Results 131 to 140 of about 1,306,732 (153)
Long lifetime and tissue-specific accumulation of lamin A/C in Hutchinson-Gilford progeria syndrome. [PDF]
J Cell BiolHasper J +5 more
europepmc +1 more source
The Use of Peripheral Nerve Block and Intra-articular Steroid Injection for Pain Management in an Adolescent with Hutchinson-Gilford Progeria Syndrome: A Case Report. [PDF]
Acta Med PhilippEndencia MCS, Sy Su KMC, Reyes CRB.
europepmc +1 more source
Aging of Hutchinson–Gilford Progeria Syndrome Fibroblasts Is Characterised by Hyperproliferation and Increased Apoptosis [PDF]
Experimental Gerontology, 2004 Hutchinson-Gilford progeria syndrome is a rare genetic disorder that mimics certain aspects of aging prematurely. Recent work has revealed that mutations in the lamin A gene are a cause of the disease.
Joanna M Bridger, Ian R Kill
exaly +7 more sources
Mechanisms of Premature Vascular Aging in Children With Hutchinson-Gilford Progeria Syndrome
Hypertension, 2012 Hutchinson-Gilford progeria syndrome is a rare, segmental premature aging syndrome of accelerated atherosclerosis and early death from myocardial infarction or stroke.
Armin Schwartzman +2 more
exaly +2 more sources
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Progeria Syndromes and Ageing: What Is the Connection?
Nature Reviews Molecular Cell Biology, 2010Brian K Kennedy
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Recent Progress in Lynch Syndrome and Other Familial Colorectal Cancer Syndromes
Ca-A Cancer Journal for Clinicians, 2018Patrick Boland +2 more
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Telomere Length in Hutchinson-Gilford Progeria Syndrome
Mechanisms of Ageing and Development, 2009Peter Lansdorp
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