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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

150 related articles for article (PubMed ID: 19236595)

  • 1. Hutchinson-Gilford progeria syndrome: oral and craniofacial phenotypes.
    Domingo DL; Trujillo MI; Council SE; Merideth MA; Gordon LB; Wu T; Introne WJ; Gahl WA; Hart TC
    Oral Dis; 2009 Apr; 15(3):187-95. PubMed ID: 19236595
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical and radiographic features of Hutchinson-Gilford progeria syndrome: A case report.
    Alves DB; Silva JM; Menezes TO; Cavaleiro RS; Tuji FM; Lopes MA; Zaia AA; Coletta RD
    World J Clin Cases; 2014 Mar; 2(3):67-71. PubMed ID: 24653988
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Hutchinson-Gilford progeria syndrome: review of the phenotype.
    Hennekam RC
    Am J Med Genet A; 2006 Dec; 140(23):2603-24. PubMed ID: 16838330
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Craniofacial abnormalities in Hutchinson-Gilford progeria syndrome.
    Ullrich NJ; Silvera VM; Campbell SE; Gordon LB
    AJNR Am J Neuroradiol; 2012 Sep; 33(8):1512-8. PubMed ID: 22460337
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hutchinson-Gilford progeria syndrome with G608G LMNA mutation.
    Kim HK; Lee JY; Bae EJ; Oh PS; Park WI; Lee DS; Kim JI; Lee HJ
    J Korean Med Sci; 2011 Dec; 26(12):1642-5. PubMed ID: 22148005
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Dermal fibroblasts in Hutchinson-Gilford progeria syndrome with the lamin A G608G mutation have dysmorphic nuclei and are hypersensitive to heat stress.
    Paradisi M; McClintock D; Boguslavsky RL; Pedicelli C; Worman HJ; Djabali K
    BMC Cell Biol; 2005 Jun; 6():27. PubMed ID: 15982412
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical imaging findings in a girl with Hutchinson-Gilford progeria syndrome.
    Chen CP; Lin SP; Lin DS; Liu YP; Hsu LJ; Wang W
    Genet Couns; 2012; 23(1):1-7. PubMed ID: 22611635
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Phenotype and course of Hutchinson-Gilford progeria syndrome.
    Merideth MA; Gordon LB; Clauss S; Sachdev V; Smith AC; Perry MB; Brewer CC; Zalewski C; Kim HJ; Solomon B; Brooks BP; Gerber LH; Turner ML; Domingo DL; Hart TC; Graf J; Reynolds JC; Gropman A; Yanovski JA; Gerhard-Herman M; Collins FS; Nabel EG; Cannon RO; Gahl WA; Introne WJ
    N Engl J Med; 2008 Feb; 358(6):592-604. PubMed ID: 18256394
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Bilateral stenosis of carotid siphon in Hutchinson-Gilford progeria syndrome.
    Narazaki R; Makimura M; Sanefuji M; Fukamachi S; Akiyoshi H; So H; Yamamura K; Doisaki S; Kojima S; Ihara K; Hara T; Ohga S
    Brain Dev; 2013 Aug; 35(7):690-3. PubMed ID: 23141186
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Variability of the cranial and dental phenotype in Williams syndrome.
    Axelsson S
    Swed Dent J Suppl; 2005; (170):3-67. PubMed ID: 15762376
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Oral and maxillofacial surgical considerations for a case of Hutchinson-Gilford progeria.
    Batstone MD; Macleod AW
    Int J Paediatr Dent; 2002 Nov; 12(6):429-32. PubMed ID: 12452985
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Ocular manifestations in the Hutchinson-Gilford progeria syndrome.
    Chandravanshi SL; Rawat AK; Dwivedi PC; Choudhary P
    Indian J Ophthalmol; 2011; 59(6):509-12. PubMed ID: 22011502
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hutchinson-Gilford progeria syndrome with severe skin calcinosis.
    Nakamura S; Makita Y; Takagi A; Hashimoto Y; Takahashi H; Ishida-Yamamoto A; Iizuka H
    Clin Exp Dermatol; 2007 Sep; 32(5):525-8. PubMed ID: 17459069
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hutchinson-Gilford progeria syndrome.
    Ullrich NJ; Gordon LB
    Handb Clin Neurol; 2015; 132():249-64. PubMed ID: 26564085
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Three cases of Hutchinson-Gilford progeria syndrome].
    Doubaj Y; Lamzouri A; Elalaoui SC; Laarabi FZ; Sefiani A
    Arch Pediatr; 2011 Feb; 18(2):156-9. PubMed ID: 21251803
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hutchinson-Gilford Progeria syndrome: Report of the first Togolese case.
    Guedenon KM; Doubaj Y; Akolly DAE; Barry Moussa W; Saka B; Adjenou K; Belo M; Pio M; Mihluedo-Agbolan KA; Vonor K; Amedome KM; Tchaou M; Atakouma YD; Gbadoe AD; Dossou CF; Fiawoo M; Gnassingbe K; Pitche P; Agbèrè DA; Gnamey DK
    Am J Med Genet A; 2020 Jun; 182(6):1316-1320. PubMed ID: 32297714
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hutchinson-Gilford progeria syndrome.
    Pollex RL; Hegele RA
    Clin Genet; 2004 Nov; 66(5):375-81. PubMed ID: 15479179
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Analysis of a case with typical Hutchinson-Gilford progeria syndrome with scleroderma-like skin changes and review of literature].
    Huang S; Liang Y; Wu W; Fu X; Liao L; Luo X
    Zhonghua Er Ke Za Zhi; 2014 Feb; 52(2):112-6. PubMed ID: 24739722
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.