Results 61 to 70 of about 5,283 (174)

Optimizing Biopsy Decisions in Benign Longitudinal Melanonychia: A Dermoscopic‐Pathologic Study of Nail Matrix Nevus vs. Melanocytic Activation

open access: yesSkin Research and Technology, Volume 32, Issue 8, August 2026.
ABSTRACT Background Longitudinal melanonychia (LM) is a common clinical manifestation of nail melanocytic lesions and poses diagnostic challenges in distinguishing benign melanocytic activation (MA) from melanocytic hyperplasia such as nail matrix nevus(NMN).
Qilin Sun   +7 more
wiley   +1 more source

Azoospermia, Atrophy, and Asymmetry: Unilateral Sertoli Cell Tumor as a Rare and Overlooked Cause of Male Infertility: A Case Report and Literature Review

open access: yesClinical Case Reports, Volume 14, Issue 7, July 2026.
ABSTRACT Sertoli cell tumors are uncommon sex‐cord stromal tumors making up < 2% of testicular tumors and have been reported to be associated with endocrine dysfunction that could compromise male fertility. Herein, we present a 34‐year‐old Pakistani male with primary infertility, azoospermia, enlargement of right testis, and contralateral severe ...
Rao Nouman Ali   +7 more
wiley   +1 more source

Unusual Palatal Pigmentation in a 71‐Year‐Old Patient

open access: yes
Oral Diseases, EarlyView.
Lucía Lago‐Méndez   +3 more
wiley   +1 more source

Gingival and Periodontal Diseases and Conditions in Children and Adolescents: Consensus Report

open access: yesJournal of Clinical Periodontology, Volume 53, Issue 7, Page 1068-1099, July 2026.
ABSTRACT Background The objectives of this Focused Workshop were to update the epidemiology, aetiology, risk factors, diagnosis and management of gingival and periodontal diseases and conditions in children and adolescents, and to explore the applicability of the 2018 Classification in children and adolescents.
Iain Chapple   +30 more
wiley   +1 more source

Distinct Germline Mutation Landscape and Clinical Implications in Chinese Colorectal Cancer: A Large‐Scale Genomic Analysis of 1094 Patients

open access: yesCancer Medicine, Volume 15, Issue 6, June 2026.
ABSTRACT Objective To investigate the prevalence, characteristics, and clinical implications of germline mutations in a consecutive cohort of Chinese colorectal cancer (CRC) patients, providing insights that may inform population‐specific genetic testing strategies.
Liting Lu   +8 more
wiley   +1 more source

Unveiling Candidate Markers for Drug Resistance or Synthetic Lethality in Cervical Cancer: Integrative Analysis of Genetic and Pharmacoprofiling

open access: yesCancer Reports, Volume 9, Issue 6, June 2026.
ABSTRACT Introduction Systemic cervical cancer management continues to be challenging. Numerous chemotherapies have been approved, but predicting response is difficult due to the lack of biomarkers. Here, we analyze the genetic and protein profiles of 20 cervical cancer cell lines (CCCLs) and explore their correlation with drug response patterns to ...
Suzy Scholl   +10 more
wiley   +1 more source

Peutz-Jeghers syndrome: presentation of a patient and literature review

open access: yesZdravniški Vestnik, 2009
Introduction: Colorectal cancer carcinogenesis is a complex, long-lasting multistep process. Patients with diff erent polyposis syndromes, including Peutz-Jeghers, have signifi cantly increased risk for diff erent types of cancer.Patients and methods: In
Pavel Skok   +3 more
doaj  

Colorectal Precancerous Lesions: Molecular Mechanisms, Research Tools, and Natural Product‐Based Clinical Translation

open access: yesMedComm – Oncology, Volume 5, Issue 2, June 2026.
This article systematically elucidates the molecular mechanisms of colorectal precancerous lesions, introduces cutting‐edge research tools like multi‐omics and organoids, and highlights the potential and prospects of natural products such as berberine, resveratrol, and curcumin in preventing and intervening in colorectal carcinogenesis by modulating ...
Shunji Liu   +6 more
wiley   +1 more source

Peutz-Jeghers Syndrome: In Siblings with Palmer-Plantar Pigmentation

open access: yesJournal of Indian Academy of Oral Medicine and Radiology, 2011
Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant disorder characterized by typical pigmented perioral maculesn pigmented spots in the oral mucosa and digits along with hamartomatous polyps in the gastrointestinal tract.
K V Suresh   +2 more
doaj   +1 more source

Peutz-Jeghers syndrome

open access: yesBangladesh Journal of Medicine, 2016
Abstract not availableBangladesh J Medicine Jan 2016; 27(1 ...
Shohael M Arafat, Mihir Kanti Adhikari
openaire   +2 more sources

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