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

Year Number of Results
1943 1
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1946 1
1947 4
1948 5
1949 7
1950 23
1951 19
1952 13
1953 8
1954 8
1955 9
1956 11
1957 16
1958 5
1959 12
1960 16
1961 16
1962 13
1963 17
1964 13
1965 17
1966 13
1967 9
1968 6
1969 19
1970 17
1971 12
1972 15
1973 8
1974 25
1975 41
1976 43
1977 40
1978 45
1979 38
1980 44
1981 24
1982 38
1983 39
1984 34
1985 28
1986 34
1987 43
1988 43
1989 38
1990 39
1991 32
1992 51
1993 58
1994 38
1995 46
1996 48
1997 46
1998 51
1999 46
2000 71
2001 46
2002 56
2003 53
2004 62
2005 61
2006 77
2007 95
2008 74
2009 87
2010 103
2011 97
2012 81
2013 116
2014 103
2015 100
2016 84
2017 93
2018 104
2019 116
2020 109
2021 124
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2026 44

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3,501 results

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Page 1
Parkes Weber syndrome-Diagnostic and management paradigms: A systematic review.
Banzic I, Brankovic M, Maksimović Ž, Davidović L, Marković M, Rančić Z. Banzic I, et al. Phlebology. 2017 Jul;32(6):371-383. doi: 10.1177/0268355516664212. Epub 2016 Aug 9. Phlebology. 2017. PMID: 27511883
Objectives Parkes Weber syndrome is a congenital vascular malformation which consists of capillary malformation, venous malformation, lymphatic malformation, and arteriovenous malformation. ...Arteriovenous malformation presents the criterion for distinguishi …
Objectives Parkes Weber syndrome is a congenital vascular malformation which consists of capillary malformation, venous …
Parkes-Weber syndrome.
Manresa-Manresa F, Iribarren-Marín MA, Gómez-Ruiz FT. Manresa-Manresa F, et al. Rev Esp Cardiol (Engl Ed). 2015 Jan;68(1):67. doi: 10.1016/j.rec.2014.02.022. Epub 2014 Jun 27. Rev Esp Cardiol (Engl Ed). 2015. PMID: 25553944 No abstract available.
Parkes Weber syndrome.
Kumar V, Jorwal P, Biswas A, Deorari V. Kumar V, et al. QJM. 2019 Dec 1;112(12):936. doi: 10.1093/qjmed/hcz101. QJM. 2019. PMID: 31086946 No abstract available.
Sturge-Weber syndrome.
Baselga E. Baselga E. Semin Cutan Med Surg. 2004 Jun;23(2):87-98. doi: 10.1016/j.sder.2004.01.002. Semin Cutan Med Surg. 2004. PMID: 15295918 Review.
Sturge-Weber syndrome is a sporadic neurocutaneous disease characterized by facial port-wine stain, ocular abnormalities (glaucoma and choroidal hemangioma) and leptomeningeal angioma. ...Early neuroimaging features are important to recognize. Management of p …
Sturge-Weber syndrome is a sporadic neurocutaneous disease characterized by facial port-wine stain, ocular abnormalitie …
Parkes-Weber syndrome in the emergency department.
Patel R, Durant EJ, Freed R. Patel R, et al. BMJ Case Rep. 2021 Sep 20;14(9):e241649. doi: 10.1136/bcr-2021-241649. BMJ Case Rep. 2021. PMID: 34544698 Free PMC article.
After multiple visits to the ED and workups with rheumatology, dermatology, interventional radiology and genetics, she was finally diagnosed with Parkes-Weber syndrome. The purpose of this case report is to illustrate the common and uncommon presentations, mi …
After multiple visits to the ED and workups with rheumatology, dermatology, interventional radiology and genetics, she was finally diagnosed …
Major Limb Amputation in Parkes-Weber Syndrome With Refractory Ulceration: A Case Report and Literature Review.
He B, Sun MS, Liu JW, Nie QQ, Fan XQ, Liu P. He B, et al. Int J Low Extrem Wounds. 2023 Mar;22(1):168-173. doi: 10.1177/1534734620986683. Epub 2021 Feb 2. Int J Low Extrem Wounds. 2023. PMID: 33527869 Review.
Parkes-Weber syndrome (PWS) is a rare congenital vascular syndrome consisting of capillary, venous, lymphatic, and arteriovenous malformation. ...
Parkes-Weber syndrome (PWS) is a rare congenital vascular syndrome consisting of capillary, venous, lymphatic, a …
Parkes Weber syndrome: a rare cause of foot drop.
Kyriakides DE, Michaelides D, Lambrianides S. Kyriakides DE, et al. BMJ Case Rep. 2023 Oct 4;16(10):e254455. doi: 10.1136/bcr-2022-254455. BMJ Case Rep. 2023. PMID: 37793841 Free PMC article.
This case report describes a patient in her late 60s, previously diagnosed with Klippel-Trenaunay syndrome who presented with difficulty walking. A year prior to her presentation she had a fall which made her notice a painless foot drop on the right. ...The patient's diffe …
This case report describes a patient in her late 60s, previously diagnosed with Klippel-Trenaunay syndrome who presented with difficu …
Capillary Malformations.
Escobar K, Pandher K, Jahnke MN. Escobar K, et al. Dermatol Clin. 2022 Oct;40(4):425-433. doi: 10.1016/j.det.2022.06.005. Epub 2022 Sep 16. Dermatol Clin. 2022. PMID: 36243429 Review.
Most of the CMs occur without any syndromic findings; the association between CMs systemic anomalies in some patients, however, makes the recognition of additional syndrome features critical. Some genetic disorders discussed, which feature CMs, include Sturge-Web …
Most of the CMs occur without any syndromic findings; the association between CMs systemic anomalies in some patients, however, makes the re …
[Parkes-Weber syndrome].
KAUFMANN W. KAUFMANN W. Arztl Wochensch. 1960 Mar 4;15:187-90. Arztl Wochensch. 1960. PMID: 14404910 German. No abstract available.
3,501 results