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Results: 1 to 20 of 105

1.

Musculo-skeletal abnormalities in patients with Marfan syndrome.

Al Kaissi A, Zwettler E, Ganger R, Schreiner S, Klaushofer K, Grill F.

Clin Med Insights Arthritis Musculoskelet Disord. 2013;6:1-9. doi: 10.4137/CMAMD.S10279. Epub 2013 Jan 29.

PMID:
23399831
[PubMed]
Free PMC Article
2.

Protrusio acetabuli in Marfan syndrome: age-related prevalence and associated hip function.

Sponseller PD, Jones KB, Ahn NU, Erkula G, Foran JR, Dietz HC 3rd.

J Bone Joint Surg Am. 2006 Mar;88(3):486-95.

PMID:
16510812
[PubMed - indexed for MEDLINE]
3.

Protrusio acetabuli in Marfan syndrome. History, diagnosis, and treatment.

Van de Velde S, Fillman R, Yandow S.

J Bone Joint Surg Am. 2006 Mar;88(3):639-46. Review.

PMID:
16510833
[PubMed - indexed for MEDLINE]
4.

Radiographic findings in Shprintzen-Goldberg syndrome.

Nishimura G, Nagai T.

Pediatr Radiol. 1996 Nov;26(11):775-8.

PMID:
8929375
[PubMed - indexed for MEDLINE]
5.

Surgical treatment for scoliosis in patients with Shprintzen-Goldberg syndrome.

Watanabe K, Okada E, Kosaki K, Tsuji T, Ishii K, Nakamura M, Chiba K, Toyama Y, Matsumoto M.

J Pediatr Orthop. 2011 Mar;31(2):186-93. doi: 10.1097/BPO.0b013e3182093da5.

PMID:
21307714
[PubMed - indexed for MEDLINE]
6.

De novo exon 1 missense mutations of SKI and Shprintzen-Goldberg syndrome: two new cases and a clinical review.

Au PY, Racher HE, Graham JM Jr, Kramer N, Lowry RB, Parboosingh JS, Innes AM; FORGE Canada Consortium.

Am J Med Genet A. 2014 Mar;164A(3):676-84. doi: 10.1002/ajmg.a.36340. Epub 2013 Dec 19. Review.

PMID:
24357594
[PubMed - indexed for MEDLINE]
7.

Fibrillin 1 gene with R2726W mutation is absent in patients with primary protrusio acetabuli and developmental dysplasia of the hip.

Ghosh S, Fryer AA, Hoban PR, Wynn-Jones C, Maffulli N.

Med Sci Monit. 2009 May;15(5):CR199-202.

PMID:
19396033
[PubMed - indexed for MEDLINE]
8.

Cardiovascular characteristics in Marfan syndrome and their relation to the genotype.

De Backer J.

Verh K Acad Geneeskd Belg. 2009;71(6):335-71. Review.

PMID:
20232788
[PubMed - indexed for MEDLINE]
9.

Fibrillin-1 mutations in Marfan syndrome and other type-1 fibrillinopathies.

Hayward C, Brock DJ.

Hum Mutat. 1997;10(6):415-23. Review.

PMID:
9401003
[PubMed - indexed for MEDLINE]
10.

Infantile scoliosis in Marfan syndrome.

Sponseller PD, Sethi N, Cameron DE, Pyeritz RE.

Spine (Phila Pa 1976). 1997 Mar 1;22(5):509-16.

PMID:
9076882
[PubMed - indexed for MEDLINE]
11.

Sensitive detection of abnormal aortic architecture in Marfan syndrome with high-frequency ultrasonic tissue characterization.

Recchia D, Sharkey AM, Bosner MS, Kouchoukos NT, Wickline SA.

Circulation. 1995 Feb 15;91(4):1036-43.

PMID:
7850939
[PubMed - indexed for MEDLINE]
Free Article
12.

Ascending aortic aneurysm with or without features of Marfan syndrome and other fibrillinopathies: new insights.

Furthmayr H, Francke U.

Semin Thorac Cardiovasc Surg. 1997 Jul;9(3):191-205. Review.

PMID:
9263339
[PubMed - indexed for MEDLINE]
13.

Orthopedic aspects of the Marfan phenotype.

Joseph KN, Kane HA, Milner RS, Steg NL, Williamson MB Jr, Bowen JR.

Clin Orthop Relat Res. 1992 Apr;(277):251-61.

PMID:
1555349
[PubMed - indexed for MEDLINE]
14.

Are Marfan syndrome and marfanoid patients distinguishable on long-term follow-up?

Svensson LG, Blackstone EH, Feng J, de Oliveira D, Gillinov AM, Thamilarasan M, Grimm RA, Griffin B, Hammer D, Williams T, Gladish DH, Lytle BW.

Ann Thorac Surg. 2007 Mar;83(3):1067-74.

PMID:
17307461
[PubMed - indexed for MEDLINE]
15.

Spontaneous spinal cerebrospinal fluid leaks and minor skeletal features of Marfan syndrome: a microfibrillopathy.

Schrijver I, Schievink WI, Godfrey M, Meyer FB, Francke U.

J Neurosurg. 2002 Mar;96(3):483-9.

PMID:
11883832
[PubMed - indexed for MEDLINE]
16.

Protrusio acetabuli in Marfan syndrome: indication for surgery in skeletally immature Marfan patients.

Van de Velde S, Fillman R, Yandow S.

J Pediatr Orthop. 2005 Sep-Oct;25(5):603-6.

PMID:
16199939
[PubMed - indexed for MEDLINE]
17.

The usefulness of multidetector computed tomographic angiography for the diagnosis of Marfan syndrome by Ghent criteria.

Sohn GH, Jang SY, Moon JR, Yang JH, Sung K, Ki CS, Oh JK, Choe YH, Kim DK.

Int J Cardiovasc Imaging. 2011 Jun;27(5):679-88. doi: 10.1007/s10554-011-9867-5. Epub 2011 Apr 19.

PMID:
21503706
[PubMed - indexed for MEDLINE]
18.

Shprintzen-Goldberg syndrome: a clinical analysis.

Greally MT, Carey JC, Milewicz DM, Hudgins L, Goldberg RB, Shprintzen RJ, Cousineau AJ, Smith WL Jr, Judisch GF, Hanson JW.

Am J Med Genet. 1998 Mar 19;76(3):202-12. Review.

PMID:
9508238
[PubMed - indexed for MEDLINE]
19.

Improving clinical recognition of Marfan syndrome.

Sponseller PD, Erkula G, Skolasky RL, Venuti KD, Dietz HC 3rd.

J Bone Joint Surg Am. 2010 Aug 4;92(9):1868-75. doi: 10.2106/JBJS.I.00892.

PMID:
20686061
[PubMed - indexed for MEDLINE]
20.

Fatal aortic dissection in a patient with a family history of Marfan syndrome.

Birsner ML, Farber JL, Berghella V.

Obstet Gynecol. 2008 Aug;112(2 Pt 2):472-5. doi: 10.1097/AOG.0b013e3181743312.

PMID:
18669769
[PubMed - indexed for MEDLINE]

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