137 related articles for article (PubMed ID: 38226450)
1. Morbus Fabry and Parkinson's Disease-More Evidence for a Possible Genetic Link.
Müller S; Kassubek J; Hold ST; Kasper DC; Mayer B; Müller K; Freischmidt A; Siebert R; Braak H; Ludolph AC; Del Tredici K
Mov Disord; 2024 Feb; 39(2):449-451. PubMed ID: 38226450
[No Abstract] [Full Text] [Related]
2. Cerebral hemorrhage in Fabry's disease.
Nakamura K; Sekijima Y; Nakamura K; Hattori K; Nagamatsu K; Shimizu Y; Yasude T; Ushiyama M; Endo F; Fukushima Y; Ikeda S
J Hum Genet; 2010 Apr; 55(4):259-61. PubMed ID: 20300124
[TBL] [Abstract][Full Text] [Related]
3. Genetics and Gene Therapy of Anderson-Fabry Disease.
Simonetta I; Tuttolomondo A; Di Chiara T; Miceli S; Vogiatzis D; Corpora F; Pinto A
Curr Gene Ther; 2018; 18(2):96-106. PubMed ID: 29618309
[TBL] [Abstract][Full Text] [Related]
4. Megadolichobasilar anomaly with thrombosis in a family with Fabry's disease and a novel mutation in the alpha-galactosidase A gene.
Garzuly F; Maródi L; Erdös M; Grubits J; Varga Z; Gelpi E; Rohonyi B; Mázló M; Molnár A; Budka H
Brain; 2005 Sep; 128(Pt 9):2078-83. PubMed ID: 15947062
[TBL] [Abstract][Full Text] [Related]
5. Molecular genetic, biochemical, and clinical studies in three families with cardiac Fabry's disease.
Yoshitama T; Nakao S; Takenaka T; Teraguchi H; Sasaki T; Kodama C; Tanaka A; Kisanuki A; Tei C
Am J Cardiol; 2001 Jan; 87(1):71-5. PubMed ID: 11137837
[TBL] [Abstract][Full Text] [Related]
6. Parkinsonism and Anderson Fabry's disease: a case report.
Buechner S; De Cristofaro MT; Ramat S; Borsini W
Mov Disord; 2006 Jan; 21(1):103-7. PubMed ID: 16149089
[TBL] [Abstract][Full Text] [Related]
7. An atypical variant of Fabry's disease in men with left ventricular hypertrophy.
Nakao S; Takenaka T; Maeda M; Kodama C; Tanaka A; Tahara M; Yoshida A; Kuriyama M; Hayashibe H; Sakuraba H
N Engl J Med; 1995 Aug; 333(5):288-93. PubMed ID: 7596372
[TBL] [Abstract][Full Text] [Related]
8. Screening for Fabry disease in a series of Parkinson's disease patients and literature review.
Perillo S; Palmieri GR; Del Moral MO; De Michele G; Giglio A; Cuomo N; Pane C; Bauer P; De Michele G; De Rosa A
Neurol Sci; 2023 Apr; 44(4):1235-1241. PubMed ID: 36547780
[TBL] [Abstract][Full Text] [Related]
9. [A case of Fabry's disease with chronic renal failure].
Suzuki T; Fujino T; Sugasawa M; Kohara Y; Toyama K; Sato T; Yasuda T; Sugiyama M; Maeba T; Owada S; Ishida M
Nihon Jinzo Gakkai Shi; 1999 Jun; 41(4):448-53. PubMed ID: 10441995
[TBL] [Abstract][Full Text] [Related]
10. [Fabry's disease (alpha-galactosidase-A deficiency): physiopathology, clinical signs, and genetic aspects].
Germain DP
J Soc Biol; 2002; 196(2):161-73. PubMed ID: 12360745
[TBL] [Abstract][Full Text] [Related]
11. A case of Fabry's disease with congenital agammaglobulinemia.
Lee KY; Jeon SY; Hong JW; Kim SE; Song KH; Kim YH; Kim KH
J Korean Med Sci; 2011 Jul; 26(7):966-70. PubMed ID: 21738355
[TBL] [Abstract][Full Text] [Related]
12. The kidney in Fabry's disease.
Pisani A; Visciano B; Imbriaco M; Di Nuzzi A; Mancini A; Marchetiello C; Riccio E
Clin Genet; 2014 Oct; 86(4):301-9. PubMed ID: 24645664
[TBL] [Abstract][Full Text] [Related]
13. Renal involvement in Fabry's disease.
Okuda S
Intern Med; 2000 Aug; 39(8):601-2. PubMed ID: 10939529
[No Abstract] [Full Text] [Related]
14. GLA Gene Mutation in Hypertrophic Cardiomyopathy with a New Variant Description: Is it Fabry's Disease?
Chaves-Markman ÂV; Markman M; Calado EB; Pires RF; Santos-Veloso MAO; Pereira CMF; Lordsleem ABMDS; Lima SG; Markman Filho B; Oliveira DC
Arq Bras Cardiol; 2019 Jul; 113(1):77-84. PubMed ID: 31291414
[TBL] [Abstract][Full Text] [Related]
15. Endothelial nitric oxide synthase gene polymorphisms in Fabry's disease.
Heltianu C; Costache G; Azibi K; Poenaru L; Simionescu M
Clin Genet; 2002 Jun; 61(6):423-9. PubMed ID: 12121349
[TBL] [Abstract][Full Text] [Related]
16. Pseudo-clinical Fabry's disease without alpha galactosidase deficiency.
Peltier A; Herbeuval E; Brondeau MT; Belleville F; Nabet P
Biomedicine; 1977 May; 26(3):194-201. PubMed ID: 407951
[TBL] [Abstract][Full Text] [Related]
17. Functional evaluation of a novel GLA causative mutation in Fabry disease.
Li P; Zhang L; Xiong Q; Wang Z; Cui X; Zhou YA; Wang Y; Xiao H; Wu C
Mol Genet Genomic Med; 2019 Sep; 7(9):e864. PubMed ID: 31321922
[TBL] [Abstract][Full Text] [Related]
18. [Heterozygous Fabry's disease. Case report with electron microscopic studies].
Luderschmidt C; Wolff HH
Hautarzt; 1980 Jul; 31(7):372-5. PubMed ID: 6249775
[TBL] [Abstract][Full Text] [Related]
19. Identification of Fabry's disease by the screening of alpha-galactosidase A activity in male and female hemodialysis patients.
Tanaka M; Ohashi T; Kobayashi M; Eto Y; Miyamura N; Nishida K; Araki E; Itoh K; Matsushita K; Hara M; Kuwahara K; Nakano T; Yasumoto N; Nonoguchi H; Tomita K
Clin Nephrol; 2005 Oct; 64(4):281-7. PubMed ID: 16240899
[TBL] [Abstract][Full Text] [Related]
20. [Angiokeratoma corporis diffusum universale (Fabry disease)].
Frank J; Jansen-Genzel W; Lentner A; Wienert V
Hautarzt; 1996 Oct; 47(10):776-9. PubMed ID: 9036128
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
