scholarly journals New ZMPSTE24 (FACE1) mutations in patients affected with restrictive dermopathy or related progeroid syndromes and mutation update

2013 ◽  
Vol 22 (8) ◽  
pp. 1002-1011 ◽  
Author(s):  
Claire Laure Navarro ◽  
Vera Esteves-Vieira ◽  
Sébastien Courrier ◽  
Amandine Boyer ◽  
Thuy Duong Nguyen ◽  
...  
Keyword(s):  
Progeroid Syndromes ◽  
Restrictive Dermopathy

scholarly journals Lack of resemblance between Myhre syndrome and other “segmental progeroid” syndromes warrants restraint in applying this classification

GeroScience ◽  
2021 ◽  
Author(s):  
Angela E. Lin ◽  
◽  
Nicola Brunetti-Pierri ◽  
Bert Callewaert ◽  
Valérie Cormier-Daire ◽  
...  
Keyword(s):  
Progeroid Syndromes ◽  
Myhre Syndrome

scholarly journals DNA damage responses in progeroid syndromes arise from defective maturation of prelamin A

2006 ◽  
Vol 119 (22) ◽  
pp. 4644-4649 ◽  
Author(s):  
Y. Liu ◽  
A. Rusinol ◽  
M. Sinensky ◽  
Y. Wang ◽  
Y. Zou
Keyword(s):  
Dna Damage ◽  
Prelamin A ◽  
Progeroid Syndromes ◽  
Dna Damage Responses

Use of Dermal Filler to Improve Exposure Keratopathy in a Patient with Restrictive Dermopathy

Orbit ◽  
2013 ◽  
Vol 32 (1) ◽  
pp. 70-72 ◽  
Author(s):  
Qiang Kwong ◽  
Raman Malhotra ◽  
Ana M. S. Morley ◽  
Shehla Mohammed ◽  
Jonathan H. Norris
Keyword(s):  
Dermal Filler ◽  
Restrictive Dermopathy

scholarly journals Restrictive dermopathy and associated prenatal ultrasound findings: case report

1997 ◽  
Vol 10 (2) ◽  
pp. 140-141 ◽  
Author(s):  
J. G. van der Stege ◽  
H. L. M. van Straaten ◽  
A. C. van der Walt ◽  
J. van Eyck
Keyword(s):  
Case Report ◽  
Prenatal Ultrasound ◽  
Ultrasound Findings ◽  
Restrictive Dermopathy

LMNA Mutations in Progeroid Syndromes

2008 ◽  
pp. 197-207 ◽  
Author(s):  
Shurong Huang ◽  
Brian K. Kennedy ◽  
Junko Oshima
Keyword(s):  
Progeroid Syndromes

scholarly journals Altered Nuclear Functions in Progeroid Syndromes: a Paradigm for Aging Research

2009 ◽  
Vol 9 ◽  
pp. 1449-1462 ◽  
Author(s):  
Baomin Li ◽  
Sonali Jog ◽  
Jose Candelario ◽  
Sita Reddy ◽  
Lucio Comai
Keyword(s):  
Werner Syndrome ◽  
Accelerated Aging ◽  
Natural Aging ◽  
Aging Research ◽  
Cellular Processes ◽  
Functional Connections ◽  
Age Related ◽  
Progeroid Syndromes ◽  
Progeria Syndrome ◽  
Hutchinson Gilford Progeria Syndrome

Syndromes of accelerated aging could provide an entry point for identifying and dissecting the cellular pathways that are involved in the development of age-related pathologies in the general population. However, their usefulness for aging research has been controversial, as it has been argued that these diseases do not faithfully reflect the process of natural aging. Here we review recent findings on the molecular basis of two progeroid diseases, Werner syndrome (WS) and Hutchinson-Gilford progeria syndrome (HGPS), and highlight functional connections to cellular processes that may contribute to normal aging.

scholarly journals Shared Phenotypes Among Segmental Progeroid Syndromes Suggest Underlying Pathways of Aging

2005 ◽  
Vol 60 (1) ◽  
pp. 10-20 ◽  
Author(s):  
A. C. Hofer ◽  
R. T. Tran ◽  
O. Z. Aziz ◽  
W. Wright ◽  
G. Novelli ◽  
...  
Keyword(s):  
Progeroid Syndromes
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