Results 241 to 250 of about 2,218,154 (303)

Emergency 33-Week Cesarean Section With 3.4 cm Type A Aortic Dissection Repair in a Patient With Marfan Syndrome: A Multidisciplinary Approach. [PDF]

Cureus
Jones A, Bcharah G, Islam N, Pan H, Smiley S.   +4 more
europepmc   +1 more source

Asymptomatic aortic dissection in Marfan syndrome

, 2002
Tom Wong
openalex   +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

Developing a more accurate population frequency of Marfan syndrome from predicted pathogenic FBN1 variants in the gnomAD cohorts. [PDF]

Sci Rep
Choi K, Huang M, Savige J.
europepmc   +1 more source

FBN1: The disease-causing gene for Marfan syndrome and other genetic disorders.

Gene, 2016
L. Sakai, D. Keene, M. Renard, J. De Backer   +3 more
semanticscholar   +1 more source

Looking for the missing links : challenges in the search for genotype-phenotype correlation in Marfan syndrome

, 2018
Campens, Laurence, De Backer, Julie, Muiño Mosquera, Laura   +2 more
core   +1 more source

Functional analysis of a novel <i>FBN1</i> deep intronic variant causing Marfan syndrome in a Chinese patient. [PDF]

Front Genet
Wang Q, Zhang F, Zhou X, Li H, Zhao J, Yuan H.   +5 more
europepmc   +1 more source

Differential Oral Microbiota and Serum Cytokine Signatures in Age-Grouped Patients with Marfan Syndrome. [PDF]

Biomedicines
Ordaz-Robles ER, Soto ME, Hernández-Ruiz P, Escalona-Montaño AR, Constantino-Jonapa LA, Amedei A, Aguirre-García MM.   +6 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