kw.\*:("PROGERIA")
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Neonatal progeroid syndrome: more than one disease?HAGADORN, J. I; WILSON, W. G; HOGGE, W. A et al.American journal of medical genetics. 1990, Vol 35, Num 1, pp 91-94, issn 0148-7299Article
PREMATURE AGING SYNDROMES AFFECTING THE SKINGILCHREST BA.1981; BIRTH DEFECTS, ORIG. ARTIC. SER.; ISSN 0547-6844; USA; DA. 1981; VOL. 17; NO 2; PP. 227-241; BIBL. 50 REF.Conference Paper
Progeria de Hutchinson-Gilford néonatale = Neonatal Hutchinson-Gilford ProgeriaGALLET, M; KRIM, G; KREMP, O et al.La Médecine infantile (Paris). 1990, Num 1, pp 45-46, issn 0025-6773Article
Does progeria provide the best model of accelerated ageing in humans ?MILLS, R. G; WEISS, A. S.Gerontology (Basel). 1990, Vol 36, Num 2, pp 84-98, issn 0304-324XArticle
DRUG METABOLISM IN A CASE OF PROGERIA.CALDWELL J; SMITH RL; DAVIES SA et al.1978; GERONTOLOGIE; CHE; DA. 1978; VOL. 24; NO 5; PP. 373-380; BIBL. 22 REF.Article
Prelamin A Acts to Accelerate Smooth Muscle Cell Senescence and Is a Novel Biomarker of Human Vascular AgingRAGNAUTH, Cassandra D; WARREN, Derek T; YIWEN LIU et al.Circulation (New York, N.Y.). 2010, Vol 121, Num 20, pp 2200-2210, issn 0009-7322, 11 p.Article
An association of Hutchinson-Gilford progeria and malignancySHALEV, Stavit A; DE SANDRE-GIOVANNOLI, Annachiara; SHANI, Ayelet Adir et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 16, pp 1821-1826, issn 1552-4825, 6 p.Article
Somatic and gonadal mosaicism in hutchinson-gilford progeriWUYTS, Wim; BIERVLIET, Martine; REYNIERS, Edwin et al.American journal of medical genetics. 2005, Vol 135A, Num 1, pp 66-68, issn 0148-7299, 3 p.Article
miR-9: la sentinelle des neurones dans la progéria = miR-9: the sentinel of neurons in progeriaBLONDEL, Sophie; NAVARRO, Claire; LEVY, Nicolas et al.MS. Médecine sciences. 2012, Vol 28, Num 6-7, pp 663-666, issn 0767-0974, 4 p.Article
Report on a case of Hutchinson-Gilford progeria, with special reference to orthopedic problemsFERNANDEZ-PALAZZI, F; MCLAREN, A. T; SLOWIE, D. F et al.European journal of pediatric surgery. 1992, Vol 2, Num 6, pp 378-382, issn 0939-7248Article
The truncated prelamin A in Hutchinson-Gilford progeria syndrome alters segregation of A-type and B-type lamin homopolymersDELBARRE, Erwan; TRAMIER, Marc; COPPEY-MOISAN, Maïté et al.Human molecular genetics (Print). 2006, Vol 15, Num 7, pp 1113-1122, issn 0964-6906, 10 p.Article
Anaesthesia for a child with progeriaNGUYEN, Nhung H; MAYHEW, James F.Paediatric anaesthesia (Paris). 2001, Vol 11, Num 3, pp 370-371, issn 1155-5645Article
Conduite anesthésique d'un malade avec syndrome de Hutchinson-GilfordARIYOSHI, S; YOROZUYA, Y; OGATA, R et al.Masui. 1987, Vol 36, Num 3, pp 422-426, issn 0021-4892Article
AN UNIDENTIFIED NEONATAL PROGEROID SYNDROME: FOLLOW-UP REPORTWIEDEMANN HR.1979; EUROP. J. PEDIATR.; DEU; DA. 1979; VOL. 130; NO 1; PP. 65-70; BIBL. 10 REF.Article
PROGERIA IN SIBLINGS.FRANKLYN PP.1976; CLIN. RADIOL.; G.B.; DA. 1976; VOL. 27; NO 3; PP. 327-333; BIBL. 23 REF.Article
ProgeriaBADAME, A. J.Archives of dermatology (1960). 1989, Vol 125, Num 4, pp 540-544, issn 0003-987XArticle
Schizophrenia as segmental progeriaPAPANASTASIOU, Evangelos; GAUGHRAN, Fiona; SMITH, Shubulade et al.Journal of the Royal Society of Medicine. 2011, Vol 104, Num 11, pp 475-484, issn 0141-0768, 10 p.Article
Paternal origin of LMNA mutations in Hutchinson-Gilford progeriaD'APICE, M. R; TENCONI, R; MAMMI, I et al.Clinical genetics. 2004, Vol 65, Num 1, pp 52-54, issn 0009-9163, 3 p.Article
Syndrome de vieillissement accéléré : le coupable identifié = Accelerated ageing syndromeBEUZARD, Marie.Biofutur (Puteaux). 2003, Vol 234, issn 0294-3506, p. 10Article
Progeria: report of two cases and literature reviewCHAWLA, V; TAWODZERA, P. B. P; CHUKWU, J. N et al.East African medical journal. 1986, Vol 63, Num 11, pp 749-755, issn 0012-835XArticle
Epigenetic Involvement in Hutchinson-Gilford Progeria Syndrome: A Mini-ReviewARANCIO, Walter; PIZZOLANTI, Giuseppe; GENOVESE, Swonild I et al.Gerontology (Basel). 2014, Vol 60, Num 3, pp 197-203, issn 0304-324X, 7 p.Article
A novel homozygous p.Arg527Leu LMNA mutation in two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndromeAL-HAGGAR, Mohammad; MADEJ-PILARCZYK, Agnieszka; KOZLOWSKI, Lukasz et al.European journal of human genetics. 2012, Vol 20, Num 11, pp 1134-1140, issn 1018-4813, 7 p.Article
Telomere length in Hutchinson-Gilford Progeria SyndromeDECKER, Michelle L; CHAVEZ, Elizabeth; VULTO, Irma et al.Mechanisms of ageing and development. 2009, Vol 130, Num 6, pp 377-383, issn 0047-6374, 7 p.Article
p53 and a human premature ageing disorderO'NEILL, Mary; NUNEZ, Fatima; MELTON, David W et al.Mechanisms of ageing and development. 2003, Vol 124, Num 5, pp 599-603, issn 0047-6374, 5 p.Article
Neurologic features of Hutchinson-Gilford progeria syndrome after lonafarnib treatmentULLRICH, Nicole J; KIERAN, Mark W; MILLER, David T et al.Neurology. 2013, Vol 81, Num 5, pp 427-430, issn 0028-3878, 4 p.Article