Rita Clementi - Concepedia

Author

Rita Clementi

Istituti di Ricovero e Cura a Carattere Scientifico

Also Known As

R CLEMENTI, R Clementi, R. Clementi, Rita Clementi

Publications

1.4K

Citations

H-Index

Concepts

All Affiliations

Istituti di Ricovero e Cura a Carattere Scientifico University of Pavia Policlinico San Matteo Fondazione Università degli Studi del Piemonte Orientale “Amedeo Avogadro”Sapienza University of Rome

About

Rita Clementi is an author at Istituti di Ricovero e Cura a Carattere Scientifico specializing in immunology, medicine, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	224
2	Immunology	6	6	224
3	Health Sciences	3	3	100
4	Cell Biology	3	3	64
5	Neurology	1	1	42

Rita Clementi

Publications

1.1K

Citations

H-Index

Page 1

	Year	Citations
A proportion of patients with lymphoma may harbor mutations of the perforin gene Rita Clementi Blood	2005	184
SAP controls the cytolytic activity of CD8+ T cells against EBV-infected cells Grazia Andolfi, Stuart G. Tangye, Rita Clementi, Blood	2005	176
Hemophagocytic lymphohistiocytosis due to germline mutations inSH2D1A, the X-linked lymphoproliferative disease gene Maurizio Aricò, Shinsaku Imashuku, Rita Clementi, Blood	2001	161
Familial hemophagocytic lymphohistiocytosis: how late can the onset be? Michaela Allen, Carmela Fusco, Frédéric Legrand, PubMed	2001	80
Haemophagocytic lymphohistiocytosis: proposal of a diagnostic algorithm based on perforin expression Maurizio Aricò, Michaela Allen, Simona Brusa, British Journal of Haematology	2002	74
Inherited Perforin and<i>Fas</i>Mutations in a Patient with Autoimmune Lymphoproliferative Syndrome and Lymphoma Rita Clementi, Lorenzo Dagna, Umberto Dianzani, New England Journal of Medicine ImmunodeficienciesGeneticsImmunologyPathologyDisease Gene Identification	2004	70
Variations of the perforin gene in patients with autoimmunity/lymphoproliferation and defective Fas function Rita Clementi, Annalisa Chiocchetti, Giuseppe Cappellano, Blood	2006	62
Atypical features of familial hemophagocytic lymphohistiocytosis Rosanna Busiello, Marsilio Adriani, Franco Locatelli, Blood	2004	55
Patients of African ancestry with hemophagocytic lymphohistiocytosis share a common haplotype of PRF1 with a 50delT mutation Susan Molleran Lee, János Sümegi, Joyce Villanueva, The Journal of Pediatrics Common HaplotypeImmunohematologyAfrican AncestryGenetic EpidemiologyImmunology	2006	48
Variations of the perforin gene in patients with multiple sclerosis Giuseppe Cappellano, Elisabetta Orilieri, Cristoforo Comi, Genes and Immunity Neurodegenerative DiseasesAutoimmune DiseaseNeurological DisorderMedicineImmunology	2008	42

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