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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1964 1
1966 1
1967 2
1969 1
1970 3
1971 1
1972 2
1973 4
1974 7
1975 4
1976 4
1977 4
1978 4
1979 3
1980 2
1981 2
1982 2
1983 2
1984 5
1985 3
1986 1
1987 4
1988 5
1989 4
1990 3
1991 7
1992 5
1993 7
1994 8
1995 9
1996 6
1997 8
1998 6
1999 4
2000 9
2001 23
2002 36
2003 28
2004 27
2005 20
2006 32
2007 49
2008 25
2009 35
2010 41
2011 32
2012 29
2013 46
2014 37
2015 34
2016 34
2017 40
2018 35
2019 39
2020 51
2021 53
2022 40
2023 38
2024 14

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894 results

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Page 1
Fabry Disease and the Heart: A Comprehensive Review.
Azevedo O, Cordeiro F, Gago MF, Miltenberger-Miltenyi G, Ferreira C, Sousa N, Cunha D. Azevedo O, et al. Int J Mol Sci. 2021 Apr 23;22(9):4434. doi: 10.3390/ijms22094434. Int J Mol Sci. 2021. PMID: 33922740 Free PMC article. Review.
Fabry disease (FD) is an X-linked lysosomal storage disorder caused by mutations of the GLA gene that result in a deficiency of the enzymatic activity of alpha-galactosidase A and consequent accumulation of glycosphingolipids in body fluids and lysosomes of the cell …
Fabry disease (FD) is an X-linked lysosomal storage disorder caused by mutations of the GLA gene that result in a deficiency o …
Fabry Disease: Current and Novel Therapeutic Strategies. A Narrative Review.
Palaiodimou L, Kokotis P, Zompola C, Papagiannopoulou G, Bakola E, Papadopoulou M, Zouvelou V, Petras D, Vlachopoulos C, Tsivgoulis G. Palaiodimou L, et al. Curr Neuropharmacol. 2023;21(3):440-456. doi: 10.2174/1570159X20666220601124117. Curr Neuropharmacol. 2023. PMID: 35652398 Free PMC article. Review.
BACKGROUND: Fabry disease (FD) is an inherited lysosomal storage disorder, leading to multisystemic manifestations and causing significant morbidity and mortality. ...RESULTS: A multidisciplinary symptomatic treatment is recommended for FD patients, personalized acc …
BACKGROUND: Fabry disease (FD) is an inherited lysosomal storage disorder, leading to multisystemic manifestations and causing …
[Fabry disease: A review].
Michaud M, Mauhin W, Belmatoug N, Bedreddine N, Garnotel R, Catros F, Lidove O, Gaches F. Michaud M, et al. Rev Med Interne. 2021 Feb;42(2):110-119. doi: 10.1016/j.revmed.2020.08.019. Epub 2020 Nov 7. Rev Med Interne. 2021. PMID: 33172708 Review. French.
Fabry disease is the second most frequent lysosomal storage disorder. ...Recognition of Fabry disease is important because treatments are available, but it may be challenging. ...
Fabry disease is the second most frequent lysosomal storage disorder. ...Recognition of Fabry disease is importa …
A Review of Fabry Disease.
Chan B, Adam DN. Chan B, et al. Skin Therapy Lett. 2018 Mar;23(2):4-6. Skin Therapy Lett. 2018. PMID: 29562089 Free article. Review.
Fabry disease (FD) is an X-linked lysosomal storage disease. A lack of alpha-galactosidase activity results in the accumulation of globotriaosylceramide in cells of various systems, leading to multi-systemic effects. ...
Fabry disease (FD) is an X-linked lysosomal storage disease. A lack of alpha-galactosidase activity results in the accu …
Fabry's disease--a comprehensive review on pathogenesis, diagnosis and treatment.
Mahmud HM. Mahmud HM. J Pak Med Assoc. 2014 Feb;64(2):189-94. J Pak Med Assoc. 2014. PMID: 24640811 Review.
Fabry's is a progressive, destructive and life threatening disease which reduces significantly life expectancy of the affected individual. ...Specific therapy for Fabry's disease is enzyme replacement with recombinant human alpha-galactosidase A. ...
Fabry's is a progressive, destructive and life threatening disease which reduces significantly life expectancy of the affected …
Fabry disease revisited: Management and treatment recommendations for adult patients.
Ortiz A, Germain DP, Desnick RJ, Politei J, Mauer M, Burlina A, Eng C, Hopkin RJ, Laney D, Linhart A, Waldek S, Wallace E, Weidemann F, Wilcox WR. Ortiz A, et al. Mol Genet Metab. 2018 Apr;123(4):416-427. doi: 10.1016/j.ymgme.2018.02.014. Epub 2018 Feb 28. Mol Genet Metab. 2018. PMID: 29530533 Free article. Review.
Fabry disease is an X-linked lysosomal storage disorder caused by mutations in the GLA gene leading to deficient alpha-galactosidase A activity, glycosphingolipid accumulation, and life-threatening complications. ...Updated monitoring and treatment guidelines for pe …
Fabry disease is an X-linked lysosomal storage disorder caused by mutations in the GLA gene leading to deficient alpha-galacto …
Cardiac Involvement in Fabry Disease: JACC Review Topic of the Week.
Pieroni M, Moon JC, Arbustini E, Barriales-Villa R, Camporeale A, Vujkovac AC, Elliott PM, Hagege A, Kuusisto J, Linhart A, Nordbeck P, Olivotto I, Pietilä-Effati P, Namdar M. Pieroni M, et al. J Am Coll Cardiol. 2021 Feb 23;77(7):922-936. doi: 10.1016/j.jacc.2020.12.024. J Am Coll Cardiol. 2021. PMID: 33602475 Free article. Review.
Fabry disease (FD) is a rare X-linked inherited lysosomal storage disorder caused by deficient alpha-galactosidase A activity that leads to an accumulation of globotriasylceramide (Gb3) in affected tissues, including the heart. ...Following the introduction of enzym …
Fabry disease (FD) is a rare X-linked inherited lysosomal storage disorder caused by deficient alpha-galactosidase A activity …
Fabry disease: genetics, pathology, and treatment.
Bernardes TP, Foresto RD, Kirsztajn GM. Bernardes TP, et al. Rev Assoc Med Bras (1992). 2020 Jan 13;66Suppl 1(Suppl 1):s10-s16. doi: 10.1590/1806-9282.66.S1.10. Rev Assoc Med Bras (1992). 2020. PMID: 31939530 Free article. Review.
Fabry disease (FD) is a recessive monogenic inheritance disease linked to chromosome X, secondary to mutations in the GLA gene. ...It is considered that the specific treatment should be initiated as soon as a diagnosis is obtained, which can change the progno …
Fabry disease (FD) is a recessive monogenic inheritance disease linked to chromosome X, secondary to mutations in the G …
Migalastat: A Review in Fabry Disease.
McCafferty EH, Scott LJ. McCafferty EH, et al. Drugs. 2019 Apr;79(5):543-554. doi: 10.1007/s40265-019-01090-4. Drugs. 2019. PMID: 30875019 Free PMC article. Review.
Fabry disease is a rare lysosomal disorder characterized by deficient or absent alpha-galactosidase A activity resulting from mutations in the GLA gene. ...Given its convenient oral regimen and the limited therapeutic options available, migalastat is an important tr …
Fabry disease is a rare lysosomal disorder characterized by deficient or absent alpha-galactosidase A activity resulting from …
When and How to Diagnose Fabry Disease in Clinical Pratice.
Michaud M, Mauhin W, Belmatoug N, Garnotel R, Bedreddine N, Catros F, Ancellin S, Lidove O, Gaches F. Michaud M, et al. Am J Med Sci. 2020 Dec;360(6):641-649. doi: 10.1016/j.amjms.2020.07.011. Epub 2020 Jul 10. Am J Med Sci. 2020. PMID: 32723516 Review.
Fabry disease may present as "classical", as "late-onset" or "non-classical" forms. ...In this review, we aimed to summarize main clinical manifestations of Fabry disease to know when to evoke Fabry disease and propose a practical diagnos …
Fabry disease may present as "classical", as "late-onset" or "non-classical" forms. ...In this review, we aimed to summarize m …
894 results