J. Heimall

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Severe malnutrition resulting from use of rice milk in food elimination diets for atopic dermatitis.

A. Cianferoni, M. Keller, Michele Shuker, 2012, The Israel Medical Association journal : IMAJ.

Disorders of CTLA-4 expression, how they lead to CVID and dysregulated immune responses.

J. Heimall, Di Sun, 2019, Current opinion in allergy and clinical immunology.

Risk Factors and Clinical Significance of Lymphopenia in Survivors of the Fontan Procedure for Single-Ventricle Congenital Cardiac Disease.

J. Rychik, K. Sullivan, L. Forbes, 2016, The journal of allergy and clinical immunology. In practice.

Geographical distribution of allergy/immunology providers in the United States and association with median income.

J. Heimall, Di Sun, 2020, The journal of allergy and clinical immunology. In practice.

The immune deficiency of chromosome 22q11.2 deletion syndrome

K. Sullivan, J. Heimall, M. Morsheimer, 2017, American journal of medical genetics. Part A.

Mini Review: Screening and Management of Late Effects in Patients with Severe Combined Immunodeficiency after Allogeneic Hematopoietic Cell Transplantation

blockquote, J. Heimall, Danielle E Arnold, 2018 .

Subcutaneous immunoglobulin replacement following CD19‐specific chimeric antigen receptor T‐cell therapy for B‐cell acute lymphoblastic leukemia in pediatric patients

S. Grupp, C. Callahan, S. Maude, 2019, Pediatric blood & cancer.

Growth in Children with a Fontan Circulation.

J. Rychik, D. Goldberg, Kathryn M. Dodds, 2021, The Journal of pediatrics.

Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis.

L. Notarangelo, G. Giardino, C. Pignata, 2019, American journal of human genetics.

Pathogenesis of Hyper IgE Syndrome

S. Holland, A. Freeman, J. Heimall, 2010, Clinical reviews in allergy & immunology.

Cost Utility of Lifelong Immunoglobulin Replacement Therapy vs Hematopoietic Stem Cell Transplant to Treat Agammaglobulinemia.

M. Greenhawt, N. Romberg, N. Bunin, 2021, JAMA pediatrics.

Differences in egg and milk food challenge outcomes based on tolerance to the baked form.

P. Capucilli, N. Pawlowski, R. Saltzman, 2018, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

Advances in atopic dermatitis in 2017

J. Spergel, J. Heimall, Katie Kennedy, 2018, The Journal of allergy and clinical immunology.

A Review of Chronic Granulomatous Disease

J. Heimall, Danielle E Arnold, Danielle E. Arnold, 2017, Advances in Therapy.

Identification of 22q11.2 Deletion Syndrome via Newborn Screening for Severe Combined Immunodeficiency

E. Zackai, K. Sullivan, D. McDonald-McGinn, 2017, Journal of Clinical Immunology.

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.

Therapeutic options for CTLA-4 Insufficiency.

V. Lougaris, T. Morio, K. Sullivan, 2021, The Journal of allergy and clinical immunology.

Filaggrin Mutations and the Atopic March

J. Spergel, J. Heimall, 2014 .

Filaggrin mutations and atopy: consequences for future therapeutics

J. Spergel, J. Heimall, 2012, Expert review of clinical immunology.

Food , drug , insect sting allergy , and anaphylaxis Omalizumab facilitates rapid oral desensitization for peanut allergy

K. Nadeau, D. Umetsu, L. Schneider, 2017 .

Reduced-Intensity/Reduced-Toxicity Conditioning Approaches Are Tolerated in XIAP Deficiency but Patients Fare Poorly with Acute GVHD

S. Choo, S. Ehl, A. Worth, 2021, Journal of clinical immunology.

At-home Dosing Adherence During Characterized Oral Desensitization Immunotherapy (CODIT) for Peanut Allergy

E. Crestani, A. Burks, B. Vickery, 2017 .

Chronic Granulomatous Disease

J. Heimall, Danielle E Arnold, Danielle E. Arnold, 2021, Primary and Secondary Immunodeficiency.

Immunodeficiency in 22q11.2 duplication syndrome.

S. Jyonouchi, J. Heimall, Di Sun, 2020, The journal of allergy and clinical immunology. In practice.

Long term outcomes of severe combined immunodeficiency: therapy implications

M. Cowan, J. Heimall, 2017, Expert review of clinical immunology.

Use of Genetic Testing for Primary Immunodeficiency Patients

J. Orange, J. Chou, T. Torgerson, 2018, Journal of Clinical Immunology.

Healing of Granulomatous Skin Changes in Ataxia‐Telangiectasia After Treatment with Intravenous Immunoglobulin and Topical Mometasone 0.1% Ointment

J. Treat, A. Yan, G. Ram, 2014, Pediatric dermatology.

What to Do with an Abnormal Newborn Screen for Severe Combined Immune Deficiency.

J. Heimall, H. Chong, Scott H. Maurer, 2019, Immunology and allergy clinics of North America.

A critical role for STAT3 transcription factor signaling in the development and maintenance of human T cell memory.

S. Holland, D. Douek, J. Brenchley, 2011, Immunity.

Granulocyte Transfusions in Patients with Chronic Granulomatous Disease Undergoing Hematopoietic Cell Transplantation or Gene Therapy

L. Notarangelo, J. Puck, T. Torgerson, 2022, Journal of Clinical Immunology.

Gain-of-Function STAT1 Mutation With Familial Lymphadenopathy and Hodgkin Lymphoma

L. Forbes, S. Henrickson, G. Brodeur, 2019, Front. Pediatr..

Heterozygous OAS1 gain-of-function variants cause an autoinflammatory immunodeficiency

H. Kanegane, C. Klein, T. Morio, 2021, Science Immunology.

Current Knowledge and Priorities for Future Research in Late Effects after Hematopoietic Stem Cell Transplantation (HCT) for Severe Combined Immunodeficiency Patients: A Consensus Statement from the Second Pediatric Blood and Marrow Transplant Consortium International Conference on Late Effects afte

L. Notarangelo, J. Puck, A. Gennery, 2017, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Gastrointestinal Manifestations of STAT3-Deficient Hyper-IgE Syndrome

S. Holland, D. Kleiner, A. Venkatesan, 2017, Journal of Clinical Immunology.

Expectations and experience: Parent and patient perspectives regarding treatment for Severe Combined Immunodeficiency (SCID).

J. Puck, M. Cowan, C. Scalchunes, 2021, Clinical immunology.

Immune reconstitution and survival of 100 SCID patients post-hematopoietic cell transplant: a PIDTC natural history study.

L. Notarangelo, J. Puck, K. Sullivan, 2017, Blood.

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

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

Efficacy and Safety of AR101 in Oral Immunotherapy for Peanut Allergy: Results of ARC001, a Randomized, Double-Blind, Placebo-Controlled Phase 2 Clinical Trial.

E. Crestani, A. Burks, B. Vickery, 2018, The journal of allergy and clinical immunology. In practice.

SCID genotype and 6-month posttransplant CD4 count predict survival and immune recovery.

L. Notarangelo, J. Puck, K. Sullivan, 2018, Blood.

Protein and lymphatic loss conditions

Joyce E. Yu, J. Heimall, 2020 .

Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease

Phillip A. Richmond, A. Hoischen, J. Casanova, 2022, medRxiv.

The Natural History of Children with Severe Combined Immunodeficiency: Baseline Features of the First Fifty Patients of the Primary Immune Deficiency Treatment Consortium Prospective Study 6901

L. Notarangelo, J. Puck, S. Pai, 2013, Journal of Clinical Immunology.

Patients with common variable immunodeficiency with autoimmune cytopenias exhibit hyperplastic yet inefficient germinal center responses

C. Cunningham-Rundles, K. Sullivan, E. Meffre, 2019, The Journal of allergy and clinical immunology.

Reduced‐intensity conditioning for hematopoietic cell transplantation of chronic granulomatous disease

N. Bunin, B. Oshrine, J. Heimall, 2015, Pediatric blood & cancer.

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.

Immune Reconstitution Following TCRαβ/CD19-Depleted Hematopoietic Cell Transplantation for Hematologic Malignancy in Pediatric Patients.

D. Monos, A. Seif, S. Grupp, 2021, Transplantation and cellular therapy.

Now Is the Time to Use Molecular Gene Testing for the Diagnosis of Primary Immune Deficiencies.

J. Heimall, 2019, The journal of allergy and clinical immunology. In practice.

Genetic Testing to Diagnose Primary Immunodeficiency Disorders and to Identify Targeted Therapy.

J. Heimall, 2019, Immunology and allergy clinics of North America.

Follow-Up for an Abnormal Newborn Screen for Severe Combined Immunodeficiencies (NBS SCID): A Clinical Immunology Society (CIS) Survey of Current Practices

T. Torgerson, N. Wright, R. Abraham, 2020, International journal of neonatal screening.

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

S. Holland, Joie Davis, A. Hsu, 2011, Clinical immunology.

Identification of 22q11.2 Deletion Syndrome via Newborn Screening for Severe Combined Immunodeficiency

E. Zackai, K. Sullivan, D. McDonald-McGinn, 2017, Journal of Clinical Immunology.

Chronic Granulomatous Disease-Associated IBD Resolves and Does Not Adversely Impact Survival Following Allogeneic HCT

L. Notarangelo, J. Puck, T. Torgerson, 2019, Journal of Clinical Immunology.

Reduced-Intensity/Reduced-Toxicity Conditioning Approaches Are Tolerated in XIAP Deficiency but Patients Fare Poorly with Acute GVHD

S. Choo, S. Ehl, A. Worth, 2021, Journal of Clinical Immunology.

The diagnosis of severe combined immunodeficiency: Implementation of the PIDTC 2022 Definitions

L. Notarangelo, J. Puck, K. Sullivan, 2022, The Journal of allergy and clinical immunology.

The diagnosis of severe combined immunodeficiency (SCID): The Primary Immune Deficiency Treatment Consortium (PIDTC) 2022 Definitions

L. Notarangelo, J. Puck, S. Pai, 2022, The Journal of allergy and 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.

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

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

Recommendations for Screening and Management of Late Effects in Patients with Severe Combined Immunodeficiency after Allogenic Hematopoietic Cell Transplantation: A Consensus Statement from the Second Pediatric Blood and Marrow Transplant Consortium International Conference on Late Effects after Ped

L. Notarangelo, J. Puck, A. Gennery, 2017, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Immunologic recovery in children after alternative donor allogeneic transplantation for hematologic malignancies: comparison of recipients of partially T cell-depleted peripheral blood stem cells and umbilical cord blood.

D. Teachey, D. Barrett, Yimei Li, 2013, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

A Toolkit and Framework for Optimal Laboratory Evaluation of Individuals with Suspected Primary Immunodeficiency.

Karin Chen, D. Vinh, M. Lawrence, 2021, The journal of allergy and clinical immunology. In practice.

Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorder.

Joseph T. Glessner, Ivan K. Chinn, J. Glessner, 2016, The Journal of allergy and clinical immunology.

Pharmacokinetics, Safety, and Tolerability of Subcutaneous Immune Globulin Injection (Human), 10 % Caprylate/Chromatography Purified (GAMUNEX®-C) in Pediatric Patients with Primary Immunodeficiency Disease

J. Church, G. Kleiner, J. Heimall, 2016, Journal of Clinical Immunology.

Common variable immunodeficiency-associated endotoxemia promotes early commitment to the T follicular lineage.

K. Sullivan, S. Henrickson, S. Jyonouchi, 2019, The Journal of allergy and clinical immunology.

Plasma metalloproteinase levels are dysregulated in signal transducer and activator of transcription 3 mutated hyper-IgE syndrome.

L. Dodd, S. Holland, A. Hsu, 2011, The Journal of allergy and clinical immunology.

T‐cell receptor sequencing demonstrates persistence of virus‐specific T cells after antiviral immunotherapy

Christopher A. Lazarski, D. Douek, S. Darko, 2019, British journal of haematology.

Distinct immune trajectories in patients with chromosome 22q11.2 deletion syndrome and immune-mediated diseases.

K. Sullivan, I. Campbell, M. Lambert, 2021, The Journal of allergy and clinical immunology.

Resolution of CGD Related Colitis after Allogeneic Hematopoietic Stem Cell Transplantation in Patients with Chronic Granulomatous Disease—Early Results From the 6903 Study of the Primary Immune Deficiency Treatment Consortium (PIDTC)

L. Notarangelo, J. Puck, K. Sullivan, 2018 .

A Path FORWARD: Development of a Comprehensive Multidisciplinary Clinic to Create Health and Wellness for the Child and Adolescent with a Fontan Circulation

J. Rychik, Nicholas P. Seivert, D. Goldberg, 2022, Pediatric Cardiology.

End‐Organ Function and Exercise Performance in Patients With Fontan Circulation: What Characterizes the High Performers?

J. Rychik, S. Paridon, D. Burstein, 2020, Journal of the American Heart Association.

Correction to: A Path FORWARD: Development of a Comprehensive Multidisciplinary Clinic to Create Health and Wellness for the Child and Adolescent with a Fontan Circulation

J. Rychik, Nicholas P. Seivert, D. Goldberg, 2022, Pediatric Cardiology.

Adoptive immunotherapy for primary immunodeficiency disorders with virus-specific T lymphocytes.

G. Lucchini, J. Orange, A. Gennery, 2016, The Journal of allergy and clinical immunology.

Viral-Specific T Lymphocytes for Treatment of Viral Infections in Primary Immunodeficiency

P. Hanley, C. Bollard, S. Jyonouchi, 2015 .

Immunologic, Molecular, and Clinical Profile of Patients with Chromosome 22q11.2 Duplications

E. Zackai, K. Sullivan, D. McDonald-McGinn, 2023, Journal of Clinical Immunology.

Defining complementary and alternative medicine in allergies and asthma

L. Bielory, J. Heimall, 2004, Clinical reviews in allergy & immunology.

Clinical immunology: literature review 2022

J. Heimall, 2022, Annals of Allergy, Asthma & Immunology.

Gastrointestinal Manifestations of STAT3-Deficient Hyper-IgE Syndrome

S. Holland, D. Kleiner, A. Venkatesan, 2017, Journal of Clinical Immunology.

Life after Peanut Immunotherapy

A. Cianferoni, J. Spergel, A. Reddy, 2017 .

Natural history of infants with non-SCID T cell lymphopenia identified on newborn screen.

M. Lawrence, H. Lederman, M. Keller, 2022, Clinical immunology.

The genetic landscape of severe combined immunodeficiency in the United States and Canada in the current era (2010-2018).

L. Notarangelo, J. Puck, T. Torgerson, 2019, The Journal of allergy and clinical immunology.

CMV-Seropositive Mothers of SCID: To Breastfeed or Not?

J. Walter, J. Heimall, 2019, The journal of allergy and clinical immunology. In practice.

Food Protein-Induced Enterocolitis Syndrome Food Challenges: Experience from a Large Referral Center.

N. Pawlowski, R. Saltzman, A. Cianferoni, 2019, The journal of allergy and clinical immunology. In practice.

Review of complementary and alternative medicine in treatment of ocular allergies

L. Bielory, J. Heimall, 2003, Current opinion in allergy and clinical immunology.

Allogeneic hematopoietic stem cell transplantation in adolescent patients with chronic granulomatous disease.

K. Sullivan, A. Seif, S. Jyonouchi, 2019, The journal of allergy and clinical immunology. In practice.

New pathways for itching in patients with atopic dermatitis?

J. Spergel, J. Heimall, 2017, The Journal of allergy and clinical immunology.

A Retrospective Review of Revaccination Patterns in Pediatric Hematopoietic Stem Cell Transplantation Recipients.

Talene A. Metjian, B. Fisher, J. Freedman, 2023, Journal of pediatric hematology/oncology nursing.

Safety and Efficacy of Hizentra® Following Pediatric Hematopoietic Cell Transplant for Treatment of Primary Immunodeficiencies.

T. Torgerson, N. Patel, M. Thakar, 2023, Journal of clinical immunology.

J. Church, G. Kleiner, J. Heimall, 2016, Journal of Clinical Immunology.

Early Hematopoietic Cell Transplant (HCT) Outcomes of Children with Severe Combined Immunodeficiency Disease (SCID): The First Seventy Four Patients of the Primary Immune Deficiency Treatment Consortium (PIDTC) Prospective Study 6901

L. Notarangelo, J. Puck, K. Sullivan, 2015 .

Measuring the effect of newborn screening on survival after haematopoietic cell transplantation for severe combined immunodeficiency: a 36-year longitudinal study from the Primary Immune Deficiency Treatment Consortium

L. Notarangelo, J. Puck, T. Torgerson, 2023, The Lancet.

The Efficacy of AR101, a Peanut-Derived Pharmaceutical for Oral Immunotherapy (OIT), Is Maintained and Tolerability Is Increased with Low-Dose Maintenance Therapy

E. Crestani, A. Burks, B. Vickery, 2016 .

Evaluation and subsequent safe administration of rabies vaccine to a child presumably allergic to the gelatin content of PCECV Rabavert.

S. Sindher, R. Saltzman, J. Heimall, 2015, Journal of Allergy and Clinical Immunology: In Practice.

Monogenic Early-Onset Lymphoproliferation and Autoimmunity: The Natural History of STAT3 GOF Syndrome.

K. Schwarz, M. Weinrich, F. Rieux-Laucat, 2022, The Journal of allergy and clinical immunology.

Rapid resolution of diffuse warts following initiation of dupilumab for severe atopic dermatitis

J. Treat, P. Sockler, J. Heimall, 2023, Pediatric dermatology.

S. Holland, K. Sullivan, N. Bunin, 2016, The Journal of allergy and clinical immunology.

Hematopoietic Stem Cell Transplant for the Treatment of X-MAID

M. Deardorff, S. Henrickson, B. Neven, 2019, Front. Pediatr..

Autoimmune Phenotypes in Patients with Autosomal dominant Hyper-IgE/Job's Syndrome

S. Holland, J. Milner, A. Freeman, 2010 .

Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease

Phillip A. Richmond, A. Hoischen, W. Wasserman, 2023, The Journal of experimental medicine.

Use of Genetic Testing for Primary Immunodeficiency Patients

J. Orange, J. Chou, T. Torgerson, 2018, Journal of Clinical Immunology.

COVID-19 Vaccination in Patients with Inborn Errors of Immunity Reduces Hospitalization and Critical Care Needs Related to COVID-19: a USIDNET Report

G. Giardino, C. Pignata, J. Puck, 2024, Journal of clinical immunology.

Diagnosis of 22q11.2 Deletion Syndrome and Artemis Deficiency in Two Children with T-B-NK+ Immunodeficiency

D. McDonald-McGinn, D. Moshous, M. Markert, 2012, Journal of Clinical Immunology.

A Path FORWARD: Development of a Comprehensive Multidisciplinary Clinic to Create Health and Wellness for the Child and Adolescent with a Fontan Circulation

J. Rychik, Nicholas P. Seivert, D. Goldberg, 2022, Pediatric Cardiology.

Intestinal microbiome and metabolome signatures in patients with chronic granulomatous disease.

C. Deming, S. Conlan, J. Segre, 2023, The Journal of allergy and clinical immunology.

Relevance of lymphocyte proliferation to PHA in severe combined immunodeficiency (SCID) and T cell lymphopenia.

J. Puck, T. Torgerson, S. Pai, 2024, Clinical immunology.

Genotype, Oxidase Status, and Preceding Infection or Autoinflammation Do Not Affect Allogeneic HCT Outcomes for CGD.

L. Notarangelo, J. Puck, T. Torgerson, 2023, Blood.

Healing of Granulomatous Skin Changes in Ataxia‐Telangiectasia After Treatment with Intravenous Immunoglobulin and Topical Mometasone 0.1% Ointment

J. Treat, A. Yan, G. Ram, 2014, Pediatric dermatology.