Alpha 2.0
Login Register
» Authors » Robert P E Sarkany

Robert P E Sarkany

Explore the profile of Robert P E Sarkany including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 17
Citations 207
Followers 0
Related Specialties
Dermatology
Biology
Neurology
Top 10 Co-Authors
Antony R Young
Hiva Fassihi
Alan R Lehmann
Paola Giunti
Shehla Mohammed
Damilola Fajuyigbe
Einapak Boontaveeyuwat
Thierry Douki
David McGibbon
Karl P Lawrence
Published In
Photodermatol Photoimmunol Photomed
J Invest Dermatol
Arch Dis Child Educ Pract Ed
Photochem Photobiol
Br J Dermatol
Affiliations
Soon will be listed here.
Recent Articles
11.
Melanin distribution in human epidermis affords localized protection against DNA photodamage and concurs with skin cancer incidence difference in extreme phototypes
Fajuyigbe D, Lwin S, Diffey B, Baker R, Tobin D, Sarkany R, et al.
FASEB J . 2018 Feb; 32(7):3700-3706. PMID: 29394104
Epidermal DNA damage, especially to the basal layer, is an established cause of keratinocyte cancers (KCs). Large differences in KC incidence (20- to 60-fold) between white and black populations are...
12.
Xeroderma pigmentosum is a definite cause of Huntington's disease-like syndrome
Garcia-Moreno H, Fassihi H, Sarkany R, Phukan J, Warner T, Lehmann A, et al.
Ann Clin Transl Neurol . 2018 Jan; 5(1):102-108. PMID: 29376097
Xeroderma pigmentosum is characterized by cutaneous, ophthalmological, and neurological features. Although it is typical of childhood, late presentations can mimic different neurodegenerative conditions. We report two families presenting as Huntington's...
13.
A 'spot' diagnosis
Sebaratnam D, Sarkany R, Fassihi H
Arch Dis Child Educ Pract Ed . 2016 Apr; 102(4):220-221. PMID: 27117973
No abstract available.
14.
Deep phenotyping of 89 xeroderma pigmentosum patients reveals unexpected heterogeneity dependent on the precise molecular defect
Fassihi H, Sethi M, Fawcett H, Wing J, Chandler N, Mohammed S, et al.
Proc Natl Acad Sci U S A . 2016 Feb; 113(9):E1236-45. PMID: 26884178
Xeroderma pigmentosum (XP) is a rare DNA repair disorder characterized by increased susceptibility to UV radiation (UVR)-induced skin pigmentation, skin cancers, ocular surface disease, and, in some patients, sunburn and...
15.
A Distinct Genotype of XP Complementation Group A: Surprisingly Mild Phenotype Highly Prevalent in Northern India/Pakistan/Afghanistan
Sethi M, Haque S, Fawcett H, Wing J, Chandler N, Mohammed S, et al.
J Invest Dermatol . 2016 Jan; 136(4):869-872. PMID: 26743599
No abstract available.
16.
Erythropoietic uroporphyria associated with myeloid malignancy is likely distinct from autosomal recessive congenital erythropoietic porphyria
Sarkany R, Ibbotson S, Whatley S, Lawrence C, Gover P, Mufti G, et al.
J Invest Dermatol . 2011 Feb; 131(5):1172-5. PMID: 21326293
No abstract available.
17.
Making sense of the porphyrias
Sarkany R
Photodermatol Photoimmunol Photomed . 2008 Mar; 24(2):102-8. PMID: 18353093
Patients with cutaneous porphyrias can be worrying for dermatologists. The diseases are rare enough to be unfamiliar, are associated with internal diseases, can have genetic implications, and are associated with...