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

Year Number of Results
1965 1
1970 2
1971 1
1973 2
1974 1
1975 1
1977 1
1978 2
1980 2
1981 2
1982 1
1983 7
1984 6
1985 4
1986 1
1987 4
1988 1
1989 6
1990 3
1991 10
1992 3
1993 2
1994 3
1995 12
1996 7
1997 2
1998 16
1999 10
2000 14
2001 10
2002 17
2003 14
2004 10
2005 20
2006 12
2007 11
2008 13
2009 14
2010 14
2011 20
2012 16
2013 21
2014 24
2015 22
2016 26
2017 20
2018 19
2019 24
2020 21
2021 15
2022 12
2023 10
2024 3

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463 results

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Quoted phrase not found in phrase index: "Telangiectasia of the skin"
Page 1
Dermatomyositis.
Callen JP. Callen JP. Lancet. 2000 Jan 1;355(9197):53-7. doi: 10.1016/S0140-6736(99)05157-0. Lancet. 2000. PMID: 10615903 Review.
Dermatomyositis is one of the idiopathic inflammatory myopathies with characteristic cutaneous manifestations including the heliotrope rash, Gottron's papules, cuticular changes including periungual telangiectasia, a photodistributed erythema or poikiloderma, and a scaly a …
Dermatomyositis is one of the idiopathic inflammatory myopathies with characteristic cutaneous manifestations including the heliotrope rash, …
Blepharochalasis.
Bergin DJ, McCord CD, Berger T, Friedberg H, Waterhouse W. Bergin DJ, et al. Br J Ophthalmol. 1988 Nov;72(11):863-7. doi: 10.1136/bjo.72.11.863. Br J Ophthalmol. 1988. PMID: 3207663 Free PMC article.
Ptosis with excellent levator function, laxity of the lateral canthal structures with rounding of the lateral canthal angle, nasal fat pad atrophy, and redundant eyelid skin develop after many episodes of eyelid swelling. Fine wrinkling, atrophy, and telangiectasias charac …
Ptosis with excellent levator function, laxity of the lateral canthal structures with rounding of the lateral canthal angle, nasal fat pad a …
Facial involvement in genodermatoses.
Schaffer JV. Schaffer JV. Clin Dermatol. 2014 Nov-Dec;32(6):772-83. doi: 10.1016/j.clindermatol.2014.02.017. Epub 2014 Mar 1. Clin Dermatol. 2014. PMID: 25441471 Review.
In this contribution, facial involvement in genodermatoses is divided into five morphologic categories based on the most prominent feature: Papules, scaling, photosensitivity/findings associated with aging (eg, telangiectasias, atrophy, lentigines), blisters/erosions, and …
In this contribution, facial involvement in genodermatoses is divided into five morphologic categories based on the most prominent feature: …
Inherited skin disorders presenting with poikiloderma.
Rayinda T, van Steensel M, Danarti R. Rayinda T, et al. Int J Dermatol. 2021 Nov;60(11):1343-1353. doi: 10.1111/ijd.15498. Epub 2021 Mar 19. Int J Dermatol. 2021. PMID: 33739439 Review.
Poikiloderma is a skin condition that combines atrophy, telangiectasia, and macular pigment changes (hypo- as well as hyperpigmentation). ...Prompt diagnosis at the time of presentation could help to prevent complications and mitigate the course of the disease. This …
Poikiloderma is a skin condition that combines atrophy, telangiectasia, and macular pigment changes (hypo- as well as hyperpigmentati …
Skin and mucosal telangiectatic lesions in hereditary hemorrhagic telangiectasia patients.
Hyldahl SJ, El-Jaji MQ, Schuster A, Kjeldsen AD. Hyldahl SJ, et al. Int J Dermatol. 2022 Dec;61(12):1497-1505. doi: 10.1111/ijd.16320. Epub 2022 Jul 6. Int J Dermatol. 2022. PMID: 35792874 Free PMC article. Review.
BACKGROUND: The diagnostic criteria for hereditary hemorrhagic telangiectasia (HHT) include the presence of telangiectatic lesions in common sites (nose, fingers, oral cavity, and lips). ...The presentation of telangiectatic lesions may vary a little between HHT1 and HHT2 …
BACKGROUND: The diagnostic criteria for hereditary hemorrhagic telangiectasia (HHT) include the presence of telangiectatic lesions in …
Treating vascular lesions.
Astner S, Anderson RR. Astner S, et al. Dermatol Ther. 2005 May-Jun;18(3):267-81. doi: 10.1111/j.1529-8019.2005.05025.x. Dermatol Ther. 2005. PMID: 16229727 Review.
ATM Mutations in Cancer: Therapeutic Implications.
Choi M, Kipps T, Kurzrock R. Choi M, et al. Mol Cancer Ther. 2016 Aug;15(8):1781-91. doi: 10.1158/1535-7163.MCT-15-0945. Epub 2016 Jul 13. Mol Cancer Ther. 2016. PMID: 27413114 Review.
Activation of checkpoint arrest and homologous DNA repair are necessary for maintenance of genomic integrity during DNA replication. Germ-line mutations of the ataxia telangiectasia mutated (ATM) gene result in the well-characterized ataxia telangiectasia syndrome, …
Activation of checkpoint arrest and homologous DNA repair are necessary for maintenance of genomic integrity during DNA replication. Germ-li …
Genetic immunodeficiency disorders.
Paller AS. Paller AS. Clin Dermatol. 2005 Jan-Feb;23(1):68-77. doi: 10.1016/j.clindermatol.2004.09.011. Clin Dermatol. 2005. PMID: 15708291 Review.
Among these cutaneous abnormalities are alopecia, cutaneous granulomas, cutaneous infections, atopic-like or seborrheic-like dermatitis, petechiae or purpura, silvery pigmentation, poor wound healing, and telangiectasias. Immunodeficiency should be considered in children w …
Among these cutaneous abnormalities are alopecia, cutaneous granulomas, cutaneous infections, atopic-like or seborrheic-like dermatitis, pet …
Vascular anomalies associated with hepatic shunting.
Schmalz MJ, Radhakrishnan K. Schmalz MJ, et al. World J Gastroenterol. 2020 Nov 14;26(42):6582-6598. doi: 10.3748/wjg.v26.i42.6582. World J Gastroenterol. 2020. PMID: 33268948 Free PMC article. Review.
Today many patients with these shunts carry good long-term prognosis thanks to advances in imaging to better detect shunts earlier and classify them. ...Congenital hepatic shunts are not the only vascular condition affecting the liver. Hereditary hemorrhagic telangiecta …
Today many patients with these shunts carry good long-term prognosis thanks to advances in imaging to better detect shunts earlier an …
Pulmonary Manifestations of Skin Disorders in Children.
Cohen BA, Turcios NL. Cohen BA, et al. Pediatr Clin North Am. 2021 Feb;68(1):261-276. doi: 10.1016/j.pcl.2020.09.009. Pediatr Clin North Am. 2021. PMID: 33228937 Review.
These conditions include both inherited multisystem genetic disorders such as yellow-nail syndrome, neurofibromatosis type 1, tuberous sclerosis complex, hereditary hemorrhagic telangiectasia, Klippel-Trenaunay-Weber syndrome, cutis laxa, Ehlers-Danlos syndrome, dyskeratos …
These conditions include both inherited multisystem genetic disorders such as yellow-nail syndrome, neurofibromatosis type 1, tuberous scler …
463 results