Results 201 to 210 of about 2,210,543 (259)

A case of aortic root replacement for acute type A dissection in Marfan syndrome with twin pregnancy. [PDF]

Interdiscip Cardiovasc Thorac Surg
Yang Y, Jia B, Li C, Zhu J.
europepmc   +1 more source

Characterization of pain, disability, and psychological burden in Marfan syndrome

American Journal of Medical Genetics. Part A, 2017
T. Speed, V. Mathur, M. Hand, B. Christensen, P. Sponseller, K. Williams, C. Campbell   +6 more
semanticscholar   +1 more source

Endovascular treatment of a giant arteria lusoria aneurysm in a young female with Marfan syndrome. [PDF]

BJR Case Rep
Fraund-Cremer S, Rusch R, Uebing A, Voges I, Schäfer P.   +4 more
europepmc   +1 more source

A novel missense variant of <i>FBN1</i> gene in a Sardinian family with Marfan syndrome: a case report. [PDF]

Front Pediatr
Marsan M, Brutti M, Meloni F, Marica M, Soddu C, Lai F, Martorana D, Savasta S.   +7 more
europepmc   +1 more source

Unexpected Tracheomalacia in Marfan Syndrome During General Anesthesia for Correction of Scoliosis

, 2002
Ah Young Oh, Yang Hyun Kim, Bo Kyung Kim, Hee‐Soo Kim, Chong Sung Kim   +4 more
openalex   +1 more source

A Case of a Short Stature Patient With Marfan Syndrome: A Tale of Wide Mediastinum. [PDF]

Cureus
Hegazy Y, Abdallah A, Salem A, Assaker A, Elmogy A.   +4 more
europepmc   +1 more source

Corneal Biomechanics Are Associated With FBN1 Mutations in Patients With Marfan Syndrome and Ectopia Lentis. [PDF]

Invest Ophthalmol Vis Sci
Huo QY, Zhang RZ, Jia WN, Wang YL, Shen X, Chen XY, Chen TH, Liu Y, Song LH, Wang X, Lv Y, Chen ZX, Jiang YX.   +12 more
europepmc   +1 more source

Allelic variation in normal human FBN1 expression in a family with Marfan syndrome: a potential modifier of phenotype?

, 2003
Sarah Hutchinson
openalex   +1 more source

The Reclassification of a <i>FBN1</i> Variant of Unknown Significance Associated With Marfan Syndrome Through Careful Clinical Correlation and Family-Based Evaluation. [PDF]

Case Rep Med
Bouhamdani D, Allain V, Bouhamdani N, Ben Amor M.   +3 more
europepmc   +1 more source

Identification and functional validation of a novel FBN1 variant in a Marfan syndrome family using a zebrafish model. [PDF]

BMC Genomics
Huang S, Chen J, Wang Q, Zhang R, Zhuang J, Huang R, Yu C, Fang M, Zhao H, Lei L.   +9 more
europepmc   +1 more source