Concepedia

Author

Emanuela Pappalardo

University of MilanORCID

Also Known As

E Pappalardo, E. Pappalardo, Emanuela Maria Pappalardo, Emanuela Pappalardo

49

Publications

1.6K

Citations

18

H-Index

44

Concepts

All Affiliations

University of MilanFondazione IRCCS Ca' Granda Ospedale Maggiore PoliclinicoIstituti di Ricovero e Cura a Carattere ScientificoEginition HospitalMcMaster University
EP

About

Emanuela Pappalardo is an author at University of Milan specializing in medicine, pathology, and vascular biology.

Top Concepts

#ConceptH-IndexPublicationsCitations

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Medicine

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Arts

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3

Health Sciences

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Public Health

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Emergency Medicine

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Emanuela Pappalardo

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21

Publications

1.3K

Citations

16

H-Index

YearCitations

Frequent de novo mutations and exon deletions in the C1inhibitor gene of patients with angioedema

Emanuela Pappalardo, Marco Cicardi, Christiane Duponchel,

Journal of Allergy and Clinical Immunology

2000

244

Angioedema without urticaria: a large clinical survey

Lorenza C. Zingale, L. Beltrami, Andrea Zanichelli,

Canadian Medical Association Journal

2006

213

Risk factors for thrombophilia in extrahepatic portal vein obstruction†

Massimo Primignani, Ida Martinelli, Paolo Bucciarelli,

Hepatology

2005

206

Mutation screening of C1 inhibitor gene in 108 unrelated families with hereditary angioedema: Functional and structural correlates

Emanuela Pappalardo, Sonia Caccia, Chiara Suffritti,

Molecular Immunology

2008

128

Platelet to Lymphocyte Ratio and Neutrophil to Lymphocyte Ratio as Risk Factors for Venous Thrombosis

Andrea Artoni, Maria Abbattista, Paolo Bucciarelli,

Clinical and Applied Thrombosis/Hemostasis

2017

71

Increased expression of C1-inhibitor mRNA in patients with hereditary angioedema treated with Danazol

Emanuela Pappalardo, Lorenza C. Zingale, Marco Cicardi

Immunology Letters

2003

67

Risk factors for idiopathic sudden sensorineural hearing loss and their association with clinical outcome

Serena M. Passamonti, Federica Di Berardino, Paolo Bucciarelli,

Thrombosis Research

2015

67

Next‐generation sequencing study finds an excess of rare, coding single‐nucleotide variants of ADAMTS13 in patients with deep vein thrombosis

Luca A. Lotta, Giacomo Tuana, Jin Yu,

Journal of Thrombosis and Haemostasis

2013

54

Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genes

Luca A. Lotta, Mark L. Wang, Jin Yu,

BMC Medical Genomics

2012

39

C1 inhibitor gene expression in patients with hereditary angioedema: Quantitative evaluation by means of real-time RT-PCR

Emanuela Pappalardo, Lorenza C. Zingale, Marco Cicardi

Journal of Allergy and Clinical Immunology

2004

36

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