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For: Ozen A. CHAPLE syndrome uncovers the primary role of complement in a familial form of Waldmann's disease. Immunol Rev 2019;287:20-32. [PMID: 30565236 DOI: 10.1111/imr.12715] [Cited by in Crossref: 13] [Cited by in F6Publishing: 14] [Article Influence: 4.3] [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 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]
3 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:izac001. [PMID: 35134932 DOI: 10.1093/ibd/izac001] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Aydemir S, Islek A, Nepesov S, Yaman Y, Baysoy G, Beser OF, Cokugras FC, Baris S, Karakoc-Aydiner E, Cokugras H, Hubrack SZ, Kendir Demirkol Y, Lo B, Kiykim A, Ozen A. Inflammatory Bowel Disease and Guillain Barre Syndrome in FCHO1 Deficiency. J Clin Immunol 2021;41:1406-10. [PMID: 33950325 DOI: 10.1007/s10875-021-01042-2] [Reference Citation Analysis]
5 Bandikatla S, Maharaj S, Dadlani A, Ramsubiek K, Rojan A. Thrombosis secondary to protein-losing enteropathy (PLE): A case report and review. Thrombosis Update 2021;3:100050. [DOI: 10.1016/j.tru.2021.100050] [Reference Citation Analysis]
6 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]
7 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]
8 Shariat M, Heydrzadeh M, Abolhassani H, Bemanian MH, Yazdani R. Complement deficiencies. Inborn Errors of Immunity 2021. [DOI: 10.1016/b978-0-12-821028-4.00011-7] [Reference Citation Analysis]
9 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]
10 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]
11 Yu JE, Heimall J. Protein and lymphatic loss conditions. Stiehm's Immune Deficiencies 2020. [DOI: 10.1016/b978-0-12-816768-7.00050-8] [Reference Citation Analysis]
12 Lenardo MJ, Holland SM. Introduction: Continuing insights into the healthy and diseased immune system through human genetic investigation. Immunol Rev 2019;287:5-8. [PMID: 30565248 DOI: 10.1111/imr.12730] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
13 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]
14 Blei F. Update February 2019. Lymphatic Research and Biology 2019;17:87-117. [DOI: 10.1089/lrb.2018.29057.fb] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]