Maurizia Grasso - Concepedia

Author

Maurizia Grasso

Istituti di Ricovero e Cura a Carattere Scientifico ORCID

Also Known As

Boezeman, EHJF, Francesco Montorsi, G Parenti, Grasso Maurizia, Grasso, Maurizia, M GRASSO, M Grasso, M. GRASSO, M. Grasso, Marco Grasso

186

Publications

6.2K

Citations

H-Index

Concepts

All Affiliations

Istituti di Ricovero e Cura a Carattere Scientifico University of Pavia Policlinico San Matteo Fondazione University of Milan Assistance Publique – Hôpitaux de Paris

About

Maurizia Grasso is an author at Istituti di Ricovero e Cura a Carattere Scientifico specializing in medicine, cardiology, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	22	30	2.3K
2	Public Health	6	6	760
3	Social Sciences	2	2	96
4	Engineering	1	1	10
5	Natural Sciences	1	1	49

Maurizia Grasso

Publications

Citations

H-Index

Page 1

	Year	Citations
Atlas of the clinical genetics of human dilated cardiomyopathy Jan Haas, Karen Frese, Barbara Peil, European Heart Journal	2014	556
Long-Term Outcome and Risk Stratification in Dilated Cardiolaminopathies Michele Pasotti, Catherine Klersy, Andrea Pilotto, Journal of the American College of Cardiology Heart FailureCardiovascular DiseaseAtherosclerosisAcute Myocardial InfarctionPublic Health	2008	387
Autosomal dominant dilated cardiomyopathy with atrioventricular block: a lamin A/C defect-related disease Eloisa Arbustini, Andrea Pilotto, Alessandra Repetto, Journal of the American College of Cardiology Autosomal DominantCardiomyopathyHeart FailureStructural Heart DiseaseCardiovascular Disease	2002	357
Mitochondrial DNA Mutations and Mitochondrial Abnormalities in Dilated Cardiomyopathy Eloisa Arbustini, Marta Diegoli, Roberta Fasani, American Journal Of Pathology	1998	238
Desmin Accumulation Restrictive Cardiomyopathy and Atrioventricular Block Associated with Desmin Gene Defects Eloisa Arbustini, Michele Pasotti, Andrea Pilotto, European Journal of Heart Failure	2005	184
Clinical and Molecular Study of 320 Children With Marfan Syndrome and Related Type I Fibrillinopathies in a Series of 1009 Probands With Pathogenic <i>FBN1</i> Mutations Laurence Faivre, Alice Masurel‐Paulet, Gwenaëlle Collod‐Béroud, PEDIATRICS GeneticsGenetic EpidemiologyPathologyMolecular GeneticsRelated Type	2008	173
Hereditary Hyperferritinemia-Cataract Syndrome: Relationship Between Phenotypes and Specific Mutations in the Iron-Responsive Element of Ferritin Light-Chain mRNA Mario Cazzola, Gaetano Bergamaschi, Laura Tonon, Blood	1997	159
Coronary atherosclerotic plaques with and without thrombus in ischemic heart syndromes: A morphologic, immunohistochemical, and biochemical study Eloisa Arbustini, Maurizia Grasso, Marta Diegoli, The American Journal of Cardiology ThrombosisVascular DiseaseCoronary Atherosclerotic PlaquesCardiovascular DiseasePathology	1991	159
Gender-Specific Differences in Major Cardiac Events and Mortality in Lamin A/C Mutation Carriers Ingrid A.W. van Rijsingen, Eline A. Nannenberg, Eloisa Arbustini, European Journal of Heart Failure	2012	143
Restrictive Cardiomyopathy, Atrioventricular Block and Mild to Subclinical Myopathy in Patients With Desmin-Immunoreactive Material Deposits Eloisa Arbustini, Patrizia Morbini, Maurizia Grasso, Journal of the American College of Cardiology CardiomyopathyHeart FailurePathologyDesmin-immunoreactive Material DepositsRestrictive Cardiomyopathy	1998	122

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