Results 191 to 200 of about 33,087 (280)
Factors Related to Nevus-Associated Cutaneous Melanoma: A Case-Case Study.
Journal of Investigative Dermatology, 2018 N. Pandeya +12 more
semanticscholar +1 more source
Persistent Gingival Bleeding After Scaling: A Diagnostic Clue to von Willebrand Disease
Clinical Case Reports, Volume 14, Issue 9, September 2026.ABSTRACT Von Willebrand disease (VWD) is not a rare inherited bleeding disorder. However, it is frequently underdiagnosed because early mucocutaneous bleeding manifestations are often attributed to local factors such as inflammation or anatomical abnormalities, leading to delayed recognition of the underlying systemic disease. A 31‐year‐old Han Chinese
Huihui Zhang +3 more
wiley +1 more source
What Is Your Diagnosis? Dermal Mass From the Left Forelimb of a Dog
Veterinary Clinical Pathology, EarlyView.
Heather D. McDavid +3 more
wiley +1 more source
Clinical and Translational Medicine, Volume 16, Issue 9, September 2026.PRAME promotes SACC invasion and metastasis by inducing EMT via Twist1 upregulation and by destabilizing RARα through Cullin2‑mediated ubiquitination, a mechanism that may limit ATRA efficacy. In vivo, PRAME enhances subcutaneous growth and lung metastasis, highlighting its oncogenic role in SACC.
Xudong Wang +8 more
wiley +1 more source
Iris nevus diagnosis: convolutional neural network and deep belief network
Turkish J. Electr. Eng. Comput. Sci., 2017 O. Oyedotun, A. Khashman
semanticscholar +1 more source
Nevus Sebaceus: A Cross‐Specialty Survey of Clinical Management in Ireland
JEADV Clinical Practice, Volume 5, Issue 3, Page 925-927, September 2026.ABSTRACT Background Nevus sebaceus (NS) is a congenital benign hamartomatous malformation typically appearing on the scalp and face as a yellow/orange hairless plaque. Benign secondary tumours can develop but malignant transformation is exceptionally rare.
B. Nolan, M. Murphy, C. O'Connor
wiley +1 more source
Postzygotic Mutations in Beta-Actin Are Associated with Becker's Nevus and Becker's Nevus Syndrome.
Journal of Investigative Dermatology, 2017 Emily D. Cai +8 more
semanticscholar +1 more source
Molecular Genetics &Genomic Medicine, Volume 14, Issue 9, September 2026.We report a case of a 22‐year‐old woman with predominantly cutaneous involvement in whom whole‐exome sequencing from both blood‐ and hair‐derived DNA samples identified somatic mosaicism for the rare HRAS p.Gly13Asp variant. This case expands the phenotypic spectrum of Costello syndrome and underscores the importance of multitissue genomic analysis ...
Jovan Lalosevic +6 more
wiley +1 more source
Effectiveness and Safety of Setmelanotide in a Patient With a Heterozygous PCSK1 Deficiency
Obesity, Volume 34, Issue S2, Page 70-74, September 2026.ABSTRACT Setmelanotide, a melanocortin 4 receptor (MC4R) agonist, is a promising pharmacological treatment option for people with rare monogenic obesity conditions affecting the leptin‐melanocortin signaling pathway, including proprotein convertase subtilisin/kexin type 1 (PCSK1) gene mutations.
Ellina Lytvyak +2 more
wiley +1 more source
Association of Patient Risk Factors and Frequency of Nevus-Associated Cutaneous Melanomas.
JAMA dermatology, 2016 H. Haenssle +7 more
semanticscholar +1 more source