These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
4. Neonatal progeroid syndrome: more than one disease? Hagadorn JI; Wilson WG; Hogge WA; Callicott JH; Beale EF Am J Med Genet; 1990 Jan; 35(1):91-4. PubMed ID: 2301475 [TBL] [Abstract][Full Text] [Related]
5. [Gilford progeria. A case report]. Lê DL; Hoeffel CC; Nguyen QK; Nguyen HN Ann Med Interne (Paris); 1999 Oct; 150(6):512-8. PubMed ID: 10615539 [TBL] [Abstract][Full Text] [Related]
6. The neonatal progeroid syndrome (Wiedemann-Rautenstrauch): a model for the study of human aging? Arboleda G; Ramírez N; Arboleda H Exp Gerontol; 2007 Oct; 42(10):939-43. PubMed ID: 17728088 [TBL] [Abstract][Full Text] [Related]
7. Study of a family with a new progeroid syndrome. Welsh O Birth Defects Orig Artic Ser; 1975; 11(5):25-38. PubMed ID: 1240776 [TBL] [Abstract][Full Text] [Related]
8. A new case of neonatal progeroid syndrome with agenesis of corpus callosum. Abdel-Salam GM; Czeizel AE Genet Couns; 1999; 10(4):377-81. PubMed ID: 10631926 [TBL] [Abstract][Full Text] [Related]
9. Progeria infantum (Hutchinson-Gilford syndrome) associated with scleroderma-like lesions and acro-osteolysis: a case report and brief review of the literature. Jansen T; Romiti R Pediatr Dermatol; 2000; 17(4):282-5. PubMed ID: 10990576 [TBL] [Abstract][Full Text] [Related]
10. Wiedemann-Rautenstrauch syndrome. A case report and review of the literature. Stoll C; Labay F; Geisert J; Alembik Y Genet Couns; 1998; 9(2):119-24. PubMed ID: 9664208 [TBL] [Abstract][Full Text] [Related]
12. Aging of Hutchinson-Gilford progeria syndrome fibroblasts is characterised by hyperproliferation and increased apoptosis. Bridger JM; Kill IR Exp Gerontol; 2004 May; 39(5):717-24. PubMed ID: 15130666 [TBL] [Abstract][Full Text] [Related]
13. Skeletal abnormalities of acrogeria, a progeroid syndrome. Ho A; White SJ; Rasmussen JE Skeletal Radiol; 1987; 16(6):463-8. PubMed ID: 3659993 [TBL] [Abstract][Full Text] [Related]
15. New progeroid disorder. Penttinen M; Niemi KM; Vinkka-Puhakka H; Johansson R; Aula P Am J Med Genet; 1997 Mar; 69(2):182-7. PubMed ID: 9056558 [TBL] [Abstract][Full Text] [Related]
16. [Neonatal progeroid syndrome (Wiedemann-Rautenstrauch syndrome): case report and review of the literature]. Hoppen T; Hausser I; Theile U; Ferrari R; Müller W; Rister M Klin Padiatr; 2000; 212(2):71-6. PubMed ID: 10812556 [TBL] [Abstract][Full Text] [Related]
17. The Hutchinson-Gilford Progeria Syndrome: a case report. Russo-Menna I; Arancibias C Minerva Anestesiol; 2010 Feb; 76(2):151-4. PubMed ID: 20150858 [TBL] [Abstract][Full Text] [Related]
19. The Wiedemann-Rautenstrauch or neonatal progeroid syndrome: report of a patient with hypospadias. Tunc T; Bulbul A; Erdinc K; Sarici SU; Gul D; Ozcan O Genet Couns; 2009; 20(4):367-71. PubMed ID: 20162872 [TBL] [Abstract][Full Text] [Related]
20. Hutchinson-Gilford progeria syndrome: clinical findings in three patients carrying the G608G mutation in LMNA and review of the literature. Mazereeuw-Hautier J; Wilson LC; Mohammed S; Smallwood D; Shackleton S; Atherton DJ; Harper JI Br J Dermatol; 2007 Jun; 156(6):1308-14. PubMed ID: 17459035 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]