Zobrazeno 1 - 10
of 68
pro vyhledávání: '"Peter R Hull"'
Publikováno v:
SAGE Open Medical Case Reports, Vol 9 (2021)
We represent a pediatric case of the congenital disorder caused by zinc malabsorption, acrodermatitis enteropathica, presenting with acute onsetof blisters. Although blisters can be seen in this condition, it is not always a key feature and can there
Externí odkaz:
https://doaj.org/article/c5632c2d880b44a792252839e3388bd7
Autor:
Alexandra Rogers, BSc, Michael L. MacGillivary, MD, Peter R. Hull, MBBCh, MMed (Derm), PhD, Sorin Selegean, MD, Lorenzo Cerroni, MD
Publikováno v:
JAAD Case Reports, Vol 51, Iss , Pp 10-13 (2024)
Externí odkaz:
https://doaj.org/article/ada1a369aa9649ad88c02517a005da7e
Publikováno v:
Journal of Cutaneous Medicine and Surgery. 26:473-476
Background Melanoma is one of the most common cancers in Canada, 1 with the highest incidence in Nova Scotia (NS). Objectives To describe the demographics, lesion characteristics, and diagnostic accuracy of suspected melanomas excised at the largest
Publikováno v:
Clinical and Experimental Dermatology. 45:494-497
Autor:
Kristina Roche, Glenda R Wright, Penelope Poyah, Laurette Geldenhuys, Michael West, Joel C. Bergman, Noreen M. Walsh, Peter R. Hull
Publikováno v:
Canadian Journal of Kidney Health and Disease, Vol 8 (2021)
Canadian Journal of Kidney Health and Disease
Canadian Journal of Kidney Health and Disease
Rationale: Primary hyperoxaluria (PH) is a rare autosomal recessive disorder more commonly diagnosed in children or adolescents. Owing to its rarity and heterogeneous phenotype, it is often underrecognized, resulting in delayed diagnosis, including d
Autor:
Lydia E. Vos, Gijs W. E. Santen, Claudia A. L. Ruivenkamp, Youssef Elhaji, Tessa M.A. van Henten, Peter R. Hull, Mathew Nightingale
Publikováno v:
JID Innovations, Vol 1, Iss 3, Pp 100022-(2021)
Basan syndrome is an autosomal dominant genodermatosis characterized by congenital adermatoglyphia, transient congenital facial milia, neonatal acral bullae, and absent or reduced sweating. Basan syndrome is rare and has been reported in only 10 kind
Autor:
Cherise E. Hedlin, Anu Nath, Youssef Elhaji, Emma L. Price, Peter R. Hull, Christopher Gallant, Stacey A. Northgrave
Publikováno v:
Journal of Cutaneous Medicine and Surgery. 24:28-32
Background: Punctate palmoplantar keratoderma type 1 (PPPK1) presents in late childhood to adulthood with multiple small discrete hyperkeratotic papules on palms and soles. PPPK1 is an autosomal dominant skin disease caused by AAGAB mutations. It has
Autor:
Ivan V. Litvinov, Raed Alhusayen, Philip Surmanowicz, Arunima Sivanand, Youwen Zhou, Robert Gniadecki, Peter R. Hull
Publikováno v:
Journal of Cutaneous Medicine and Surgery. 23:537-544
Mycosis fungoides (MF) and Sézary syndrome (SS) are chronic, progressive primary cutaneous T-cell lymphomas (CTCLs) for which there are no curative treatments. Skin-directed therapies, such as phototherapy, radiation therapy, or topical nitrogen mus
Autor:
Youssef, Elhaji, Tessa M A, van Henten, Claudia A L, Ruivenkamp, Mathew, Nightingale, Gijs We, Santen, Lydia E, Vos, Peter R, Hull
Publikováno v:
JID Innovations
Basan syndrome is an autosomal dominant genodermatosis characterized by congenital adermatoglyphia, transient congenital facial milia, neonatal acral bullae, and absent or reduced sweating. Basan syndrome is rare and has been reported in only 10 kind
Autor:
Martin Oti, Bjørn Ivar Haukanes, Thandiswa Ngcungcu, Stine Buechmann-Moller, Tomasz Stokowy, Wayne Grayson, Olav Sundnes, Edward J. Oakeley, Fan Yang, Ivonne M.J.J. van Vlijmen-Willems, Han G. Brunner, Michèle Ramsay, Hans van Bokhoven, Robert Bruccoleri, Jiang Zhu, Thomas Morgan, Kari Merete Ersland, Bolan Linghu, Charlotte von der Lippe, Huiqing Zhou, Torunn Fiskerstrand, Frank Staedtler, Marc Sultan, Joost Schalkwijk, Jan Cezary Sitek, Vidar M. Steen, Joseph D. Szustakowski, Peter R. Hull, Nanguneri Nirmala
Publikováno v:
American Journal of Human Genetics, 100, 5, pp. 737-750
American Journal of Human Genetics, 100, 737-750
American Journal of Human Genetics, 100(5), 737-750. Cell Press
American Journal of Human Genetics, 100, 737-750
American Journal of Human Genetics, 100(5), 737-750. Cell Press
Contains fulltext : 174194.pdf (Publisher’s version ) (Open Access) Keratolytic winter erythema (KWE) is a rare autosomal-dominant skin disorder characterized by recurrent episodes of palmoplantar erythema and epidermal peeling. KWE was previously