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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 diagnosis
Laureano 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 infarction
Margherita 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 correlations
Daniela 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 syndrome
Alessandro Pecci, Ginevra Biino, Tiziana Fierro, et al.
Haematologica
|
July 6, 2019
Eltrombopag for the treatment of inherited thrombocytopenias: a phase II clinical trial
Carlo 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 deficiency
Roberta 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 apoptosis
Vittorio 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 Disease
Eva 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 thrombocytopenia
Daniela De Rocco, Federica Melazzini, Caterina Marconi, et al.
Page
of 13
Search research articles
Search
Showing results (81-90 of 121) with videos related to
Sort By:
Page
of 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 diagnosis
Laureano 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 infarction
Margherita 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 correlations
Daniela 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 syndrome
Alessandro Pecci, Ginevra Biino, Tiziana Fierro, et al.
Haematologica
|
July 6, 2019
Eltrombopag for the treatment of inherited thrombocytopenias: a phase II clinical trial
Carlo 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 deficiency
Roberta 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 apoptosis
Vittorio 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 Disease
Eva 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 thrombocytopenia
Daniela De Rocco, Federica Melazzini, Caterina Marconi, et al.
Page
of 13