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

Year Number of Results
1964 2
1967 1
1968 2
1969 3
1970 2
1972 1
1975 1
1976 1
1977 1
1982 1
1987 2
1988 2
1989 4
1990 1
1991 2
1992 4
1993 1
1995 3
1996 3
1997 1
1998 1
1999 3
2000 3
2001 2
2002 5
2003 3
2004 6
2005 2
2006 4
2007 1
2008 2
2009 4
2010 5
2011 6
2012 3
2013 10
2014 4
2015 4
2016 7
2017 6
2018 9
2019 5
2020 9
2021 3
2022 3
2023 4
2024 0

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146 results

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Page 1
[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.
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.
The cutaneous hallmark of FD is a specific distribution of angiokeratoma. Other common symptoms include cornea verticillata, acroparesthesia, and sweating abnormalities. FD-specific symptoms, history, as well as examination of angiokeratoma can assist in the differe …
The cutaneous hallmark of FD is a specific distribution of angiokeratoma. Other common symptoms include cornea verticillata, acropare …
Fabry disease.
Germain DP. Germain DP. Orphanet J Rare Dis. 2010 Nov 22;5:30. doi: 10.1186/1750-1172-5-30. Orphanet J Rare Dis. 2010. PMID: 21092187 Free PMC article. Review.
Classically affected hemizygous males, with no residual alpha-galactosidase A activity may display all the characteristic neurological (pain), cutaneous (angiokeratoma), renal (proteinuria, kidney failure), cardiovascular (cardiomyopathy, arrhythmia), cochleo-vestibular an …
Classically affected hemizygous males, with no residual alpha-galactosidase A activity may display all the characteristic neurological (pain …
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.
Subsequently, symptoms related to progressive impairment appear, such as angiokeratomas, cornea verticillata, left ventricular hypertrophy, myocardial fibrosis, proteinuria, and renal insufficiency. ...
Subsequently, symptoms related to progressive impairment appear, such as angiokeratomas, cornea verticillata, left ventricular hypert …
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.
Clinical manifestations of disease are hypohidrosis, acroparesthesias, heat intolerance, angiokeratomas, corneal opacities, cardiac arrhythmias, left ventricular hypertrophy, proteinuria, renal insufficiency and cerebrovascular accidents. ...
Clinical manifestations of disease are hypohidrosis, acroparesthesias, heat intolerance, angiokeratomas, corneal opacities, cardiac a …
[Fabry disease].
Stephan F, Haber R. Stephan F, et al. Ann Dermatol Venereol. 2017 Feb;144(2):137-146. doi: 10.1016/j.annder.2016.10.010. Epub 2017 Jan 16. Ann Dermatol Venereol. 2017. PMID: 28104284 Review. French.
Fabry disease, also known as Anderson-Fabry disease or angiokeratoma corporis diffusum universale, is an X-linked recessive form of sphingolipidosis caused by total or partial deficiency of the lysosomal hydrolase, alpha-galactosidase A. ...Cutaneous, neurological, nephrol …
Fabry disease, also known as Anderson-Fabry disease or angiokeratoma corporis diffusum universale, is an X-linked recessive form of s …
Fabry disease.
Thomas AS, Hughes DA. Thomas AS, et al. Pediatr Endocrinol Rev. 2014 Sep;12 Suppl 1:88-101. Pediatr Endocrinol Rev. 2014. PMID: 25345090 Review.
Accumulation of substrate occurs in multiple cell types resulting in a multi-system disorder, affecting both males and females. Clinical features include neuropathic pain and angiokeratoma, with subsequent development of proteinuria, renal failure, left ventricular hypertr …
Accumulation of substrate occurs in multiple cell types resulting in a multi-system disorder, affecting both males and females. Clinical fea …
[Dermoscopy of genodermatoses].
Plázár D, Joura MI, Kiss N, Medvecz M. Plázár D, et al. Dermatologie (Heidelb). 2023 Apr;74(4):256-261. doi: 10.1007/s00105-023-05124-7. Epub 2023 Mar 7. Dermatologie (Heidelb). 2023. PMID: 36882583 Free PMC article. Review. German.
Cutaneous Pseudolymphomas.
Romero-Pérez D, Blanes Martínez M, Encabo-Durán B. Romero-Pérez D, et al. Actas Dermosifiliogr. 2016 Oct;107(8):640-51. doi: 10.1016/j.ad.2016.05.003. Epub 2016 Jun 8. Actas Dermosifiliogr. 2016. PMID: 27289134 Free article. Review. English, Spanish.
Fabry disease.
Schiffmann R. Schiffmann R. Handb Clin Neurol. 2015;132:231-48. doi: 10.1016/B978-0-444-62702-5.00017-2. Handb Clin Neurol. 2015. PMID: 26564084 Review.
146 results