✦ LIBER ✦

A disease of premature ageing

✍ Scribed by Inderjeet Dokal

Book ID: 117279275
Publisher: The Lancet
Year: 2001
Tongue: English
Weight: 84 KB
Volume: 358
Category: Article
ISSN: 0140-6736
DOI: 10.1016/s0140-6736(01)07040-4

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Uremia causes premature ageing of the T

Uremia causes premature ageing of the T cell compartment in end-stage renal disease patients

✍ Ruud WJ Meijers, Nicolle HR Litjens, Elly A de Wit, Anton W Langerak, Ashley van 📂 Article 📅 2012 🏛 BioMed Central 🌐 English ⚖ 248 KB

Cloning the gene for Werner syndrome: a

Cloning the gene for Werner syndrome: a disease with many symptoms of premature aging

✍ David B. Lombard; Leonard Guarente 📂 Article 📅 1996 🏛 Elsevier Science 🌐 English ⚖ 450 KB

A proteomic study of Hutchinson–Gilford

A proteomic study of Hutchinson–Gilford progeria syndrome: Application of 2D-chromotography in a premature aging disease

✍ Li Wang; Wu Yang; Weina Ju; Peirong Wang; Xinliang Zhao; Edmund C. Jenkins; W. T 📂 Article 📅 2012 🏛 Elsevier Science 🌐 English ⚖ 900 KB

Human Genome and Diseases: A new series

Human Genome and Diseases: A new series of reviews in CMLS¶Werner Syndrome: genetic and molecular basis of a premature aging disorder

✍ Lebel, M. 📂 Article 📅 2001 🏛 Springer 🌐 English ⚖ 142 KB

Prevalence of atherogenic LDL pattern B

Prevalence of atherogenic LDL pattern B in asymptomatic middle aged African Americans with a family history of premature coronary heart diseases

✍ Khurram Nasir; Diane M. Becker; Lisa R. Yanek; Taryn F. Moy; Lewis C. Becker; Ro 📂 Article 📅 2002 🏛 Elsevier Science 🌐 English ⚖ 187 KB

Age at onset–dependent presentations of

Age at onset–dependent presentations of premature hip osteoarthritis, avascular necrosis of the femoral head, or Legg-Calvé-Perthes disease in a single family, consequent upon a p.Gly1170Ser mutation of COL2A1

✍ Peiqiang Su; Ru Li; Shangli Liu; Yan Zhou; Xinguang Wang; Nilesh Patil; Christop 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 219 KB 👁 2 views

## Abstract ## Objective To identify the genetic abnormality responsible for osteoarthritis (OA), avascular necrosis (AVN) of the femoral head, and Legg‐Calvé‐Perthes disease in a single family, and to determine factors responsible for the distinct phenotypes manifested by different family members