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Extracellular matrix and vascular dynamics in the kidney of a murine model for Marfan syndrome

• Authors : de Souza, Rodrigo Barbosa; Lemes, Renan Barbosa; Foresto-Neto, Orestes

• Source: PLoS ONE. May 9, 2023, Vol. 18 Issue 5, e0285418

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From Neonates to Adults in Marfan Syndrome: Diagnosis, Progress and Transition to Adult Care.

• Authors : Stark, V. C.; Olfe, J.; Doering, K.

Subjects: MARFAN syndrome; MARFAN syndrome treatment; DISEASE progression

• Source: Thoracic & Cardiovascular Surgeon, Supplement; 2018 Supplement 2, Vol. 66, pS111-S138, 28p, 1 Chart

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Coronary involvement in marfan syndrome: The role of electrocardiographically gated computed tomography angiography

• Authors : Donato, Rocco; David, Emanuele; Blandino, Alfredo

• Source: Journal of Cardiovascular Echography. April-June, 2017, Vol. 27 Issue 2, 64

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Bilateral transient pupil closure after iris supported intraocular lens implantation in a case with Marfan syndrome

• Authors : Kara, Necip; Bozkurt, ErcüMent; Yazici, Ahmet

• Source: Middle East African Journal of Ophthalmology. April-June, 2012, Vol. 19 Issue 2, 262

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Pupillary manifestations of Marfan syndrome: from the Marfan eye consortium of Chicago.

• Authors : Shah, Sanket S.¹; Kurup, Sudhi P.^1,2; Ralay Ranaivo, Hantamalala²

Subjects: *MARFAN syndrome; *MEARES-Irlen syndrome; *CHILD patients

• Source: Ophthalmic Genetics. Jun2018, Vol. 39 Issue 3, p297-299. 3p.

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Marfan Syndrome imitates heart attack, early detection is a must.

Subjects: *AORTIC dissection; *MARFAN syndrome treatment; *MARFAN syndromeNEW York (State). Dept. of Health

• Source: Hudson Valley Business Journal. 11/08/99, Vol. 10 Issue 20, p27. 1/4p.

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Missed diagnoses: Clinically relevant lessons learned through medical mysteries solved by the Undiagnosed Diseases Network.

• Authors : Cope, Heidi; Spillmann, Rebecca; Rosenfeld, Jill A.

Subjects: GENETIC testing; GENETIC counseling; PHARMACOGENOMICS

• Source: Molecular Genetics & Genomic Medicine; Oct2020, Vol. 8 Issue 10, p1-17, 17p

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Ocular manifestations of Marfan's syndrome.

• Authors : Waduthantri, Samanthila¹

Subjects: *OCULAR manifestations of general diseases; *MARFAN syndrome; *EARLY diagnosis

• Source: Medical Journal of Dr. D.Y. Patil University. Mae/Apr2017, Vol. 10 Issue 2, p118-119. 2p.

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ADAMTSL4 assessment in ectopia lentis reveals a recurrent founder mutation in Polynesians.

• Authors : van Bysterveldt, Katherine A.; al Taie, Rasha; Ikink, Will

Subjects: MARFAN syndrome; GENETIC mutation; EYE examination

• Source: Ophthalmic Genetics; Dec2017, Vol. 38 Issue 6, p537-543, 7p

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Marfan syndrome: current perspectives.

• Authors : Pepe, Guglielmina; Giusti, Betti; Sticchi, Elena

Subjects: MARFAN syndrome; CONNECTIVE tissue diseases; MULTIDRUG resistance

• Source: Application of Clinical Genetics; May2016, Vol. 9, p55-65, 11p

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