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Progeria

Known as: Progeria [Disease/Finding], HGPS, Hutchinson-Gilford Progeria Syndromes 
An abnormal congenital condition, associated with defects in the LAMIN TYPE A gene, which is characterized by premature aging in children, where all… 
National Institutes of Health

Papers overview

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Review
2007
Review
2007
Progeria (Hutchinson-Gilford progeria syndrome) is a rare genetic disorder that offers considerable insight into the biology of… 
Highly Cited
2003
Highly Cited
2003
Les ‘glissements de type ecoulement' (flow-like landslides) constituent un risque naturel majeur dans la plupart des zones de… 
Highly Cited
1979
Highly Cited
1979
Purified peripheral blood T lymphocytes were incubated with inducers of cyclic nucleotides and examined for the numbers of T… 
Highly Cited
1971
Highly Cited
1971
Progeria is an autosomal recessive disorder showing precocious senility. The cultured skin fibroblast from both the homozygous… 
Highly Cited
1969
Highly Cited
1969
Two boys with classical progeria have been studied by a variety of laboratories in the Boston area. Evidence for unresponsiveness…