Elisa Fermo - Concepedia

Author

Elisa Fermo

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico ORCID

Also Known As

E Fermo, E. Fermo, Elisa Fermo, Fermo, E., Fermo, Elisa

166

Publications

3.5K

Citations

H-Index

Concepts

All Affiliations

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico Ospedale Maggiore University of Milan Istituti di Ricovero e Cura a Carattere Scientifico University Medical Center Utrecht

About

Elisa Fermo is an author at Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico specializing in medicine, pathology, and hematology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	21	23	1K
2	Health Sciences	5	5	242
3	Natural Sciences	5	5	197
4	Engineering	1	1	37
5	Public Health	1	1	29

Elisa Fermo

Publications

2.3K

Citations

H-Index

Page 1

	Year	Citations
Diagnostic power of laboratory tests for hereditary spherocytosis: a comparison study in 150 patients grouped according to molecular and clinical characteristics Paola Bianchi, Elisa Fermo, Cristina Vercellati, Haematologica	2011	174
Congenital dyserythropoietic anemia type II (CDAII) is caused by mutations in the<i>SEC23B</i>gene Paola Bianchi, Elisa Fermo, Cristina Vercellati, Human Mutation Red Blood CellGenetic DisorderGeneticsInherited Metabolic DiseaseHematology	2009	174
Clinical and hematologic features of 300 patients affected by hereditary spherocytosis grouped according to the type of the membrane protein defect Marcello Mariani, Wilma Barcellini, Cristina Vercellati, Haematologica	2008	161
Clinical spectrum of pyruvate kinase deficiency: data from the Pyruvate Kinase Deficiency Natural History Study Rachael F. Grace, Paola Bianchi, Eduard J. van Beers, Blood	2018	161
<i>RAS</i> Mutations Contribute to Evolution of Chronic Myelomonocytic Leukemia to the Proliferative Variant Clara Ricci, Elisa Fermo, Stefania Corti, Clinical Cancer Research	2010	136
Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiency Paola Bianchi, Elisa Fermo, Bertil Glader, American Journal of Hematology Diagnostic WorkflowPyruvate Kinase DeficiencyDiagnosisPathologyDiagnostic Guidelines	2018	88
Molecular Insights on Pathogenic Effects of Mutations Causing Phosphoglycerate Kinase Deficiency Laurent R. Chiarelli, Simone M. Morera, Paola Bianchi, PLoS ONE Clinical SymptomsGeneticsPathologyMolecular BiologyMolecular Genetics	2012	80
‘Gardos Channelopathy’: a variant of hereditary Stomatocytosis with complex molecular regulation Elisa Fermo, Anna Bogdanova, Polina Petkova‐Kirova, Scientific Reports	2017	80
Use of Laser Assisted Optical Rotational Cell Analyzer (LoRRca MaxSis) in the Diagnosis of RBC Membrane Disorders, Enzyme Defects, and Congenital Dyserythropoietic Anemias: A Monocentric Study on 202 Patients Anna Zaninoni, Elisa Fermo, Cristina Vercellati, Frontiers in Physiology	2018	76
The Significance of Bone Marrow Biopsy and<i>JAK2</i><i><sup>V617F</sup></i>Mutation in the Differential Diagnosis Between the “Early” Prepolycythemic Phase of Polycythemia Vera and Essential Thrombocythemia Umberto Gianelli, Alessandra Iurlo, Claudia Vener, American Journal of Clinical Pathology Essential ThrombocythemiaImmunologyBlood CellPathologyHypercellular Bone Marrow	2008	67

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