Results 121 to 130 of about 69,884 (306)

Topical imiquimod and in situ vulvar melanoma: A promising therapy?

open access: yesInternational Journal of Gynecology &Obstetrics, Volume 170, Issue 2, Page 608-613, August 2025.
Abstract Objectives Vulvar melanoma is a rare type of cancer that affects mainly postmenopausal women. There are no established protocols for the treatment of vulvar melanoma. From data extrapolated from the literature on cutaneous melanoma, surgical excision remains the best option for the resectable disease.
Francesca Pepe   +7 more
wiley   +1 more source

Multiple miliary osteoma cutis treatment response to Q-switched Nd:YAG laser: A case report

open access: yesSAGE Open Medical Case Reports, 2020
Facial multiple miliary osteoma cutis is a variant of osteoma cutis usually occurring in women with a previous history of acne vulgaris. Successful ablative laser treatment has been reported using both CO2 and Er:YAG lasers among other invasive treatment
Augustin C. Barolet   +2 more
doaj   +1 more source

Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)

open access: yes
Journal of Cutaneous Pathology, EarlyView.
Cathal O'Connor   +4 more
wiley   +1 more source

Quantitative susceptibility mapping of the human carotid artery: Assessing sensitivity to elastin and collagen ex vivo

open access: yesMagnetic Resonance in Medicine, Volume 94, Issue 2, Page 771-784, August 2025.
Abstract Purpose The aim is to establish the relationship between carotid susceptibility and microstructural components in diseased carotid arteries. Methods Excised cadaveric carotid arteries (n = 5) were scanned using high‐resolution QSM at 7 Tesla. After ex vivo imaging, all samples were brought to histology and stained for elastin, collagen, cells,
Alan J. Stone   +4 more
wiley   +1 more source

Calcinosis cutis universalis - a rare manifestation of systemic lupus erthymatosus

open access: yesSouth African Journal of Radiology, 2012
Calcinosis cutis (or skin and subcutaneous calcification) is a feature of a variety of rheumatic conditions, most commonly dermatomyositis and scleroderma, but is rarely reported in systemic lupus erythematosus (SLE ). When calcinosis cutis does occur in
farhana ebrahim suleman   +1 more
doaj   +1 more source

TUGS – The tactile user guidance system [PDF]

open access: yes, 2005
The Electronic System and Information Technology Research Group at Brunel University has designed a multifaceted navigation system for blind and visually impaired pedestrians.
Billett, EH   +2 more
core  

From variome to phenome : pathogenesis, diagnosis and management of ectopic mineralization disorders [PDF]

open access: yes, 2015
Ectopic mineralization - inappropriate biomineralization in soft tissues - is a frequent finding in physiological aging processes and several common disorders, which can be associated with significant morbidity and mortality.
De Vilder, eva, Vanakker, Olivier
core   +2 more sources

Calcinosis cutis of the lower legs – hyperphosphatemic familial tumoral calcinosis in a patient with GALNT3 mutation

open access: yes
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
David Ranzinger   +4 more
wiley   +1 more source

The Spectrum of Epidermolysis Bullosa in KwaZulu‐Natal, South Africa

open access: yesInternational Journal of Dermatology, Volume 64, Issue 8, Page 1425-1433, August 2025.
ABSTRACT Background Epidermolysis bullosa (EB) is a rare, heterogeneous genodermatosis characterized by skin fragility due to inherited defects in genes encoding proteins that maintain epidermal–dermal integrity. The severity and complications of EB vary by subtype, and no cure currently exists. The epidemiology is unknown in South Africa. Methods This
Antoinette Chateau   +10 more
wiley   +1 more source

Anesthesia Management in Rare Case: Cutis Laxa Syndrome

open access: yesArchives of Anesthesia and Critical Care, 2015
Cutis laxa is rare and hetrogenous group of disorders related to abnormalities in elastic tissue. It may be autosomal recessive, autosomal dominant, X linked or acquired.
Anahid Maleki   +5 more
doaj  

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