D. Buchbinder

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Impact of pre‐transplant depression on outcomes of allogeneic and autologous hematopoietic stem cell transplantation

W. Wood, M. Aljurf, J. Szer, 2017, Cancer.

B cell-intrinsic deficiency of the Wiskott-Aldrich syndrome protein (WASp) causes severe abnormalities of the peripheral B-cell compartment in mice.

J. Hartwig, L. Notarangelo, J. Walter, 2012, Blood.

Broad spectrum of autoantibodies in patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia.

L. Notarangelo, R. Geha, J. Chou, 2015, The Journal of allergy and clinical immunology.

Sedigheh Mirzaei Salehabadi, G. Armstrong, K. Krull, 2021, Journal of Cancer Survivorship.

Psychological outcomes of siblings of cancer survivors: a report from the Childhood Cancer Survivor Study

C. Recklitis, G. Armstrong, K. Krull, 2011, Psycho-oncology.

Risk factors for the development of cutaneous melanoma after allogeneic hematopoietic cell transplantation.

M. Tucker, B. Shaw, M. Flowers, 2018, Journal of the American Academy of Dermatology.

Spotlight on romiplostim in the treatment of children with chronic immune thrombocytopenia: design, development, and potential place in therapy

D. Buchbinder, D. Nugent, L. Hsieh, 2017, Drug design, development and therapy.

From 'Wizard' to 'Wicked': Adaptation Theory and Young Adult Fiction

D. Buchbinder, 2011 .

Risk of acute myeloid leukemia and myelodysplastic syndrome after autotransplants for lymphomas and plasma cell myeloma.

J. Fay, W. Wood, J. Maciejewski, 2018, Leukemia research.

“She Was a Little Social Butterfly”: A Qualitative Analysis of Parent Perception of Social Functioning in Adolescent and Young Adult Brain Tumor Survivors

K. Osann, S. Parsons, L. Wenzel, 2017, Journal of pediatric oncology nursing : official journal of the Association of Pediatric Oncology Nurses.

Tobacco Use Among Siblings of Childhood Cancer Survivors: A Report From the Childhood Cancer Survivor Study

C. Recklitis, G. Armstrong, K. Krull, 2016, Pediatric blood & cancer.

Newborn screening for severe combined immunodeficiency: an opportunity for intervention

J. Church, D. Buchbinder, A. Soni, 2013, Journal of Perinatology.

Unique Variant of NOD2 Pediatric Granulomatous Arthritis With Severe 1,25‐Dihydroxyvitamin D‐Mediated Hypercalcemia and Generalized Osteosclerosis

W. Mcalister, S. Mumm, M. Whyte, 2018, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Rubella Virus Infected Macrophages and Neutrophils Define Patterns of Granulomatous Inflammation in Inborn and Acquired Errors of Immunity

W. Al-Herz, K. Sullivan, R. Krüger, 2021, Frontiers in Immunology.

Sedigheh Mirzaei Salehabadi, G. Armstrong, K. Krull, 2021, Journal of Cancer Survivorship.

Late effects in hematopoietic cell transplant recipients with acquired severe aplastic anemia: a report from the late effects working committee of the center for international blood and marrow transplant research.

W. Wood, M. Sorror, M. Aljurf, 2012, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Diagnosis and clinical management of Wiskott–Aldrich syndrome: current and emerging techniques

H. Ochs, D. Buchbinder, Corey Cavannaugh, 2022, Expert review of clinical immunology.

Wiskott–Aldrich syndrome: diagnosis, current management, and emerging treatments

D. Buchbinder, D. Nugent, Alexandra H Fillipovich, 2014, The application of clinical genetics.

Non-Graft-versus-Host Disease Ocular Complications after Hematopoietic Cell Transplantation: Expert Review from the Late Effects and Quality of Life Working Committee of the Center for International Blood and Marrow Transplant Research and the Transplant Complications Working Party of the European S

M. Aljurf, R. Gale, N. Callander, 2019, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Non-GVHD ocular complications after hematopoietic cell transplantation: expert review from the Late Effects and Quality of Life Working Committee of the CIBMTR and Transplant Complications Working Party of the EBMT

M. Aljurf, R. Gale, N. Callander, 2019, Bone Marrow Transplantation.

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.

Screening for Wiskott-Aldrich syndrome by flow cytometry.

J. Bussel, Kejian Zhang, Ammar Husami, 2018, The Journal of allergy and clinical immunology.

Rash, Fever, and Pulmonary Hypertension in a 6‐Year‐Old Female

Andrew I. Shulman, R. Goldbach-Mansky, H. Brunner, 2018, Arthritis care & research.

Rubella Virus-Associated Cutaneous Granulomatous Disease: a Unique Complication in Immune-Deficient Patients, Not Limited to DNA Repair Disorders

C. Bodemer, C. Klein, H. Ochs, 2019, Journal of Clinical Immunology.

A patient with familial bone marrow failure and an inversion of chromosome 8.

D. Buchbinder, D. Nugent, T. Zadeh, 2011, Journal of pediatric hematology/oncology.

Successful autologous cord blood transplantation in a child with acquired severe aplastic anemia

I. Kirov, R. Childs, D. Margolis, 2013, Pediatric transplantation.

Quality of Life Among Parents of Adolescent and Young Adult Brain Tumor Survivors

K. Osann, S. Parsons, L. Wenzel, 2017, Journal of pediatric hematology/oncology.

Risk factors for the development of cutaneous melanoma after allogeneic hematopoietic cell transplantation.

M. Tucker, B. Shaw, M. Flowers, 2018, Journal of the American Academy of Dermatology.

Case Report: Pseudomonas can take a toll on a patient

J. Singh, D. Buchbinder, A. Arrieta, 2021, F1000Research.

Case Report: Pseudomonas can take a toll on a patient.

J. Singh, D. Buchbinder, A. Arrieta, 2021, F1000Research.

Therapeutic options for CTLA-4 Insufficiency.

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

compartment in mice (WASp) causes severe abnormalities of the peripheral B-cell intrinsic deficiency of the Wiskott-Aldrich syndrome protein - B cell

J. Hartwig, F. Frugoni, M. Massaad, 2012 .

Characteristics of Graft-versus-Host Disease (GvHD) after Post-transplant Cyclophosphamide versus Conventional GvHD Prophylaxis.

M. Perales, J. Pidala, C. Abboud, 2022, Transplantation and cellular therapy.

Second Allogeneic Hematopoietic Cell Transplantation for Patients with Fanconi Anemia and Bone Marrow Failure.

H. Deeg, J. Wagner, R. Gale, 2015, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Clinical risks and healthcare utilization of hematopoietic cell transplantation for sickle cell disease in the USA using merged databases

Michael J. Eckrich, W. Wood, Zhezhen Jin, 2017, Haematologica.

High risk of relapsed disease in patients with NK/T-cell chronic active Epstein-Barr virus disease outside of Asia

H. Heslop, C. Bollard, D. Hagin, 2021, Blood advances.

Hematopoietic Cell Transplantation for Congenital Dyserythropoietic Anemia. A Report from the Pediatric Transplant and Cellular Therapy Consortium (PTCTC).

M. Pulsipher, J. Stanek, D. Buchbinder, 2022, Transplantation and cellular therapy.

Characteristics of Late Fatal Infections after Allogeneic Hematopoietic Cell Transplantation.

M. Norkin, M. Aljurf, J. Wingard, 2019, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

What is the role of prophylaxis in the improvement of health-related quality of life of patients with hemophilia?

M. Ragni, D. Buchbinder, 2013, Hematology. American Society of Hematology. Education Program.

Lupus anticoagulant hypoprothrombinemia syndrome associated with severe thrombocytopenia in a child

A. Mahajerin, D. Buchbinder, Aimee Foord, 2017, Pediatric blood & cancer.

Successful cord blood transplantation in a patient with malignant infantile osteopetrosis and hemophilia

I. Kirov, D. Buchbinder, A. Soni, 2013, Pediatric transplantation.

Having It Both Ways: Cross-Dressing in Orton's What the Butler Saw and Churchill's Cloud Nine

D. Buchbinder, M. Macintyre, 1987 .

Kahn JM, Brazauskas R, Tecca HR, et al. Subsequent neoplasms and late mortality in children undergoing allogeneic transplantation for nonmalignant diseases. Blood Adv. 2020;4(9):2084-2094.

M. Norkin, B. George, R. Gale, 2020, Blood advances.

Predictors of lost to follow-up among pediatric and adult hematopoietic cell transplant survivors: A report from the Center for International Blood and Marrow Transplant Research.

W. Wood, M. Aljurf, A. Yoshimi, 2019, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Primary immune regulatory disorders for the pediatric hematologist and oncologist: A case‐based review

T. Torgerson, D. Buchbinder, S. Chandrakasan, 2019, Pediatric blood & cancer.

Second solid cancers after allogeneic hematopoietic cell transplantation using reduced-intensity conditioning.

M. Sorror, J. Wingard, U. Popat, 2014, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

NAPDH Oxidase-Specific Flow Cytometry Allows for Rapid Genetic Triage and Classification of Novel Variants in Chronic Granulomatous Disease

M. Cooper, R. Abraham, S. Bahna, 2019, Journal of Clinical Immunology.

Psychological status in childhood cancer survivors: a report from the Childhood Cancer Survivor Study.

C. Recklitis, Q. Lu, K. Krull, 2009, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Childhood Cancer Survivor Study

W. Leisenring, D. Buchbinder, J. Casillas, 2020, Definitions.

Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56bright NKG2A+++ Cells, and Yet Display Increased Degranulation and Higher Perforin Content

L. Notarangelo, J. Walter, V. Lougaris, 2017, Front. Immunol..

Clinical Challenges: Identification of Patients With Novel Primary Immunodeficiency Syndromes.

G. Uzel, D. Buchbinder, D. Nugent, 2017, Journal of pediatric hematology/oncology.

Meeting the Psychosocial Needs of Sibling Survivors

L. Zeltzer, D. Buchbinder, J. Casillas, 2011, Journal of pediatric oncology nursing : official journal of the Association of Pediatric Oncology Nurses.

Lymphocytes Utilize Somatic Mutations, Epigenetic Silencing, and the Proteasome to Escape Truncated WASP Expression

E. Behrens, N. Romberg, D. Buchbinder, 2022, Journal of Clinical Immunology.

Country-Level Macroeconomic Indicators Predict Early Post-Allogeneic Hematopoietic Cell Transplantation Survival in Acute Lymphoblastic Leukemia: A CIBMTR Analysis.

W. Wood, K. Sullivan, M. Aljurf, 2018, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Successful treatment of post‐transplant thrombocytopenia with romiplostim in a pediatric patient with X‐linked chronic granulomatous disease

R. Krance, D. Buchbinder, D. Nugent, 2014, Pediatric transplantation.

Successful treatment of secondary graft failure following unrelated cord blood transplant with hematopoietic growth factors in a pediatric patient with Fanconi anemia

A. Mahajerin, D. Buchbinder, A. Soni, 2015, Pediatric transplantation.

Inflammatory polyps following successful HLA‐matched cord blood transplantation in a patient with X‐linked lymphoproliferative syndrome

D. Buchbinder, A. Soni, D. Nugent, 2012, Pediatric transplantation.

L. Notarangelo, J. Walter, Karin Chen, 2016, Journal of Clinical Immunology.

Impact of T Cell Dose on Outcome of T Cell-Replete HLA-Matched Allogeneic Peripheral Blood Stem Cell Transplantation.

R. Vij, M. Aljurf, R. Gale, 2019, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Excellent Overall Survival and Low Incidence of Late Effects in Patients Undergoing Allogeneic Hematopoietic Cell Transplant for Sickle Cell Disease: A Report from the Center for International Blood and Marrow Transplant Research (CIBMTR)

B. Shaw, L. Krishnamurti, R. Phelan, 2019, Blood.

Broad-spectrum antibodies against self-antigens and cytokines in RAG deficiency.

J. B. Oliveira, R. Gelman, L. Notarangelo, 2015, The Journal of clinical investigation.

Identification of Patients with RAG Mutations Previously Diagnosed with Common Variable Immunodeficiency Disorders

Emily M. Coonrod, J. McElwee, L. Notarangelo, 2014, Journal of Clinical Immunology.

Monozygotic Twin Pair Showing Discordant Phenotype for X-linked Thrombocytopenia and Wiskott–Aldrich Syndrome: a Role for Epigenetics?

K. Nadeau, D. Buchbinder, D. Nugent, 2011, Journal of Clinical Immunology.

Application of a radiosensitivity flow assay in a patient with DNA ligase 4 deficiency.

M. Cowan, R. Abraham, D. Buchbinder, 2018, Blood advances.

Mild B-cell lymphocytosis in patients with a CARD11 C49Y mutation.

A. Fischer, A. Durandy, J. Stinson, 2015, The Journal of allergy and clinical immunology.

Hematopoietic stem cell transplantation for infantile osteopetrosis.

P. Veys, E. Horwitz, M. Ayas, 2015, Blood.

Outcomes and Treatment Strategies for Autoimmunity and Hyperinflammation in Patients with RAG Deficiency.

L. Notarangelo, J. Walter, R. Geha, 2019, The journal of allergy and clinical immunology. In practice.

Characterization of T and B cell repertoire diversity in patients with RAG deficiency

Hao Wu, L. Notarangelo, J. Walter, 2016, Science Immunology.

Broad-spectrum antibodies against self-antigens and cytokines in RAG deficiency.

J. B. Oliveira, R. Gelman, L. Notarangelo, 2016, The Journal of clinical investigation.

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.

Prevalence and clinical challenges among adults with primary immunodeficiency and recombination-activating gene deficiency.

Sri V. V. Deevi, Kenneth G. C. Smith, K. Stirrups, 2018, The Journal of allergy and clinical immunology.

X-linked Hyper IgM Syndrome: A Novel Sequence Variant Associated With An Atypical Mild Phenotype

D. Buchbinder, D. Nugent, S. Park, 2012, Journal of pediatric hematology/oncology.

Clinical efficacy of gene-modified stem cells in adenosine deaminase–deficient immunodeficiency

Barbara Engel, John Tse, David Gjertson, 2017, The Journal of clinical investigation.

Long‐term outcomes among 2‐year survivors of autologous hematopoietic cell transplantation for Hodgkin and diffuse large b‐cell lymphoma

W. Wood, Z. DeFilipp, B. Shaw, 2018, Cancer.

Late effects after ablative allogeneic stem cell transplantation for adolescent and young adult acute myeloid leukemia.

J. Liesveld, Z. DeFilipp, B. Shaw, 2020, Blood advances.

Psychosocial and financial issues after hematopoietic cell transplantation.

D. Buchbinder, N. Khera, 2021, Hematology. American Society of Hematology. Education Program.

Neurocognitive dysfunction in hematopoietic cell transplant recipients: expert review from the late effects and Quality of Life Working Committee of the CIBMTR and complications and Quality of Life Working Party of the EBMT

M. Norkin, A. Nagler, J. Szer, 2018, Bone Marrow Transplantation.

Survival and Late Effects after Allogeneic Hematopoietic Cell Transplantation for Hematologic Malignancy at Less than Three Years of Age.

M. Aljurf, L. Diller, R. Gale, 2017, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Survival improvements in adolescents and young adults after myeloablative allogeneic transplantation for acute lymphoblastic leukemia.

W. Wood, M. Aljurf, K. Ballen, 2014, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Pre-transplant marital status and hematopoietic cell transplantation outcomes.

W. Wood, K. Sullivan, M. Aljurf, 2020, Current oncology.

Return to Work Among Young Adult Survivors of Allogeneic Hematopoietic Cell Transplantation in the United States.

M. Krem, Stephanie J. Lee, K. Syrjala, 2021, Transplantation and cellular therapy.

Inappropriate sinus tachycardia after hematopoietic stem cell transplantation.

K. Shannon, T. Moore, D. Levi, 2010, Journal of pediatric hematology/oncology.

Inferior Access to Allogeneic Transplant in Disadvantaged Populations: A CIBMTR Analysis.

W. Wood, M. Aljurf, H. Lazarus, 2019, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Compound Heterozygous DOCK8 Mutations in a Patient with B Lymphoblastic Leukemia and EBV-Associated Diffuse Large B Cell Lymphoma

I. Kirov, A. Freeman, H. Su, 2019, Journal of Clinical Immunology.

Outcomes for Nitazoxanide Treatment in a Case Series of Patients with Primary Immunodeficiencies and Rubella Virus-Associated Granuloma

K. Sullivan, M. Dorsey, T. Hautala, 2019, Journal of Clinical Immunology.

Donor body mass index does not predict graft versus host disease following hematopoietic cell transplantation

M. Norkin, R. Vij, M. Horowitz, 2018, Bone Marrow Transplantation.

Copper Deficiency and Cytopenias.

D. Buchbinder, A. Nael, Sonia Morales, 2021, Journal of pediatric hematology/oncology.

Cancer Prevention and Screening Practices of Siblings of Childhood Cancer Survivors: A Report from the Childhood Cancer Survivor Study

C. Recklitis, G. Armstrong, M. Hudson, 2012, Cancer Epidemiology, Biomarkers & Prevention.

Identification of Patients with RAG Mutations Previously Diagnosed with Common Variable Immunodeficiency Disorders

J. McElwee, L. Notarangelo, J. Walter, 2015, Journal of Clinical Immunology.

Inferior Access to Allogeneic Transplant in Disadvantaged Populations: A CIBMTR Analysis.

W. Wood, M. Aljurf, H. Lazarus, 2016, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Congenital dyserythropoietic anemia type I: First report from the Congenital Dyserythropoietic Anemia Registry of North America (CDAR).

R. Lorsbach, T. McCavit, Wenying Zhang, 2020, Blood cells, molecules & diseases.

Psychosocial care providers’ perspectives: Barriers to implementing services for siblings of children with cancer

M. Alderfer, D. Buchbinder, Christina M. Sharkey, 2021, Pediatric blood & cancer.

NAPDH Oxidase-Specific Flow Cytometry Allows for Rapid Genetic Triage and Classification of Novel Variants in Chronic Granulomatous Disease

M. Cooper, R. Abraham, S. Bahna, 2019, Journal of Clinical Immunology.

D. Buchbinder, A. Soni, D. Nugent, 2012, Pediatric transplantation.

Financial hardship among siblings of long-term survivors of childhood cancer: A Childhood Cancer Survivor Study (CCSS) report.

Arti D. Desai, P. Nathan, Zhiyuan Zheng, 2023, Journal of Clinical Oncology.

Treatment of atypical central neurocytoma in a child with high dose chemotherapy and autologous stem cell rescue

N. Salamon, Joseph L. Lasky, W. Yong, 2009, Journal of Neuro-Oncology.

Moyamoya in a child treated with interferon for recurrent osteosarcoma.

D. Buchbinder, J. Casillas, M. Linetsky, 2010, Journal of pediatric hematology/oncology.

Outcomes for Nitazoxanide Treatment in a Case Series of Patients with Primary Immunodeficiencies and Rubella Virus-Associated Granuloma

K. Sullivan, M. Dorsey, T. Hautala, 2019, Journal of Clinical Immunology.

Corrigendum: Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56bright NKG2A+++ Cells, and Yet Display Increased Degranulation and Higher Perforin Content

L. Notarangelo, J. Walter, V. Lougaris, 2017, Front. Immunol..

Financial hardship in childhood cancer survivors treated with hematopoietic cell transplant: A report from the Childhood Cancer Survivor Study.

P. Nathan, G. Armstrong, Y. Yasui, 2023, Transplantation and cellular therapy.

The Application of Clinical Genetics Dovepress Wiskott–aldrich Syndrome: Diagnosis, Current Management, and Emerging Treatments

D. Buchbinder, D. Nugent, Alexandra H Fillipovich, 2022 .

Correction: Non-GVHD ocular complications after hematopoietic cell transplantation: expert review from the Late Effects and Quality of Life Working Committee of the CIBMTR and Transplant Complications Working Party of the EBMT

M. Aljurf, R. Gale, N. Callander, 2019, Bone Marrow Transplantation.

SECOND MALIGNANCIES AFTER AUTOLOGOUS HEMATOPOIETIC CELL TRANSPLANTATION IN CHILDREN

W. Wood, M. Sorror, J. Wingard, 2012, Bone Marrow Transplantation.

Congenital Dyserythropoietic Anemia Type I Due to Biallelic CDAN1 mutations: Report from the Congenital Dyserythropoietic Anemia Registry (CDAR)

R. Lorsbach, T. McCavit, Wenying Zhang, 2019, Blood.

Pediatric resident knowledge, experience, comfort, and perceived competency in providing sibling psychosocial support

M. Alderfer, D. Buchbinder, R. Kolarik, 2020, International journal of medical education.

Psychological status in childhood cancer survivors: a report from the Childhood Cancer Survivor Study.

C. Recklitis, Q. Lu, K. Krull, 2009, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Topics in Antiviral Medicine

D. Buchbinder, MD Mph Albert Liu, 94102. Dr Liu, 2021 .

Parent proxy assessment of sibling quality of life following pediatric hematopoietic cell transplantation

L. Zeltzer, Sunita K. Patel, S. Parsons, 2019, Health and Quality of Life Outcomes.

Outcomes and Treatment Strategies for Autoimmunity and Hyperinflammation in Patients with RAG Deficiency.

L. Notarangelo, J. Walter, R. Geha, 2019, The journal of allergy and clinical immunology. In practice.

Broad-spectrum antibodies against self-antigens and cytokines in RAG deficiency.

J. B. Oliveira, R. Gelman, L. Notarangelo, 2016, The Journal of clinical investigation.