This site needs JavaScript to work properly. Please enable it to take advantage of the complete set of features!

Skip to main page content

Add to Collections

Your saved search

Name of saved search:

Search terms:

Test search terms

Would you like email updates of new search results?

Yes
No

Email: (change)

Frequency:

Which day?

Which day?

Report format:

Send at most:

Send even when there aren't any new results

Optional text in email:

Your RSS Feed

Comment

. 1992 Apr 1;42(6):857.

doi: 10.1002/ajmg.1320420627.

Newly recognized congenital progeroid disorder

PMID: 1554028
DOI: 10.1002/ajmg.1320420627

Comment

Newly recognized congenital progeroid disorder

H R Wiedemann. Am J Med Genet. 1992.

. 1992 Apr 1;42(6):857.

doi: 10.1002/ajmg.1320420627.

Author

PMID: 1554028
DOI: 10.1002/ajmg.1320420627

No abstract available

PubMed Disclaimer

Comment on

Previously unrecognized congenital progeroid disorder.
Petty EM, Laxova R, Wiedemann HR. Petty EM, et al. Am J Med Genet. 1990 Mar;35(3):383-7. doi: 10.1002/ajmg.1320350314. Am J Med Genet. 1990. PMID: 2309786

Similar articles

[Werner syndrome-like disease in 3 brothers. Differential diagnosis of progeria syndrome].
Mensing H, Schaeg G, Burck U, Meigel W. Mensing H, et al. Hautarzt. 1982 Oct;33(10):542-7. Hautarzt. 1982. PMID: 7152896 German.
Nuclear deformation characterizes Werner syndrome cells.
Adelfalk C, Scherthan H, Hirsch-Kauffmann M, Schweiger M. Adelfalk C, et al. Cell Biol Int. 2005 Dec;29(12):1032-7. doi: 10.1016/j.cellbi.2005.10.011. Epub 2005 Nov 28. Cell Biol Int. 2005. PMID: 16314120
[Convexity meningioma associated with Werner's syndrome--histopathological findings with electron microscopical and immunohistochemical findings].
Morimoto K, Yoshimine T, Saitoh Y, Yamada M, Mogami H, Yamagata S, Miyagawa J. Morimoto K, et al. No Shinkei Geka. 1987 Aug;15(8):877-82. No Shinkei Geka. 1987. PMID: 3431652 Japanese.
Gene expression and DNA repair in progeroid syndromes and human aging.
Kyng KJ, Bohr VA. Kyng KJ, et al. Ageing Res Rev. 2005 Nov;4(4):579-602. doi: 10.1016/j.arr.2005.06.008. Epub 2005 Oct 24. Ageing Res Rev. 2005. PMID: 16246641 Review.
Vascular aging: insights from studies on cellular senescence, stem cell aging, and progeroid syndromes.
Minamino T, Komuro I. Minamino T, et al. Nat Clin Pract Cardiovasc Med. 2008 Oct;5(10):637-48. doi: 10.1038/ncpcardio1324. Epub 2008 Sep 2. Nat Clin Pract Cardiovasc Med. 2008. PMID: 18762784 Review.

See all similar articles

Cited by

Whole exome sequencing identifies de novo heterozygous CAV1 mutations associated with a novel neonatal onset lipodystrophy syndrome.
Garg A, Kircher M, Del Campo M, Amato RS, Agarwal AK; University of Washington Center for Mendelian Genomics. Garg A, et al. Am J Med Genet A. 2015 Aug;167A(8):1796-806. doi: 10.1002/ajmg.a.37115. Epub 2015 Apr 21. Am J Med Genet A. 2015. PMID: 25898808 Free PMC article.
Congenital generalized lipodystrophies--new insights into metabolic dysfunction.
Patni N, Garg A. Patni N, et al. Nat Rev Endocrinol. 2015 Sep;11(9):522-34. doi: 10.1038/nrendo.2015.123. Epub 2015 Aug 4. Nat Rev Endocrinol. 2015. PMID: 26239609 Free PMC article. Review.

Publication types

Actions
Actions

MeSH terms

Actions
Actions
Actions
Actions
Actions

LinkOut - more resources

Full Text Sources
- Wiley