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]
Darre Haahr P +10 more
europepmc +1 more source
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]
Varenne F +11 more
europepmc +1 more source
A case of hereditary hemorrhagic telangiectasia with hypoxemia onset in the neonatal period. [PDF]
Zhang D +5 more
europepmc +1 more source
Hereditary Hemorrhagic Telangiectasia: A Rare Cause of Anemia [PDF]
Waseem Jan +4 more
openalex +1 more source
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
Ataxia-Telangiectasia in Resource-Limited Settings: A Diagnostic Challenge. [PDF]
Adeyemi E +4 more
europepmc +1 more source
Hereditary hemorrhagic telangiectasia in a 68-year-old man. [PDF]
Chen LL, Xie W.
europepmc +1 more source

