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Rivista Di Psichiatria
|
January 30, 2023
Similar grey matter abnormalities in 22q11.2DS and chronic schizophrenia: a voxel-based morphometry study
Marianna Frascarelli, Tommaso Accinni, Antonino Buzzanca, et al.
Children (Basel, Switzerland)
|
June 24, 2022
22q11.2 Deletion Syndrome: Impact of Genetics in the Treatment of Conotruncal Heart Defects
Carolina Putotto, Flaminia Pugnaloni, Marta Unolt, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 9, 2024
From Klinefelter Syndrome to High Grade Aneuploidies: Expanding the Gene-dosage Effect of Supernumerary X Chromosomes
Matteo Spaziani, Francesco Carlomagno, Chiara Tarantino, et al.
Canadian Journal of Physiology and Pharmacology
|
October 6, 2021
Serum prokineticin-2 in prepubertal and adult Klinefelter individuals
Marco Fiore, Luigi Tarani, Antonio Radicioni, et al.
International Journal of Molecular Sciences
|
February 25, 2023
Neuroinflammation and Oxidative Stress in Individuals Affected by DiGeorge Syndrome
Michela Menghi, Ginevra Micangeli, Francesca Tarani, et al.
Early Intervention in Psychiatry
|
March 29, 2022
Recognition of facial emotion expressions and perceptual processes in 22q11.2 deletion syndrome
Antonino Buzzanca, Tommaso Accinni, Marianna Frascarelli, 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.
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.
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.
Prenatal Diagnosis
|
April 9, 2024
Prenatal cardiac findings and 22q11.2 deletion syndrome: Fetal detection and evaluation
Elizabeth Goldmuntz, Anne S Bassett, Erik Boot, et al.
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of 6
Search research articles
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Showing results (21-30 of 57) with videos related to
Sort By:
Page
of 6
Rivista Di Psichiatria
|
January 30, 2023
Similar grey matter abnormalities in 22q11.2DS and chronic schizophrenia: a voxel-based morphometry study
Marianna Frascarelli, Tommaso Accinni, Antonino Buzzanca, et al.
Children (Basel, Switzerland)
|
June 24, 2022
22q11.2 Deletion Syndrome: Impact of Genetics in the Treatment of Conotruncal Heart Defects
Carolina Putotto, Flaminia Pugnaloni, Marta Unolt, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 9, 2024
From Klinefelter Syndrome to High Grade Aneuploidies: Expanding the Gene-dosage Effect of Supernumerary X Chromosomes
Matteo Spaziani, Francesco Carlomagno, Chiara Tarantino, et al.
Canadian Journal of Physiology and Pharmacology
|
October 6, 2021
Serum prokineticin-2 in prepubertal and adult Klinefelter individuals
Marco Fiore, Luigi Tarani, Antonio Radicioni, et al.
International Journal of Molecular Sciences
|
February 25, 2023
Neuroinflammation and Oxidative Stress in Individuals Affected by DiGeorge Syndrome
Michela Menghi, Ginevra Micangeli, Francesca Tarani, et al.
Early Intervention in Psychiatry
|
March 29, 2022
Recognition of facial emotion expressions and perceptual processes in 22q11.2 deletion syndrome
Antonino Buzzanca, Tommaso Accinni, Marianna Frascarelli, 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.
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.
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.
Prenatal Diagnosis
|
April 9, 2024
Prenatal cardiac findings and 22q11.2 deletion syndrome: Fetal detection and evaluation
Elizabeth Goldmuntz, Anne S Bassett, Erik Boot, et al.
Page
of 6