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For: Ozen A, Comrie WA, Ardy RC, Domínguez Conde C, Dalgic B, Beser ÖF, Morawski AR, Karakoc-Aydiner E, Tutar E, Baris S, Ozcay F, Serwas NK, Zhang Y, Matthews HF, Pittaluga S, Folio LR, Unlusoy Aksu A, McElwee JJ, Krolo A, Kiykim A, Baris Z, Gulsan M, Ogulur I, Snapper SB, Houwen RHJ, Leavis HL, Ertem D, Kain R, Sari S, Erkan T, Su HC, Boztug K, Lenardo MJ. CD55 Deficiency, Early-Onset Protein-Losing Enteropathy, and Thrombosis. N Engl J Med 2017;377:52-61. [PMID: 28657829 DOI: 10.1056/NEJMoa1615887] [Cited by in Crossref: 95] [Cited by in F6Publishing: 99] [Article Influence: 19.0] [Reference Citation Analysis]
Number Citing Articles
1 Sullivan KE. Inherited Complement Deficiencies. Emery and Rimoin' s Principles and Practice of Medical Genetics and Genomics 2023. [DOI: 10.1016/b978-0-12-812534-2.00001-1] [Reference Citation Analysis]
2 Bharti R, Dey G, Lin F, Lathia J, Reizes O. CD55 in cancer: Complementing functions in a non-canonical manner. Cancer Letters 2022;551:215935. [DOI: 10.1016/j.canlet.2022.215935] [Reference Citation Analysis]
3 Minović I, Schipperus MR, Mäkelburg ABU, Meijer K, Lukens MV, Kootstra-Ros JE, van der Heide F, Abbasova I, de Kleine RHJ, Meekers JH, Mulder AB. Anti-IFC antibodies in a patient with CHAPLE syndrome: Implications for blood management. Br J Haematol 2022. [PMID: 36216787 DOI: 10.1111/bjh.18509] [Reference Citation Analysis]
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6 Chongsrisawat V, Suratannon N, Chatchatee P, Ittiwut R, Ittiwut C, Weerapakorn W, Theamboonlers A, Rohlfs M, Klein C, Kotlarz D, Suphapeetiporn K. Novel CD55 Mutation Associated With Severe Small Bowel Ulceration Mimicking Inflammatory Bowel Disease in a Pair of Siblings. Inflamm Bowel Dis 2022;28:1458-61. [PMID: 35134932 DOI: 10.1093/ibd/izac001] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Arora G, Lynn GE, Tang X, Rosen CE, Hoornstra D, Sajid A, Hovius JW, Palm NW, Ring AM, Fikrig E. CD55 Facilitates Immune Evasion by Borrelia crocidurae, an Agent of Relapsing Fever. mBio 2022;:e0116122. [PMID: 36036625 DOI: 10.1128/mbio.01161-22] [Reference Citation Analysis]
8 Azabdaftari A, Jones KDJ, Kammermeier J, Uhlig HH. Monogenic inflammatory bowel disease-genetic variants, functional mechanisms and personalised medicine in clinical practice. Hum Genet 2022. [PMID: 35761107 DOI: 10.1007/s00439-022-02464-7] [Reference Citation Analysis]
9 Ko N, Shim J, Kim HJ, Lee Y, Park JK, Kwak K, Lee JW, Jin DI, Kim H, Choi K. A desirable transgenic strategy using GGTA1 endogenous promoter-mediated knock-in for xenotransplantation model. Sci Rep 2022;12:9611. [PMID: 35688851 DOI: 10.1038/s41598-022-13536-z] [Reference Citation Analysis]
10 Hoşnut FÖ, Sahin GE, Ozyazıcı A, Olgac A, Aksu AU. Congenital Rare Diseases Causing Persistent Diarrhea in the Newborn: A Single Center Experience. Z Geburtshilfe Neonatol 2022. [PMID: 35576965 DOI: 10.1055/a-1774-5005] [Reference Citation Analysis]
11 Li J, Tang H, Tu W. Mechanism of dexmedetomidine preconditioning on spinal cord analgesia in rats with functional chronic visceral pain. Acta Cir Bras 2022;37:e370203. [PMID: 35507967 DOI: 10.1590/acb370203] [Reference Citation Analysis]
12 Estrada CC, Cardona S, Guo Y, Revelo MP, D'Agati VD, Koganti S, Devaraj J, He JC, Heeger PS, Mallipattu SK. Endothelial-specific loss of Krüppel-Like Factor 4 triggers complement-mediated endothelial injury. Kidney Int 2022:S0085-2538(22)00344-1. [PMID: 35483525 DOI: 10.1016/j.kint.2022.03.025] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
13 Kurolap A, Hagin D, Freund T, Fishman S, Zunz Henig N, Brazowski E, Yeshaya J, Naiman T, Pras E, Ablin JN, Baris Feldman H. CD55-deficiency in Jews of Bukharan descent is caused by the Cromer blood type Dr(a-) variant. Hum Genet 2022. [PMID: 35314883 DOI: 10.1007/s00439-021-02428-3] [Reference Citation Analysis]
14 Mulenga C, Sviben S, Chandwe K, Amadi B, Kayamba V, Fitzpatrick JAJ, Mudenda V, Kelly P. Epithelial Abnormalities in the Small Intestine of Zambian Children With Stunting. Front Med 2022;9:849677. [DOI: 10.3389/fmed.2022.849677] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
15 Liu D, Duan L, Cyster JG. Chemo- and mechanosensing by dendritic cells facilitate antigen surveillance in the spleen. Immunol Rev 2022;306:25-42. [PMID: 35147233 DOI: 10.1111/imr.13055] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
16 Vuyyuru SK, Kedia S, Sahu P, Ahuja V. Immune‐mediated inflammatory diseases of the gastrointestinal tract: Beyond Crohn's disease and ulcerative colitis. JGH Open. [DOI: 10.1002/jgh3.12706] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
17 Redmond MT, Scherzer R, Prince BT. Novel Genetic Discoveries in Primary Immunodeficiency Disorders. Clin Rev Allergy Immunol 2022. [PMID: 35020168 DOI: 10.1007/s12016-021-08881-2] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
18 Kayes T, Bonnichsen M, Willmann L, Lorenzo A, Das A, El-haddad C, Househ Z, Ng W, Ng W, Williams A, Prince D, Connor SJ. Menetrier’s disease exacerbating ulcerative colitis and relieved by gastrectomy. BMJ Open Gastroenterol 2021;8:e000806. [DOI: 10.1136/bmjgast-2021-000806] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
19 Ploier R. Primäre intestinale Lymphangiektasie und proteinverlierende Enteropathie bei Kindern und Jugendlichen. Monatsschr Kinderheilkd 2021;169:1160-1166. [DOI: 10.1007/s00112-020-01005-8] [Reference Citation Analysis]
20 Buphamalai P, Kokotovic T, Nagy V, Menche J. Network analysis reveals rare disease signatures across multiple levels of biological organization. Nat Commun 2021;12:6306. [PMID: 34753928 DOI: 10.1038/s41467-021-26674-1] [Cited by in Crossref: 5] [Cited by in F6Publishing: 8] [Article Influence: 5.0] [Reference Citation Analysis]
21 Pouw RB, Ricklin D. Tipping the balance: intricate roles of the complement system in disease and therapy. Semin Immunopathol 2021;43:757-71. [PMID: 34698894 DOI: 10.1007/s00281-021-00892-7] [Cited by in Crossref: 10] [Cited by in F6Publishing: 6] [Article Influence: 10.0] [Reference Citation Analysis]
22 Freyberger F, Kokotović T, Krnjak G, Frković SH, Nagy V. Expanding the known phenotype of Mullegama-Klein-Martinez syndrome in male patients. Hum Genome Var 2021;8:37. [PMID: 34580287 DOI: 10.1038/s41439-021-00169-3] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
23 Martínez-Alarcón L, Liarte S, Quereda JJ, Sáez-Acosta A, Torre-Minguela C, Mendonça L, Abellaneda JM, Majado MJ, Ríos A, Ramírez P, Muñoz A, Ramis G. Profiling Human CD55 Transgene Performance Assist in Selecting Best Suited Specimens and Tissues for Swine Organ Xenotransplantation. Biology (Basel) 2021;10:747. [PMID: 34439979 DOI: 10.3390/biology10080747] [Reference Citation Analysis]
24 Santos NB, Vaz da Silva ZE, Gomes C, Reis CA, Amorim MJ. Complement Decay-Accelerating Factor is a modulator of influenza A virus lung immunopathology. PLoS Pathog 2021;17:e1009381. [PMID: 34197564 DOI: 10.1371/journal.ppat.1009381] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
25 Goto M, Tsuchida Y, Terada K, Takahashi H, Sugimori Y, Komai T, Iwasaki Y, Shoda H, Fujio K. ANCA-associated vasculitis with protein-losing enteropathy is characterized by hypocomplementemia. Rheumatol Int 2021. [PMID: 34156527 DOI: 10.1007/s00296-021-04923-2] [Reference Citation Analysis]
26 Oskay Halacli S. Flow Cytometric Approach in the Diagnosis of Primary Immunodeficiencies. Cell Interaction - Molecular and Immunological Basis for Disease Management 2021. [DOI: 10.5772/intechopen.96004] [Reference Citation Analysis]
27 Garred P, Tenner AJ, Mollnes TE. Therapeutic Targeting of the Complement System: From Rare Diseases to Pandemics. Pharmacol Rev 2021;73:792-827. [PMID: 33687995 DOI: 10.1124/pharmrev.120.000072] [Cited by in Crossref: 42] [Cited by in F6Publishing: 45] [Article Influence: 42.0] [Reference Citation Analysis]
28 Wang L, Aschenbrenner D, Zeng Z, Cao X, Mayr D, Mehta M, Capitani M, Warner N, Pan J, Wang L, Li Q, Zuo T, Cohen-Kedar S, Lu J, Ardy RC, Mulder DJ, Dissanayake D, Peng K, Huang Z, Li X, Wang Y, Wang X, Li S, Bullers S, Gammage AN, Warnatz K, Schiefer AI, Krivan G, Goda V, Kahr WHA, Lemaire M, Lu CY, Siddiqui I, Surette MG, Kotlarz D, Engelhardt KR, Griffin HR, Rottapel R, Decaluwe H, Laxer RM, Proietti M, Hambleton S, Elcombe S, Guo CH, Grimbacher B, Dotan I, Ng SC, Freeman SA, Snapper SB, Klein C, Boztug K, Huang Y, Li D, Uhlig HH, Muise AM; Genomics England Research Consortium. Gain-of-function variants in SYK cause immune dysregulation and systemic inflammation in humans and mice. Nat Genet 2021;53:500-10. [PMID: 33782605 DOI: 10.1038/s41588-021-00803-4] [Cited by in Crossref: 18] [Cited by in F6Publishing: 20] [Article Influence: 18.0] [Reference Citation Analysis]
29 Peter HH, Ochs HD, Cunningham-Rundles C, Vinh DC, Kiessling P, Greve B, Jolles S. Targeting FcRn for immunomodulation: Benefits, risks, and practical considerations. J Allergy Clin Immunol 2020;146:479-491.e5. [PMID: 32896308 DOI: 10.1016/j.jaci.2020.07.016] [Cited by in Crossref: 20] [Cited by in F6Publishing: 16] [Article Influence: 20.0] [Reference Citation Analysis]
30 Santos NB, Vaz da Silva ZE, Gomes C, Reis CA, Amorim MJ. Complement Decay-Accelerating Factor is a modulator of influenza A virus lung immunopathology.. [DOI: 10.1101/2021.02.16.431406] [Reference Citation Analysis]
31 Adesanya TMA, Campbell CM, Cheng L, Ogbogu PU, Kahwash R. C1 Esterase Inhibition: Targeting Multiple Systems in COVID-19. J Clin Immunol 2021;41:729-32. [PMID: 33474624 DOI: 10.1007/s10875-021-00972-1] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 6.0] [Reference Citation Analysis]
32 Dernstedt A, Leidig J, Holm A, Kerkman PF, Mjösberg J, Ahlm C, Henriksson J, Hultdin M, Forsell MNE. Regulation of Decay Accelerating Factor Primes Human Germinal Center B Cells for Phagocytosis. Front Immunol 2020;11:599647. [PMID: 33469456 DOI: 10.3389/fimmu.2020.599647] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
33 Ozen A, Kasap N, Vujkovic-Cvijin I, Apps R, Cheung F, Karakoc-Aydiner E, Akkelle B, Sari S, Tutar E, Ozcay F, Uygun DK, Islek A, Akgun G, Selcuk M, Sezer OB, Zhang Y, Kutluk G, Topal E, Sayar E, Celikel C, Houwen RHJ, Bingol A, Ogulur I, Eltan SB, Snow AL, Lake C, Fantoni G, Alba C, Sellers B, Chauvin SD, Dalgard CL, Harari O, Ni YG, Wang MD, Devalaraja-Narashimha K, Subramanian P, Ergelen R, Artan R, Guner SN, Dalgic B, Tsang J, Belkaid Y, Ertem D, Baris S, Lenardo MJ. Broadly effective metabolic and immune recovery with C5 inhibition in CHAPLE disease. Nat Immunol 2021;22:128-39. [PMID: 33398182 DOI: 10.1038/s41590-020-00830-z] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 11.0] [Reference Citation Analysis]
34 Brownell JN, Piccoli DA. Protein-Losing Enteropathy. Pediatric Gastrointestinal and Liver Disease 2021. [DOI: 10.1016/b978-0-323-67293-1.00033-5] [Reference Citation Analysis]
35 Murakami Y. Diseases Associated With GPI Anchors. Comprehensive Glycoscience 2021. [DOI: 10.1016/b978-0-12-819475-1.00025-0] [Reference Citation Analysis]
36 Liu C, Ahearn JM. Complement and SLE. Lahita's Systemic Lupus Erythematosus 2021. [DOI: 10.1016/b978-0-12-820583-9.00019-1] [Reference Citation Analysis]
37 Ediger TR, Erdman SH. Maldigestion and Malabsorption. Pediatric Gastrointestinal and Liver Disease 2021. [DOI: 10.1016/b978-0-323-67293-1.00031-1] [Reference Citation Analysis]
38 de Boer ECW, van Mourik AG, Jongerius I. Therapeutic Lessons to be Learned From the Role of Complement Regulators as Double-Edged Sword in Health and Disease. Front Immunol 2020;11:578069. [PMID: 33362763 DOI: 10.3389/fimmu.2020.578069] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
39 Ort M, Dingemanse J, van den Anker J, Kaufmann P. Treatment of Rare Inflammatory Kidney Diseases: Drugs Targeting the Terminal Complement Pathway. Front Immunol 2020;11:599417. [PMID: 33362783 DOI: 10.3389/fimmu.2020.599417] [Cited by in Crossref: 15] [Cited by in F6Publishing: 15] [Article Influence: 7.5] [Reference Citation Analysis]
40 van Rijn JM, Werner L, Aydemir Y, Spronck JMA, Pode-Shakked B, van Hoesel M, Shimshoni E, Polak-Charcon S, Talmi L, Eren M, Weiss B, H J Houwen R, Barshack I, Somech R, Nieuwenhuis EES, Sagi I, Raas-Rothschild A, Middendorp S, Shouval DS. Enhanced Collagen Deposition in the Duodenum of Patients with Hyaline Fibromatosis Syndrome and Protein Losing Enteropathy. Int J Mol Sci 2020;21:E8200. [PMID: 33147779 DOI: 10.3390/ijms21218200] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
41 Dernstedt A, Leidig J, Holm A, Mjösberg J, Ahlm C, Henriksson J, Hultdin M, Forsell MN. Regulation of Decay Accelerating Factor primes human germinal center B cells for phagocytosis.. [DOI: 10.1101/2020.08.27.271148] [Reference Citation Analysis]
42 Krüger R, Martin E, Dmytrus J, Feiterna-Sperling C, Meisel C, Unterwalder N, Kölsch U, Wahn V, Hofmann J, Korn P, Latour S, Boztug K, von Bernuth H. CD70 Deficiency Associated With Chronic Epstein-Barr Virus Infection, Recurrent Airway Infections and Severe Gingivitis in a 24-Year-Old Woman. Front Immunol 2020;11:1593. [PMID: 32849540 DOI: 10.3389/fimmu.2020.01593] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
43 Salzer E, Zoghi S, Kiss MG, Kage F, Rashkova C, Stahnke S, Haimel M, Platzer R, Caldera M, Ardy RC, Hoeger B, Block J, Medgyesi D, Sin C, Shahkarami S, Kain R, Ziaee V, Hammerl P, Bock C, Menche J, Dupré L, Huppa JB, Sixt M, Lomakin A, Rottner K, Binder CJ, Stradal TEB, Rezaei N, Boztug K. The cytoskeletal regulator HEM1 governs B cell development and prevents autoimmunity. Sci Immunol 2020;5:eabc3979. [PMID: 32646852 DOI: 10.1126/sciimmunol.abc3979] [Cited by in Crossref: 26] [Cited by in F6Publishing: 25] [Article Influence: 13.0] [Reference Citation Analysis]
44 Ouahed J, Spencer E, Kotlarz D, Shouval DS, Kowalik M, Peng K, Field M, Grushkin-Lerner L, Pai SY, Bousvaros A, Cho J, Argmann C, Schadt E, Mcgovern DPB, Mokry M, Nieuwenhuis E, Clevers H, Powrie F, Uhlig H, Klein C, Muise A, Dubinsky M, Snapper SB. Very Early Onset Inflammatory Bowel Disease: A Clinical Approach With a Focus on the Role of Genetics and Underlying Immune Deficiencies. Inflamm Bowel Dis 2020;26:820-42. [PMID: 31833544 DOI: 10.1093/ibd/izz259] [Cited by in Crossref: 53] [Cited by in F6Publishing: 46] [Article Influence: 26.5] [Reference Citation Analysis]
45 Klee KMC, Janecke AR, Civan HA, Rosipal Š, Heinz-Erian P, Huber LA, Müller T, Vogel GF. AP1S1 missense mutations cause a congenital enteropathy via an epithelial barrier defect. Hum Genet 2020;139:1247-59. [PMID: 32306098 DOI: 10.1007/s00439-020-02168-w] [Cited by in Crossref: 15] [Cited by in F6Publishing: 11] [Article Influence: 7.5] [Reference Citation Analysis]
46 Reis ES, Mastellos DC, Hajishengallis G, Lambris JD. New insights into the immune functions of complement. Nat Rev Immunol 2019;19:503-16. [PMID: 31048789 DOI: 10.1038/s41577-019-0168-x] [Cited by in Crossref: 157] [Cited by in F6Publishing: 170] [Article Influence: 78.5] [Reference Citation Analysis]
47 Brodszki N, Frazer-Abel A, Grumach AS, Kirschfink M, Litzman J, Perez E, Seppänen MRJ, Sullivan KE, Jolles S. European Society for Immunodeficiencies (ESID) and European Reference Network on Rare Primary Immunodeficiency, Autoinflammatory and Autoimmune Diseases (ERN RITA) Complement Guideline: Deficiencies, Diagnosis, and Management. J Clin Immunol 2020;40:576-91. [PMID: 32064578 DOI: 10.1007/s10875-020-00754-1] [Cited by in Crossref: 31] [Cited by in F6Publishing: 34] [Article Influence: 15.5] [Reference Citation Analysis]
48 Lentze MJ. Eiweißverlierende Enteropathie. Pädiatrie 2020. [DOI: 10.1007/978-3-662-60300-0_155] [Reference Citation Analysis]
49 Frank MM, Sullivan KE. Complement deficiencies. Stiehm's Immune Deficiencies 2020. [DOI: 10.1016/b978-0-12-816768-7.00042-9] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
50 Olcina MM, Balanis NG, Kim RK, Aksoy BA, Kodysh J, Thompson MJ, Hammerbacher J, Graeber TG, Giaccia AJ. Mutations in an Innate Immunity Pathway Are Associated with Poor Overall Survival Outcomes and Hypoxic Signaling in Cancer. Cell Rep 2018;25:3721-3732.e6. [PMID: 30590044 DOI: 10.1016/j.celrep.2018.11.093] [Cited by in Crossref: 16] [Cited by in F6Publishing: 17] [Article Influence: 5.3] [Reference Citation Analysis]
51 Pazmandi J, Kalinichenko A, Ardy RC, Boztug K. Early-onset inflammatory bowel disease as a model disease to identify key regulators of immune homeostasis mechanisms. Immunol Rev 2019;287:162-85. [PMID: 30565237 DOI: 10.1111/imr.12726] [Cited by in Crossref: 34] [Cited by in F6Publishing: 36] [Article Influence: 11.3] [Reference Citation Analysis]
52 Fan Y, Bai B, Ren Y, Liu Y, Zhou F, Lou X, Zi J, Hou G, Zhao Q, Liu S. Protein profiling reveals the characteristic changes of complement cascade pathway in the tissues of gastric signet ring cell carcinoma.. [DOI: 10.1101/816272] [Reference Citation Analysis]
53 Lee AS, Rusch J, Lima AC, Usmani A, Huang N, Lepamets M, Vigh-Conrad KA, Worthington RE, Mägi R, Wu X, Aston KI, Atkinson JP, Carrell DT, Hess RA, O'Bryan MK, Conrad DF. Rare mutations in the complement regulatory gene CSMD1 are associated with male and female infertility. Nat Commun 2019;10:4626. [PMID: 31604923 DOI: 10.1038/s41467-019-12522-w] [Cited by in Crossref: 11] [Cited by in F6Publishing: 13] [Article Influence: 3.7] [Reference Citation Analysis]
54 Pérez-Alós L, Bayarri-Olmos R, Skjoedt MO, Garred P. Combining MAP-1:CD35 or MAP-1:CD55 fusion proteins with pattern-recognition molecules as novel targeted modulators of the complement cascade. FASEB J 2019;33:12723-34. [PMID: 31469600 DOI: 10.1096/fj.201901643R] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
55 Cagdas D, Halaçlı SO, Tan Ç, Lo B, Çetinkaya PG, Esenboğa S, Karaatmaca B, Matthews H, Balcı-Hayta B, Arıkoğlu T, Ezgü F, Aladağ E, Saltık-Temizel İN, Demir H, Kuşkonmaz B, Okur V, Gümrük F, Göker H, Çetinkaya D, Boztuğ K, Lenardo M, Sanal Ö, Tezcan İ. A Spectrum of Clinical Findings from ALPS to CVID: Several Novel LRBA Defects. J Clin Immunol 2019;39:726-38. [PMID: 31432443 DOI: 10.1007/s10875-019-00677-6] [Cited by in Crossref: 34] [Cited by in F6Publishing: 24] [Article Influence: 11.3] [Reference Citation Analysis]
56 Patary B, Das K, Pyne S, Chatterjee N. Excruciating Headache in a Case of Malabsorption Syndrome. Bengal Physician Journal 2019;6:31-32. [DOI: 10.5005/jp-journals-10070-6116] [Reference Citation Analysis]
57 Hanna RM, Hasnain H, Abdelnour L, Yanny B, Burwick RM. Atypical hemolytic uremic syndrome in a patient with protein-losing enteropathy. J Int Med Res 2019;47:4027-32. [PMID: 31364428 DOI: 10.1177/0300060519864808] [Cited by in Crossref: 4] [Cited by in F6Publishing: 6] [Article Influence: 1.3] [Reference Citation Analysis]
58 Mohammad L, Omran R, Ibrahim A, Hourieh MA, Ibrahim A. Primary intestinal lymphangiectasia in a 23-month- old girl. Oxf Med Case Reports 2019;2019:omz065. [PMID: 31333853 DOI: 10.1093/omcr/omz065] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
59 Kurolap A, Eshach Adiv O, Hershkovitz T, Tabib A, Karbian N, Paperna T, Mory A, Vachyan A, Slijper N, Steinberg R, Zohar Y, Mevorach D, Baris Feldman H. Eculizumab Is Safe and Effective as a Long-term Treatment for Protein-losing Enteropathy Due to CD55 Deficiency. J Pediatr Gastroenterol Nutr 2019;68:325-33. [PMID: 30418410 DOI: 10.1097/MPG.0000000000002198] [Cited by in Crossref: 12] [Cited by in F6Publishing: 11] [Article Influence: 4.0] [Reference Citation Analysis]
60 Lentze MJ. Eiweißverlierende Enteropathie bei Kindern und Jugendlichen. Pädiatrie 2019. [DOI: 10.1007/978-3-642-54671-6_155-2] [Reference Citation Analysis]
61 Ozen A, Karakoc-aydiner E, Ertem D. Chronic Diarrhea, Recurrent Edema and Respiratory Infections. Pediatric Immunology 2019. [DOI: 10.1007/978-3-030-21262-9_122] [Reference Citation Analysis]
62 Furniss RCD, Low WW, Mavridou DAI, Dagley LF, Webb AI, Tate EW, Clements A. Plasma membrane profiling during enterohemorrhagic E. coli infection reveals that the metalloprotease StcE cleaves CD55 from host epithelial surfaces. J Biol Chem 2018;293:17188-99. [PMID: 30190327 DOI: 10.1074/jbc.RA118.005114] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.3] [Reference Citation Analysis]
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