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You searched for: Author/Creator Wheeler, Matthew T.

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1. "Doctors can read about it, they can know about it, but they've never lived with it": How parents use social media throughout the diagnostic odyssey. Issue 6 (6th June 2021)

2. A toolkit for genetics providers in follow‐up of patients with non‐diagnostic exome sequencing. Issue 2 (9th April 2019)

3. Allele-Specific Silencing Ameliorates Restrictive Cardiomyopathy Attributable to a Human Myosin Regulatory Light Chain Mutation. Issue 9 (27th August 2019)

4. Applying Cardiopulmonary Exercise Testing to the Evaluation of Left Ventricular Function for Patients Ventricular Assist Device Therapy: 1948 June 1 4. (May 2017)

5. Atypical Alexander disease with dystonia, retinopathy, and a brain mass mimicking astrocytoma. (August 2018)

6. Baseline Characteristics of the VANISH Cohort. (December 2019)

7. Compound heterozygous KCTD7 variants in progressive myoclonus epilepsy. (3rd April 2021)

8. Contractile reserve and cardiopulmonary exercise parameters in patients with dilated cardiomyopathy, the two dimensions of exercise testing. Issue 8 (6th July 2017)

9. Developing a genomics rotation: Practical training around variant interpretation for genetic counseling students. Issue 2 (1st February 2019)

10. Effect of beta‐blocker therapy on the response to mavacamten in patients with symptomatic obstructive hypertrophic cardiomyopathy. (1st February 2023)