185 related articles for article (PubMed ID: 26552470)
21. Is standard GLA gene mutation analysis definitive for the diagnosis of Fabry disease?
Mignani R; Morrone A
Kidney Int; 2009 May; 75(10):1115-6; author reply 1115. PubMed ID: 19404287
[No Abstract] [Full Text] [Related]
22. Fabry Disease Screening in Patients With Kidney Transplant: A Single-Center Study in Turkey.
Erdogmus S; Kutlay S; Kumru G; Ors Sendogan D; Erturk S; Keven K; Ceylaner G; Sengul S
Exp Clin Transplant; 2020 Aug; 18(4):444-449. PubMed ID: 32281532
[TBL] [Abstract][Full Text] [Related]
23. New mutation in female patient with renal variant of Fabry disease and HIV.
Solis MA; Pascual B; Boscá M; Ramos V; Carda C; Monteagudo C; Torregrosa I; Pons S; Miguel A
J Nephrol; 2010; 23(2):231-3. PubMed ID: 20155722
[TBL] [Abstract][Full Text] [Related]
24. A Case Report of Henoch-Schonlein Purpura and IgA Nephropathy Associated With Rivaroxaban.
Chung EY; Chen J; Roxburgh S
Nephrology (Carlton); 2018 Mar; 23(3):289-290. PubMed ID: 29461002
[No Abstract] [Full Text] [Related]
25. A classical phenotype of Anderson-Fabry disease in a female patient with intronic mutations of the GLA gene: a case report.
Pisani A; Imbriaco M; Zizzo C; Albeggiani G; Colomba P; Alessandro R; Iemolo F; Duro G
BMC Cardiovasc Disord; 2012 Jun; 12():39. PubMed ID: 22682330
[TBL] [Abstract][Full Text] [Related]
26. Raynaud's phenomenon associated with Fabry disease.
Germain DP; Atanasiu OI; Akrout-Marouene J; Benistan K
J Inherit Metab Dis; 2015 Mar; 38(2):367-8. PubMed ID: 25511234
[No Abstract] [Full Text] [Related]
27. A case of IgA-related enteropathy complicated with gastrointestinal bleeding and progressive IgA nephropathy: a possible variant Henoch-Schönlein purpura?
Nakamura S; Hisamatsu T; Kikuchi J; Adachi M; Yamagishi Y; Imaeda H; Hosoe N; Naganuma M; Ebinuma H; Okamoto S; Kanai T; Ogata H; Hanaoka H; Furuya Y; Kawano Y; Bokuda K; Sasamura H; Uchida H; Endo T; Hashiguchi A; Kameyama K; Mukai M; Hibi T
Intern Med; 2010; 49(16):1755-61. PubMed ID: 20720354
[TBL] [Abstract][Full Text] [Related]
28. Berger disease: Henoch-Schönlein syndrome without the rash.
Meadow SR; Scott DG
J Pediatr; 1985 Jan; 106(1):27-32. PubMed ID: 2981307
[TBL] [Abstract][Full Text] [Related]
29. Evolution of IgA nephropathy into anaphylactoid purpura in six cases--further evidence that IgA nephropathy and Henoch-Schonlein purpura nephritis share common pathogenesis.
Kamei K; Ogura M; Sato M; Ito S; Ishikura K
Pediatr Nephrol; 2016 May; 31(5):779-85. PubMed ID: 26679340
[TBL] [Abstract][Full Text] [Related]
30. [Henoch-Schönlein purpura in the adult].
Pillebout E; Verine J
Rev Med Interne; 2014 Jun; 35(6):372-81. PubMed ID: 24657040
[TBL] [Abstract][Full Text] [Related]
31. Recurrent adult onset Henoch-Schonlein Purpura: a case report.
Gaskill N; Guido B; Magro CM
Dermatol Online J; 2016 Aug; 22(8):. PubMed ID: 27617937
[TBL] [Abstract][Full Text] [Related]
32. Henoch-Schönlein purpura nephritis.
Fervenza FC
Int J Dermatol; 2003 Mar; 42(3):170-7. PubMed ID: 12653909
[No Abstract] [Full Text] [Related]
33. [Clinical course and pathogenesis of Schönlein-Henoch nephropathy].
Zurowska A
Pediatr Pol; 1986 May; 61(5):315-9. PubMed ID: 3537947
[No Abstract] [Full Text] [Related]
34. What is Schönlein-Henoch purpura, and why should we care?
Piette WW
Arch Dermatol; 1997 Apr; 133(4):515-8. PubMed ID: 9126029
[No Abstract] [Full Text] [Related]
35. A novel small insertion mutation, C.1030_1031ins (T) in α-galactosidase A leads to renal variant fabry disease.
Choi JS; Kim CS; Park JW; Bae EH; Ma SK; Choi YD; Kim GH; Yoo HW; Kim SW
Ren Fail; 2012; 34(3):390-3. PubMed ID: 22260214
[TBL] [Abstract][Full Text] [Related]
36. Abnormal IgA glycosylation in Henoch-Schönlein purpura restricted to patients with clinical nephritis.
Allen AC; Willis FR; Beattie TJ; Feehally J
Nephrol Dial Transplant; 1998 Apr; 13(4):930-4. PubMed ID: 9568852
[TBL] [Abstract][Full Text] [Related]
37. Henoch-Schönlein purpura presenting with anuria in an adult.
Weiser JA; Rogers HD; Stokes MB; Grossman ME
Cutis; 2010 Oct; 86(4):181-4. PubMed ID: 21140925
[TBL] [Abstract][Full Text] [Related]
38. [Fabry disease from the neurologist's point of view: is it a rare cause of strokes?].
Marti-Martinez S; Climent V; Pampliega-Perez A; Martin-Estefania C; Leiva-Santana C
Rev Neurol; 2015 Jan; 60(2):93-5. PubMed ID: 25583594
[No Abstract] [Full Text] [Related]
39. Screening, diagnosis, and management of patients with Fabry disease: conclusions from a "Kidney Disease: Improving Global Outcomes" (KDIGO) Controversies Conference.
Schiffmann R; Hughes DA; Linthorst GE; Ortiz A; Svarstad E; Warnock DG; West ML; Wanner C;
Kidney Int; 2017 Feb; 91(2):284-293. PubMed ID: 27998644
[TBL] [Abstract][Full Text] [Related]
40. Clinical characteristics and mutation spectrum of GLA in Korean patients with Fabry disease by a nationwide survey: Underdiagnosis of late-onset phenotype.
Choi JH; Lee BH; Heo SH; Kim GH; Kim YM; Kim DS; Ko JM; Sohn YB; Hong YH; Lee DH; Kook H; Lim HH; Kim KH; Kim WS; Hong GR; Kim SH; Park SH; Kim CD; Kim SM; Seo JS; Yoo HW
Medicine (Baltimore); 2017 Jul; 96(29):e7387. PubMed ID: 28723748
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]