M. Dorsey

发表

Immune deficiencies, infection, and systemic immune disordersDominant gain-of-function STAT1 mutations in FOXP3 wild-type immune dysregulation–polyendocrinopathy–enteropathy–X-linked–like syndrome

J. Yim, S. Holland, T. Torgerson, 2013 .

Fiscal implications of newborn screening in the diagnosis of severe combined immunodeficiency.

A. Zbrozek, M. Dorsey, Catherine Kubiak, 2014, The journal of allergy and clinical immunology. In practice.

Update on the use of immunoglobulin in human disease: A review of evidence

Ivan K. Chinn, J. Orange, E. Hossny, 2017, The Journal of allergy and clinical immunology.

Impaired specific antibody response and increased B-cell population in transient hypogammaglobulinemia of infancy.

J. Orange, M. Dorsey, 2006, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

Supporting caregivers during hematopoietic cell transplantation for children with primary immunodeficiency disorders.

M. Dorsey, V. Yank, C. Mangurian, 2019, The Journal of allergy and clinical immunology.

Transfer of monoclonal antibodies into breastmilk in neurologic and non-neurologic diseases

Sara C. LaHue, M. Dorsey, R. Bove, 2020, Neurology: Neuroimmunology & Neuroinflammation.

Influenza vaccine in 55 patients with egg allergy

M. Dorsey, H. Oettgen, L. Schneider, 2005 .

Dominant gain-of-function STAT1 mutations in FOXP3 WT IPEX-like Syndrome

Anahita, J. Yim, S. Holland, 2013 .

Disease Progression of WHIM Syndrome in an International Cohort of 66 Pediatric and Adult Patients

Shannon M. McNulty, J. Walter, H. Kanegane, 2022, Journal of Clinical Immunology.

Complete DiGeorge syndrome associated with CHD7 mutation.

M. Dorsey, J. Sleasman, M. Loscalzo, 2007, The Journal of allergy and clinical immunology.

IMPROVING ASTHMA OUTCOMES AND SELF-MANAGEMENT BEHAVIORS OF INNER-CITY CHILDREN

L. Schneider, M. Dorsey, 2003, Pediatrics.

Extended Follow-up After Hematopoietic Cell Transplantation for IκBα Deficiency with Disseminated Mycobacterium avium Infection

J. Puck, M. Dorsey, C. Dvorak, 2019, Journal of Clinical Immunology.

Alterations in Regulatory T Cell Subpopulations Seen in Preterm Infants

M. Dorsey, N. Funderburg, A. Luciano, 2014, PloS one.

Subcutaneous Immunoglobulin Replacement Therapy with Hizentra® is Safe and Effective in Children Less Than 5 Years of Age

H. Ochs, E. Haddad, N. Patel, 2015, Journal of Clinical Immunology.

Long‐term outcomes of 176 patients with X‐linked hyper‐IgM syndrome treated with or without hematopoietic cell transplantation

L. Notarangelo, J. Chou, C. Cunningham-Rundles, 2017, The Journal of allergy and clinical immunology.

Assessment of adrenal suppression in children with asthma treated with inhaled corticosteroids: use of dehydroepiandrosterone sulfate as a screening test.

L. Cohen, M. Dorsey, W. Phipatanakul, 2006, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

Newborn Screening for Severe Combined Immunodeficiency and T-cell Lymphopenia in California, 2010–2017

J. Puck, J. Church, S. Sciortino, 2019, Pediatrics.

Eczema and Petechiae in an Infant.

M. Dorsey, K. Cordoro, K. Shimano, 2022, Pediatrics in review.

FOXP3 expression following bone marrow transplantation for IPEX syndrome after reduced-intensity conditioning

M. Dorsey, J. Sleasman, A. Petrovič, 2009, Immunologic research.

Treatment of infants identified as having severe combined immunodeficiency by means of newborn screening

J. Puck, M. Dorsey, C. Dvorak, 2017, The Journal of allergy and clinical immunology.

Chronic granulomatous disease associated colitis leading to profound zinc deficiency.

M. Dorsey, E. Perez, H. T. Ladinsky, 2014, The journal of allergy and clinical immunology. In practice.

Drug Sensitivity of Vaccine-Derived Rubella Viruses and Quasispecies Evolution in Granulomatous Lesions of Two Ataxia-Telangiectasia Patients Treated with Nitazoxanide

K. Sullivan, M. Dorsey, J. Icenogle, 2022, Pathogens.

Lentiviral gene therapy for X-linked chronic granulomatous disease

Luca Biasco, Adrian J. Thrasher, David A. Williams, 2020, Nature Medicine.

Infectious vaccine-derived rubella viruses emerge, persist, and evolve in cutaneous granulomas of children with primary immunodeficiencies

D. Gordenin, A. Zharkikh, K. Sullivan, 2019, PLoS pathogens.

Diagnostic Interpretation of Genetic Studies in Patients with Primary Immunodeficiency Diseases: A Working Group Report of the Primary Immunodeficiency Diseases Committee of the American Academy of Allergy, Asthma, and Immunology.

Ivan K. Chinn, J. Orange, J. Walter, 2019, The Journal of allergy and clinical immunology.

TASP1 mutation in a female with craniofacial anomalies, anterior segment dysgenesis, congenital immunodeficiency and macrocytic anemia

J. Pomerantz, M. Dorsey, A. Slavotinek, 2019, Molecular genetics & genomic medicine.

Clinical Experience With an L-Proline–Stabilized 10 % Intravenous Immunoglobulin (Privigen®): Real-Life Effectiveness and Tolerability

P. Soler-Palacín, M. Dorsey, M. Rojavin, 2014, Journal of Clinical Immunology.

Outcomes Following Treatment for Adenosine Deaminase Deficient Severe Combined Immunodeficiency: A Report from the PIDTC.

L. Notarangelo, J. Puck, T. Torgerson, 2022, Blood.

AR101 Oral Immunotherapy for Peanut Allergy

William H. Yang, N. Rupp, G. Toit, 2018, The New England journal of medicine.

Use of a fish oil-based lipid emulsion to treat essential fatty acid deficiency in a soy allergic patient receiving parenteral nutrition.

M. Dorsey, W. Phipatanakul, C. Duggan, 2005, Clinical nutrition.

T Cell Defects

M. Dorsey, M. Cowan, 2018 .

Hematopoietic Cell Transplantation in Patients With Primary Immune Regulatory Disorders (PIRD): A Primary Immune Deficiency Treatment Consortium (PIDTC) Survey

L. Notarangelo, J. Walter, J. Puck, 2020, Frontiers in Immunology.

Hematopoietic stem cell transplantation for pediatric patients with primary immunodeficiency diseases at All Children’s Hospital/University of South Florida

M. Dorsey, A. Petrovič, J. Miotke, 2009, Immunologic research.

Unconditioned unrelated donor bone marrow transplantation for IL7Rα- and Artemis-deficient SCID

J. Puck, M. Dorsey, C. Dvorak, 2017, Bone Marrow Transplantation.

Practical Approach to Genetic Testing for Primary Immunodeficiencies.

M. Lawrence, M. Dorsey, J. Chinen, 2019, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

Infections in Infants with SCID: Isolation, Infection Screening, and Prophylaxis in PIDTC Centers

L. Notarangelo, J. Puck, T. Torgerson, 2020, Journal of Clinical Immunology.

Infections in Infants with SCID: Isolation, Infection Screening, and Prophylaxis in PIDTC Centers

L. Notarangelo, J. Puck, T. Torgerson, 2020, Journal of Clinical Immunology.

A Novel Mutation CHS1 (LYST) Mutation: Osteomyelitis in a Child with Chediak-Higashi Syndrome

M. Dorsey, J. Sleasman, A. Petrovič, 2010 .

When Screening for Severe Combined Immunodeficiency (SCID) with T Cell Receptor Excision Circles Is Not SCID: a Case-Based Review

J. Walter, J. Puck, M. Dorsey, 2021, Journal of Clinical Immunology.

Low Exposure Busulfan Conditioning to Achieve Sufficient Multilineage Chimerism in Patients with Severe Combined Immunodeficiency.

J. Puck, James N. Huang, M. Dorsey, 2019, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Gastrointestinal Manifestations in X-linked Agammaglobulinemia

J. Walter, H. Ochs, M. Dorsey, 2017, Journal of Clinical Immunology.

Neurologic event-free survival demonstrates a benefit for SCID patients diagnosed by newborn screening.

J. Puck, M. Dorsey, C. Dvorak, 2017, Blood advances.

Mutations in the iron-sulfur cluster ligands of the human ferrochelatase lead to erythropoietic protoporphyria

M. Dorsey, X. Schneider-Yin, J. Deybach, 2000 .

Mutations in the iron-sulfur cluster ligands of the human ferrochelatase lead to erythropoietic protoporphyria.

M. Dorsey, X. Schneider-Yin, J. Deybach, 2000, Blood.

Mechanisms of genotype‐phenotype correlation in autosomal dominant anhidrotic ectodermal dysplasia with immune deficiency

J. Casanova, R. Geha, H. Kanegane, 2017, The Journal of allergy and clinical immunology.

disease and greater impairment of NF-κB activation in IκBa point mutants versus truncation mutants in autosomal dominant anhidrotic ectodermal dysplasia with immune deficiency

J. Casanova, R. Geha, H. Kanegane, 2017 .