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Isabella Ceccherini

Showing results (161-170 of 180) with videos related to

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The Journal of Rheumatology|September 17, 2017
Cryopyrin-associated Periodic Syndromes in Italian Patients: Evaluation of the Rate of Somatic NLRP3 Mosaicism and Phenotypic CharacterizationDenise Lasigliè, Anna Mensa-Vilaro, Denise Ferrera, et al.
Molecular Medicine (Cambridge, Mass.)|May 27, 2026
Machine learning, whole genome sequencing, and Mendelian randomization support a role of CRP on COVID-19 severityFrancesca Lantieri, Stefania Croci, Sergio Decherchi, et al.
Hemasphere|February 27, 2023
Autoimmune Lymphoproliferative Syndrome (ALPS) Disease and ALPS Phenotype: Are They Two Distinct Entities?Elena Palmisani, Maurizio Miano, Alice Grossi, et al.
Hemasphere|January 14, 2026
Application of machine learning in the diagnostic work-up of telomere biology disordersErika Massaccesi, Luca Arcuri, Giacomo Cavalca, et al.
Frontiers in Immunology|April 5, 2021
Spectrum of Systemic Auto-Inflammatory Diseases in India: A Multi-Centric ExperienceDeepti Suri, Amit Rawat, Ankur Kumar Jindal, et al.
Annals of the Rheumatic Diseases|May 20, 2017
ADA2 deficiency (DADA2) as an unrecognised cause of early onset polyarteritis nodosa and stroke: a multicentre national studyRoberta Caorsi, Federica Penco, Alice Grossi, et al.
American Journal of Human Genetics|April 4, 2015
Functional loss of semaphorin 3C and/or semaphorin 3D and their epistatic interaction with ret are critical to Hirschsprung disease liabilityQian Jiang, Stacey Arnold, Tiffany Heanue, et al.
American Journal of Human Genetics|July 6, 2010
Differential contributions of rare and common, coding and noncoding Ret mutations to multifactorial Hirschsprung disease liabilityEileen Sproat Emison, Merce Garcia-Barcelo, Elizabeth A Grice, et al.
Gastroenterology|December 14, 2011
CLMP is required for intestinal development, and loss-of-function mutations cause congenital short-bowel syndromeChristine S Van Der Werf, Tara D Wabbersen, Nai-Hua Hsiao, et al.
Blood Advances|November 18, 2020
Late-onset and long-lasting autoimmune neutropenia: an analysis from the Italian Neutropenia RegistryFrancesca Fioredda, Gioacchino Andrea Rotulo, Piero Farruggia, et al.
Pageof 18

Showing results (161-170 of 180) with videos related to

Sort By:
Pageof 18
The Journal of Rheumatology|September 17, 2017
Cryopyrin-associated Periodic Syndromes in Italian Patients: Evaluation of the Rate of Somatic NLRP3 Mosaicism and Phenotypic CharacterizationDenise Lasigliè, Anna Mensa-Vilaro, Denise Ferrera, et al.
Molecular Medicine (Cambridge, Mass.)|May 27, 2026
Machine learning, whole genome sequencing, and Mendelian randomization support a role of CRP on COVID-19 severityFrancesca Lantieri, Stefania Croci, Sergio Decherchi, et al.
Hemasphere|February 27, 2023
Autoimmune Lymphoproliferative Syndrome (ALPS) Disease and ALPS Phenotype: Are They Two Distinct Entities?Elena Palmisani, Maurizio Miano, Alice Grossi, et al.
Hemasphere|January 14, 2026
Application of machine learning in the diagnostic work-up of telomere biology disordersErika Massaccesi, Luca Arcuri, Giacomo Cavalca, et al.
Frontiers in Immunology|April 5, 2021
Spectrum of Systemic Auto-Inflammatory Diseases in India: A Multi-Centric ExperienceDeepti Suri, Amit Rawat, Ankur Kumar Jindal, et al.
Annals of the Rheumatic Diseases|May 20, 2017
ADA2 deficiency (DADA2) as an unrecognised cause of early onset polyarteritis nodosa and stroke: a multicentre national studyRoberta Caorsi, Federica Penco, Alice Grossi, et al.
American Journal of Human Genetics|April 4, 2015
Functional loss of semaphorin 3C and/or semaphorin 3D and their epistatic interaction with ret are critical to Hirschsprung disease liabilityQian Jiang, Stacey Arnold, Tiffany Heanue, et al.
American Journal of Human Genetics|July 6, 2010
Differential contributions of rare and common, coding and noncoding Ret mutations to multifactorial Hirschsprung disease liabilityEileen Sproat Emison, Merce Garcia-Barcelo, Elizabeth A Grice, et al.
Gastroenterology|December 14, 2011
CLMP is required for intestinal development, and loss-of-function mutations cause congenital short-bowel syndromeChristine S Van Der Werf, Tara D Wabbersen, Nai-Hua Hsiao, et al.
Blood Advances|November 18, 2020
Late-onset and long-lasting autoimmune neutropenia: an analysis from the Italian Neutropenia RegistryFrancesca Fioredda, Gioacchino Andrea Rotulo, Piero Farruggia, et al.
Pageof 18