Results 181 to 190 of about 7,521 (211)
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Hutchinson-Gilford progeria syndrome.
Journal of the Medical Association of Thailand = Chotmaihet thangphaet, 1999Hutchinson-Gilford progeria syndrome is an extremely rare condition of premature aging. It is characterized by growth retardation and accelerated degenerative changes of cutaneous, musculoskeletal and cardiovascular systems. The pathogenesis of the disease is unknown. The patients usually appear normal at birth. Typical manifestations develop gradually
W, Wisuthsarewong, S, Viravan
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Hutchinson-Gilford Progeria Syndrome
Southern Medical Journal, 1978P, Runge +3 more
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Hip Disease in Hutchinson-Gilford Progeria Syndrome
Journal of Pediatric Orthopaedics, 1984Two cases of Hutchinson-Gilford progeria syndrome are presented with a focus on hip disease. A severe coxa valga is the first abnormality. The femoral head becomes increasingly uncovered as the acetabulum becomes more dysplastic. The center edge angle decreases, the acetabular index increases, and the medial wall of the acetabulum widens.
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Vascular dysfunction in Hutchinson–Gilford progeria syndrome
Trends in Molecular MedicineMost patients with Hutchinson-Gilford progeria syndrome (HGPS) succumb to cardiovascular disease. Recent studies by Barettino et al., Cardoso et al., and Vakili et al. utilized progeria mouse models to elucidate novel mechanisms by which vascular smooth muscle cell (VSMC) and endothelial cell (EC) dysfunction accelerate the progress of the disease ...
Yaping Zhao, Li Wang, Suowen Xu
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In vivo base editing rescues Hutchinson–Gilford progeria syndrome in mice
Nature, 2021Luke W Koblan +2 more
exaly
Rhinoplasty on Hutchinson–Gilford Progeria Syndrome Patient
Aesthetic Plastic Surgery, 2021Mauro Barone +3 more
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Phenotype and Course of Hutchinson–Gilford Progeria Syndrome
New England Journal of Medicine, 2008Leslie B Gordon +2 more
exaly

