140 related articles for article (PubMed ID: 16755670)
1. Coexistent Marfan's syndrome and ankylosing spondylitis.
Kiss C; Jónap I; Gergely P; Poór G
J Rheumatol; 2006 Jun; 33(6):1199-200. PubMed ID: 16755670
[TBL] [Abstract][Full Text] [Related]
2. Is fibrillin-1 the link between ankylosing spondylitis and Marfan's syndrome?
Fietta P; Manganelli P
J Rheumatol; 2002 Aug; 29(8):1808. PubMed ID: 12180757
[No Abstract] [Full Text] [Related]
3. Coexistent Marfan's syndrome and ankylosing spondylitis: a case report.
Fietta P; Manganelli P
Clin Rheumatol; 2001; 20(2):140-2. PubMed ID: 11346228
[TBL] [Abstract][Full Text] [Related]
4. A novel mutation in the fibrillin gene (FBN1) in familial arachnodactyly.
Hayward C; Porteous ME; Brock DJ
Mol Cell Probes; 1994 Aug; 8(4):325-7. PubMed ID: 7870075
[TBL] [Abstract][Full Text] [Related]
5. A molecular approach to the stratification of cardiovascular risk in families with Marfan's syndrome.
Pereira L; Levran O; Ramirez F; Lynch JR; Sykes B; Pyeritz RE; Dietz HC
N Engl J Med; 1994 Jul; 331(3):148-53. PubMed ID: 8008028
[TBL] [Abstract][Full Text] [Related]
6. [Acute lymphoblastic leukemia in a pediatric patient with Marfan's syndrome].
Miyajima Y; Kitase Y; Mizuno S; Sakai H; Matsumoto N; Ogawa A
Rinsho Ketsueki; 2011 Jan; 52(1):28-31. PubMed ID: 21378479
[TBL] [Abstract][Full Text] [Related]
7. Marfan's syndrome and other disorders of fibrillin.
Francke U; Furthmayr H
N Engl J Med; 1994 May; 330(19):1384-5. PubMed ID: 8152453
[No Abstract] [Full Text] [Related]
8. [Contribution of genetics to pathogenicity and diagnosis of Marfan syndrome].
Boileau C; Collod G; Bonnet D
Arch Mal Coeur Vaiss; 1997 Dec; 90(12 Suppl):1707-12. PubMed ID: 9587455
[TBL] [Abstract][Full Text] [Related]
9. Muscle fibrillin deficiency in Marfan's syndrome myopathy.
Behan WM; Longman C; Petty RK; Comeglio P; Child AH; Boxer M; Foskett P; Harriman DG
J Neurol Neurosurg Psychiatry; 2003 May; 74(5):633-8. PubMed ID: 12700307
[TBL] [Abstract][Full Text] [Related]
10. Severe periodontitis in Marfan's syndrome: a case report.
Straub AM; Grahame R; Scully C; Tonetti MS
J Periodontol; 2002 Jul; 73(7):823-6. PubMed ID: 12146542
[TBL] [Abstract][Full Text] [Related]
11. Variability of aortic stiffness is not associated with the fibrillin 1 genotype in patients with Marfan's syndrome.
De Backer J; Nollen GJ; Devos D; Pals G; Coucke P; Verstraete K; van der Wall EE; De Paepe A; Mulder BJ
Heart; 2006 Jul; 92(7):977-8. PubMed ID: 16775108
[No Abstract] [Full Text] [Related]
12. Novel non-synonymous mutation in the transforming growth factor beta binding protein-like (TB) domain of the fibrillin-1 (FBN1) gene in a Han Chinese family with Marfan syndrome (MFS).
Qin Y; Yan J; Simpson JL; Gu HF; Wang LC; Chen ZJ
Neuro Endocrinol Lett; 2007 Oct; 28(5):629-32. PubMed ID: 17984934
[TBL] [Abstract][Full Text] [Related]
13. Therapy insight: aortic aneurysm and dissection in Marfan's syndrome.
Ramirez F; Dietz HC
Nat Clin Pract Cardiovasc Med; 2004 Nov; 1(1):31-6. PubMed ID: 16265257
[TBL] [Abstract][Full Text] [Related]
14. FBN1 mutation in Chinese patients with Marfan syndrome and its gene diagnosis using haplotype linkage analysis.
Wang B; Hu D; Xia J; Li Q; Yang J; Lu G
Chin Med J (Engl); 2003 Jul; 116(7):1043-6. PubMed ID: 12890380
[TBL] [Abstract][Full Text] [Related]
15. The FBN1 (R2726W) mutation is not fully penetrant.
Buoni S; Zannolli R; Macucci F; Ansaldi S; Grasso M; Arbustini E; Fois A
Ann Hum Genet; 2004 Nov; 68(Pt 6):633-8. PubMed ID: 15598221
[TBL] [Abstract][Full Text] [Related]
16. [AFBN1 gene in patients with Marfan syndrome].
Valiev RR; Khusainova RI; Kutuev IA; Khusnutdinova EK
Mol Biol (Mosk); 2006; 40(6):1021-30. PubMed ID: 17209430
[TBL] [Abstract][Full Text] [Related]
17. [Computer construction and analysis of protein models of mutant fibrillin-1 gene in Marfan's syndrome].
Shentu XC; Tang XJ; Ye PP; Jin CF; Wang W; Yao K
Zhonghua Yan Ke Za Zhi; 2009 Aug; 45(8):699-702. PubMed ID: 20021881
[TBL] [Abstract][Full Text] [Related]
18. Fibrillin abnormalities and prognosis in Marfan syndrome and related disorders.
Aoyama T; Francke U; Gasner C; Furthmayr H
Am J Med Genet; 1995 Aug; 58(2):169-76. PubMed ID: 8533811
[TBL] [Abstract][Full Text] [Related]
19. Novel fibrillin 1 mutation in a case of neonatal Marfan syndrome: the increasing importance of early recognition.
Sutherell J; Zarate Y; Tinkle BT; Markham LW; Cripe LH; Hyland JC; Witte D; Hopkin RJ; Hinton RB
Congenit Heart Dis; 2007; 2(5):342-6. PubMed ID: 18377451
[TBL] [Abstract][Full Text] [Related]
20. Identification of 29 novel and nine recurrent fibrillin-1 (FBN1) mutations and genotype-phenotype correlations in 76 patients with Marfan syndrome.
Rommel K; Karck M; Haverich A; von Kodolitsch Y; Rybczynski M; Müller G; Singh KK; Schmidtke J; Arslan-Kirchner M
Hum Mutat; 2005 Dec; 26(6):529-39. PubMed ID: 16220557
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
