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

Year Number of Results
1962 1
1963 3
1964 1
1967 1
1968 3
1969 1
1970 1
1971 1
1973 7
1974 1
1975 5
1977 1
1978 1
1979 2
1981 3
1982 1
1983 1
1984 4
1985 1
1987 2
1988 1
1989 2
1990 1
1991 4
1992 3
1993 4
1994 5
1995 5
1996 4
1997 6
1998 2
1999 4
2000 3
2001 9
2002 4
2003 5
2004 5
2005 8
2006 4
2007 7
2008 2
2009 5
2010 5
2011 10
2012 7
2013 8
2014 5
2015 12
2016 11
2017 9
2018 9
2019 10
2020 7
2021 3
2022 5
2023 4
2024 7

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219 results

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Page 1
Pseudoxanthoma elasticum.
Germain DP. Germain DP. Orphanet J Rare Dis. 2017 May 10;12(1):85. doi: 10.1186/s13023-017-0639-8. Orphanet J Rare Dis. 2017. PMID: 28486967 Free PMC article. Review.
Pseudoxanthoma elasticum (PXE) is a genetic metabolic disease with autosomal recessive inheritance caused by mutations in the ABCC6 gene. ...
Pseudoxanthoma elasticum (PXE) is a genetic metabolic disease with autosomal recessive inheritance caused by mutations in the …
Pseudoxanthoma elasticum.
Roach ES, Islam MP. Roach ES, et al. Handb Clin Neurol. 2015;132:215-21. doi: 10.1016/B978-0-444-62702-5.00015-9. Handb Clin Neurol. 2015. PMID: 26564082 Review.
Pseudoxanthoma elasticum (PXE) is characterized by elastic tissue fragmentation and calcification. ...
Pseudoxanthoma elasticum (PXE) is characterized by elastic tissue fragmentation and calcification. ...
[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.
In ectopic mineralization and lysosomal storage disorders (pseudoxanthoma elasticum and Fabry disease, respectively), cutaneous manifestations may indicate involvement of other organs. ...
In ectopic mineralization and lysosomal storage disorders (pseudoxanthoma elasticum and Fabry disease, respectively), cutaneou …
Cutaneous Elastic Tissue Anomalies.
Andrés-Ramos I, Alegría-Landa V, Gimeno I, Pérez-Plaza A, Rütten A, Kutzner H, Requena L. Andrés-Ramos I, et al. Am J Dermatopathol. 2019 Feb;41(2):85-117. doi: 10.1097/DAD.0000000000001275. Am J Dermatopathol. 2019. PMID: 30688725 Review.
Cutaneous disorders characterized by increased and/or abnormal elastic tissue in the dermis include elastoma, also named nevus elasticus, dermatosis lenticularis disseminata, pseudoxanthoma elasticum, late-onset focal dermal elastosis, linear focal elastosis, elasto …
Cutaneous disorders characterized by increased and/or abnormal elastic tissue in the dermis include elastoma, also named nevus elasticus, de …
Pseudoxanthoma elasticum.
Laube S, Moss C. Laube S, et al. Arch Dis Child. 2005 Jul;90(7):754-6. doi: 10.1136/adc.2004.062075. Arch Dis Child. 2005. PMID: 15970621 Free PMC article. Review.
Pseudoxanthoma elasticum (PXE) is a rare multisystem disorder characterised by progressive calcification and fragmentation of elastic fibres. ...
Pseudoxanthoma elasticum (PXE) is a rare multisystem disorder characterised by progressive calcification and fragmentation of …
The Human Face of ABCC6.
Terry SF. Terry SF. FEBS Lett. 2020 Dec;594(23):4151-4157. doi: 10.1002/1873-3468.14002. Epub 2020 Dec 8. FEBS Lett. 2020. PMID: 33211322 Free article. Review.
As the field has grown, so has its contribution to human disease. Pseudoxanthoma elasticum (PXE) International, an advocacy organization established by non-scientists, began supporting research and convenings on these transporters, specifically ABCC6, the gene assoc …
As the field has grown, so has its contribution to human disease. Pseudoxanthoma elasticum (PXE) International, an advocacy or …
Mid-dermal elastolysis revisited.
Gambichler T. Gambichler T. Arch Dermatol Res. 2010 Mar;302(2):85-93. doi: 10.1007/s00403-009-1004-0. Arch Dermatol Res. 2010. PMID: 19936772 Review.
First-line differential diagnoses may include closely related conditions such as anetoderma, annular elastolytic giant cell granuloma, cutis laxa acquisita and pseudoxanthoma elasticum-like papillary dermal elastolysis. Future therapeutic approaches in MDE patients …
First-line differential diagnoses may include closely related conditions such as anetoderma, annular elastolytic giant cell granuloma, cutis …
Pseudoxanthoma elasticum.
Ohtani T, Furukawa F. Ohtani T, et al. J Dermatol. 2002 Oct;29(10):615-20. doi: 10.1111/j.1346-8138.2002.tb00190.x. J Dermatol. 2002. PMID: 12432991 Review.
Pseudoxanthoma elasticum (PXE) is a heritable disease characterized by dermal, ocular, and vascular lesions that result from degeneration of the elastic fibers. ...
Pseudoxanthoma elasticum (PXE) is a heritable disease characterized by dermal, ocular, and vascular lesions that result from d …
Reticular pseudodrusen: current understanding.
Wightman AJ, Guymer RH. Wightman AJ, et al. Clin Exp Optom. 2019 Sep;102(5):455-462. doi: 10.1111/cxo.12842. Epub 2018 Oct 8. Clin Exp Optom. 2019. PMID: 30298528 Free article. Review.
Reticular pseudodrusen are also found in other diseases, most notably Sorsby's fundus dystrophy, pseudoxanthoma elasticum and acquired vitelliform lesions. They are found more frequently in females, with increased age and more commonly bilaterally than unilaterally. …
Reticular pseudodrusen are also found in other diseases, most notably Sorsby's fundus dystrophy, pseudoxanthoma elasticum and …
Pseudoxanthoma elasticum - Genetics, pathophysiology, and clinical presentation.
Pfau K, Lengyel I, Ossewaarde-van Norel J, van Leeuwen R, Risseeuw S, Leftheriotis G, Scholl HPN, Feltgen N, Holz FG, Pfau M. Pfau K, et al. Prog Retin Eye Res. 2024 Sep;102:101274. doi: 10.1016/j.preteyeres.2024.101274. Epub 2024 May 28. Prog Retin Eye Res. 2024. PMID: 38815804 Free article. Review.
Pseudoxanthoma elasticum (PXE) is an autosomal-recessively inherited multisystem disease. Mutations in the ABCC6-gene are causative, coding for a transmembrane transporter mainly expressed in hepatocytes, which promotes the efflux of adenosine triphosphate (ATP). .. …
Pseudoxanthoma elasticum (PXE) is an autosomal-recessively inherited multisystem disease. Mutations in the ABCC6-gene are caus …
219 results