening programs in the United States.

M. Watson, L. Notarangelo, J. Walter, 2014, JAMA.

Two-tiered universal newborn screening strategy for severe combined immunodeficiency.

Edward R B McCabe, Sean A McGhee, E. McCabe, 2005, Molecular genetics and metabolism.

Potential costs and benefits of newborn screening for severe combined immunodeficiency.

E. Stiehm, E. McCabe, S. Mcghee, 2005, The Journal of pediatrics.

Long-term Sinonasal Outcomes of Aspirin Desensitization in Aspirin Exacerbated Respiratory Disease

K. Nadeau, P. Hwang, E. Soudry, 2014, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

Pediatric eosinophilic esophagitis outcomes vary with co-morbid eczema and pollen food syndrome

A. Goyal, S. Sindher, Yiwen Wang, 2022, Frontiers in Allergy.

Representational oligonucleotide microarray analysis (ROMA) and comparison of binning and change‐point methods of analysis: application to detection of del22q11.2 (DiGeorge) Syndrome

M. Suchard, Zugen Chen, S. Mcghee, 2008, Human mutation.

DOCK8 Immune Deficiency as a Model for Primary Cytoskeletal Dysfunction

T. Chatila, S. Mcghee, S. McGhee, 2010, Disease markers.

How the practice of allergy shows the promise and challenge of personalized medicine.

S. Mcghee, S. McGhee, 2011, Molecular genetics and metabolism.

Primary Immune Deficiency Treatment Consortium (PIDTC) report.

M. van der Burg, L. Notarangelo, H. Bobby Gaspar, 2014, The Journal of allergy and clinical immunology.

Genome-wide Testing: Genomic Medicine: Commentary on the article by Bar-Shira et al. on page 353

E. McCabe, S. Mcghee, S. McGhee, 2006, Pediatric Research.

Anaphylaxis to invasive chlorhexidine administration despite tolerance of topical chlorhexidine use.

Anna Postolova, D. Parris, Joseph D Hernandez, 2017, The journal of allergy and clinical immunology. In practice.

Consensus Guidelines for the Diagnosis and Management of Food Protein-Induced Enterocolitis Syndrome

R. A. Wood, A. Muraro, A. Burks, 2017 .

Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome (vol 124, pg 1289, 2009)

T. Chatila, J. Puck, S. Ehl, 2010 .

Is Dupilumab Effective in Treating Uncontrolled Moderate-to-Severe Asthma?

S. Mcghee, R. Lo, Rachelle M Lo, 2019, The journal of allergy and clinical immunology. In practice.

Disease Long-term Sinonasal Outcomes of Aspirin Desensitization in Aspirin Exacerbated Respiratory

K. Nadeau, P. Hwang, E. Soudry, 2014 .

Role of nonspecific cross-reacting antigen, a CD66 cluster antigen, in activation of human granulocytes

S. Hefta, S. Mcghee, L. Stevens, 1996, Infection and immunity.

granulocytes . CD 66 cluster antigen , in activation of human Role of nonspecific cross-reacting antigen , a

S. Hefta, L. Stevens, M. Klein, 1996 .