Results 141 to 150 of about 41,467 (301)

Keratosis of the Nipples [PDF]

Proceedings of the Royal Society of Medicine, 1936
openaire   +3 more sources

Severe Nerve Enlargement in SOS2‐Related Noonan Syndrome

American Journal of Medical Genetics Part A, Volume 197, Issue 10, October 2025.
ABSTRACT Noonan syndrome is a genetic multisystem congenital disorder, caused by pathogenic variants in genes that encode components of the RAS/MAPK signaling pathway. Pathogenic variants in SOS2 represent less than 2% of cases with NS. The phenotype includes a particularly high prevalence (65%) of lymphatic disease. Recently, severe nerve enlargements
Erika Leenders, Fieke Draaisma, Corrie E. Erasmus, Catelijne Coppens, Lotte E. R. Kleimeier, Melanie Burgers, Tuula Rinne, Martin Zenker, Laura Mazzanti, Wesley Reintjes, Nens van Alfen, Jos M. T. Draaisma   +11 more
wiley   +1 more source

Loss-of-function mutations in the cathepsin C gene result in periodontal disease and palmoplantar keratosis [PDF]

, 1999
Carmel Toomes, Jacqueline A. James, Andrew J. Wood, Chu Wu, D. McCormick, Nicholas Lench, Chelsee Hewitt, Leanne Moynihan, Emma Roberts, C. Geoffrey Woods, Alexander F. Markham, Melanie Wong, Richard P Widmer, Khaled Abdel Ghaffar, Michael Pemberton, Ibtessam R. Hussein, Samia A. Temtamy, Robin Davies, Andrew Read, Philip Sloan, Michael J. Dixon, Nalin Thakker   +21 more
openalex   +1 more source

Williams Syndrome Associated With Facial Port‐Wine Stain and Phacomatosis Pigmentovascularis: A Case Report

Clinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT Williams syndrome (WS) is a rare congenital multi‐systemic condition due to gene deletion. We present a rare case of co‐existence of WS, port wine stains, and phacomatosis pigmentovascularis. This case emphasizes the importance of recognizing the co‐occurrence of such conditions and WS for accurate diagnosis and management.
Bahareh Abtahi‐Naeini, Omid Yaghini, Zahra Razavi   +2 more
wiley   +1 more source

Development of Carcinoma in a Case of Laryngeal Keratosis Diagnosed 3 years Before

, 1963
Seiichi Kawata, Kensuke Hisaki
openalex   +2 more sources

Buschke–Fischer–Brauer Keratoderma: A Case Report of a Rare Skin Disorder

Clinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT Buschke–Fischer–Brauer keratoderma is a rare autosomal dominant disorder presenting as hyperkeratotic lesions on the palms and soles. Diagnosis requires clinical and histopathological evaluation. Management is symptomatic with keratolytics like salicylic acid and urea. Early recognition and ongoing care improve the quality of life for patients
Dyala Sayed Ahmad, Rim Nasser, Moatasem Hussein Al‐janabi, Fouz Hassan   +3 more
wiley   +1 more source

Secondary Localized Cutaneous Amyloidosis Associated with Actinic Keratosis

, 1973
Ken Hashimoto, Lloyd E. King
openalex   +1 more source

Role of endothelin-1 in hyperpigmentation in seborrhoeic keratosis [PDF]

, 1996
Emiko Teraki, Shingo Tajima, Izumi Manaka, Makoto Kawashima, M. MIYACLSHI, Genji Imokawa   +5 more
openalex   +1 more source

Autophagy‐Targeting Nanomedicine: Strike at the Heart of the Cancer via Precise Modulation of Autophagy

Exploration, Volume 5, Issue 5, October 2025.
This review emphasizes the critical role of autophagy in cancer treatment, highlighting the development of autophagy‐targeting nanomedicines and their applications in combination therapies. It explores how nanoplatforms can effectively regulate autophagy, underscoring the potential of integrating autophagy modulation with other treatment strategies to ...
Zhouyi Sun, Huali Zuo, Kai Zhang, Yang Liu, Qianwen Wang, Qitao Hu, Jiwei Qian, Andreas Lundqvist, Bo Zhang, Weiyu Chen, Zhe Tang   +10 more
wiley   +1 more source

Lichenoid keratosis successfully treated with topical imiquimod

JAAD Case Reports, 2020
Hessah BinJadeed, MD, Nouf Aljomah, MD, Norah Alsubait, MD, Fahad Alsaif, PhD, Ahmed AlHumidi, PhD   +4 more
doaj   +1 more source