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M Pinotti

Showing results (21-30 of 51) with videos related to

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Human Molecular Genetics|May 1, 1993
In-frame deletion of von Willebrand factor A domains in a dominant type of von Willebrand diseaseF Bernardi, P Patracchini, D Gemmati, et al.
Pest Management Science|April 2, 2024
First use of unmanned aerial vehicles to monitor Halyomorpha halys and recognize it using artificial intelligenceDaniele Giannetti, Niccolò Patelli, Lorenzo Palazzetti, et al.
Thrombosis and Haemostasis|May 1, 1995
Protein S mRNA in patients with protein S deficiencyE Sacchi, M Pinotti, G Marchetti, et al.
Epidemiology (Cambridge, Mass.)|September 1, 1996
Amyotrophic lateral sclerosis after long-term exposure to drinking water with high selenium contentM Vinceti, D Guidetti, M Pinotti, et al.
Clinical Biomechanics (Bristol, Avon)|June 22, 2011
Improvement of hand function in children with cerebral palsy via an orthosis that provides wrist extension and thumb abductionP N Barroso, S D Vecchio, Y R Xavier, et al.
Journal of Thrombosis and Haemostasis : JTH|April 17, 2014
An engineered U1 small nuclear RNA rescues splicing defective coagulation F7 gene expression in miceD Balestra, A Faella, P Margaritis, et al.
Journal of Thrombosis and Haemostasis : JTH|June 18, 2015
The carboxyl-terminal region is NOT essential for secreted and functional levels of coagulation factor XA Branchini, M Baroni, F Burini, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|May 22, 2008
[Hepatitis type A with atypical course]M Fuoti, M Pinotti, M C Villa, et al.
European Journal of Gynaecological Oncology|June 17, 2003
Breast cancer metastatic to uterine leiomyosarcoma. A case report and review of the literatureM D Ricci, M Pinotti, A H G Giribela, et al.
British Journal of Haematology|August 1, 1995
Molecular bases of CRM+ factor X deficiency: a frequent mutation (Ser334Pro) in the catalytic domain and a substitution (Glu102Lys) in the second EGF-like domainG Marchetti, G Castaman, M Pinotti, et al.
Pageof 6

Showing results (21-30 of 51) with videos related to

Sort By:
Pageof 6
Human Molecular Genetics|May 1, 1993
In-frame deletion of von Willebrand factor A domains in a dominant type of von Willebrand diseaseF Bernardi, P Patracchini, D Gemmati, et al.
Pest Management Science|April 2, 2024
First use of unmanned aerial vehicles to monitor Halyomorpha halys and recognize it using artificial intelligenceDaniele Giannetti, Niccolò Patelli, Lorenzo Palazzetti, et al.
Thrombosis and Haemostasis|May 1, 1995
Protein S mRNA in patients with protein S deficiencyE Sacchi, M Pinotti, G Marchetti, et al.
Epidemiology (Cambridge, Mass.)|September 1, 1996
Amyotrophic lateral sclerosis after long-term exposure to drinking water with high selenium contentM Vinceti, D Guidetti, M Pinotti, et al.
Clinical Biomechanics (Bristol, Avon)|June 22, 2011
Improvement of hand function in children with cerebral palsy via an orthosis that provides wrist extension and thumb abductionP N Barroso, S D Vecchio, Y R Xavier, et al.
Journal of Thrombosis and Haemostasis : JTH|April 17, 2014
An engineered U1 small nuclear RNA rescues splicing defective coagulation F7 gene expression in miceD Balestra, A Faella, P Margaritis, et al.
Journal of Thrombosis and Haemostasis : JTH|June 18, 2015
The carboxyl-terminal region is NOT essential for secreted and functional levels of coagulation factor XA Branchini, M Baroni, F Burini, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|May 22, 2008
[Hepatitis type A with atypical course]M Fuoti, M Pinotti, M C Villa, et al.
European Journal of Gynaecological Oncology|June 17, 2003
Breast cancer metastatic to uterine leiomyosarcoma. A case report and review of the literatureM D Ricci, M Pinotti, A H G Giribela, et al.
British Journal of Haematology|August 1, 1995
Molecular bases of CRM+ factor X deficiency: a frequent mutation (Ser334Pro) in the catalytic domain and a substitution (Glu102Lys) in the second EGF-like domainG Marchetti, G Castaman, M Pinotti, et al.
Pageof 6