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M Bertoli

Showing results (71-80 of 168) with videos related to

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Journal of Medical Genetics|February 6, 2004
A study of gene--environment interaction on the gene for angiotensin converting enzyme: a combined functional and population based approachF A Sayed-Tabatabaei, A F C Schut, A Hofman, et al.
Nederlands Tijdschrift Voor Geneeskunde|May 23, 2013
[Patients with aneurysms and osteoarthritis: Marfan syndrome ruled out, so what is it?]Denise van der Linde, Ingrid M B H van de Laar, Adriaan Moelker, et al.
Journal of Medical Genetics|January 7, 2005
Angiotensin converting enzyme gene polymorphism and cardiovascular morbidity and mortality: the Rotterdam StudyF A Sayed-Tabatabaei, A F C Schut, A Arias Vásquez, et al.
Orphanet Journal of Rare Diseases|January 3, 2012
Congenital dyserythropoietic anemia type II: molecular analysis and expression of the SEC23B geneFrancesca Punzo, Aida M Bertoli-Avella, Saverio Scianguetta, et al.
Lupus|September 19, 2009
Factors associated with arterial vascular events in PROFILE: a Multiethnic Lupus CohortA M Bertoli, L M Vilá, G S Alarcón, et al.
Neurogenetics|April 28, 2009
A novel 16p locus associated with BSCL2 hereditary motor neuronopathy: a genetic modifier?Esther Brusse, Danielle Majoor-Krakauer, Bianca M de Graaf, et al.
Leukemia Research|January 1, 1987
Abnormal splenic megakaryopoiesis in MPSV-induced myeloproliferative diseaseM C Le Bousse-Kerdiles, R Fernandez-Delgado, F Smadja-Joffe, et al.
Journal of Clinical Rheumatology : Practical Reports on Rheumatic & Musculoskeletal Diseases|October 9, 2007
Systemic lupus erythematosus in a multiethnic US cohort (LUMINA L II): relationship between vascular events and the use of hormone replacement therapy in postmenopausal womenMónica Fernández, Jaime Calvo-Alén, Ana M Bertoli, et al.
Clinical Genetics|December 23, 2020
Biallelic loss-of-function HACD1 variants are a bona fide cause of congenital myopathyLia Abbasi-Moheb, Ana Westenberger, Maha Alotaibi, et al.
Neurobiology of Aging|May 27, 2005
ACE gene is associated with Alzheimer's disease and atrophy of hippocampus and amygdalaKristel Sleegers, Tom den Heijer, Ewoud J van Dijk, et al.
Pageof 17

Showing results (71-80 of 168) with videos related to

Sort By:
Pageof 17
Journal of Medical Genetics|February 6, 2004
A study of gene--environment interaction on the gene for angiotensin converting enzyme: a combined functional and population based approachF A Sayed-Tabatabaei, A F C Schut, A Hofman, et al.
Nederlands Tijdschrift Voor Geneeskunde|May 23, 2013
[Patients with aneurysms and osteoarthritis: Marfan syndrome ruled out, so what is it?]Denise van der Linde, Ingrid M B H van de Laar, Adriaan Moelker, et al.
Journal of Medical Genetics|January 7, 2005
Angiotensin converting enzyme gene polymorphism and cardiovascular morbidity and mortality: the Rotterdam StudyF A Sayed-Tabatabaei, A F C Schut, A Arias Vásquez, et al.
Orphanet Journal of Rare Diseases|January 3, 2012
Congenital dyserythropoietic anemia type II: molecular analysis and expression of the SEC23B geneFrancesca Punzo, Aida M Bertoli-Avella, Saverio Scianguetta, et al.
Lupus|September 19, 2009
Factors associated with arterial vascular events in PROFILE: a Multiethnic Lupus CohortA M Bertoli, L M Vilá, G S Alarcón, et al.
Neurogenetics|April 28, 2009
A novel 16p locus associated with BSCL2 hereditary motor neuronopathy: a genetic modifier?Esther Brusse, Danielle Majoor-Krakauer, Bianca M de Graaf, et al.
Leukemia Research|January 1, 1987
Abnormal splenic megakaryopoiesis in MPSV-induced myeloproliferative diseaseM C Le Bousse-Kerdiles, R Fernandez-Delgado, F Smadja-Joffe, et al.
Journal of Clinical Rheumatology : Practical Reports on Rheumatic & Musculoskeletal Diseases|October 9, 2007
Systemic lupus erythematosus in a multiethnic US cohort (LUMINA L II): relationship between vascular events and the use of hormone replacement therapy in postmenopausal womenMónica Fernández, Jaime Calvo-Alén, Ana M Bertoli, et al.
Clinical Genetics|December 23, 2020
Biallelic loss-of-function HACD1 variants are a bona fide cause of congenital myopathyLia Abbasi-Moheb, Ana Westenberger, Maha Alotaibi, et al.
Neurobiology of Aging|May 27, 2005
ACE gene is associated with Alzheimer's disease and atrophy of hippocampus and amygdalaKristel Sleegers, Tom den Heijer, Ewoud J van Dijk, et al.
Pageof 17