47 results on '"Kinnamon, Daniel D."'
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2. Abstract 14707: Electrocardiographic Abnormalities Are Common in DCM Patients’ Family Members With Early Manifestations of DCM
3. Response to "assessment of risk of ALS conferred by the GGGGCC hexanucleotide expansion in C9orf72 among first-degree relatives of patients with ALS carrying the repeat expansion".
4. Differences in Cardiac Mechanics among Genetically At-Risk First-Degree Relatives: The DCM Precision Medicine Study
5. Screening for Dilated Cardiomyopathy in At-Risk First-Degree Relatives
6. Genetic Architecture of Dilated Cardiomyopathy in Individuals of African and European Ancestry.
7. Knowledge of Genome Sequencing and Trust in Medical Researchers Among Patients of Different Racial and Ethnic Groups With Idiopathic Dilated Cardiomyopathy
8. Single Marker Family-Based Association Analysis Conditional on Parental Information
9. Toward Genetics-Driven Early Intervention in Dilated Cardiomyopathy: Design and Implementation of the DCM Precision Medicine Study
10. TTR variants in patients with dilated cardiomyopathy: An investigation of the DCM Precision Medicine Study
11. Communal Coping as a Strategy to Enhance Family Engagement in Dilated Cardiomyopathy
12. Validating an Idiopathic Dilated Cardiomyopathy Diagnosis Using Cardiovascular Magnetic Resonance: The Dilated Cardiomyopathy Precision Medicine Study
13. Effectiveness of the Family Heart Talk Communication Tool in Improving Family Member Screening for Dilated Cardiomyopathy: Results of a Randomized Trial.
14. Effectiveness of the Family Heart TalkCommunication Tool in Improving Family Member Screening for Dilated Cardiomyopathy: Results of a Randomized Trial
15. The Complex and Diverse Genetic Architecture of Dilated Cardiomyopathy
16. Changes in macronutrient intake among HIV-infected children between 1995 and 2004
17. Associations between neurohormonal and inflammatory activation and heart failure in children
18. Variant Interpretation for Dilated Cardiomyopathy (DCM): Refinement of the ACMG/ClinGen Guidelines for the DCM Precision Medicine Study
19. Antenatal hydronephrosis as a predictor of postnatal outcome: a meta-analysis
20. Expanded newborn screening for biochemical disorders: the effect of a false-positive result
21. Cerebellar hemorrhage in the preterm infant: ultrasonographic findings and risk factors
22. Prevalence and Cumulative Risk of Familial Idiopathic Dilated Cardiomyopathy.
23. Attitudes of Dilated Cardiomyopathy Patients and Investigators Toward Genomic Study Enrollment, Consent Process, and Return of Genetic Results
24. SOS1 Gain-of-Function Variants in Dilated Cardiomyopathy
25. Common Susceptibility Variants Examined for Association with Dilated Cardiomyopathy
26. BLADDER GROWTH AND DEVELOPMENT AFTER COMPLETE PRIMARY REPAIR OF BLADDER EXSTROPHY IN THE NEWBORN WITH COMPARISON TO STAGED APPROACH
27. SMALLER MANDIBULAR SIZE IN INFANTS WITH A HISTORY OF AN APPARENT LIFE-THREATENING EVENT
28. Understanding BRCA Mutation Carriers’ Preferences for Communication of Genetic Modifiers of Breast Cancer Risk
29. Attitudes of Dilated Cardiomyopathy Patients and Investigators Toward Genomic Study Enrollment, Consent Process, and Return of Genetic Results.
30. Multigenic Disease and Bilineal Inheritance in Dilated Cardiomyopathy Is Illustrated in Nonsegregating LMNA Pedigrees
31. Understanding Mutation Carriers' Preferences for Communication of Genetic Modifiers of Breast Cancer Risk.
32. The central role of family-based approaches in understanding the genetic architecture of left ventricular noncompaction
33. Valid Monte Carlo Permutation Tests for Genetic Case-Control Studies With Missing Genotypes
34. Reconsidering Association Testing Methods Using Single-Variant Test Statistics as Alternatives to Pooling Tests for Sequence Data with Rare Variants
35. The Effect of a Structured Exercise Program on Nutrition and Fitness Outcomes in Human Immunodeficiency Virus-Infected Children
36. An improved estimator for the hydration of fat-free mass fromin vivomeasurements subject to additive technical errors
37. Associations between neurohormonal and inflammatory activation and heart failure in children
38. TTRvariants in patients with dilated cardiomyopathy: An investigation of the DCM Precision Medicine Study
39. Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease.
40. Whole exome sequencing of rare variants in EIF4G1and VPS35in Parkinson disease
41. Prospective phase 1/2 study of rituximab in childhood and adolescent chronic immune thrombocytopenic purpura
42. Validity of High-Sensitivity C-Reactive Protein in Pediatric Heart Failure
43. Abstract 14186: Cardiac Magnetic Resonance Identifies Early Dilated Cardiomyopathy Phenotype in Genetically At-Risk Family Members.
44. Differences in Cardiac Mechanics among Genetically At-Risk First-Degree Relatives: The DCM Precision Medicine Study.
45. Variant Interpretation for Dilated Cardiomyopathy: Refinement of the American College of Medical Genetics and Genomics/ClinGen Guidelines for the DCM Precision Medicine Study.
46. Single Marker Family-Based Association Analysis Conditional on Parental Information.
47. An improved estimator for the hydration of fat-free mass from in vivo measurements subject to additive technical errors.
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