Results 51 to 60 of about 2,571 (160)
Molecular Genetics &Genomic Medicine, Volume 14, Issue 8, August 2026.Major symptoms of dyskeratosis congenita. Predicted nuclear localization site at N‐terminus of DKC1 protein. Comparison of nuclear localization for DKC1 showing normal localization for wild‐type versus disruption of localization for p.Ala2Val. ABSTRACT Background Dyskeratosis congenita (DKC) is typically characterized by the triad of abnormal cutaneous
Taimoor I. Sheikh, John B. Vincent
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Autologous immunotherapy for periocular and oral cavity papillomatosis in a dog
Veterinary Record Case Reports, Volume 14, Issue 3, August 2026.Abstract Papillomaviruses induce epithelial hyperplasia and exophytic warts in dogs. In young immunocompetent animals, lesions are typically self‐limiting and regress spontaneously; however, persistent infections may rarely be associated with malignant transformation.
Marcelo Martínez‐Barbitta +4 more
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Pellagra in Contemporary Clinical Practice (2000–2023): A Systematic Review
International Journal of Dermatology, Volume 65, Issue 8, Page 1590-1599, August 2026.This systematic review (2000–2023) of 1212 cases highlights pellagra's evolving etiology. While primary dietary deficiency (85%) persists in humanitarian crises, secondary forms from alcohol misuse (9.6%), isoniazid (14.3% of drug‐related cases), and malabsorption are rising.
Noureddine Litaiem +2 more
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Dermkielia cavawata sp. nov. gen. nov., Isolated From Plantar Eczema
Mycoses, Volume 69, Issue 8, August 2026.ABSTRACT Background Human skin is naturally exposed to diverse fungi. New taxa, including species with unknown pathogenic potential, continue to be isolated from human skin. Objective To characterize a hitherto unknown hyphomycete isolated from human eczema and to assess its habitat and pathogenic abilities.
Jochen Brasch +4 more
wiley +1 more source
Peutz-Jeghers Syndrome: A Case Report and Literature Review in Indonesia
The Indonesian Journal of Gastroenterology, Hepatology and Digestive EndoscopyBackground: Peutz-Jeghers Syndrome (PJS) is a rare hereditary polyposis syndrome that is autosomal dominant and has the main characteristics of hamartoma polyps, mucocutaneous pigmentation, and increased susceptibility to malignancy.
Kaka Renaldi, Yudha Friatna
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Mucocutaneous manifestations in patients with chronic kidney disease: A cross-sectional study
Indian Dermatology Online Journal, 2018 Background: Chronic kidney disease (CKD)-associated mucocutaneous manifestations significantly impair the quality of life but often remain understudied.
Rattan S Rashpa +6 more
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Unveiling Saint Theobald: A Multidisciplinary Bioanthropological Investigation
International Journal of Osteoarchaeology, Volume 36, Issue 4, Page 945-953, July/August 2026.ABSTRACT Saint Theobald of Provins (1033–1066), a French nobleman who embraced voluntary poverty, hermitism, and pilgrimage, represents an early figure in the medieval ascetic movement. He holds historical significance for the diffusion of 11th‐century ascetic ideals, as a hermit saint associated with the Camaldolese order and venerated across northern
Nicola Carrara +6 more
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Findings from the Peutz-Jeghers syndrome registry of uruguay. [PDF]
PLoS ONE, 2013 BACKGROUND: Peutz-Jeghers syndrome (PJS) is characterized by intestinal polyposis, mucocutaneous pigmentation and an increased cancer risk, usually caused by mutations of the STK11 gene.
Asadur Tchekmedyian +7 more
doaj +1 more source
Clinical Case Reports, Volume 14, Issue 6, June 2026.ABSTRACT Syphilis is a re‐emerging global public health concern; recently, its incidence has significantly increased in all demographic groups. However, acute syphilitic posterior placoid chorioretinitis (ASPPC) and syphilitic optic neuropathy in a patient with human immunodeficiency virus (HIV) co‐infection are extremely uncommon.
Shengsheng Liu +3 more
wiley +1 more source