These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
110 related articles for article (PubMed ID: 7369233)
1. Familial partial deficiency of the third component of complement (C3) and the hypocomplementemic cutaneous vasculitis syndrome. McLean RH; Weinstein A; Chapitis J; Lowenstein M; Rothfield NF Am J Med; 1980 Apr; 68(4):549-58. PubMed ID: 7369233 [TBL] [Abstract][Full Text] [Related]
2. [Hypocomplementemic urticarial vasculitis syndrome. Successful therapy with intravenous immunoglobulins]. Staubach-Renz P; von Stebut E; Bräuninger W; Maurer M; Steinbrink K Hautarzt; 2007 Aug; 58(8):693-7. PubMed ID: 17453168 [TBL] [Abstract][Full Text] [Related]
8. Glomerular disease in two patients with urticaria-cutaneous vasculitis and hypocomplementemia. Schultz DR; Perez GO; Volanakis JE; Pardo V; Moss SH Am J Kidney Dis; 1981 Nov; 1(3):157-65. PubMed ID: 7332008 [TBL] [Abstract][Full Text] [Related]
9. A hypocomplementemic vasculitic urticarial syndrome. Report of four new cases and definition of the disease. Zeiss CR; Burch FX; Marder RJ; Furey NL; Schmid FR; Gewurz H Am J Med; 1980 Jun; 68(6):867-75. PubMed ID: 6770684 [TBL] [Abstract][Full Text] [Related]
10. Hereditary partial deficiency of the third component of complement associated with minimal change nephrotic syndrome. Springate JE; McLean RH; Winkelstein JA; Feld LG Pediatr Nephrol; 1987 Oct; 1(4):608-10. PubMed ID: 3153340 [TBL] [Abstract][Full Text] [Related]
11. Hypocomplementemic urticarial vasculitis or systemic lupus erythematosus? Trendelenburg M; Courvoisier S; Späth PJ; Moll S; Mihatsch M; Itin P; Schifferli JA Am J Kidney Dis; 1999 Oct; 34(4):745-51. PubMed ID: 10516358 [TBL] [Abstract][Full Text] [Related]
12. Inherited deficiency of the third component of complement associated with recurrent pyogenic infections, circulating immune complexes, and vasculitis in a Dutch family. Roord JJ; Daha M; Kuis W; Verbrugh HA; Verhoef J; Zegers BJ; Stoop JW Pediatrics; 1983 Jan; 71(1):81-7. PubMed ID: 6848983 [TBL] [Abstract][Full Text] [Related]
13. [Severe membranoproliferative glomerulonephritis with polyadenopathy associated with hypocomplementemic urticarial vasculitis syndrome]. Gheerbrant H; Giovannini D; Falque L; Andry F; Lugosi M; Deroux A Presse Med; 2017 May; 46(5):547-550. PubMed ID: 28502374 [No Abstract] [Full Text] [Related]
14. [Hypocomplementemic vasculitis treated with dapsone]. Hérault M; Mazet J; Beurey P; Cuny JF; Barbaud A; Schmutz JL; Bursztejn AC Ann Dermatol Venereol; 2010; 137(8-9):541-5. PubMed ID: 20804899 [TBL] [Abstract][Full Text] [Related]
15. Dermal C4d Deposition and Neutrophil Alignment Along the Dermal-Epidermal Junction as a Diagnostic Adjunct for Hypocomplementemic Urticarial Vasculitis (Anti-C1q Vasculitis) and Underlying Systemic Disease. Damman J; Mooyaart AL; Seelen MAJ; van Doorn MBA Am J Dermatopathol; 2020 Jun; 42(6):399-406. PubMed ID: 31436578 [TBL] [Abstract][Full Text] [Related]
16. Hypocomplementaemic urticarial vasculitis syndrome: a mimicker of systemic lupus erythematosus. Roy K; Talukdar A; Kumar B; Sarkar S BMJ Case Rep; 2013 May; 2013():. PubMed ID: 23704433 [TBL] [Abstract][Full Text] [Related]
17. C3 metabolism in a patient with deficiency of the second component of complement (C2) and discoid lupus erythematosus. Wild JH; Zvaifler NJ; Müller-Eberhard HJ; Wilson CB Clin Exp Immunol; 1976 May; 24(2):238-48. PubMed ID: 1084239 [TBL] [Abstract][Full Text] [Related]
18. Role of Direct Immunofluorescence in Cutaneous Small-Vessel Vasculitis: Experience From a Tertiary Center. Lath K; Chatterjee D; Saikia UN; Saikia B; Minz R; De D; Handa S; Radotra B Am J Dermatopathol; 2018 Sep; 40(9):661-666. PubMed ID: 29672364 [TBL] [Abstract][Full Text] [Related]
19. Hereditary deficiency of the third component of complement in two sisters with systemic lupus erythematosus-like symptoms. Sano Y; Nishimukai H; Kitamura H; Nagaki K; Inai S; Hamasaki Y; Maruyama I; Igata A Arthritis Rheum; 1981 Oct; 24(10):1255-60. PubMed ID: 7306227 [TBL] [Abstract][Full Text] [Related]
20. Hypocomplementemia in systemic lupus erythematosus and primary antiphospholipid syndrome: prevalence and clinical significance in 667 patients. Ramos-Casals M; Campoamor MT; Chamorro A; Salvador G; Segura S; Botero JC; Yagüe J; Cervera R; Ingelmo M; Font J Lupus; 2004; 13(10):777-83. PubMed ID: 15540510 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]