Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Alessandro Pecci

Showing results (81-90 of 121) with videos related to

Pageof 13
Sort By:
British Journal of Haematology|October 8, 2024
Two novel families with RUNX1 variants indicate glycine 168 as a new mutational hotspot: Implications for FPD/AML diagnosisLaureano J Kamiya, Serena Barozzi, Federica Isidori, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 25, 2002
Genetics, clinical and pathological features of glomerulonephritis associated with mutations of nonmuscle myosin IIA (Fechtner syndrome)Gian Marco Ghiggeri, Gianluca Caridi, Umberto Magrini, et al.
Blood|September 4, 2004
Increased circulating hematopoietic and endothelial progenitor cells in the early phase of acute myocardial infarctionMargherita Massa, Vittorio Rosti, Maurizio Ferrario, et al.
European Journal of Medical Genetics|November 6, 2012
MYH9-related disease: five novel mutations expanding the spectrum of causative mutations and confirming genotype/phenotype correlationsDaniela De Rocco, Barbara Zieger, Helen Platokouki, et al.
Plos One|May 5, 2012
Alteration of liver enzymes is a feature of the MYH9-related disease syndromeAlessandro Pecci, Ginevra Biino, Tiziana Fierro, et al.
Haematologica|July 6, 2019
Eltrombopag for the treatment of inherited thrombocytopenias: a phase II clinical trialCarlo Zaninetti, Paolo Gresele, Antonella Bertomoro, et al.
Haematologica|October 27, 2012
Correlation between platelet phenotype and NBEAL2 genotype in patients with congenital thrombocytopenia and α-granule deficiencyRoberta Bottega, Alessandro Pecci, Erica De Candia, et al.
Autophagy|July 20, 2022
Lack of COL6/collagen VI causes megakaryocyte dysfunction by impairing autophagy and inducing apoptosisVittorio Abbonante, Alessandro Malara, Martina Chrisam, et al.
Ear and Hearing|July 31, 2015
Nonmuscle Myosin Heavy Chain IIA Mutation Predicts Severity and Progression of Sensorineural Hearing Loss in Patients With MYH9-Related DiseaseEva J J Verver, Vedat Topsakal, Henricus P M Kunst, et al.
American Journal of Hematology|February 28, 2017
Mutations of RUNX1 in families with inherited thrombocytopeniaDaniela De Rocco, Federica Melazzini, Caterina Marconi, et al.
Pageof 13

Showing results (81-90 of 121) with videos related to

Sort By:
Pageof 13
British Journal of Haematology|October 8, 2024
Two novel families with RUNX1 variants indicate glycine 168 as a new mutational hotspot: Implications for FPD/AML diagnosisLaureano J Kamiya, Serena Barozzi, Federica Isidori, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 25, 2002
Genetics, clinical and pathological features of glomerulonephritis associated with mutations of nonmuscle myosin IIA (Fechtner syndrome)Gian Marco Ghiggeri, Gianluca Caridi, Umberto Magrini, et al.
Blood|September 4, 2004
Increased circulating hematopoietic and endothelial progenitor cells in the early phase of acute myocardial infarctionMargherita Massa, Vittorio Rosti, Maurizio Ferrario, et al.
European Journal of Medical Genetics|November 6, 2012
MYH9-related disease: five novel mutations expanding the spectrum of causative mutations and confirming genotype/phenotype correlationsDaniela De Rocco, Barbara Zieger, Helen Platokouki, et al.
Plos One|May 5, 2012
Alteration of liver enzymes is a feature of the MYH9-related disease syndromeAlessandro Pecci, Ginevra Biino, Tiziana Fierro, et al.
Haematologica|July 6, 2019
Eltrombopag for the treatment of inherited thrombocytopenias: a phase II clinical trialCarlo Zaninetti, Paolo Gresele, Antonella Bertomoro, et al.
Haematologica|October 27, 2012
Correlation between platelet phenotype and NBEAL2 genotype in patients with congenital thrombocytopenia and α-granule deficiencyRoberta Bottega, Alessandro Pecci, Erica De Candia, et al.
Autophagy|July 20, 2022
Lack of COL6/collagen VI causes megakaryocyte dysfunction by impairing autophagy and inducing apoptosisVittorio Abbonante, Alessandro Malara, Martina Chrisam, et al.
Ear and Hearing|July 31, 2015
Nonmuscle Myosin Heavy Chain IIA Mutation Predicts Severity and Progression of Sensorineural Hearing Loss in Patients With MYH9-Related DiseaseEva J J Verver, Vedat Topsakal, Henricus P M Kunst, et al.
American Journal of Hematology|February 28, 2017
Mutations of RUNX1 in families with inherited thrombocytopeniaDaniela De Rocco, Federica Melazzini, Caterina Marconi, et al.
Pageof 13