Charles F. Harris, Robert Hutohison
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Characterization of the craniofacial abnormalities of the homozygous G608G progeria mouse model
IntroductionHutchinson-Gilford Progeria Syndrome (HGPS) is a rare genetic condition characterized by premature aging, impacting multiple organ systems, including cardiovascular, musculoskeletal, and integumentary.
Indeevar Beeram +13 more
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The potential of human induced pluripotent stem cells for modelling diabetic wound healing in vitro [PDF]
Aasen +150 more
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Hutchinson-Gilford syndrome (progeria)
Progeria is a rare, autosomal dominant, progeroid disorder. In the world literature less than 100 cases have been reported to date. We present this case because of its rarity.
Surjushe Amar +3 more
doaj
Epidural hematoma in a pediatric patient with Hutchinson-Gilford progeria syndrome: management considerations: a case report. [PDF]
Ozmarasali AI, Sivas ZZ, Uguz I, Oto A.
europepmc +1 more source
General anesthesia in patient with Hutchinson-Gilford Progeria syndrome: two case reports of dental treatment in the one patient. [PDF]
Mankovsky B +3 more
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LAV-BPIFB4 reverses progeria-associated cardiac aging by restoring diastolic function and reducing senescence. [PDF]
Chae U +4 more
europepmc +1 more source
Periosteal mitochondria DNA structures drive aging-associated poor skeletal repair. [PDF]
Wu Y +11 more
europepmc +1 more source
Transcriptional profiling of Hutchinson-Gilford progeria patients identifies primary target pathways of progerin. [PDF]
Vidak S, Kim S, Misteli T.
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