Results 71 to 80 of about 21,965 (216)

A theoretical investigation of human skin thermal response to near-infrared laser irradiation [PDF]

, 2004
Near-infrared wavelengths are absorbed less by epidermal melanin mainly located at the basal layer of epidermis (dermo-epidermal junction), and penetrate deeper into human skin dermis and blood than visible wavelengths. Therefore, laser irradiation using
Anvari, Bahman, Dai, Tianhong, Pikkula, Brian M., Wang, Lihong V.   +3 more
core  

A rare presentation of Sturge-Weber syndrome: when a port-wine stain is not the key - case report

Portuguese Journal of Pediatrics
Sturge-Weber syndrome (SWS) is a sporadic congenital vascular disorder which typically presents with a facial port-wine stain and capillary malformations affecting the brain and eye.
Miguel Labrusco, Inês Martins, Sara I. de Almeida, Sofia Quintas, Paulo Oom   +4 more
doaj   +1 more source

Transition into adulthood: Tuberous sclerosis complex, S turge‐ W eber syndrome, and R asmussen encephalitis [PDF]

, 2014
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/108590/1/epi12722 ...
Chugani, Harry T., Granata, Tiziana, Matricardi, Sara, Thiele, Elizabeth A.   +3 more
core   +1 more source

Applicability of Complementary Colors in Skin Tone Correction for Young Chinese Adults Based on Image Processing and Machine Learning

Journal of Cosmetic Dermatology, Volume 24, Issue 12, December 2025.
ABSTRACT Background and Objective Skin tone correction is an essential focus within dermatology and cosmetology, particularly in achieving a balanced and even facial appearance. The application of complementary color theory in skin tone correction remains predominantly subjective, relying on individual user experiences rather than systematic and ...
Guolong Dong, Yueheng Liu, Jianghong Ran, Fan Yi, Li Li, Hong Meng, Yue Wu   +6 more
wiley   +1 more source

Phenotypic Spectrum and Diagnostic Challenges in Klippel‐Trenaunay Syndrome: A Case Series

Clinical Case Reports, Volume 13, Issue 11, November 2025.
ABSTRACT Klippel‐Trénaunay syndrome (KTS) is a rare congenital disorder characterized by the triad of capillary malformations, venous varicosities, and soft tissue or bony hypertrophy. This case series highlights rare and atypical presentations of KTS, emphasizing the importance of a multidisciplinary diagnostic approach.
Marya Hameed, Tooba Ali, Md Ariful Haque
wiley   +1 more source

Increase in teledermatology consultations regarding suspected tinea capitis – an observation of misidentified nevi flammei

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 24, Issue 2, Page 243-244, February 2026.
Julian Kött, Johannes Dupont, Katharina Langen, Christian Drerup   +3 more
wiley   +1 more source

Toward Less Energy‐Consuming Alcoholic Fermentations in Oenology: A Laboratory‐Scale Case Study

Food Frontiers, Volume 6, Issue 6, Page 2931-2941, November 2025.
The graphical abstract outlines the experimental workflow, from fermenting nine commercial yeast strains under different sugar concentrations and temperature programs, to systematic sampling and analysis of metabolites, volatiles, and cell populations, generating the dataset used to assess the impact of temperature dynamics on fermentation.
Romain Minebois, Lainy Ramírez‐Aroca, Eva Balsa‐Canto, Amparo Querol   +3 more
wiley   +1 more source

Sturge-Weber Syndrome with Osteohypertrophy of Maxilla

Case Reports in Pediatrics, 2013
Sturge-Weber syndrome is a rare nonhereditary developmental condition with neurological and skin disorder, characterized by presence of port wine stain on the face along with ocular disorders, oral manifestations and leptomeningeal angiomas.
Prashant Babaji, Anju Bansal, Gopal Krishna Choudhury, Rashmita Nayak, Ashok Kodangala Prabhakar, Nagarathna Suratkal, Veena Raju, Suresh S. Kamble   +7 more
doaj   +1 more source

Conjunctival melanosis with retinal vessel tortuosity: An unusual presentation of Sturge–Weber syndrome

Kerala Journal of Ophthalmology, 2017
Sturge–Weber syndrome (SWS) is a rare neuro-oculocutaneous disorder. The classical signs are unilateral facial port wine stain, leptomeningeal angiomas, and their sequele with ipsilateral glaucoma.
Padma B Prabhu, Deviprasad Soman, V Babitha   +2 more
doaj   +1 more source

Plausible predicament in emergency endodontic rehabilitation of a child with Sturge-Weber syndrome: A case report

Contemporary Pediatric Dentistry, 2022
Sturge–Weber Syndrome (SWS) is a neuro-oculo-cutaneous vascular disorder that includes leptomeningeal hemangioma and port wine stains, usually ipsilaterally, with ocular manifestations and extended lesions over the oral cavity.
Amit Khatri, Namita Kalra, Rishi Tyagi, Khadeeja Kulood M, Mayank Sharma, Drishti Kaushal   +5 more
doaj   +1 more source