Concepedia

Author

Wilma Barcellini

Fondazione IRCCS Ca' Granda Ospedale Maggiore PoliclinicoORCID

Also Known As

Austin G Kulasekararaj, Barcellini Wilma, Barcellini, W., Barcellini,Wilma, Erfan Nur, W BARCELLINI, W Barcellini, W. BARCELLINI, W. Barcellini, WILMA BARCELLINI

555

Publications

11.9K

Citations

58

H-Index

149

Concepts

All Affiliations

Fondazione IRCCS Ca' Granda Ospedale Maggiore PoliclinicoUniversity of MilanOspedale MaggioreIstituti di Ricovero e Cura a Carattere ScientificoIRCCS Istituto Auxologico Italiano
WB

About

Wilma Barcellini is an author at Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico specializing in medicine, immunology, and autoimmunity.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

31

63

2.7K

2

Health Sciences

15

17

930

3

Public Health

2

2

46

4

Natural Sciences

1

1

39

5

Social Sciences

1

1

24

Wilma Barcellini

×

143

Publications

6.8K

Citations

45

H-Index

YearCitations

Clinical heterogeneity and predictors of outcome in primary autoimmune hemolytic anemia: a GIMEMA study of 308 patients

Wilma Barcellini, Bruno Fattizzo, Anna Zaninoni,

Blood

2014

359

Eltrombopag Added to Immunosuppression in Severe Aplastic Anemia

Régis Peffault de Latour, Austin Kulasekararaj, Simona Iacobelli,

New England Journal of Medicine

2022

265

Recommendations regarding splenectomy in hereditary hemolytic anemias

Achille Iolascon, Immacolata Andolfo, Wilma Barcellini,

Haematologica

2017

206

Sutimlimab in Cold Agglutinin Disease

Alexander Röth, Wilma Barcellini, Shirley D’Sa,

New England Journal of Medicine

2021

198

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

2009

174

TH1 and TH2 cytokine production by peripheral blood mononuclear cells from HIV-infected patients

Wilma Barcellini, Gian Paolo Rizzardi, Maria Orietta Borgh,

AIDS

1994

162

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

Cold agglutinin disease revisited: a multinational, observational study of 232 patients

Sigbjørn Berentsen, Wilma Barcellini, Shirley D’Sa,

Blood

2020

155

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