BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Szõcs HI, Torma K, Petrovicz E, Hársing J, Fekete G, Kárpáti S, Horváth A. Wegener's granulomatosis presenting as pyoderma gangrenosum. Int J Dermatol 2003;42:898-902. [PMID: 14636209 DOI: 10.1046/j.1365-4362.2003.01924.x] [Cited by in Crossref: 18] [Cited by in F6Publishing: 13] [Article Influence: 1.1] [Reference Citation Analysis]
Number Citing Articles
1 Dissemond J, Korber A, Grabbe S. Differential diagnosis of leg ulcers. JDDG 2006;4:627-34. [DOI: 10.1111/j.1610-0387.2006.06052.x] [Cited by in Crossref: 37] [Cited by in F6Publishing: 16] [Article Influence: 2.5] [Reference Citation Analysis]
2 Thomas DR. Managing Venous Stasis Disease and Ulcers. Clinics in Geriatric Medicine 2013;29:415-24. [DOI: 10.1016/j.cger.2013.01.006] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 1.0] [Reference Citation Analysis]
3 Donmez S, Pamuk ON, Gedik M, A K R, Bulut G. A case of granulomatosis with polyangiitis and pyoderma gangrenosum successfully treated with infliximab and rituximab. Int J Rheum Dis 2014;17:471-5. [PMID: 24460826 DOI: 10.1111/1756-185X.12274] [Cited by in Crossref: 22] [Cited by in F6Publishing: 8] [Article Influence: 3.1] [Reference Citation Analysis]
4 de Boysson H, Martin Silva N, de Moreuil C, Néel A, de Menthon M, Meyer O, Launay D, Pagnoux C, Guillevin L, Puéchal X, Bienvenu B, Aouba A; French Vasculitis Study Group, French Internal Medicine Society. Neutrophilic Dermatoses in Antineutrophil Cytoplasmic Antibody-Associated Vasculitis: A French Multicenter Study of 17 Cases and Literature Review. Medicine (Baltimore) 2016;95:e2957. [PMID: 26986103 DOI: 10.1097/MD.0000000000002957] [Cited by in Crossref: 24] [Cited by in F6Publishing: 3] [Article Influence: 4.8] [Reference Citation Analysis]
5 Genovese G, Tavecchio S, Berti E, Rongioletti F, Marzano AV. Pyoderma gangrenosum-like ulcerations in granulomatosis with polyangiitis: two cases and literature review. Rheumatol Int 2018;38:1139-51. [PMID: 29721696 DOI: 10.1007/s00296-018-4035-z] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 2.3] [Reference Citation Analysis]
6 Hoffman MD. Inflammatory ulcers. Clinics in Dermatology 2007;25:131-8. [DOI: 10.1016/j.clindermatol.2006.09.010] [Cited by in Crossref: 9] [Cited by in F6Publishing: 5] [Article Influence: 0.6] [Reference Citation Analysis]
7 Boucelma M, Hakem D, Ibrir M, Kadri N, Youcef-ouali D, Ouadahi N, Berrah A. Granulomatose de Wegener et ulcérations nécrotiques mammaires. À propos d’un cas. La Revue de Médecine Interne 2005;26:155-7. [DOI: 10.1016/j.revmed.2004.09.020] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.2] [Reference Citation Analysis]
8 Yamamoto T. Pyoderma gangrenosum: An important dermatologic condition occasionally associated with rheumatic diseases. WJR 2015;5:101. [DOI: 10.5499/wjr.v5.i2.101] [Cited by in CrossRef: 3] [Article Influence: 0.5] [Reference Citation Analysis]
9 Carlson JA, Chen K. Cutaneous Vasculitis Update: Small Vessel Neutrophilic Vasculitis Syndromes. The American Journal of Dermatopathology 2006;28:486-506. [DOI: 10.1097/01.dad.0000246646.45651.a2] [Cited by in Crossref: 130] [Cited by in F6Publishing: 71] [Article Influence: 8.7] [Reference Citation Analysis]
10 Weedon D. The vasculopathic reaction pattern. Weedon's Skin Pathology. Elsevier; 2010. pp. 195-244.e49. [DOI: 10.1016/b978-0-7020-3485-5.00009-7] [Cited by in Crossref: 11] [Article Influence: 1.0] [Reference Citation Analysis]
11 Boudny C, Nievergelt H, Braathen LR, Simon D. Wegener's granulomatosis presenting as pyoderma gangrenosum. J Dtsch Dermatol Ges 2008;6:477-9. [PMID: 18076660 DOI: 10.1111/j.1610-0387.2007.06497.x] [Cited by in Crossref: 17] [Cited by in F6Publishing: 11] [Article Influence: 1.2] [Reference Citation Analysis]
12 Subhadarshani S, Gupta V, Chahal A, Verma KK. Saddle-nose and bilateral cauliflower ear deformities with pyoderma gangrenosum-like ulcers, cavitary pulmonary lesions, digital gangrene and pulselessness in a young female. BMJ Case Rep 2017;2017:bcr-2017-220434. [PMID: 28619741 DOI: 10.1136/bcr-2017-220434] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
13 Hashem AM, Hoffman GS, Gastman B, Bernard S, Djohan R, Hendrickson M, Schwarz G, Doumit G, Gharb BB, Rampazzo A, Zins JE, Siemionow M, Papay F. Establishing the Feasibility of Face Transplantation in Granulomatosis With Polyangiitis. Am J Transplant 2016;16:2213-23. [DOI: 10.1111/ajt.13751] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]