217 results on '"Chatfield, Kathryn"'
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2. Dilated Cardiomyopathy in Children
3. ACAD9 treatment with bezafibrate and nicotinamide riboside temporarily stabilizes cardiomyopathy and lactic acidosis
4. Chronic Lactate Exposure Decreases Mitochondrial Function by Inhibition of Fatty Acid Uptake and Cardiolipin Alterations in Neonatal Rat Cardiomyocytes
5. Genomic regions associated with microdeletion/microduplication syndromes exhibit extreme diversity of structural variation
6. Abstract 15278: Cardiac Assessments and Manifestations Among Individuals With Long-Chain Fatty Acid Oxidation Disorders: A Retrospective Claims Database Analysis
7. Abstract 14415: Aortic Strain and Stiffness in Patients With Turner and Marfan Syndrome: Non-Invasive Phenotyping of Aortic Biomechanical Properties
8. Automated syndrome diagnosis by three-dimensional facial imaging.
9. Cardiac Transcriptome Remodeling and Impaired Bioenergetics in Single-Ventricle Congenital Heart Disease
10. Costello syndrome: Clinical phenotype, genotype, and management guidelines.
11. The Prevalence of Noonan Spectrum Disorders in Pediatric Patients with Pulmonary Valve Stenosis
12. The Fourth International Symposium on Genetic Disorders of the Ras/MAPK pathway
13. Elamipretide Improves Mitochondrial Function in the Failing Human Heart
14. An extensive β1-adrenergic receptor gene signaling network regulates molecular remodeling in dilated cardiomyopathies
15. In-utero idiopathic ductal constriction: a prenatal manifestation of Alagille and Williams syndrome arteriopathy
16. Kiosk 2R-TC-04 - Assessment of Abnormal Transvalvular Flow and Wall Shear Stress for Pediatric/young Adults with Bicuspid Aortic Valve: A Cross-sectional 4D Flow Study
17. Elamipretide Improves Cardiac Mitochondrial Function In Children With Single Ventricle Heart Disease
18. Megacystis Associated With an Underlying ACTA2 Variant and Diagnosis of Multisystemic Smooth Muscle Dysfunction Syndrome: A Case Report
19. Chromosomal Anomalies Associated with Congenital Heart Disease
20. General pediatric care for a patient after heart transplant: what the practitioner needs to know
21. Thromboembolic toxicity observed with concurrent trametinib and lenalidomide therapy
22. Linoleate-Enrichment of Mitochondrial Cardiolipin Molecular Species Is Developmentally Regulated and a Determinant of Metabolic Phenotype
23. Frozen elephant trunk aortic reconstruction in a patient with Loeys-Dietz syndrome
24. The heart in RASopathies
25. Mechanisms and significance of tissue-specific MICU regulation of the mitochondrial calcium uniporter complex
26. Trametinib for Refractory Chylous Effusions and Systemic Complications in Children with Noonan Syndrome
27. Dysregulation of cardiolipin biosynthesis in pediatric heart failure
28. Anesthetic Considerations for a Child With Rare B3GALT6 Mutations: A Case Report
29. Abstract 20616: Treatment of Primary Cardiomyocytes With Serum From Dilated Cardiomyopathy Patients Induces Gene Expression and Functional Changes Observed in the Pediatric Heart
30. Pathogenic variants in glutamyl-tRNAGln amidotransferase subunits cause a lethal mitochondrial cardiomyopathy disorder
31. Hepatic abnormalities in youth with Turner syndrome
32. LGG-42. Thromboembolic toxicity observed with concurrent trametinib and lenalidomide therapy
33. Thromboembolic toxicity observed with concurrent trametinib and lenalidomide therapy
34. Mutations in the accessory subunit NDUFB10 result in isolated complex I deficiency and illustrate the critical role of intermembrane space import for complex I holoenzyme assembly
35. Anesthetic Considerations for Children with Multisystem Smooth Muscle Dysfunction Syndrome and review of the literature
36. Chronic Lactate Exposure Decreases Mitochondrial Function by Inhibition of Fatty Acid Uptake and Cardiolipin Alterations in Neonatal Rat Cardiomyocytes
37. Cardiac Transcriptome Remodeling and Impaired Bioenergetics in Single Ventricle Congenital Heart Disease
38. Long‐chain fatty acid oxidation and respiratory complex I deficiencies distinguish Barth Syndrome from idiopathic pediatric cardiomyopathy
39. Trametinib for Refractory Chylous Effusions in Children with Noonan Syndrome
40. Linoleate-Enrichment of Mitochondrial Cardiolipin Molecular Species Is Developmentally Regulated and a Determinant of Metabolic Phenotype.
41. Impact of Genetic Testing for Cardiomyopathy on Emotional Well-Being and Family Dynamics: A Study of Parents and Adolescents
42. Hepatic Abnormalities in Youth With Turner Syndrome
43. Outcomes in hospitalisations of women with Turner syndrome compared to women without Turner syndrome
44. Maturation of Pluripotent Stem Cell-Derived Cardiomyocytes Enables Modeling of Human Hypertrophic Cardiomyopathy
45. Supplemental Material for Mostovoy et al., 2020
46. Chromosomal Anomalies Associated with Congenital Heart Disease
47. Principles of Human Genetics
48. Contributors
49. Congenital Heart Disease in Cornelia de Lange Syndrome: Phenotype and Genotype Analysis
50. Tafazzin deficiency impairs CoA-dependent oxidative metabolism in cardiac mitochondria
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