USIDNET is proud of the publications emerging from registry data queries. Click below to explore the reference lists!
wdt_ID | Author(s) | Title | Journal | Yr. | Vol. | Pgs. |
---|---|---|---|---|---|---|
1 | Barmettler S, Otani I, Minhas J, Abraham RS, Chang Y, Dorsey MJ, Ballas ZK, Bonilla FA, Ochs HD, Walter JE | Gastrointestinal Manifestations in X-linked Agammaglobulinemia | J Clin Immunol | 2017 | 37 (3) | 287-294 |
2 | Hajjar J, Guffey D, Minard CG, Orange JS | Increased Incidence of Fatigue in Patients with Primary Immunodeficiency Disorders: Prevalence and Associations Within the US Immunodeficiency Network Registry | J Clin Immunol | 2017 | 37 (2) | 153-165 |
3 | Hartman H, Schneider K, Hintermeyer M, Bausch-Jurken M, Fuleihan R, Sullivan KE, Cunningham-Rundles C, Bonilla FA; USIDNET Consortium, Verbsky J, Routes J | Lack of Clinical Hypersensitivity to Penicillin Antibiotics in Common Variable Immunodeficiency | J Clin Immunol | 2017 | 37 (1) | 22-24 |
4 | Mayor PC, Eng KH, Singel KL, Abrams SI, Odunsi K, Moysich KB, Fuleihan R, Garabedian E, Lugar P, Ochs HD, Bonilla FA, Buckley RH, Sullivan KE, Ballas ZK, Cunningham-Rundles C, Segal BH | Cancer in primary immunodeficiency diseases: Cancer incidence in the United States Immune Deficiency Network Registry | J Allergy Clin Immunol | 2018 | 141 (3) | 1028-1035 |
5 | Sanchez LA, Maggadottir SM, Pantell MS, Lugar P, Rundles CC, Sullivan KE, USIDNET Consortium | Two Sides of the Same Coin: Pediatric-Onset and Adult-Onset Common Variable Immune Deficiency | J Clin Immunol | 2017 | 37 (6) | 592-602 |
6 | Gernez Y, Freeman AF, Holland SM, Garabedian E, Patel NC, Puck JM, Sullivan KE, Akhter J, Secord E, Chen K, Buckley R, Haddad E, Ochs HD, Fuleihan R, Routes J, Muskat M, Lugar P, Mancini J, Cunningham-Rundles C | Autosomal Dominant Hyper-IgE Syndrome in the USIDNET Registry | J Allergy Clin Immunol Pract | 2018 | 6 (3) | 996-1001 |
7 | Feuille EJ, Anooshiravani N, Sullivan KE, Fuleihan RL, Cunningham-Rundles C | Autoimmune Cytopenias and Associated Conditions in CVID: a Report From the USIDNET Registry | J Clin Immunol | 2018 | 38 (1) | 28-34 |
8 | Farmer J, Ong MS, Barmettler S, Yonker L, Fuleihan R, Sullivan K, Cunningham-Rundles C, Walter J | Common variable immunodeficiency (CVID) non-infectious disease endotypes redefined using unbiased network clustering in large electronic datasets | Front Immunol | 2018 | 8 | 1740 |
9 | Leven E, Maffucci1 P, Ochs H, Scholl P, Buckley R, Fuleihan R, Geha R, Cunningham C, Bonilla F, Conley ME, Ferdman R, Hernandez-Trujillo V, Puck J, Sullivan K, Secord E, Ramesh M, Cunningham-Rundles, C | Hyper IgM Syndrome: a Report from the USIDNET Registry | J Clin Immunol | 2016 | 36 (5) | 490-501 |
10 | Perelygina L, Plotkin S, Russo P, Hautala T, Bonilla F, Ochs HD, Joshi A, Routes J, Patel K, Wehr C, Icenogle J, Sullivan KE | Rubella persistence in epidermal keratinocytes and granuloma M2 macrophages in patients with primary immunodeficiencies | J Allergy Clin Immunol | 2016 | 138 (5) | 1436-1439 |
11 | Al-Herz W, Notarangelo LD, Sadek A, Buckley R; USIDNET Consortium | Combined immunodeficiency in the United States and Kuwait: Comparison of patients’ characteristics and molecular diagnosis USIDNET Consortium | Clin Immunol | 2015 | 161(2) | 170-3 |
12 | Seeborg FO, Seay R, Boyle M, Boyle J, Scalchunes C, Orange JS | Perceived Health in Patients with Primary Immune Deficiency | J Clin Immunol | 2015 | 35 (7) | 638-50 |
13 | Tuano KS, Orange JS, Sullivan K, Cunningham-Rundles C, Bonilla FA, Davis CM | Food allergy in patients with primary immune deficiency diseases: prevalence within the USIDNET | J Allergy Clin Immunol | 2015 | 135(1) | 273-5 |
14 | Costa-Reis P, Weaver LK, Behrens EM, Sullivan KE | Chronic non-bacterial osteomyelitis in a patient with common variable immunodeficiency | Joint Bone Spine | 2014 | 81(2) | 193-4 |
15 | de la Morena MT, Nelson RP Jr | Recent advances in transplantation for primary immune deficiency diseases: a comprehensive review | Clin Rev Allergy Immunol | 2014 | 46(2) | 131-44 |
16 | Shearer WT, Fleisher TA, Buckley RH, Ballas Z, Ballow M, Blaese RM, Bonilla FA, Conley ME, Cunningham-Rundles C, Filipovich AH, Fuleihan R, Gelfand EW, Hernandez-Trujillo V, Holland SM, Hong R, Lederman HM, Malech HL, Miles S, Notarangelo LD, Ochs HD, Ora | Recommendations for live viral and bacterial vaccines in immunodeficient patients and their close contacts | J Allergy Clin Immunol | 2014 | 133(4) | 961-6 |
17 | Sullivan KE, Puck JM, Notarangelo LD, Fuleihan R, Caulder T, Wang C, Boyle M, Cunningham-Rundles C | USIDNET: A Strategy to Build a Community of Clinical Immunologists | J Clin Immunol | 2014 | 34(4) | 428-35 |
18 | Al-Herz W, Al-Mousa H | Combined immunodeficiency: the Middle East experience | J Allergy Clin Immunol | 2013 | 131(3) | 658-60 |
19 | Ballow M | Managing comorbid complications in patients with common variable immunodeficiency | Ann Allergy Asthma Immunol | 2013 | 111(6 Suppl) | S6-9 |
20 | Patel K, Akhter J, Kobrynski L, Benjamin Gathmann MA, Davis O, Sullivan KE, International DiGeorge Syndrome Immunodeficiency Consortium | Immunoglobulin deficiencies: the B-lymphocyte side of DiGeorge Syndrome | J Pediatr | 2012 | 161(5) | 950-3 |
21 | Jain A, Kovacs JA, Nelson DL, Migueles SA, Pittaluga S, Fanslow W, Fan X, Wong DW, Massey J, Hornung R, Brown MR, Spinner JJ, Liu S, Davey V, Hill HA, Ochs H, Fleisher TA | Partial immune reconstitution of X-linked hyper IgM syndrome with recombinant CD40 ligand | Blood | 2011 | 118(14) | 3811-7 |
22 | Fleisher T, Notarangelo L | Primary immune deficiencies, once again leading the way | Clin Immunol | 2010 | 135(2) | 167-168 |
23 | Yong PL, Orange JS, Sullivan KE | Pediatric common variable immunodeficiency: immunologic and phenotypic associations with switched memory B cells. | Pediatr Allergy Immunol | 2010 | 21(5) | 852-8 |
24 | Waldrep ML, Zhuang Y, Schroeder HW Jr | Analysis of TACI mutations in CVID & RESPI patients with HLA-DQ2, -DR7, -DR3(17), -B8 or -B44 | BMC Med Genet | 2009 | 10 | 100 |
25 | Park MA, Li JT, Hagan JB, Maddox DE, Abraham RS | Common variable immunodeficiency: a new look at an old disease | Lancet | 2008 | 372(9637) | 489-502 |
26 | Winkelstein JA, Conley ME, James C, Howard V, Boyle J | Adults with X-linked agammaglobulinemia: impact of disease on daily lives, quality of life, educational and socioeconomic status, knowledge of inheritance, and reproductive attitudes | Medicine (Baltimore) | 2008 | 87(5) | 253-8 |
27 | Cunningham-Rundles C, Knight AK | Common variable immune deficiency: reviews, continued puzzles, and a new registry | Immunol Res | 2007 | 38(1-3) | 78-86 |
28 | Mehra A, Sidi P, Doucette J, Estrella L, Rouvelas H, Cunningham-Rundles C | Subspecialty evaluation of chronically ill hospitalized patients with suspected immune defects | Ann Allergy Asthma Immunol | 2007 | 99(2) | 143-150 |
29 | Puck JM, The SCID Newborn Screening Working Group | Population-based newborn screening for severe combined immunodeficiency: Steps toward implementation | J Allergy Clin Immunol | 2007 | 120(4) | 760-8 |
30 | Howard V, Greene JM, Pahwa S, Winkelstein JA, Boyle JM, Kocak M, Conley ME | The health status and quality of life of adults with X-linked agammaglobulinemia | Clin Immunol | 2006 | 118(2-3) | 201-8 |
31 | Winkelstein JA, Marino MC, Lederman HM, Jones SM, Sullivan K, Burks AW, Conley ME, Cunningham-Rundles C, Ochs HD | X-linked agammaglobulinemia: report on a United States registry of 201 patients | Medicine (Baltimore) | 2006 | 85 (4) | 193-202 |
32 | Halsey NA, Pinto J, Espinosa-Rosales F, Faure-Fontenla MA, da Silva E, Khan AJ, Webster AD, Minor P, Dunn G, Asturias E, Hussain H, Pallansch MA, Kew OM, Winkelstein J, Sutter R; Polio Project Team | Search for poliovirus carriers among people with primary immune deficiency diseases in the United States, Mexico, Brazil, and the United Kingdom | Bull World Health Organ | 2004 | 82(1) | 3-8 |
33 | Marciano BE, Wesley R, De Carlo ES, Anderson VL, Barnhart LA, Darnell D, Malech HL, Gallin JI, Holland SM | Long-term interferon-gamma therapy for patients with chronic granulomatous disease | Clin Infect Dis | 2004 | 39(5) | 692-9 |
34 | Shearer WT, Cunningham-Rundles C, Ochs HD | Primary immunodeficiency: Looking backwards, looking forwards | J Allergy Clin Immunol | 2004 | 113(4) | 607-609 |
35 | Gallin JI, Alling DW, Malech HL, Wesley R, Koziol D, Marciano B, Eisenstein EM, Turner ML, DeCarlo ES, Starling JM, Holland SM | Itraconazole to prevent fungal infections in chronic granulomatous disease | N Engl J Med | 2003 | 348(24) | 2416-22 |
36 | Winkelstein JA, Marino MC, Ochs H, Fuleihan R, Scholl PR, Geha R, Stiehm ER, Conley ME | The X-linked hyper-IgM syndrome: clinical and immunologic features of 79 patients | Medicine (Baltimore) | 2003 | 82(6) | 373-84 |
37 | Horwitz ME, Barrett AJ, Brown MR, Carter CS, Childs R, Gallin JI, Holland SM, Linton GF, Miller JA, Leitman SF, Read EJ, Malech HL. | Treatment of chronic granulomatous disease with nonmyeloablative conditioning and a T-cell-depleted hematopoietic allograft | N Engl J Med | 2001 | 344(12) | 881-8 |
38 | Razvi S, Schneider L, Jonas MM, Cunningham-Rundles C | Outcome of intravenous immunoglobulin-transmitted hepatitis C virus infection in primary immunodeficiency | Clin Immunol | 2001 | 101(3) | 284-8 |
39 | Rogers MH, Lwin R, Fairbanks L, Gerritsen B, Gaspar HB | Cognitive and behavioral abnormalities in adenosine deaminase deficient severe combined immunodeficiency | J Pediatr | 2001 | 139(1) | 44-50 |
40 | Chanock SJ, Roesler J, Zhan S, Hopkins P, Lee P, Barrett DT, Christensen BL, Curnutte JT, Görlach A. | Genomic structure of the human p47-phox (NCF1) gene | Blood Cells Mol Dis | 2000 | 26(1) | 37-46 |
41 | Winkelstein JA, Marino MC, Johnston RB Jr, Boyle J, Curnutte J, Gallin JI, Malech HL, Holland SM, Ochs H, Quie P, Buckley RH, Foster CB, Chanock SJ, Dickler H | Chronic granulomatous disease. Report on a national registry of 368 patients | Medicine (Baltimore) | 2000 | 79(3) | 155-69 |
42 | Chanock SJ, Foster CB | SNPing away at innate immunity | J Clin Invest | 1999 | 104(4) | 369-70 |
43 | Stonebraker JS, Hajjar J, Orange JS | Latent therapeutic demand model for the immunoglobulin replacement therapy of primary immune deficiency disorders in the USA | Vox Sang | 2018 | 113(5) | 430-440 |
44 | Ruffner MA, USIDNET Body Weight Group, Sullivan KE | Complications Associated with Underweight Primary Immunodeficiency Patients: Prevalence and Associations Within the USIDNET Registry | J Clin Immunol | 2018 | 38 (3) | 283-293 |
45 | Sacco K, Garabedian E, Sullivan K, USIDNET Consortium, Joshi A | Renal Disease in Chronic Granulomatous Disease: Data from the USIDNET Registry | J Clin Immunol | 2018 | 38 (5) | 556-557 |
47 | Gutierrez M, Sullivan K, Fuleihan R, Bingham O | Phenotypic Characterization of Patients With Rheumatologic Manifestations of Common Variable Immunodeficiency | Semin Arthritis Rheum | 2018 | 48(2) | 318-326 |
48 | Leung J, Sullivan KE, Perelygina L, Icenogle JP, Fuleihan RL, Lanzieri TM | Prevalence of Granulomas in Patients With Primary Immunodeficiency Disorders, United States: Data From National Health Care Claims and the US Immunodeficiency Network Registry | J Clin Immunol | 2018 | 38 (6) | 717-726 |
49 | de la Morena MT, Leonard D, Torgerson TR, Cabral-Marques O, Slatter M, Aghamohammadi A, Chandra S, Murguia-Favela L, Bonilla FA, Kanariou M, Damrongwatanasuk R, Kuo CY, Dvorak CC, Meyts I, Chen K, Kobrynski L, Kapoor N,... | Long-term outcomes of 176 patients with X-linked hyper-IgM syndrome treated with or without hematopoietic cell transplantation | J Allergy Clin Immunol | 2017 | 139(4) | 1282-1292 |
51 | Yonkof J, Gupta AO, Fu P, Garabedian E, Dalal JD | Early Transplant Improves Outcomes in Patients with Chronic Granulomatous Disease: Results from United States Immunodeficiency Network (USIDNET) | Blood | 2017 | 130 | 671 |
52 | Kellner ES, Fuleihan R, Cunningham-Rundles C, USIDNET Consortium, Wechsler JB | Cellular Defects in CVID Patients with Chronic Lung Disease in the USIDNET Registry. | J Clin Immunol | 2019 | 39(6) | 569–576 |
53 | Yonkof JR, Gupta A, Fu P, Garabedian E, Dalal J, USIDNET Consortium | Role of Allogeneic Hematopoietic Stem Cell Transplant for Chronic Granulomatous Disease (CGD): a Report of the United States Immunodeficiency Network. | J Clin Immunol | 2019 | 39 (4) | 448-458 |
54 | Weinberger T, Fuleihan R, Cunningham-Rundles, C, Maglione, P | Factors Beyond Lack of Antibody Govern Pulmonary Complications in Primary Antibody Deficiency | J Clin Immunol | 2019 | 39(4) | 440-447 |
55 | Lawrence MG, Palacios-Kibler TV, Workman LJ, Schuyler AJ, Steinke JW, Payne SC, McGowan EC, Patrie J, Fuleihan RL, Sullivan KE, Lugar PL, Hernandez CL, Beakes DE, Verbsky JW, Platts-Mills TAE, Cunningham-Rundles C, Routes JM, Borish L | Low Serum IgE Is a Sensitive and Specific Marker for Common Variable Immunodeficiency (CVID) | J Clin Immunol | 2018 | 38 (3) | 225-233 |
56 | Correa-Jimenez O, Restrepo-Gualteros S, Villamil-Osorio M, Cunningham-Rundles C, Sullivan KE, Fuleihan R, Gutierrez, MJ | Respiratory Comorbidities Associated with Bronchiectasis in Patients with Common Variable Immunodeficiency | J Allergy Clin Immunol | 2019 | 143 (2) | AB13 |
57 | Kelsen JR, Russo P, Sullivan KE | Early-Onset Inflammatory Bowel Disease | Immunol Allergy Clin North Am | 2019 | 39(1) | 63-79 |
58 | Patrawala M, Cui Y, Peng L, Fuleihan R, Garabedian E, Patel K, Guglani L | Pulmonary Disease Burden in Primary Immune Deficiency Disorders: Data from USIDNET Registry | J Clin Immunol | 2020 | 40(2) | 340–349 |
59 | Yakaboski E, Fuleihan RL, Sullivan KE, Cunningham-Rundles C, Feuille E | Lymphoproliferative Disease in CVID: a Report of Types and Frequencies from a US Patient Registry | J Clin Immunol | 2020 | 40 | 524-530 |
60 | Kuo CY, Garabedian E, Puck J, Cowan MJ, Sullivan KE, Buckley RH., ... & Kohn DB | Adenosine Deaminase (ADA)–Deficient Severe Combined Immune Deficiency (SCID) in the US Immunodeficiency Network (USIDNet) Registry | J Clin Immunol | 2020 | 40(8) | 1124–1131 |
61 | Lee M, Nguyen J, Fuleihan R, Gundling K, Cunningham-Rundles C, Otani IM | Neurologic Conditions and Symptoms Reported Among Common Variable Immunodeficiency Patients in the USIDNET | J Clin Immunol | 2020 | 40(8) | 1181–1183 |
62 | Zhang S, Kline M, Fuleihan RL, Consortium U, Scalchunes C, Sullivan KE, Jongco AM | PROMIS-29 survey confirms major impact of fatigue on health-related quality of life in common variable immunodeficiency | Immunol Res | 2020 | 68(6) | 379–388 |
63 | Pickett G, Motazedi T, Kutac C, Cahill G, Cunningham-Rundles C, Fuleihan RL, Sullivan KE, Rider NL | Infection Phenotypes Among Patients with Primary Antibody Deficiency Mined from a US Patient Registry | J Clin Immunol | 2021 | 41 (2) | 374-381 |
64 | Khan F, Person H, Dekio F, Ogawa M, Ho HE, Dunkin D, Secord E, Cunningham-Rundles C, Ward SC | Crohn’s-like Enteritis in X-Linked Agammaglobulinemia: A Case Series and Systematic Review | J Allergy Clin Immunol Pract | 2021 | 9(9) | 3466-3478 |
65 | Deshpande DR, Demirdag YY, Marsh RA, Sullivan KE, & Orange JS | Relationship Between Severity of T Cell Lymphopenia and Immune Dysregulation in Patients with DiGeorge Syndrome (22q11.2 Deletions and/or Related TBX1 Mutations): a USIDNET Study | J Clin Immunol | 2021 | 41(1) | 29-37 |
66 | Wallace L, Ware M, Cunningham-Rundles C, Fuleihan R, Maglione P | Clinical disparity of primary antibody deficiency patients at a safety net hospital | J Allergy Clin Immunol Pract | 2021 | 9(7) | 2923-2925 |
67 | Soshnick SH, Joseph T, Bennett NJ | Humoral Immunodeficiency and Immune Globulin Replacement Therapy (IGRT) Usage in DiGeorge Syndrome | J Clin Immunol | 2021 | 41(6) | 1208-1212 |
68 | Oh J, Garabedian E, Fuleihan R, Cunningham-Rundles C | Clinical Manifestations and Outcomes of Activated Phosphoinositide 3-Kinase δ Syndrome from the USIDNET Cohort | J Allergy Clin Immunol Pract | 2021 | 9(11) | 4095-4102 |
70 | Smith KL, Dai D, Modi BP, Sara R, Garabedian E, Marsh RA, Puck J, Secord E, Sullivan KE, Turvey SE, Biggs CM, USIDNET Consortium | Inborn Errors of Immunity Associated With Type 2 Inflammation in the USIDNET Registry | Front Immunol | 2022 | 13 | Article 831279 |
71 | LaBere B, Gutierrez MJ, Wright H, Garabedian E, Ochs HD, Fuleihan RL, Secord E, Marsh R, Sullivan, KE, Cunningham-Rundles C, Notarangelo LD, Chen K | Chronic Granulomatous Disease with Inflammatory Bowel Disease: Clinical Presentation, Treatment, and Outcomes From the USIDNET Registry | J Allergy Clin Immunol Pract | 2022 | 10(5) | 1325-1333.e5 |
72 | Durkee-Shock J, Zhang A, Liang H, Wright H, Magnusson J, Garabedian E, Marsh R, Sullivan KE, Keller M, USIDNET Consortium | Morbidity, Mortality, and Therapeutics in Combined Immunodeficiency: Data from the USIDNET Registry | J Allergy Clin Immunol Pract | 2022 | 10(5) | 1334-1341.e6 |
73 | Lopes JP, Cunningham-Rundles C | The importance of primary immune deficiency registries: the United States immunodeficiency network registry | Immunol Allergy Clin North Am | 2020 | 40(3) | 385-402 |
74 | Padem N, Wright H, Fuleihan R, Garabedian E, Suez D, Cunningham-Rundles C, Marsh RA, Khojah A | Rheumatologic diseases in patients with inborn errors of immunity in the USIDNET registry | Clin Rheumatol | 2022 | 41(7) | 2197-2203 |
75 | O’Toole D, Groth D, Wright H, Bonilla FA, Fuleihan RL, Cunningham-Rundles C, Sullivan KE, Ochs HD, Marsh R, Feuille E | X-Linked Agammaglobulinemia: Infection Frequency and Infection-Related Mortality in the USIDNET Registry | J Clin Immunol | 2022 | 42(4) | 827-836 |
76 | Pham MN, Fuleihan RL, Sullivan KE, Cunningham-Rundles C | Ocular Manifestations in Primary Immunodeficiency Disorders: A Report from the United States Immunodeficiency Network (USIDNET) Registry | J Allergy Clin Immunol Pract | 2022 | 10(7) | 1788-1796 |
77 | El-Sayed, ZA, El-Ghoneimy, DH, Ortega-Martell, JA, Radwan, N, Aldave, JC, Al-Herz, W, ... & Sullivan, K | Allergic manifestations of inborn errors of immunity and their impact on the diagnosis: A worldwide study | World Allergy Organization Journal | 2022 | 15(6) | 100657 |
78 | Syed MN, Kutac C, Miller JM, Marsh R, Sullivan KE, Cunningham-Rundles C, Fuleihan RL, Kheradmand F, Hajjar J | Risk Factors of Pneumonia in Primary Antibody Deficiency Patients Receiving Immunoglobulin Therapy: Data from the US Immunodeficiency Network (USIDNET) | J Clin Immunol | 2022 | 42(7) | 1545–1552 |
79 | Krase IZ, Garabedian E, Fuleihan R, Sacco K | Prevalence of coccidioidomycosis in primary immunodeficiency: Data from the USIDNET registry | J Clin Immunol | 2022 | 245 | 109135 |
80 | Tran P, Gober L, Garabedian EK, Fuleihan RL, Puck JM, Sullivan KE, Spergel JM, Ruffner MA | Eosinophilic gastrointestinal disorders in patients with inborn errors of immunity: Data from the USIDNET registry | Front Immunol | 2022 | 13 | Article 987895 |
81 | O'Toole, D, Groth, D, Wright, H, Bonilla, FA, Cunningham-Rundles, C, Sullivan, KE, Ochs HD, Marsh RA, Feuille E, Fuleihan, RL | Outcomes Among Racial and Ethnic Minority Groups with X-linked Agammaglobulinemia from the USIDNET Registry | J Allergy Clin Immunol Pract | 2023 | 11(6) | 1945-1946 |
82 | Hernandez-Trujillo, V., Zhou, C., Scalchunes, C., Ochs, H.D., Sullivan, K.E., Cunningham-Rundles, C., Fuleihan, R.L., Bonilla, F.A., Petrovic, A., Rawlings, D.J. and de la Morena, M.T. | A Registry Study of 240 Patients with X-Linked Agammaglobulinemia Living in the USA | J Clin Immunol | 2023 | 43(6) | 1468-1477 |
83 | Méndez Barrera, J.A., Rocha Guzmán, S., Hierro Cascajares, E., Garabedian, E.K., Fuleihan, R.L., Sullivan, K.E., & Lugo Reyes, S.O. | Who’s your data? Primary immune deficiency differential diagnosis prediction via machine learning and data mining of the USIDNET registry | Clin Immunol | 2023 | 225 | Article 109759 |
84 | Correa-Jimenez O, Restrepo-Gualteros S, Nino G, Cunningham-Rundles C, Sullivan KE, Fuleihan RL, Gutierrez MJ | Respiratory Comorbidities Associated with Bronchiectasis in Patients with Common Variable Immunodeficiency in the USIDNET Registry | J Clin Immunol | 2023 | Online ahead of print |