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

Year Number of Results
1963 1
1964 3
1965 1
1966 2
1967 5
1968 11
1969 3
1970 12
1971 11
1972 10
1973 13
1974 11
1975 9
1976 13
1977 11
1978 11
1979 13
1980 16
1981 14
1982 8
1983 11
1984 21
1985 16
1986 11
1987 15
1988 16
1989 34
1990 30
1991 26
1992 27
1993 29
1994 40
1995 46
1996 51
1997 57
1998 43
1999 63
2000 69
2001 79
2002 52
2003 67
2004 78
2005 74
2006 105
2007 87
2008 95
2009 70
2010 67
2011 88
2012 102
2013 107
2014 91
2015 94
2016 117
2017 105
2018 96
2019 82
2020 105
2021 110
2022 76
2023 67
2024 19

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2,602 results

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Page 1
Rosacea management: A comprehensive review.
Sharma A, Kroumpouzos G, Kassir M, Galadari H, Goren A, Grabbe S, Goldust M. Sharma A, et al. J Cosmet Dermatol. 2022 May;21(5):1895-1904. doi: 10.1111/jocd.14816. Epub 2022 Feb 14. J Cosmet Dermatol. 2022. PMID: 35104917 Review.
Rosacea is a chronic cutaneous disorder affecting primarily the face, characterized by erythema, transient or persistent, telangiectasia, and inflammatory lesions including papulo-pustules and swelling. ...
Rosacea is a chronic cutaneous disorder affecting primarily the face, characterized by erythema, transient or persistent, telangiectasia …
Ataxia-telangiectasia: recommendations for multidisciplinary treatment.
van Os NJH, Haaxma CA, van der Flier M, Merkus PJFM, van Deuren M, de Groot IJM, Loeffen J, van de Warrenburg BPC, Willemsen MAAP; A-T Study Group. van Os NJH, et al. Dev Med Child Neurol. 2017 Jul;59(7):680-689. doi: 10.1111/dmcn.13424. Epub 2017 Mar 20. Dev Med Child Neurol. 2017. PMID: 28318010 Free article. Review.
Ataxia-telangiectasia is a rare, neurodegenerative, and multisystem disease, characterized by cerebellar ataxia, oculocutaneous telangiectasia, immunodeficiency, progressive respiratory failure, and an increased risk of malignancies. It demands specialized care tail …
Ataxia-telangiectasia is a rare, neurodegenerative, and multisystem disease, characterized by cerebellar ataxia, oculocutaneous te …
Ataxia-telangiectasia: A review of clinical features and molecular pathology.
Amirifar P, Ranjouri MR, Yazdani R, Abolhassani H, Aghamohammadi A. Amirifar P, et al. Pediatr Allergy Immunol. 2019 May;30(3):277-288. doi: 10.1111/pai.13020. Epub 2019 Mar 20. Pediatr Allergy Immunol. 2019. PMID: 30685876 Review.
Ataxia-telangiectasia (A-T) is an autosomal recessive primary immunodeficiency (PID) disease that is caused by mutations in ataxia-telangiectasia mutated (ATM) gene encoding a serine/threonine protein kinase. A-T patients represent a broad range of clinical manifest …
Ataxia-telangiectasia (A-T) is an autosomal recessive primary immunodeficiency (PID) disease that is caused by mutations in ataxia- …
Coats disease: An overview of classification, management and outcomes.
Sen M, Shields CL, Honavar SG, Shields JA. Sen M, et al. Indian J Ophthalmol. 2019 Jun;67(6):763-771. doi: 10.4103/ijo.IJO_841_19. Indian J Ophthalmol. 2019. PMID: 31124484 Free PMC article. Review.
Coats disease is an idiopathic retinal vascular disorder with retinal telangiectasia with intraretinal and/or subretinal exudation without appreciable retinal or vitreal traction. ...
Coats disease is an idiopathic retinal vascular disorder with retinal telangiectasia with intraretinal and/or subretinal exudation wi …
Hereditary hemorrhagic telangiectasia: diagnosis and management from the hematologist's perspective.
Kritharis A, Al-Samkari H, Kuter DJ. Kritharis A, et al. Haematologica. 2018 Sep;103(9):1433-1443. doi: 10.3324/haematol.2018.193003. Epub 2018 May 24. Haematologica. 2018. PMID: 29794143 Free PMC article. Review.
Hereditary hemorrhagic telangiectasia (HHT), also known as Osler-Weber-Rendu syndrome, is an autosomal dominant disorder that causes abnormal blood vessel formation. The diagnosis of hereditary hemorrhagic telangiectasia is clinical, based on the Curacao criteria. G …
Hereditary hemorrhagic telangiectasia (HHT), also known as Osler-Weber-Rendu syndrome, is an autosomal dominant disorder that causes …
Global epidemiology and clinical spectrum of rosacea, highlighting skin of color: Review and clinical practice experience.
Alexis AF, Callender VD, Baldwin HE, Desai SR, Rendon MI, Taylor SC. Alexis AF, et al. J Am Acad Dermatol. 2019 Jun;80(6):1722-1729.e7. doi: 10.1016/j.jaad.2018.08.049. Epub 2018 Sep 19. J Am Acad Dermatol. 2019. PMID: 30240779 Free article. Review.
In fact, rosacea might be underreported and underdiagnosed in populations with skin of color because of the difficulty of discerning erythema and telangiectasia in dark skin. The susceptibility of persons with highly pigmented skin to dermatologic conditions like rosacea, …
In fact, rosacea might be underreported and underdiagnosed in populations with skin of color because of the difficulty of discerning erythem …
Adult-onset Coats disease.
Banerjee M, Nayak S, Kumar S, Bhayana AA, Kumar V. Banerjee M, et al. Surv Ophthalmol. 2023 Jul-Aug;68(4):591-600. doi: 10.1016/j.survophthal.2023.03.002. Epub 2023 Mar 17. Surv Ophthalmol. 2023. PMID: 36933772 Review.
Coats disease is an idiopathic retinal vasculopathy characterized by telangiectasia and aneurysm of retinal vessels along with intra and subretinal exudation and fluid. ...
Coats disease is an idiopathic retinal vasculopathy characterized by telangiectasia and aneurysm of retinal vessels along with intra …
Cosmetic sclerotherapy.
Watson JJ, Mansour MA. Watson JJ, et al. J Vasc Surg Venous Lymphat Disord. 2017 May;5(3):437-445. doi: 10.1016/j.jvsv.2017.02.002. J Vasc Surg Venous Lymphat Disord. 2017. PMID: 28411713 Free article. Review.
Telangiectasias and spider veins are considered a common cosmetic concern for both women and men. ...This article reviews the pathophysiology and diagnosis of telangiectasias and reticular veins as well as the currently available agents and techniques of sclerothera …
Telangiectasias and spider veins are considered a common cosmetic concern for both women and men. ...This article reviews the pathoph …
Non-vasogenic cystoid maculopathies.
Gaudric A, Audo I, Vignal C, Couturier A, Boulanger-Scemama É, Tadayoni R, Cohen SY. Gaudric A, et al. Prog Retin Eye Res. 2022 Nov;91:101092. doi: 10.1016/j.preteyeres.2022.101092. Epub 2022 Aug 1. Prog Retin Eye Res. 2022. PMID: 35927124 Free article. Review.
In inherited retinal dystrophies, cystoid spaces may be part of the disease as in X-linked retinoschisis or enhanced S-cone syndrome, or occur occasionally as in bestrophinopathies, retinitis pigmentosa and allied diseases, congenital microphthalmia, choroideremia, gyrate atrophy …
In inherited retinal dystrophies, cystoid spaces may be part of the disease as in X-linked retinoschisis or enhanced S-cone syndrome, or occ …
Hereditary haemorrhagic telangiectasia.
Rimmer J, Lund VJ. Rimmer J, et al. Rhinology. 2015 Sep;53(3):195-203. doi: 10.4193/Rhino14.274. Rhinology. 2015. PMID: 26460394 Review.
BACKGROUND: Hereditary haemorrhagic telangiectasia is an autosomal dominant vascular disease characterized by recurrent epistaxis, mucocutaneous telangiectasia and visceral arteriovenous malformations. ...The current management options, both medical and surgical, ar …
BACKGROUND: Hereditary haemorrhagic telangiectasia is an autosomal dominant vascular disease characterized by recurrent epistaxis, mu …
2,602 results