151 related articles for article (PubMed ID: 26602202)
21. Fabry disease due to G171S
Prencipe M; Posarelli C; Figus M; Gabbriellini G
Eur J Ophthalmol; 2021 Nov; 31(6):NP53-NP57. PubMed ID: 32586128
[TBL] [Abstract][Full Text] [Related]
22. Cardiac Anderson-Fabry disease: lessons from a 25-year-follow up.
Brito D; Miltenberger-Miltenyi G; Moldovan O; Navarro C; Madeira HC
Rev Port Cardiol; 2014 Apr; 33(4):247.e1-7. PubMed ID: 24830310
[TBL] [Abstract][Full Text] [Related]
23. Identification of a novel mutation and prevalence study for fabry disease in Japanese dialysis patients.
Nishino T; Obata Y; Furusu A; Hirose M; Shinzato K; Hattori K; Nakamura K; Matsumoto T; Endo F; Kohno S
Ren Fail; 2012; 34(5):566-70. PubMed ID: 22563919
[TBL] [Abstract][Full Text] [Related]
24. Phenotypical characterization of α-galactosidase A gene mutations identified in a large Fabry disease screening program in stroke in the young.
De Brabander I; Yperzeele L; Ceuterick-De Groote C; Brouns R; Baker R; Belachew S; Delbecq J; De Keulenaer G; Dethy S; Eyskens F; Fumal A; Hemelsoet D; Hughes D; Jeangette S; Nuytten D; Redondo P; Sadzot B; Sindic C; Sheorajpanday R; Thijs V; Van Broeckhoven C; De Deyn PP
Clin Neurol Neurosurg; 2013 Jul; 115(7):1088-93. PubMed ID: 23219219
[TBL] [Abstract][Full Text] [Related]
25. A family with Fabry disease diagnosed by a single angiokeratoma.
Corry A; Feighery C; Alderdice D; Stewart F; Walsh M; Dolan OM
Dermatol Online J; 2011 Apr; 17(4):5. PubMed ID: 21549080
[TBL] [Abstract][Full Text] [Related]
26. Fabry disease in a female patient due to a de novo point mutation at position 691 of exon 5.
Brokalaki EI; Hentschke M; Grabbe S; Jansen T
Eur J Med Res; 2006 Jul; 11(7):306-8. PubMed ID: 16899426
[TBL] [Abstract][Full Text] [Related]
27. [Cardiological follow-up in patients with Fabry disease].
Pieruzzi F; Pieroni M; Chimenti C; Frustaci A; Sarais C; Cecchi F;
G Ital Cardiol (Rome); 2010; 11(7-8):566-72. PubMed ID: 21033333
[TBL] [Abstract][Full Text] [Related]
28. [Left ventricular hypertrophy and end-stage renal failure of unknown etiology: Fabry disease?].
Arévalo-Gómez A; Rivera-García S; López-Muñiz A; Barriales-Villa R
Rev Clin Esp; 2012 May; 212(5):265-6. PubMed ID: 22112280
[No Abstract] [Full Text] [Related]
29. A family with various symptomatology suggestive of Anderson-Fabry disease and a genetic polymorphism of alpha galactosidase A gene.
Tuttolomondo A; Duro G; Pecoraro R; Simonetta I; Miceli S; Colomba P; Zizzo C; Di Chiara T; Scaglione R; Della Corte V; Corpora F; Pinto A
Clin Biochem; 2015 Jan; 48(1-2):55-62. PubMed ID: 25281798
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. Case report:
Simonetta I; Riolo R; Todaro F; Donadio V; Incensi A; Miceli S; Colomba P; Duro G; Tuttolomondo A
Front Genet; 2023; 14():1122893. PubMed ID: 37779915
[No Abstract] [Full Text] [Related]
32. [Early diagnosis of Fabry disease in children].
Genoni G; Demarchi I; Bellone S; Petri A; Settanni F; Dondi E; Negro M; Cortese L; Prodam F; Bona G
Minerva Pediatr; 2011 Oct; 63(5):425-30. PubMed ID: 21946453
[TBL] [Abstract][Full Text] [Related]
33. Hemizygous Fabry disease associated with membranous nephropathy: A rare case report
.
Zhou W; Ni Z; Zhang M
Clin Nephrol; 2018 Sep; 90(3):227-231. PubMed ID: 29792392
[TBL] [Abstract][Full Text] [Related]
34. Screening for Fabry disease in male patients with end-stage renal disease in western France.
Vigneau C; Germain DP; Larmet D; Jabbour F; Hourmant M;
Nephrol Ther; 2021 Jun; 17(3):180-184. PubMed ID: 33994139
[TBL] [Abstract][Full Text] [Related]
35. [Clinical courses of two male siblings on hemodialysis for Fabry disease ].
Itoh K; Tanaka M; Matsushita K; Miyamura N; Nishida K; Araki E; Nonoguchi H; Tomita K
Nihon Jinzo Gakkai Shi; 2005; 47(2):121-7. PubMed ID: 15859134
[TBL] [Abstract][Full Text] [Related]
36. Identification of a novel mutation in the alpha-galactosidase A gene in patients with Fabry disease.
Colomba P; Nucera A; Zizzo C; Albeggiani G; Francofonte D; Iemolo F; Tuttolomondo A; Pinto A; Duro G
Clin Biochem; 2012 Jul; 45(10-11):839-41. PubMed ID: 22465271
[TBL] [Abstract][Full Text] [Related]
37. Fabry disease in hemodialysis patients in southern Brazil: prevalence study and clinical report.
Porsch DB; Nunes AC; Milani V; Rossato LB; Mattos CB; Tsao M; Netto C; Burin M; Pereira F; Matte U; Giugliani R; Barros EJ
Ren Fail; 2008; 30(9):825-30. PubMed ID: 18925518
[TBL] [Abstract][Full Text] [Related]
38. Differences in Fabry cardiomyopathy between female and male patients: consequences for diagnostic assessment.
Niemann M; Herrmann S; Hu K; Breunig F; Strotmann J; Beer M; Machann W; Voelker W; Ertl G; Wanner C; Weidemann F
JACC Cardiovasc Imaging; 2011 Jun; 4(6):592-601. PubMed ID: 21679893
[TBL] [Abstract][Full Text] [Related]
39. A missense mutation, A156T, in the alpha-galactosidase A gene causes typical Fabry disease.
Konoshita T; Mutoh H; Yokoi T; Koni I; Miyamori I; Mabuchi H
Clin Nephrol; 2001 Mar; 55(3):243-7. PubMed ID: 11316246
[TBL] [Abstract][Full Text] [Related]
40. Fabry disease in children: a federal screening programme in Russia.
Namazova-Baranova LS; Baranov AA; Pushkov AA; Savostyanov KV
Eur J Pediatr; 2017 Oct; 176(10):1385-1391. PubMed ID: 28871487
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
