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Daniela De Rocco

Showing results (11-20 of 37) with videos related to

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Plos One|November 22, 2013
Fanconi anemia patients are more susceptible to infection with tumor virus SV40Manola Comar, Daniela De Rocco, Enrico Cappelli, et al.
Annals of Hematology|March 12, 2010
MYH9-related disease: Report on five German families and description of a novel mutationAnna Savoia, Manuela Germeshausen, Daniela De Rocco, et al.
Biochimica Et Biophysica Acta|December 12, 2013
Mutations of cytochrome c identified in patients with thrombocytopenia THC4 affect both apoptosis and cellular bioenergeticsDaniela De Rocco, Cristina Cerqua, Paola Goffrini, et al.
Platelets|October 29, 2009
MYH9 related disease: a novel missense Ala95Asp mutation of the MYH9 geneDaniela de Rocco, Paula G Heller, Giorgia Girotto, et al.
Haematologica|December 22, 2010
Clinical and genetic aspects of Bernard-Soulier syndrome: searching for genotype/phenotype correlationsAnna Savoia, Annalisa Pastore, Daniela De Rocco, et al.
European Journal of Haematology|December 17, 2009
MYH9 related disease: four novel mutations of the tail domain of myosin-9 correlating with a mild clinical phenotypeAlessandro Pecci, Emanuele Panza, Daniela De Rocco, et al.
EMBO Molecular Medicine|December 2, 2017
Thrombopoietin mutation in congenital amegakaryocytic thrombocytopenia treatable with romiplostimAlessandro Pecci, Iman Ragab, Valeria Bozzi, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|June 3, 2015
Clinical aspects of Fanconi anemia individuals with the same mutation of FANCF identified by next generation sequencingElena Nicchia, Francesco Benedicenti, Daniela De Rocco, 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.
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.
Pageof 4

Showing results (11-20 of 37) with videos related to

Sort By:
Pageof 4
Plos One|November 22, 2013
Fanconi anemia patients are more susceptible to infection with tumor virus SV40Manola Comar, Daniela De Rocco, Enrico Cappelli, et al.
Annals of Hematology|March 12, 2010
MYH9-related disease: Report on five German families and description of a novel mutationAnna Savoia, Manuela Germeshausen, Daniela De Rocco, et al.
Biochimica Et Biophysica Acta|December 12, 2013
Mutations of cytochrome c identified in patients with thrombocytopenia THC4 affect both apoptosis and cellular bioenergeticsDaniela De Rocco, Cristina Cerqua, Paola Goffrini, et al.
Platelets|October 29, 2009
MYH9 related disease: a novel missense Ala95Asp mutation of the MYH9 geneDaniela de Rocco, Paula G Heller, Giorgia Girotto, et al.
Haematologica|December 22, 2010
Clinical and genetic aspects of Bernard-Soulier syndrome: searching for genotype/phenotype correlationsAnna Savoia, Annalisa Pastore, Daniela De Rocco, et al.
European Journal of Haematology|December 17, 2009
MYH9 related disease: four novel mutations of the tail domain of myosin-9 correlating with a mild clinical phenotypeAlessandro Pecci, Emanuele Panza, Daniela De Rocco, et al.
EMBO Molecular Medicine|December 2, 2017
Thrombopoietin mutation in congenital amegakaryocytic thrombocytopenia treatable with romiplostimAlessandro Pecci, Iman Ragab, Valeria Bozzi, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|June 3, 2015
Clinical aspects of Fanconi anemia individuals with the same mutation of FANCF identified by next generation sequencingElena Nicchia, Francesco Benedicenti, Daniela De Rocco, 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.
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.
Pageof 4