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38 results on '"Unolt, M."'

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

2. Long-term incidence of arrhythmias in extracardiac conduit Fontan and comparison between systemic left and right ventricle.

3. Prenatal vs postnatal diagnosis of 22q11.2 deletion syndrome: cardiac and noncardiac outcomes through 1 year of age.

4. Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS.

5. Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome.

6. Cardiac function in adolescents and young adults with 22q11.2 deletion syndrome without congenital heart disease.

7. Improved Outcomes in Patients with 22q11.2 Deletion Syndrome and Diagnosis of Interrupted Aortic Arch Prior to Birth Hospital Discharge, a Retrospective Study.

8. Clinical Risk Factors for Aortic Root Dilation in Patients with 22q11.2 Deletion Syndrome: A Longitudinal Single-Center Study.

9. 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.

10. 22q11.2 Deletion Syndrome: Impact of Genetics in the Treatment of Conotruncal Heart Defects.

11. Congenital heart defects in molecularly confirmed KBG syndrome patients.

12. Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion.

13. Cardiac Defects and Genetic Syndromes: Old Uncertainties and New Insights.

14. Left ventricular (LV) pacing in newborns and infants: Echo assessment of LV systolic function and synchrony at 5-year follow-up.

15. Atypical cardiac defects in patients with RASopathies: Updated data on CARNET study.

16. Myoclonic epilepsy, parkinsonism, schizophrenia and left-handedness as common neuropsychiatric features in 22q11.2 deletion syndrome.

17. Pathogenic variants in CDC45 on the remaining allele in patients with a chromosome 22q11.2 deletion result in a novel autosomal recessive condition.

18. Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects.

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

20. Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers.

21. What is new with 22q? An update from the 22q and You Center at the Children's Hospital of Philadelphia.

22. Use of a Pediatric Syncope Unit Improves Diagnosis and Lowers Costs: A Hospital-Based Experience.

23. 22q and two: 22q11.2 deletion syndrome and coexisting conditions.

24. Primary lymphedema and other lymphatic anomalies are associated with 22q11.2 deletion syndrome.

25. Some Isolated Cardiac Malformations Can Be Related to Laterality Defects.

26. Congenital heart disease and genetic syndromes: new insights into molecular mechanisms.

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

28. Congenital diaphragmatic hernia in 22q11.2 deletion syndrome.

29. Sprengel anomaly in deletion 22q11.2 (DiGeorge/Velo-Cardio-Facial) syndrome.

31. Transposition of great arteries: new insights into the pathogenesis.

33. Double outlet right ventricle versus aortic dextroposition: morphologically distinct defects.

35. [Congenital heart diseases in women].

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