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1. C06 Genetic variation in MSH3 that lowers its expression ameliorates disease course and limits repeat expansion in huntington's disease and myotonic dystrophy type 1. (September 2018)

2. Community-wide HIV testing, linkage case management, and defaulter tracing in Bukoba, Tanzania: pre-intervention and post-intervention, population-based survey evaluation. Issue 10 (October 2020)

3. Feasibility, Acceptability, and Adherence with Short-Term HIV Preexposure Prophylaxis in Female Sexual Partners of Migrant Miners in Mozambique. (1st December 2017)

4. Identification and Functional Characterization of CLCN1 Mutations Found in Nondystrophic Myotonia Patients. Issue 1 (28th October 2015)

5. Individual-specific levels of CTGCAG somatic instability are shared across multiple tissues in myotonic dystrophy type 1. Issue 4 (13th September 2022)

6. Longitudinal increases in somatic mosaicism of the expanded CTG repeat in myotonic dystrophy type 1 are associated with variation in age-at-onset. (30th June 2020)

8. Myotonic dystrophy type 1 (DM1) clinical subtypes and CTCF site methylation status flanking the CTG expansion are mutant allele length-dependent. Issue 2 (25th August 2021)

9. Patient-level outcomes and virologic suppression rates in HIV-infected patients receiving antiretroviral therapy in Rwanda. (August 2018)