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Maria Lombardi

Showing results (31-40 of 108) with videos related to

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Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|October 26, 2005
Confirmation of the value of a modified long-distance polymerase chain reaction in the detection of inversion intron 22 in severe hemophilia a: a technical noteAnna Maria Lombardi, Laura Cabrio, Ezio Zanon, et al.
Cardiovascular & Hematological Disorders Drug Targets|September 12, 2017
Congenital FX Deficiency Rio Tercero: A New Heterozygous Missense Mutation (Cys241Gly) with a Potentiating Effect by a Polymorphism (c. 503-57C>T)Antonio Girolami, Salvador Minoldo, Silvia Ferrari, et al.
Acta Haematologica|January 21, 2006
Pregnancy and oral contraceptives in congenital bleeding disorders of the vitamin K-dependent coagulation factorsAntonio Girolami, Maria Luigia Randi, Elisabetta Ruzzon, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 30, 2003
A novel type I factor X variant (factor X Cys350Phe) due to loss of a disulfide bond in the catalytic domainFabrizio Vianello, Anna Maria Lombardi, Federico Dal Bello, et al.
Thrombosis Research|November 5, 2002
Conformation sensitive gel electrophoresis for detection of factor X gene mutationsFabrizio Vianello, Anna Maria Lombardi, Federico Dal Bello, et al.
Thrombosis and Haemostasis|December 4, 2003
Severe prekallikrein (Fletcher factor) deficiency due to a compound heterozygosis (383Trp stop codon and Cys529Tyr)Anna Maria Lombardi, Maria Teresa Sartori, Laura Cabrio, et al.
World Journal of Clinical Oncology|June 30, 2021
Long-term complete response in metastatic poorly-differentiated neuroendocrine rectal carcinoma with a multimodal approach: A case reportSilvia Della Torre, Germana de Nucci, Pietro Maria Lombardi, et al.
European Journal of Haematology|October 18, 2011
A cluster of factor XI-deficient patients due to a new mutation (Ile 436 Lys) in northeastern ItalyAntonio Girolami, Pamela Scarparo, Emanuela Bonamigo, et al.
Updates in Surgery|March 29, 2023
Facing adenocarcinoma of distal esophagus and esophagogastric junction: a CROSS versus FLOT propensity score-matched analysis of oncological outcomes in a high-volume institutionPietro Maria Lombardi, Andrea Pansa, Silvia Basato, et al.
European Journal of Haematology|April 30, 2013
Discrepant ratios of arterial vs. venous thrombosis in hemophilias A and B as compared to FVII deficiencyAntonio Girolami, Giulia Berti de Marinis, Irene Bertozzi, et al.
Pageof 11

Showing results (31-40 of 108) with videos related to

Sort By:
Pageof 11
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|October 26, 2005
Confirmation of the value of a modified long-distance polymerase chain reaction in the detection of inversion intron 22 in severe hemophilia a: a technical noteAnna Maria Lombardi, Laura Cabrio, Ezio Zanon, et al.
Cardiovascular & Hematological Disorders Drug Targets|September 12, 2017
Congenital FX Deficiency Rio Tercero: A New Heterozygous Missense Mutation (Cys241Gly) with a Potentiating Effect by a Polymorphism (c. 503-57C>T)Antonio Girolami, Salvador Minoldo, Silvia Ferrari, et al.
Acta Haematologica|January 21, 2006
Pregnancy and oral contraceptives in congenital bleeding disorders of the vitamin K-dependent coagulation factorsAntonio Girolami, Maria Luigia Randi, Elisabetta Ruzzon, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 30, 2003
A novel type I factor X variant (factor X Cys350Phe) due to loss of a disulfide bond in the catalytic domainFabrizio Vianello, Anna Maria Lombardi, Federico Dal Bello, et al.
Thrombosis Research|November 5, 2002
Conformation sensitive gel electrophoresis for detection of factor X gene mutationsFabrizio Vianello, Anna Maria Lombardi, Federico Dal Bello, et al.
Thrombosis and Haemostasis|December 4, 2003
Severe prekallikrein (Fletcher factor) deficiency due to a compound heterozygosis (383Trp stop codon and Cys529Tyr)Anna Maria Lombardi, Maria Teresa Sartori, Laura Cabrio, et al.
World Journal of Clinical Oncology|June 30, 2021
Long-term complete response in metastatic poorly-differentiated neuroendocrine rectal carcinoma with a multimodal approach: A case reportSilvia Della Torre, Germana de Nucci, Pietro Maria Lombardi, et al.
European Journal of Haematology|October 18, 2011
A cluster of factor XI-deficient patients due to a new mutation (Ile 436 Lys) in northeastern ItalyAntonio Girolami, Pamela Scarparo, Emanuela Bonamigo, et al.
Updates in Surgery|March 29, 2023
Facing adenocarcinoma of distal esophagus and esophagogastric junction: a CROSS versus FLOT propensity score-matched analysis of oncological outcomes in a high-volume institutionPietro Maria Lombardi, Andrea Pansa, Silvia Basato, et al.
European Journal of Haematology|April 30, 2013
Discrepant ratios of arterial vs. venous thrombosis in hemophilias A and B as compared to FVII deficiencyAntonio Girolami, Giulia Berti de Marinis, Irene Bertozzi, et al.
Pageof 11