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Laura Masi

Showing results (61-70 of 123) with videos related to

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International Journal of Pediatric Otorhinolaryngology|July 10, 2017
Airway stenting in a child with spondyloepiphyseal dysplasia congenita: 13-Year survivalRaffaella Nenna, Fabio Midulla, Laura Masi, et al.
Physics in Medicine and Biology|April 18, 2019
ADAM phantom to test 4D medical imaging and dose delivery devicesStefania Pallotta, Silvia Calusi, Laura Masi, et al.
Clinical Cases in Mineral and Bone Metabolism : the Official Journal of the Italian Society of Osteoporosis, Mineral Metabolism, and Skeletal Diseases|March 31, 2012
The role of osteoprotegerin (OPG) and estrogen receptor (ER-α) gene polymorphisms in rheumatoid arthritisLaura Masi, Susanna Maddali Bongi, Chiara Angotti, et al.
European Journal of Clinical Investigation|July 27, 2010
Genetic aspects of the Paget's disease of bone: concerns on the introduction of DNA-based tests in the clinical practice. Advantages and disadvantages of its applicationAlberto Falchetti, Falchetti Alberto, Francesca Marini, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|January 29, 2003
Analysis of estrogen receptor (ERalpha and ERbeta) and progesterone receptor (PR) polymorphisms in uterine leiomyomasFrancesco Massart, Lucia Becherini, Francesca Marini, et al.
Physics in Medicine and Biology|August 10, 2017
Is the PTW 60019 microDiamond a suitable candidate for small field reference dosimetry?Vanessa De Coste, Paolo Francescon, Marco Marinelli, et al.
The Journal of Clinical Endocrinology and Metabolism|December 22, 2021
ALPL Genotypes in Patients With Atypical Femur Fractures or Other Biochemical and Clinical Signs of HypophosphatasiaFrancesca Marini, Laura Masi, Francesca Giusti, et al.
Arthritis Research & Therapy|November 10, 2005
Segregation of a M404V mutation of the p62/sequestosome 1 (p62/SQSTM1) gene with polyostotic Paget's disease of bone in an Italian familyAlberto Falchetti, Marco Di Stefano, Francesca Marini, et al.
European Journal of Endocrinology|February 9, 2012
A novel germline inactivating mutation in the CASR gene in an Italian kindred affected by familial hypocalciuric hypercalcemiaAlberto Falchetti, Alessia Gozzini, Annalisa Terranegra, et al.
Clinical Cases in Mineral and Bone Metabolism : the Official Journal of the Italian Society of Osteoporosis, Mineral Metabolism, and Skeletal Diseases|July 9, 2014
CYP19 and ESR1 gene polymorphisms: response of the bone mineral density in post-menopausal women to hormonal replacement therapyLaura Masi, Silva Ottanelli, Rossella Berni, et al.
Pageof 13

Showing results (61-70 of 123) with videos related to

Sort By:
Pageof 13
International Journal of Pediatric Otorhinolaryngology|July 10, 2017
Airway stenting in a child with spondyloepiphyseal dysplasia congenita: 13-Year survivalRaffaella Nenna, Fabio Midulla, Laura Masi, et al.
Physics in Medicine and Biology|April 18, 2019
ADAM phantom to test 4D medical imaging and dose delivery devicesStefania Pallotta, Silvia Calusi, Laura Masi, et al.
Clinical Cases in Mineral and Bone Metabolism : the Official Journal of the Italian Society of Osteoporosis, Mineral Metabolism, and Skeletal Diseases|March 31, 2012
The role of osteoprotegerin (OPG) and estrogen receptor (ER-α) gene polymorphisms in rheumatoid arthritisLaura Masi, Susanna Maddali Bongi, Chiara Angotti, et al.
European Journal of Clinical Investigation|July 27, 2010
Genetic aspects of the Paget's disease of bone: concerns on the introduction of DNA-based tests in the clinical practice. Advantages and disadvantages of its applicationAlberto Falchetti, Falchetti Alberto, Francesca Marini, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|January 29, 2003
Analysis of estrogen receptor (ERalpha and ERbeta) and progesterone receptor (PR) polymorphisms in uterine leiomyomasFrancesco Massart, Lucia Becherini, Francesca Marini, et al.
Physics in Medicine and Biology|August 10, 2017
Is the PTW 60019 microDiamond a suitable candidate for small field reference dosimetry?Vanessa De Coste, Paolo Francescon, Marco Marinelli, et al.
The Journal of Clinical Endocrinology and Metabolism|December 22, 2021
ALPL Genotypes in Patients With Atypical Femur Fractures or Other Biochemical and Clinical Signs of HypophosphatasiaFrancesca Marini, Laura Masi, Francesca Giusti, et al.
Arthritis Research & Therapy|November 10, 2005
Segregation of a M404V mutation of the p62/sequestosome 1 (p62/SQSTM1) gene with polyostotic Paget's disease of bone in an Italian familyAlberto Falchetti, Marco Di Stefano, Francesca Marini, et al.
European Journal of Endocrinology|February 9, 2012
A novel germline inactivating mutation in the CASR gene in an Italian kindred affected by familial hypocalciuric hypercalcemiaAlberto Falchetti, Alessia Gozzini, Annalisa Terranegra, et al.
Clinical Cases in Mineral and Bone Metabolism : the Official Journal of the Italian Society of Osteoporosis, Mineral Metabolism, and Skeletal Diseases|July 9, 2014
CYP19 and ESR1 gene polymorphisms: response of the bone mineral density in post-menopausal women to hormonal replacement therapyLaura Masi, Silva Ottanelli, Rossella Berni, et al.
Pageof 13