Amelia Morrone - Concepedia

Author

Amelia Morrone

University of Florence ORCID

Also Known As

A Morrone, A. Luigi Morrone, A. MORRONE, A. Morrone, Amelia Morrone, Antima Morrone, D. Sperlì, E Zammarchi

192

Publications

Citations

H-Index

127

Concepts

All Affiliations

University of Florence Meyer Children's Hospital Azienda Ospedaliera San Gerardo Istituti di Ricovero e Cura a Carattere Scientifico Istituto Giannina Gaslini

About

Amelia Morrone is an author at University of Florence specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	24	39	1.4K
2	Natural Sciences	6	6	175
3	Public Health	4	4	121
4	Engineering	3	3	95
5	Health Sciences	3	3	181

Amelia Morrone

Publications

4.1K

Citations

H-Index

Page 1

	Year	Citations
Senescence‐associated β‐galactosidase is lysosomal β‐galactosidase Bo Yun Lee, Jung A Han, Jun Sub Im, Aging Cell	2006	1.4K
GM1 gangliosidosis and Morquio B disease: An update on genetic alterations and clinical findings Anna Caciotti, Scott C. Garman, Yadilette Rivera-Colón, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease GeneticsGenetic EpidemiologyImmunologyPathologyMorquio B Disease	2011	151
Coronary Microvascular Dysfunction is an Early Feature of Cardiac Involvement in Patients with Anderson–Fabry Disease Benedetta Tomberli, Franco Cecchi, Roberto Sciagrà, European Journal of Heart Failure	2013	74
RNA metabolism in myotonic dystrophy: patient muscle shows decreased insulin receptor RNA and protein consistent with abnormal insulin resistance. Amelia Morrone, Elena Pegoraro, C. Angelini, Journal of Clinical Investigation GeneticsProtein Kinase GeneTotal RnaDisease Gene IdentificationInsulin Signaling	1997	74
Fabry disease: molecular studies in Italian patients and X inactivation analysis in manifesting carriers Amelia Morrone Journal of Medical Genetics Heart FailureAnderson-fabry DiseaseGeneticsPathologyStructural Heart Disease	2003	71
?-galactosidase gene mutations affecting the lysosomal enzyme and the elastin-binding protein in GM1-gangliosidosis patients with cardiac involvement Amelia Morrone, Tiziana Bardelli, Maria Alice Donati, Human Mutation	2000	66
Hypocitrullinemia in expanded newborn screening by LC–MS/MS is not a reliable marker for ornithine transcarbamylase deficiency Catia Cavicchi, Sabrina Malvagia, Giancarlo la Marca, Journal of Pharmaceutical and Biomedical Analysis Expanded Newborn ScreeningReliable MarkerHematologyPediatricsPathology	2009	60
Molecular testing of 163 patients with Morquio A (Mucopolysaccharidosis IVA) identifies 39 novel GALNS mutations Amelia Morrone, Karen Tylee, Moeenaldeen AlSayed, Molecular Genetics and Metabolism	2014	56
Intrafamilial phenotypic variability in four families with Anderson‐Fabry disease Miriam Rigoldi, Daniela Concolino, Amelia Morrone, Clinical Genetics	2013	53
Human Acid β‐Glucosidase Inhibition by Carbohydrate Derived Iminosugars: Towards New Pharmacological Chaperones for Gaucher Disease Camilla Parmeggiani, Serena Catarzi, Camilla Matassini, ChemBioChem	2015	53

Page 1