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Laterality, heterotaxy, and isolated congenital heart defects

Genome medicine, 2024-08, Vol.16 (1), p.1-3

2024

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From Klinefelter Syndrome to High Grade Aneuploidies: Expanding the Gene-dosage Effect of Supernumerary X Chromosomes

The journal of clinical endocrinology and metabolism, 2024-01, Vol.109 (8), p.e1564-e1573

2024

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Neuroinflammation and Oxidative Stress in Individuals Affected by DiGeorge Syndrome

International journal of molecular sciences, 2023-02, Vol.24 (4), p.4242

2023

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Neuroinflammatory Markers in the Serum of Prepubertal Children with Down Syndrome

Journal of Immunology Research, 2020, Vol.2020 (2020), p.1-10

2020

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Anatomical substrate for biventricular repair in patients with left isomerism

Annals of pediatric cardiology, 2021-04, Vol.14 (2), p.250-251

2021

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Impaction of regurgitation jet on anterior mitral leaflet is associated with diastolic dysfunction in patients with bicuspid aortic valve and mild insufficiency: a cardiovascular magnetic resonance study

The International Journal of Cardiovascular Imaging, 2022-01, Vol.38 (1), p.211-221

2022

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Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice

PloS one, 2019-04, Vol.14 (4), p.e0211170-e0211170

2019

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Commentary: sVEGFR1 Is Enriched in Hepatic Vein Blood—Evidence for a Provisional Hepatic Factor Candidate?

Frontiers in pediatrics, 2021-11, Vol.9, p.782779-782779

2021

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Genetics of atrioventricular canal defects

Italian journal of pediatrics, 2020-05, Vol.46 (1), p.61-61, Article 61

2020

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Neuroimmune Dysregulation in Prepubertal and Adolescent Individuals Affected by Klinefelter Syndrome

Endocrine, metabolic & immune disorders drug targets, 2023-01, Vol.23 (1), p.105-114

2023

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22q11.2 Deletion Syndrome: Impact of Genetics in the Treatment of Conotruncal Heart Defects

Children (Basel), 2022-05, Vol.9 (6), p.772

2022

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Long-term outcome of a patient with Transcobalamin deficiency caused by the homozygous c.1115_1116delCA mutation in TCN2 gene: a case report

Italian journal of pediatrics, 2021-03, Vol.47 (1), p.54-54, Article 54

2021

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Factors That Negatively Affect the Prognosis of Pediatric Community-Acquired Pneumonia in District Hospital in Tanzania

International journal of molecular sciences, 2017-03, Vol.18 (3), p.623-623

2017

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Some Isolated Cardiac Malformations Can Be Related to Laterality Defects

Journal of cardiovascular development and disease, 2018-05, Vol.5 (2), p.24

2018

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Congenital Heart Defects in Patients with Molecularly Confirmed Sotos Syndrome

Diagnostics (Basel), 2024-03, Vol.14 (6), p.594

2024

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Variable Effects of Laterality Genes on Disharmony Between Different Thoraco-Abdominal Organs and Between Individual Cardiac Segments

Pediatric cardiology, 2024-09

2024

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Double-Orifice Left Atrioventricular Valve in Patients With Atrioventricular Septal Defect With and Without Down Syndrome

The Annals of thoracic surgery, 2013-05, Vol.95 (5), p.1843-1844

2013

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Aortic arch interruption without ductus arteriosus and no ventricular septal defect

The Journal of thoracic and cardiovascular surgery, 2013, Vol.145 (1), p.311-311

2013

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Efficacy and safety of clozapine in treatment-resistant psychotic patients with DiGeorge syndrome (22q11.2 deletion syndrome): a case series

International clinical psychopharmacology, 2024-07, Vol.39 (4), p.284-287

2024

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Is Aripiprazole Useful for Treatment of Psychotic Symptoms in a Patient With 22q11.2 Deletion Syndrome?: A Case Series

Journal of clinical psychopharmacology, 2023-07, Vol.43 (4), p.384-386

2023

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Laterality, heterotaxy, and isolated congenital heart defects : The genetic basis of the segmental nature of the heart

Genome medicine, 2024-08, Vol.16 (1), p.100, Article 100

2024

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RASopathy Syndrome: Do Not Overlook Mitral Valve Anomalies

JACC. Case reports, 2024-10, Vol.29 (19), p.102604

2024

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RASopathy Syndrome

JACC. Case reports, 2024-10, Vol.29 (19), p.102604, Article 102604

2024

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Anatomically corrected malposition of the great arteries (S,L,D) with mutation of Nodal gene

Cardiology in the young, 2023-01, Vol.33 (1), p.160-162

2023

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Transpositions of the great arteries versus aortic dextropositions. A review of some embryogenetic and morphological aspects

Anatomical record (Hoboken, N.J. : 2007), 2023-03, Vol.306 (3), p.502-514

2023

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Laterality, heterotaxy, and isolated congenital heart defects

From Klinefelter Syndrome to High Grade Aneuploidies: Expanding the Gene-dosage Effect of Supernumerary X Chromosomes

Neuroinflammation and Oxidative Stress in Individuals Affected by DiGeorge Syndrome

Neuroinflammatory Markers in the Serum of Prepubertal Children with Down Syndrome

Anatomical substrate for biventricular repair in patients with left isomerism

Impaction of regurgitation jet on anterior mitral leaflet is associated with diastolic dysfunction in patients with bicuspid aortic valve and mild insufficiency: a cardiovascular magnetic resonance study

Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice

Commentary: sVEGFR1 Is Enriched in Hepatic Vein Blood—Evidence for a Provisional Hepatic Factor Candidate?

Genetics of atrioventricular canal defects

Neuroimmune Dysregulation in Prepubertal and Adolescent Individuals Affected by Klinefelter Syndrome

22q11.2 Deletion Syndrome: Impact of Genetics in the Treatment of Conotruncal Heart Defects

Long-term outcome of a patient with Transcobalamin deficiency caused by the homozygous c.1115_1116delCA mutation in TCN2 gene: a case report

Factors That Negatively Affect the Prognosis of Pediatric Community-Acquired Pneumonia in District Hospital in Tanzania

Some Isolated Cardiac Malformations Can Be Related to Laterality Defects

Congenital Heart Defects in Patients with Molecularly Confirmed Sotos Syndrome

Variable Effects of Laterality Genes on Disharmony Between Different Thoraco-Abdominal Organs and Between Individual Cardiac Segments

Double-Orifice Left Atrioventricular Valve in Patients With Atrioventricular Septal Defect With and Without Down Syndrome

Aortic arch interruption without ductus arteriosus and no ventricular septal defect

Efficacy and safety of clozapine in treatment-resistant psychotic patients with DiGeorge syndrome (22q11.2 deletion syndrome): a case series

Is Aripiprazole Useful for Treatment of Psychotic Symptoms in a Patient With 22q11.2 Deletion Syndrome?: A Case Series

Laterality, heterotaxy, and isolated congenital heart defects : The genetic basis of the segmental nature of the heart

RASopathy Syndrome: Do Not Overlook Mitral Valve Anomalies

RASopathy Syndrome

Anatomically corrected malposition of the great arteries (S,L,D) with mutation of Nodal gene

Transpositions of the great arteries versus aortic dextropositions. A review of some embryogenetic and morphological aspects

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