Search research articles
Contact Us
Filters
Showing results (11-20 of 137) with videos related to
Page
of 14
Sort By:
Journal of Cardiovascular Medicine (Hagerstown, Md.)
|
April 29, 2006
22q11 deletion syndrome: a review of some developmental biology aspects of the cardiovascular system
Angelo Restivo, Anna Sarkozy, Maria Cristina Digilio, et al.
European Journal of Pediatrics
|
November 9, 2006
Familial recurrence of congenital heart disease: an overview and review of the literature
Giulio Calcagni, M Cristina Digilio, Anna Sarkozy, et al.
European Journal of Neurology
|
September 9, 2024
Relationship between growth and ambulation loss in Duchenne muscular dystrophy boys on steroids
Georgia Stimpson, Deborah Ridout, Anna Sarkozy, et al.
Frontiers in Molecular Neuroscience
|
August 28, 2020
LAMA2-Related Dystrophies: Clinical Phenotypes, Disease Biomarkers, and Clinical Trial Readiness
Anna Sarkozy, A Reghan Foley, Alberto A Zambon, et al.
European Journal of Pediatrics
|
May 31, 2006
PTPN11 gene mutations: linking the Gln510Glu mutation to the "LEOPARD syndrome phenotype"
M Cristina Digilio, Anna Sarkozy, Giuseppe Pacileo, et al.
American Journal of Medical Genetics. Part A
|
August 8, 2006
Additional evidence that PTPN11 mutations play only a minor role in the pathogenesis of non-syndromic atrioventricular canal defect
Anna Sarkozy, Francesca Lepri, Bruno Marino, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)
|
January 27, 2007
Genetics of congenital heart diseases in syndromic and non-syndromic patients: new advances and clinical implications
Gerardo Piacentini, M Cristina Digilio, Anna Sarkozy, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)
|
October 24, 2013
Skeletal muscle involvement in cardiomyopathies
Giuseppe Limongelli, Raffaella D'Alessandro, Valeria Maddaloni, et al.
Journal of Vascular Surgery
|
April 9, 2004
LEOPARD syndrome: a new polyaneurysm association and an update on the molecular genetics of the disease
Marineh Yagubyan, Jean M Panneton, Noralane M Lindor, et al.
Journal of Neuromuscular Diseases
|
March 29, 2025
Signs and symptoms of carriers of non-<i>DMD</i> X-linked neuromuscular diseases: A scoping review
Job Simons, Amanda Dekker, Rosanne Govaarts, et al.
Page
of 14
Search research articles
Search
Showing results (11-20 of 137) with videos related to
Sort By:
Page
of 14
Journal of Cardiovascular Medicine (Hagerstown, Md.)
|
April 29, 2006
22q11 deletion syndrome: a review of some developmental biology aspects of the cardiovascular system
Angelo Restivo, Anna Sarkozy, Maria Cristina Digilio, et al.
European Journal of Pediatrics
|
November 9, 2006
Familial recurrence of congenital heart disease: an overview and review of the literature
Giulio Calcagni, M Cristina Digilio, Anna Sarkozy, et al.
European Journal of Neurology
|
September 9, 2024
Relationship between growth and ambulation loss in Duchenne muscular dystrophy boys on steroids
Georgia Stimpson, Deborah Ridout, Anna Sarkozy, et al.
Frontiers in Molecular Neuroscience
|
August 28, 2020
LAMA2-Related Dystrophies: Clinical Phenotypes, Disease Biomarkers, and Clinical Trial Readiness
Anna Sarkozy, A Reghan Foley, Alberto A Zambon, et al.
European Journal of Pediatrics
|
May 31, 2006
PTPN11 gene mutations: linking the Gln510Glu mutation to the "LEOPARD syndrome phenotype"
M Cristina Digilio, Anna Sarkozy, Giuseppe Pacileo, et al.
American Journal of Medical Genetics. Part A
|
August 8, 2006
Additional evidence that PTPN11 mutations play only a minor role in the pathogenesis of non-syndromic atrioventricular canal defect
Anna Sarkozy, Francesca Lepri, Bruno Marino, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)
|
January 27, 2007
Genetics of congenital heart diseases in syndromic and non-syndromic patients: new advances and clinical implications
Gerardo Piacentini, M Cristina Digilio, Anna Sarkozy, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)
|
October 24, 2013
Skeletal muscle involvement in cardiomyopathies
Giuseppe Limongelli, Raffaella D'Alessandro, Valeria Maddaloni, et al.
Journal of Vascular Surgery
|
April 9, 2004
LEOPARD syndrome: a new polyaneurysm association and an update on the molecular genetics of the disease
Marineh Yagubyan, Jean M Panneton, Noralane M Lindor, et al.
Journal of Neuromuscular Diseases
|
March 29, 2025
Signs and symptoms of carriers of non-<i>DMD</i> X-linked neuromuscular diseases: A scoping review
Job Simons, Amanda Dekker, Rosanne Govaarts, et al.
Page
of 14