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European Journal of Human Genetics : EJHG
|
March 20, 2019
Genotype-phenotype correlation study in 364 osteogenesis imperfecta Italian patients
Margherita Maioli, Maria Gnoli, Manila Boarini, et al.
Heart Failure Clinics
|
March 12, 2018
Clinical Presentation and Natural History of Hypertrophic Cardiomyopathy in RASopathies
Giulio Calcagni, Rachele Adorisio, Simone Martinelli, et al.
Frontiers in Pediatrics
|
May 8, 2026
Morphological and functional echocardiographic findings in pediatric patients diagnosed with hypermobile Ehlers-Danlos syndrome
Walter Vignaroli, Gioia Mastromoro, Carolina Putotto, et al.
American Journal of Medical Genetics. Part A
|
May 2, 2022
Crossed pulmonary arteries: An underestimated cardiovascular variant with a strong association with genetic syndromes-A report of 74 cases with systematic review of the literature
Gioia Mastromoro, Giulio Calcagni, Walter Vignaroli, et al.
Current Medicinal Chemistry
|
August 20, 2020
Nerve Growth Factor, Stress and Diseases
Flavio Maria Ceci, Giampiero Ferraguti, Carla Petrella, et al.
Genes
|
December 23, 2022
Clinical Risk Factors for Aortic Root Dilation in Patients with 22q11.2 Deletion Syndrome: A Longitudinal Single-Center Study
Carolina Putotto, Federica Pulvirenti, Flaminia Pugnaloni, et al.
American Journal of Medical Genetics. Part A
|
April 3, 2021
Smith-Magenis syndrome: Report of morphological and new functional cardiac findings with review of the literature
Roberta Onesimo, Paolo Versacci, Angelica Bibiana Delogu, et al.
Frontiers in Pediatrics
|
January 7, 2021
Echocardiography-Guided Management of Preterms With Patent Ductus Arteriosus Influences the Outcome: A Cohort Study
Gianluca Terrin, Maria Di Chiara, Giovanni Boscarino, et al.
American Journal of Medical Genetics. Part A
|
August 5, 2011
Ebstein anomaly: Genetic heterogeneity and association with microdeletions 1p36 and 8p23.1
Maria Cristina Digilio, Laura Bernardini, Francesca Lepri, et al.
Journal of Immunology Research
|
April 14, 2020
Neuroinflammatory Markers in the Serum of Prepubertal Children with Down Syndrome
Luigi Tarani, Valentina Carito, Giampiero Ferraguti, et al.
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of 9
Search research articles
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Showing results (51-60 of 84) with videos related to
Sort By:
Page
of 9
European Journal of Human Genetics : EJHG
|
March 20, 2019
Genotype-phenotype correlation study in 364 osteogenesis imperfecta Italian patients
Margherita Maioli, Maria Gnoli, Manila Boarini, et al.
Heart Failure Clinics
|
March 12, 2018
Clinical Presentation and Natural History of Hypertrophic Cardiomyopathy in RASopathies
Giulio Calcagni, Rachele Adorisio, Simone Martinelli, et al.
Frontiers in Pediatrics
|
May 8, 2026
Morphological and functional echocardiographic findings in pediatric patients diagnosed with hypermobile Ehlers-Danlos syndrome
Walter Vignaroli, Gioia Mastromoro, Carolina Putotto, et al.
American Journal of Medical Genetics. Part A
|
May 2, 2022
Crossed pulmonary arteries: An underestimated cardiovascular variant with a strong association with genetic syndromes-A report of 74 cases with systematic review of the literature
Gioia Mastromoro, Giulio Calcagni, Walter Vignaroli, et al.
Current Medicinal Chemistry
|
August 20, 2020
Nerve Growth Factor, Stress and Diseases
Flavio Maria Ceci, Giampiero Ferraguti, Carla Petrella, et al.
Genes
|
December 23, 2022
Clinical Risk Factors for Aortic Root Dilation in Patients with 22q11.2 Deletion Syndrome: A Longitudinal Single-Center Study
Carolina Putotto, Federica Pulvirenti, Flaminia Pugnaloni, et al.
American Journal of Medical Genetics. Part A
|
April 3, 2021
Smith-Magenis syndrome: Report of morphological and new functional cardiac findings with review of the literature
Roberta Onesimo, Paolo Versacci, Angelica Bibiana Delogu, et al.
Frontiers in Pediatrics
|
January 7, 2021
Echocardiography-Guided Management of Preterms With Patent Ductus Arteriosus Influences the Outcome: A Cohort Study
Gianluca Terrin, Maria Di Chiara, Giovanni Boscarino, et al.
American Journal of Medical Genetics. Part A
|
August 5, 2011
Ebstein anomaly: Genetic heterogeneity and association with microdeletions 1p36 and 8p23.1
Maria Cristina Digilio, Laura Bernardini, Francesca Lepri, et al.
Journal of Immunology Research
|
April 14, 2020
Neuroinflammatory Markers in the Serum of Prepubertal Children with Down Syndrome
Luigi Tarani, Valentina Carito, Giampiero Ferraguti, et al.
Page
of 9