ARBUSTINI E

Last name: ARBUSTINI E

1998 (v1)

Publication

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Evolution of childhood central diabetes insipidus into panhypopituitarism with a large hypothalamic mass: is 'lymphocytic infundibuloneurohypophysitis' in children a different entity?

MAGHNIE, MOHAMAD Genovese E Sommaruga MG

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Uploaded on: April 14, 2023
2020 (v1)

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Clinical outcomes of calcified nodules detected by optical coherence tomography: a sub-analysis of the CLIMA study

Prati F Gatto L Fabbiocchi F

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Uploaded on: February 14, 2024
2005 (v1)

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Identification of sixty-two novel and twelve known FBN1 mutations in eighty-one unrelated probands with Marfan syndrome and other fibrillinopathies.

Arbustini E Grasso M Ansaldi S

Marfan Syndrome (MFS) is an autosomal dominant disorder of the connective tissue due to mutations of Fibrillin-1 gene (FBN1) in more than 90% of cases and Transforming Growth Factor-Beta-Receptor2 gene (TGFB2R) in a minority of cases. Genotyping is relevant for diagnosis and genotype-phenotype correlations. We describe the FBN1 genotypes and...

Uploaded on: April 14, 2023
2014 (v1)

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Comprehensive overview of definitions for optical coherence tomography-based plaque and stent analyses

Di Vito L Yoon JH Kato K

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Uploaded on: May 13, 2023
2021 (v1)

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Prevalence and quantitative assessment of macrophages in coronary plaques

Gatto L Paoletti G Marco V

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Uploaded on: February 14, 2024
2020 (v1)

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Relationship between coronary plaque morphology of the left anterior descending artery and 12 months clinical outcome: the CLIMA study

Prati F Romagnoli E Gatto L

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Uploaded on: February 14, 2024

ARBUSTINI E

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