1. | Brennan, S., Marmor, I., Schafer, C., Ko, J., Torres Garcia, J.A., Rosman, I.S., Coughlin, C., Coverstone, A. and White, A.J.. Serum sickness‐like reaction following initiation of elexacaftor/tezacaftor/ivacaftor therapy. doi:10.1002/ppul.25072 Pediatric Pulmonology. 2020. |
2. | Philipsborn, Rebecca Pass MD, MPA; Sheffield, Perry MD, MPH; White, Andrew MD; Osta, Amanda MD; Anderson, Marsha S. MD; Bernstein, Aaron MD, MPH. Climate Change and the Practice of Medicine Academic Medicine. 2020. |
3. | Marie E. Faughnan, MD, MSc; Johannes J. Mager, MD, PhD; Steven Hetts, MD; Valerie A. Palda, MD, MSc; Kelly Lang-Robertson;Elisabetta Buscarini, MD; Erik Deslandres, MD; Raj S. Kasthuri, MD; Andrea Lausman, MD; David Poetker, MD,MA; Felix Ratjen, MD;Mark S. Chesnutt, MD; Marianne Clancy, RDH, MPA; Kevin J. Whitehead, MD; Hanny Al-Samkari, MD; Murali Chakinala, MD;Miles Conrad, MD; Daniel Cortes, BscPhm; Claudia Crocione; Jama Darling, MD; Els de Gussem, MD; Carol Derksen;Sophie Dupuis-Girod, MD, PhD; Patrick Foy, MD; Urban Geisthoff, MD; James R. Gossage, MD; Adrienne Hammill, MD; Ketil Heimdal, MD;Katharine Henderson, MS, CGC; Vivek N. Iyer, MD, MPH; Anette D. Kjeldsen, MD; Masaki Komiyama, MD; Kevin Korenblatt, MD;Jamie McDonald, MS, CGC; Jack McMahon; Justin McWilliams, MD; Mary E. Meek, MD; Meir Mei-Zahav, MD; Scott Olitsky, MD, MBA;Sara Palmer, PhD; Rose Pantalone, RN; Jay F. Piccirillo, MD; Beth Plahn, RN, MHA; Mary E.M. Porteous, MD; Marco C. Post, MD, PhD;Ivan Radovanovic, MD; Paul J. Rochon, MD; Josanna Rodriguez-Lopez, MD; Carlo Sabba, MD; Marcelo Serra, MD; Claire Shovlin, PhD, MA;Dennis Sprecher, MD; Andrew J. White, MD; Ingrid Winship, MBChB, MD; and Roberto Zarrabeitia,MD. Second International Guidelines for the Diagnosis and Management of Hereditary Hemorrhagic Telangiectasia Annals of Internal Medicine. 2020. |
4. | Kilian, A.; Latino, G.A.; White, A.J.; Clark, D.; Chakinala, M.M.; Ratjen, F.; McDonald, J.; Whitehead, K.; Gossage, J.R.; Lin, D.; Henderson, K.; Pollak, J.; McWilliams, J.P.; Kim, H.; Lawton, M.T.; Faughnan, M.E.; the Brain Vascular Malformation Consortium HHT Investigator Group.. Genotype–Phenotype Correlations in Children with HHT J. Clin. Med. 2020, 9, 2714.. 2020. |
5. | Choi H, Conrad MB, Oh SP, Roman BL, White AJ. Highlights of the 13th International Hereditary Hemorrhagic Telangiectasia Scientific conference. Angiogenesis. 2019;22(4):583-584. PMID:31606769 |
6. | Pahl KS, Choudhury A, Wusik K, Hammill A, White A, Henderson K, Pollak J, Kasthuri RS. Applicability of the Curaçao Criteria for the Diagnosis of Hereditary Hemorrhagic Telangiectasia in the Pediatric Population. J Pediatr. 2018. PMID:29655863 |
7. | Panupattanapong S, Stwalley DL, White AJ, Olsen MA, French AR, Hartman ME. Epidemiology and Outcomes of Granulomatosis with Polyangiitis (GPA) in Pediatric and Working-age Adults Populations in the United States: Analysis of a Large National Claims Database. Arthritis Rheumatol. 2018. PMID:29806148 |
8. | Mowers KL, Sekarski L, White AJ, Grady RM. EXPRESS: Pulmonary Arteriovenous Malformations in Children with Hereditary Hemorrhagic Telangiectasia: A longitudinal study. Pulm Circ. 2018;2045894018786696. PMID:29916764 |
9. | Cortez VS, Ulland TK, Cervantes-Barragan L, Bando JK, Robinette ML, Wang Q, White AJ, Gilfillan S, Cella M, Colonna M. SMAD4 impedes the conversion of NK cells into ILC1-like cells by curtailing non-canonical TGF-β signaling. Nat Immunol. 2017;18(9):995-1003. PMID:28759002 |
10. | Kasthuri RS, Montifar M, Nelson J, Kim H, Lawton MT, Faughnan ME, Brain Vascular Malformation Consortium HHT Investigator Group.. Prevalence and predictors of anemia in hereditary hemorrhagic telangiectasia. Am J Hematol. 2017. PMID:28639385 |
11. | Gefen AM, White AJ. Asymptomatic pulmonary arteriovenous malformations in children with hereditary hemorrhagic telangiectasia. Pediatr Pulmonol. 2017. PMID:28608633 |
12. | Ahmad FA, White AJ, Hiller KM, Amini R, Jeffe DB. An assessment of residents' and fellows' personal finance literacy: an unmet medical education need. Int J Med Educ. 2017;8:192-204. PMCID:PMC5457786 PMID:28557777 |
13. | Phillippi K, Hoeltzel M, Byun Robinson A, Kim S, Childhood Arthritis and Rheumatology Research Alliance (CARRA) Legacy Registry Investigators. Race, Income, and Disease Outcomes in Juvenile Dermatomyositis. J Pediatr. 2017;184:38-44.e1. PMCID:PMC5410644 PMID:28410093 |
14. | Khan A, Coffey M, Litterer KP, Baird JD, Furtak SL, Garcia BM, Ashland MA, Calaman S, Kuzma NC, O'Toole JK, Patel A, Rosenbluth G, Destino LA, Everhart JL, Good BP, Hepps JH, Dalal AK, Lipsitz SR, Yoon CS, Zigmont KR, Srivastava R, Starmer AJ, Sectish TC, Spector ND, West DC, Landrigan CP, and the Patient and Family Centered I-PASS Study Group., Allair BK, Alminde C, Alvarado-Little W, Atsatt M, Aylor ME, Bale JF Jr, Balmer D, Barton KT, Beck C, Bismilla Z, Blankenberg RL, Chandler D, Choudhary A, Christensen E, Coghlan-McDonald S, Cole FS, Corless E, Cray S, Da Silva R, Dahale D, Dreyer B, Growdon AS, Gubler L, Guiot A, Harris R, Haskell H, Kocolas I, Kruvand E, Lane MM, Langrish K, Ledford CJ, Lewis K, Lopreiato JO, Maloney CG, Mangan A, Markle P, Mendoza F, Micalizzi DA, Mittal V, Obermeyer M, O'Donnell KA, Ottolini M, Patel SJ, Pickler R, Rogers JE, Sanders LM, Sauder K, Shah SS, Sharma M, Simpkin A, Subramony A, Thompson ED Jr, Trueman L, Trujillo T, Turmelle MP, Warnick C, Welch C, White AJ, Wien MF, Winn AS, Wintch S, Wolf M, Yin HS, Yu CE. Families as Partners in Hospital Error and Adverse Event Surveillance. JAMA Pediatr. 2017;171(4):372-381. PMID:28241211 |
15. | Orandi AB, Eutsler E, Ferguson C, White AJ, Kitcharoensakkul M. Sarcoidosis presenting as granulomatous myositis in a 16-year-old adolescent. Pediatr Rheumatol Online J. 2016;14(1):59. PMCID:PMC5105277 PMID:27832822 |
16. | G.J. Palagallo, S.R. McWilliams, L.A. Sekarski, A. Sharma, M.S. Goyal and A.J. White. The Prevalence of Malformations of Cortical Development in a Pediatric Hereditary Hemorrhagic Telangiectasia Population American Journal of Neuroradiology. 2016;1-4. PMID:28059706 |
17. | Fotis L, Baszis KW, White AJ, French AR. Four Cases of Anti-PM/Scl Antibody-positive Juvenile Overlap Syndrome with Features of Myositis and Systemic Sclerosis. J Rheumatol. 2016;43(9):1768-9. PMID:27587018 |
18. | Warren JT, Miller CP, White AJ. 7-Year-Old With a Painful Rash. JAMA Pediatr. 2016;170(8):801-2. PMID:27479116 |
19. | Abraham G, Fehr J, Ahmad F, Jeffe DB, Copper T, Yu F, White AJ, Auerbach M, Schnadower D. Emergency Information Forms for Children With Medical Complexity: A Simulation Study. Pediatrics. 2016;138(2). PMID:27436504 |
20. | Fotis L, Tuttle PV 4th, Baszis KW, Pepmueller PH, Moore TL, White AJ. Azathioprine therapy for steroid-resistant Henoch-Schönlein purpura: a report of 6 cases. Pediatr Rheumatol Online J. 2016;14(1):37. PMCID:PMC4918135 PMID:27333803 |
21. | Cabral DA, Canter DL, Muscal E, Nanda K, Wahezi DM, Spalding SJ, Twilt M, Benseler SM, Campillo S, Charuvanij S, Dancey P, Eberhard BA, Elder ME, Hersh A, Higgins G, Huber AM, Khubchandani R, Kim S, Klein-Gitelman M, Kostik M, Lawson E, Lee T, Lubieniecka JM, McCurdy D, Moorthy LN, Morishita KA, Nielsen SM, O'Neil KM, Reiff A, Ristic G, Robinson AB, Sarmiento A, Shenoi S, Toth MB, Van Mater H, Wagner-Weiner L, Weiss JE, White AJ, Yeung RS, ARChiVe Investigators Network within the PedVas initiative. Comparing presenting clinical features of 48 children with microscopic polyangiitis (MPA) against 183 having granulomatosis with polyangiitis (GPA). An ARChiVe study. Arthritis Rheumatol. 2016. PMID:27111558 |
22. | Pawlikowska L, Nelson J, Guo DE, McCulloch CE, Lawton MT, Young WL, Kim H, Faughnan ME, Brain Vascular Malformation Consortium HHT Investigator Group. The ACVRL1 c.314-35A>G polymorphism is associated with organ vascular malformations in hereditary hemorrhagic telangiectasia patients with ENG mutations, but not in patients with ACVRL1 mutations. Am J Med Genet A. 2015;167(6):1262-7. PMCID:PMC4449292 PMID:25847705 |
23. | Kim H, Nelson J, Krings T, terBrugge KG, McCulloch CE, Lawton MT, Young WL, Faughnan ME, Brain Vascular Malformation Consortium HHT Investigator Group. Hemorrhage rates from brain arteriovenous malformation in patients with hereditary hemorrhagic telangiectasia. Stroke. 2015;46(5):1362-4. doi:10.1161/STROKEAHA.114.007367 PMCID:PMC4415515 PMID:25858236 |
24. | Krings T, Kim H, Power S, Nelson J, Faughnan ME, Young WL, terBrugge KG, Brain Vascular Malformation Consortium HHT Investigator Group. Neurovascular manifestations in hereditary hemorrhagic telangiectasia: imaging features and genotype-phenotype correlations. AJNR Am J Neuroradiol. 2015;36(5):863-70. PMCID:PMC4433843 PMID:25572952 |
25. | Fotis L, Baszis KW, French AR, Cooper MA, White AJ. Mesenteric vasculitis in children with systemic lupus erythematosus. Clin Rheumatol. 2015. doi:10.1007/s10067-015-2892-3 PMID:25687984 |
26. | Milner JD, Vogel TP, Forbes L, Ma CA, Stray-Pedersen A, Niemela JE, Lyons JJ, Engelhardt KR, Zhang Y, Topcagic N, Roberson ED, Matthews H, Verbsky JW, Dasu T, Vargas-Hernandez A, Varghese N, McClain KL, Karam LB, Nahmod K, Makedonas G, Mace EM, Sorte HS, Perminow G, Rao VK, O'Connell MP, Price S, Su HC, Butrick M, McElwee J, Hughes JD, Willet J, Swan D, Xu Y, Santibanez-Koref M, Slowik V, Dinwiddie DL, Ciaccio CE, Saunders CJ, Septer S, Kingsmore SF, White AJ, Cant AJ, Hambleton S, Cooper MA. Early-onset lymphoproliferation and autoimmunity caused by germline STAT3 gain-of-function mutations. Blood. 2015;125(4):591-9. doi:10.1182/blood-2014-09-602763 PMCID:PMC4304103 PMID:25359994 |
27. | Latino GA, Kim H, Nelson J, Pawlikowska L, Young W, Faughnan ME, Brain Vascular Malformation Consortium HHT Investigator Group. Severity score for hereditary hemorrhagic telangiectasia. Orphanet J Rare Dis. 2014;9:188. PMCID:PMC4302697 PMID:25928712 |
28. | Starmer AJ, Spector ND, Srivastava R, West DC, Rosenbluth G, Allen AD, Noble EL, Tse LL, Dalal AK, Keohane CA, Lipsitz SR, Rothschild JM, Wien MF, Yoon CS, Zigmont KR, Wilson KM, O'Toole JK, Solan LG, Aylor M, Bismilla Z, Coffey M, Mahant S, Blankenburg RL, Destino LA, Everhart JL, Patel SJ, Bale JF Jr, Spackman JB, Stevenson AT, Calaman S, Cole FS, Balmer DF, Hepps JH, Lopreiato JO, Yu CE, Sectish TC, Landrigan CP, I-PASS Study Group. Changes in medical errors after implementation of a handoff program. N Engl J Med. 2014;371(19):1803-12. doi:10.1056/NEJMsa1405556 PMID:25372088 |
29. | Ringold S, Hendrickson A, Abramson L, Beukelman T, Blier PR, Bohnsack J, Chalom EC, Gewanter HL, Gottlieb B, Hollister R, Hsu J, Hudgins A, Ilowite NT, Klein-Gitelman M, Lindsley C, Lopez Benitez JM, Lovell DJ, Mason T, Milojevic D, Moorthy LN, Nanda K, Onel K, Prahalad S, Rabinovich CE, Ray L, Rouster-Stevens K, Ruth N, Shishov M, Spalding S, Syed R, Stoll M, Vehe RK, Weiss JE, White AJ, Wallace CA, Sobel RE. Novel method to collect medication adverse events in juvenile arthritis: results from the childhood arthritis and rheumatology research alliance enhanced drug safety surveillance project. Arthritis Care Res (Hoboken). 2014. doi:10.1002/acr.22487 PMID:25331530 |
30. | Maliakkal JG, Liapis H, White AJ, Ahn SY. C1q nephropathy in the setting of granulomatosis with polyangiitis treated with tacrolimus. Clin Kidney J. 2014;7(5):499-500. doi:10.1093/ckj/sfu087 PMCID:PMC4379345 PMID:25878789 |
31. | Cheng KH, Mariampillai A, Lee KK, Vuong B, Luk TW, Ramjist J, Curtis A, Jakubovic H, Kertes P, Letarte M, Faughnan ME, Brain Vascular Malformation Consortium HHT Investigator Group, Yang VX. Histogram flow mapping with optical coherence tomography for in vivo skin angiography of hereditary hemorrhagic telangiectasia. J Biomed Opt. 2014;19(8):086015. PMCID:PMC4407667 PMID:25140883 |
32. | Tarbox JA, Keppel MP, Topcagic N, Mackin C, Ben Abdallah M, Baszis KW, White AJ, French AR, Cooper MA. Elevated double negative T cells in pediatric autoimmunity. J Clin Immunol. 2014;34(5):594-9. doi:10.1007/s10875-014-0038-z PMCID:PMC4047151 PMID:24760111 |
33. | Kitcharoensakkul M, Schulz CG, Kassel R, Khanna G, Liang S, Ngwube A, Baszis KW, Hunstad DA, White AJ. Scurvy revealed by difficulty walking: three cases in young children. J Clin Rheumatol. 2014;20(4):224-8. doi:10.1097/RHU.0000000000000101 PMID:24847751 |
34. | Robinson AB, Hoeltzel MF, Wahezi DM, Becker ML, Kessler EA, Schmeling H, Carrasco R, Huber AM, Feldman BM, Reed AM, Juvenile Myositis CARRA Subgroup, for the CARRA Registry Investigators.. Clinical characteristics of children with juvenile dermatomyositis: the Childhood Arthritis and Rheumatology Research Alliance Registry. Arthritis Care Res (Hoboken). 2014;66(3):404-10. PMCID:PMC4078654 PMID:23983017 |
35. | Morris H, Grant K, Khanna G, White AJ. Gout in a 15-year-old boy with juvenile idiopathic arthritis: a case study. Pediatr Rheumatol Online J. 2014;12(1):1. doi:10.1186/1546-0096-12-1 PMCID:PMC3895757 PMID:24393408 |
36. | Angeles-Han ST, Pelajo CF, Vogler LB, Rouster-Stevens K, Kennedy C, Ponder L, McCracken C, Lopez-Benitez J, Drews-Botsch C, Prahalad S, CARRA Registry Investigators.. Risk markers of juvenile idiopathic arthritis-associated uveitis in the Childhood Arthritis and Rheumatology Research Alliance (CARRA) Registry. J Rheumatol. 2013;40(12):2088-96. PMCID:PMC4117408 PMID:24187099 |
37. | |
38. | Slattery E, White AJ, Gauthier M, Linscott L, Hirose K. Tolosa-Hunt syndrome masquerading as Gradenigo syndrome in a teenager. Int J Pediatr Otorhinolaryngol. 2013;77(7):1219-21. doi:10.1016/j.ijporl.2013.04.023 PMID:23684166 |
39. | Ringold S, Beukelman T, Nigrovic PA, Kimura Y, CARRA Registry Site Principal Investigators.. Race, ethnicity, and disease outcomes in juvenile idiopathic arthritis: a cross-sectional analysis of the Childhood Arthritis and Rheumatology Research Alliance (CARRA) Registry. J Rheumatol. 2013;40(6):936-42. PMID:23588937 |
40. | Kimura Y, Weiss JE, Haroldson KL, Lee T, Punaro M, Oliveira S, Rabinovich E, Riebschleger M, Antón J, Blier PR, Gerloni V, Hazen MM, Kessler E, Onel K, Passo MH, Rennebohm RM, Wallace CA, Woo P, Wulffraat N, Childhood Arthritis Rheumatology Research Alliance Carra Net Investigators.. Pulmonary hypertension and other potentially fatal pulmonary complications in systemic juvenile idiopathic arthritis. Arthritis Care Res (Hoboken). 2013;65(5):745-52. PMCID:PMC4476507 PMID:23139240 |
41. | |
42. | Rosman IS, Liang LC, Patil S, Bayliss SJ, White AJ. Febrile ulceronecrotic Mucha-Habermann disease with central nervous system vasculitis. Pediatr Dermatol. 2013;30(1):90-3. doi:10.1111/j.1525-1470.2011.01669.x PMID:22276640 |
43. | Sheybani EF, Khanna G, White AJ, Demertzis JL. Imaging of juvenile idiopathic arthritis: a multimodality approach. Radiographics. 2013;33(5):1253-73. doi:10.1148/rg.335125178 PMID:24025923 |
44. | Weiss PF, Beukelman T, Schanberg LE, Kimura Y, Colbert RA, CARRA Registry Investigators.. Enthesitis-related arthritis is associated with higher pain intensity and poorer health status in comparison with other categories of juvenile idiopathic arthritis: the Childhood Arthritis and Rheumatology Research Alliance Registry. J Rheumatol. 2012;39(12):2341-51. PMCID:PMC3513507 PMID:23070991 |
45. | Mon T, L'ecuyer S, Farber NB, White AJ, Baszis KW, Hearn JK, Spiegel TE, French AR, Kitcharoensakkul M. The use of electroconvulsive therapy in a patient with juvenile systemic lupus erythematosus and catatonia. Lupus. 2012;21(14):1575-81. doi:10.1177/0961203312464803 PMID:23161578 |
46. | Morishita K, Guzman J, Chira P, Muscal E, Zeft A, Klein-Gitelman M, Uribe AG, Abramson L, Benseler SM, Eberhard A, Ede K, Hashkes PJ, Hersh AO, Higgins G, Imundo LF, Jung L, Kim S, Kingsbury DJ, Lawson EF, Lee T, Li SC, Lovell DJ, Mason T, McCurdy D, O'Neil KM, Punaro M, Ramsey SE, Reiff A, Rosenkranz M, Schikler KN, Scuccimarri R, Singer NG, Stevens AM, van Mater H, Wahezi DM, White AJ, Cabral DA, ARChiVe Investigators Network. Do adult disease severity subclassifications predict use of cyclophosphamide in children with ANCA-associated vasculitis? An analysis of ARChiVe study treatment decisions. J Rheumatol. 2012;39(10):2012-20. doi:10.3899/jrheum.120299 PMID:22859342 |
47. | Kitcharoensakkul M, Ree N, Bloomberg GR, Dehner LP, Heidingsfelder JA, White AJ, Cooper MA. Vancomycin-induced DRESS with evidence of T-cell activation in a 22-month-old patient. Ann Allergy Asthma Immunol. 2012;109(4):280-1. doi:10.1016/j.anai.2012.07.016 PMID:23010236 |
48. | Baszis KW, Singh G, White A, Thatayatikom A. Recurrent cardiac tamponade in a child with newly diagnosed systemic-onset juvenile idiopathic arthritis. J Clin Rheumatol. 2012;18(6):304-6. doi:10.1097/RHU.0b013e3182685857 PMID:22955481 |
49. | Uribe AG, Huber AM, Kim S, O'Neil KM, Wahezi DM, Abramson L, Baszis K, Benseler SM, Bowyer SL, Campillo S, Chira P, Hersh AO, Higgins GC, Eberhard A, Ede K, Imundo LF, Jung L, Kingsbury DJ, Klein-Gitelman M, Lawson EF, Li SC, Lovell DJ, Mason T, McCurdy D, Muscal E, Nassi L, Rabinovich E, Reiff A, Rosenkranz M, Schikler KN, Singer NG, Spalding S, Stevens AM, Cabral DA, ARegistry for Children with Vasculitis e-entry (ARChiVe) Network. Increased sensitivity of the European medicines agency algorithm for classification of childhood granulomatosis with polyangiitis. J Rheumatol. 2012;39(8):1687-97. doi:10.3899/jrheum.111352 PMID:22589257 |
50. | Starmer AJ, Spector ND, Srivastava R, Allen AD, Landrigan CP, Sectish TC, I-PASS Study Group. I-pass, a mnemonic to standardize verbal handoffs. Pediatrics. 2012;129(2):201-4. doi:10.1542/peds.2011-2966 PMID:22232313 |
51. | Rosman IS, Berk DR, Bayliss SJ, White AJ, Merritt DF. Acute genital ulcers in nonsexually active young girls: case series, review of the literature, and evaluation and management recommendations. Pediatr Dermatol. 2012;29(2):147-53. doi:10.1111/j.1525-1470.2011.01589.x PMID:22300420 |
52. | Baszis K, Toib D, Cooper M, French A, White A. Recurrent parotitis as a presentation of primary pediatric Sjögren syndrome. Pediatrics. 2012;129(1):e179-82. doi:10.1542/peds.2011-0716 PMID:22184654 |
53. | Baszis K, Garbutt J, Toib D, Mao J, King A, White A, French A. Clinical outcomes after withdrawal of anti-tumor necrosis factor α therapy in patients with juvenile idiopathic arthritis: a twelve-year experience. Arthritis Rheum. 2011;63(10):3163-8. doi:10.1002/art.30502 PMID:21702011 |
54. | Sectish TC, Starmer AJ, Landrigan CP, Spector ND, I-PASS Study Group. Establishing a multisite education and research project requires leadership, expertise, collaboration, and an important aim. Pediatrics. 2010;126(4):619-22. doi:10.1542/peds.2010-1793 PMID:20876168 |
55. | |
56. | Cooper MA, Willingham DL, Brown DE, French AR, Shih FF, White AJ. Rituximab for the treatment of juvenile dermatomyositis: a report of four pediatric patients. Arthritis Rheum. 2007;56(9):3107-11. doi:10.1002/art.22856 PMID:17763414 |
57. | Pachman LM, Abbott K, Sinacore JM, Amoruso L, Dyer A, Lipton R, Ilowite N, Hom C, Cawkwell G, White A, Rivas-Chacon R, Kimura Y, Ray L, Ramsey-Goldman R. Duration of illness is an important variable for untreated children with juvenile dermatomyositis. J Pediatr. 2006;148(2):247-53. doi:10.1016/j.jpeds.2005.10.032 PMID:16492437 |
58. | |
59. | Thatayatikom A, Thatayatikom S, White AJ. Infliximab treatment for severe granulomatous disease in common variable immunodeficiency: a case report and review of the literature. Ann Allergy Asthma Immunol. 2005;95(3):293-300. doi:10.1016/S1081-1206(10)61228-8 PMID:16200822 |
60. | |
61. | Verbsky JW, White AJ. Effective use of the recombinant interleukin 1 receptor antagonist anakinra in therapy resistant systemic onset juvenile rheumatoid arthritis. J Rheumatol. 2004;31(10):2071-5. PMID:15468378 |
62. | Eaton PE, White AJ. The mechanism of olefin-to-carbene rearrangement for 9-phenyl-1(9)-homocubene. 1990; 55(4):1321. J Org Chem . 1990;55(4):1321. |
63. | . Second International Guidelines for the Diagnosis and Management of Hereditary Hemorrhagic Telangiectasia Annals of Internal Medicine. PMID:32894695 |