Results 221 to 230 of about 99,459 (305)

Multiple lesion-specific somatic mutations and bi-allelic loss of ACVRL1 in a single patient with hereditary haemorrhagic telangiectasia. [PDF]

open access: yesEur J Hum Genet
Darre Haahr P   +10 more
europepmc   +1 more source

Efficacy of Intralesional Triamcinolone Acetonide Combined With Cryotherapy Compared to Intralesional Triamcinolone Acetonide Alone in Treating Limited Patchy Alopecia Areata of the Scalp and Face: A Prospective, Randomized, Within‐Subject Controlled Trial

open access: yesJournal of Cosmetic Dermatology, Volume 25, Issue 2, February 2026.
ABSTRACT Background Alopecia areata (AA) is a common autoimmune disease characterized by non‐scarring hair loss. The disease occurs in both sexes, with no racial or age‐related predilection. Many patients experience spontaneous improvement and regrowth of hair, while some patients are resistant to common therapies and others progress to more severe ...
Sama Heidari   +5 more
wiley   +1 more source

Could a macular telangiectasia type 2-like phenotype characterize retinal JC virus infection? [PDF]

open access: yesAIDS
Varenne F   +11 more
europepmc   +1 more source

Hereditary Hemorrhagic Telangiectasia: A Rare Cause of Anemia [PDF]

open access: diamond, 2019
Waseem Jan   +4 more
openalex   +1 more source

Comprehensive Evaluation of a Cream With Advanced Soothing Complex for Skin Recovery Following Intense Pulsed Light Therapy

open access: yesJournal of Cosmetic Dermatology, Volume 25, Issue 2, February 2026.
ABSTRACT Background Intense pulsed light (IPL) therapy is widely used for skin rejuvenation but frequently induces transient skin barrier impairment, erythema, and discomfort. Post‐procedure skincare targeting barrier repair and symptom relief remains a clinical priority.
Jianhua Zhang   +4 more
wiley   +1 more source

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