320 related articles for article (PubMed ID: 37443678)
1. Marfan Syndrome: Enhanced Diagnostic Tools and Follow-up Management Strategies.
Marelli S; Micaglio E; Taurino J; Salvi P; Rurali E; Perrucci GL; Dolci C; Udugampolage NS; Caruso R; Gentilini D; Trifiro' G; Callus E; Frigiola A; De Vincentiis C; Pappone C; Parati G; Pini A
Diagnostics (Basel); 2023 Jul; 13(13):. PubMed ID: 37443678
[TBL] [Abstract][Full Text] [Related]
2. Cardiovascular characteristics in Marfan syndrome and their relation to the genotype.
De Backer J
Verh K Acad Geneeskd Belg; 2009; 71(6):335-71. PubMed ID: 20232788
[TBL] [Abstract][Full Text] [Related]
3. Differences in manifestations of Marfan syndrome, Ehlers-Danlos syndrome, and Loeys-Dietz syndrome.
Meester JAN; Verstraeten A; Schepers D; Alaerts M; Van Laer L; Loeys BL
Ann Cardiothorac Surg; 2017 Nov; 6(6):582-594. PubMed ID: 29270370
[TBL] [Abstract][Full Text] [Related]
4. Genetic dissection of marfan syndrome and related connective tissue disorders: an update 2012.
Hoffjan S
Mol Syndromol; 2012 Aug; 3(2):47-58. PubMed ID: 23326250
[TBL] [Abstract][Full Text] [Related]
5. Genotype and phenotype analysis of 171 patients referred for molecular study of the fibrillin-1 gene FBN1 because of suspected Marfan syndrome.
Loeys B; Nuytinck L; Delvaux I; De Bie S; De Paepe A
Arch Intern Med; 2001 Nov; 161(20):2447-54. PubMed ID: 11700157
[TBL] [Abstract][Full Text] [Related]
6. Differences in Cardiovascular Manifestation of Marfan Syndrome Between Children and Adults.
Wozniak-Mielczarek L; Sabiniewicz R; Drezek-Nojowicz M; Nowak R; Gilis-Malinowska N; Mielczarek M; Łabuc A; Waldoch A; Wierzba J
Pediatr Cardiol; 2019 Feb; 40(2):393-403. PubMed ID: 30417312
[TBL] [Abstract][Full Text] [Related]
7. The Heart Muscle and Valve Involvement in Marfan Syndrome, Loeys-Dietz Syndromes, and Collagenopathies.
Fusco A; Mauriello A; Lioncino M; Palmiero G; Fratta F; Granato C; Cirillo A; Caiazza M; Monda E; Credendino A; Signore G; Natale F; Chiosi F; Scarano G; Della Corte A; Nistri S; Russo MG; Limongelli G; Pepe G
Heart Fail Clin; 2022 Jan; 18(1):165-175. PubMed ID: 34776077
[TBL] [Abstract][Full Text] [Related]
8. Missense mutations in FBN1 exons 41 and 42 cause Weill-Marchesani syndrome with thoracic aortic disease and Marfan syndrome.
Cecchi A; Ogawa N; Martinez HR; Carlson A; Fan Y; Penny DJ; Guo DC; Eisenberg S; Safi H; Estrera A; Lewis RA; Meyers D; Milewicz DM
Am J Med Genet A; 2013 Sep; 161A(9):2305-10. PubMed ID: 23897642
[TBL] [Abstract][Full Text] [Related]
9. The Musculoskeletal Manifestations of Marfan Syndrome: Diagnosis, Impact, and Management.
Pollock L; Ridout A; Teh J; Nnadi C; Stavroulias D; Pitcher A; Blair E; Wordsworth P; Vincent TL
Curr Rheumatol Rep; 2021 Nov; 23(11):81. PubMed ID: 34825999
[TBL] [Abstract][Full Text] [Related]
10. Mutations of FBN1 and genotype-phenotype correlations in Marfan syndrome and related fibrillinopathies.
Robinson PN; Booms P; Katzke S; Ladewig M; Neumann L; Palz M; Pregla R; Tiecke F; Rosenberg T
Hum Mutat; 2002 Sep; 20(3):153-61. PubMed ID: 12203987
[TBL] [Abstract][Full Text] [Related]
11. Marfan syndrome type II: there is more to Marfan syndrome than fibrillin 1.
Zangwill SD; Brown MD; Bryke CR; Cava JR; Segura AD
Congenit Heart Dis; 2006 Sep; 1(5):229-32. PubMed ID: 18377530
[TBL] [Abstract][Full Text] [Related]
12. Ectopia lentis as the presenting and primary feature in Marfan syndrome.
Zadeh N; Bernstein JA; Niemi AK; Dugan S; Kwan A; Liang D; Hyland JC; Hoyme HE; Hudgins L; Manning MA
Am J Med Genet A; 2011 Nov; 155A(11):2661-8. PubMed ID: 21932315
[TBL] [Abstract][Full Text] [Related]
13. Marfan syndrome: An eyesight of syndrome.
Kumar A; Agarwal S
Meta Gene; 2014 Dec; 2():96-105. PubMed ID: 25606393
[TBL] [Abstract][Full Text] [Related]
14. Optimising the mutation screening strategy in Marfan syndrome and identifying genotypes with more severe aortic involvement.
Stengl R; Bors A; Ágg B; Pólos M; Matyas G; Molnár MJ; Fekete B; Csabán D; Andrikovics H; Merkely B; Radovits T; Szabolcs Z; Benke K
Orphanet J Rare Dis; 2020 Oct; 15(1):290. PubMed ID: 33059708
[TBL] [Abstract][Full Text] [Related]
15. Clinical Characteristics of Marfan Syndrome in Korea.
Lim AY; Song JS; Kim EK; Jang SY; Chung TY; Choi SH; Sung K; Huh J; Kang IS; Choe YH; Ki CS; Kim DK
Korean Circ J; 2016 Nov; 46(6):841-845. PubMed ID: 27826344
[TBL] [Abstract][Full Text] [Related]
16. Revised Ghent Criteria is Comparable to Original Diagnostic Criteria for Marfan Syndrome with Increased Ability to Clinically Diagnose Related Disorders.
Penpattharakul W; Pithukpakorn M
J Med Assoc Thai; 2016 Jan; 99(1):34-9. PubMed ID: 27455822
[TBL] [Abstract][Full Text] [Related]
17. Recent molecular biological progress in Marfan syndrome and Marfan-associated disorders.
Gao LG; Luo F; Hui RT; Zhou XL
Ageing Res Rev; 2010 Jul; 9(3):363-8. PubMed ID: 19772952
[TBL] [Abstract][Full Text] [Related]
18. Marfan syndrome.
Milewicz DM; Braverman AC; De Backer J; Morris SA; Boileau C; Maumenee IH; Jondeau G; Evangelista A; Pyeritz RE
Nat Rev Dis Primers; 2021 Sep; 7(1):64. PubMed ID: 34475413
[TBL] [Abstract][Full Text] [Related]
19. Neonatal Marfan Syndrome.
Tognato E; Perona A; Aronica A; Bertola A; Cimminelli L; De Vecchi S; Eshraghy MR; Loperfido B; Vivenza C; Manzoni P
Am J Perinatol; 2019 Jul; 36(S 02):S74-S76. PubMed ID: 31238364
[TBL] [Abstract][Full Text] [Related]
20. Mutation analysis of the FBN1 gene in a cohort of patients with Marfan Syndrome: A 10-year single center experience.
Mannucci L; Luciano S; Salehi LB; Gigante L; Conte C; Longo G; Ferradini V; Piumelli N; Brancati F; Ruvolo G; Novelli G; Sangiuolo F
Clin Chim Acta; 2020 Feb; 501():154-164. PubMed ID: 31730815
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
