Results 161 to 170 of about 23,678,950 (225)

Neonatal Marfan syndrome: a case report of a novel fibrillin 1 mutation, with genotype-phenotype correlation and brief review of the literature. [PDF]

open access: yesItal J Pediatr
Pugnaloni F   +8 more
europepmc   +1 more source

Knockdown of fibrillin-1 suppresses retina-blood barrier dysfunction by inhibiting vascular endothelial apoptosis under diabetic conditions. [PDF]

open access: yesInt J Ophthalmol
Zhang Y   +10 more
europepmc   +1 more source

Relationship between fibrillin-1 genotype and severity of cardiovascular involvement in Marfan syndrome

open access: yesHeart, 2017
R. Franken   +9 more
semanticscholar   +1 more source

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