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.
139 related articles for article (PubMed ID: 34563317)
1. 50 Years Ago in TheJournal ofPediatrics: Distinguishing Marfan Syndrome and Related Connective Tissue Disorders. Giuffre AM; Giampietro PF J Pediatr; 2021 Oct; 237():124. PubMed ID: 34563317 [No Abstract] [Full Text] [Related]
2. 2006 Curt Stern Award Address. Marfan syndrome: from molecules to medicines. Dietz HC Am J Hum Genet; 2007 Oct; 81(4):662-7. PubMed ID: 20529617 [No Abstract] [Full Text] [Related]
3. [Antonin-Bernard Jean Marfan and Gabrielle]. Léonard JC; Morin C Arch Pediatr; 2008 Jun; 15(5):562-3. PubMed ID: 18582673 [No Abstract] [Full Text] [Related]
4. "New" syndrome of congenital contractural arachnodactyly originally described by Marfan in 1896. Hecht F; Beals RK Pediatrics; 1972 Apr; 49(4):574-9. PubMed ID: 4552107 [No Abstract] [Full Text] [Related]
5. Recent developments in the diagnosis of Marfan syndrome and related disorders. Summers KM; West JA; Hattam A; Stark D; McGill JJ; West MJ Med J Aust; 2012 Nov; 197(9):494-7. PubMed ID: 23121584 [TBL] [Abstract][Full Text] [Related]
6. 50 Years Ago in TheJournal ofPediatrics: When "Chronic Active Hepatitis" Became Autoimmune Hepatitis. Rezvani M J Pediatr; 2021 Jul; 234():204. PubMed ID: 34172160 [No Abstract] [Full Text] [Related]
8. Challenges in the diagnosis of Marfan syndrome. Summers KM; West JA; Peterson MM; Stark D; McGill JJ; West MJ Med J Aust; 2006 Jun; 184(12):627-31. PubMed ID: 16803443 [TBL] [Abstract][Full Text] [Related]
10. [The man behind the syndrome: Antonin Marfan. He introduced the discovery of congenital connective tissue diseases]. Zettergvist P; Brodin LA; Ivert T; Mogensen L Lakartidningen; 1989 Jun; 86(23):2205-6. PubMed ID: 2664382 [No Abstract] [Full Text] [Related]
11. The diagnosis of art: Rachmaninov's hand span. Ramachandran M; Aronson JK J R Soc Med; 2006 Oct; 99(10):529-30. PubMed ID: 17066567 [No Abstract] [Full Text] [Related]
12. Clinical and molecular study of 320 children with Marfan syndrome and related type I fibrillinopathies in a series of 1009 probands with pathogenic FBN1 mutations. Faivre L; Masurel-Paulet A; Collod-Béroud G; Callewaert BL; Child AH; Stheneur C; Binquet C; Gautier E; Chevallier B; Huet F; Loeys BL; Arbustini E; Mayer K; Arslan-Kirchner M; Kiotsekoglou A; Comeglio P; Grasso M; Halliday DJ; Béroud C; Bonithon-Kopp C; Claustres M; Robinson PN; Adès L; De Backer J; Coucke P; Francke U; De Paepe A; Boileau C; Jondeau G Pediatrics; 2009 Jan; 123(1):391-8. PubMed ID: 19117906 [TBL] [Abstract][Full Text] [Related]
13. Haplotype analysis enables the diagnosis of Marfan syndrome. Basel D; Kilpatrick MW; Tsipouras P Conn Med; 2004; 68(6):363-6. PubMed ID: 15266886 [TBL] [Abstract][Full Text] [Related]
14. Guidelines for the diagnosis and management of Marfan syndrome. Ades L; Heart Lung Circ; 2007 Feb; 16(1):28-30. PubMed ID: 17188935 [No Abstract] [Full Text] [Related]
16. Genetic testing of the FBN1 gene in Chinese patients with Marfan/Marfan-like syndrome. Yang H; Luo M; Chen Q; Fu Y; Zhang J; Qian X; Sun X; Fan Y; Zhou Z; Chang Q Clin Chim Acta; 2016 Aug; 459():30-35. PubMed ID: 27234404 [TBL] [Abstract][Full Text] [Related]