Dr. Richard T. Moxley M.D.
Neurologist | Neurology with Special Qualifications in Child Neurology
601 Elmwood Ave Box 278984 Rochester NY, 14642Rating
5/5
About
Dr. Richard Moxley is a distinguished Neurologist in Rochester, NY. Dr. Moxley specializes in diagnosing, treating, and managing disorders of the brain and nervous system. With expertise in handling complex conditions like epilepsy, multiple sclerosis, and migraines, Dr. Moxley employs advanced techniques and personalized treatment plans to improve patient outcomes. As a neurologist, Dr. Moxley is committed to staying abreast of the latest developments in neurological research and therapies.
Provider Details
Expert Publications
Data provided by the National Library of Medicine- American experience with low-dose thalidomide therapy for severe cutaneous lupus erythematosus.
- Reduced cerebral blood flow and impaired visual-spatial function in proximal myotonic myopathy.
- Hypothyroidism unmasking proximal myotonic myopathy.
- K-40 and dual-energy X-ray absorptiometry estimates of lean weight compared. Normals and patients with neuromuscular disease.
- A randomized efficacy and safety trial of oxandrolone in the treatment of
- Muscleblind localizes to nuclear foci of aberrant RNA in myotonic dystrophy types 1 and 2.
- Proximal myotonic myopathy: a syndrome with a favourable prognosis?
- Report of the 84th ENMC workshop: PROMM (proximal myotonic myopathy) and other myotonic dystrophy-like syndromes: 2nd workshop. 13-15th October, 2000, Loosdrecht, The Netherlands.
- Confirmation of the type 2 myotonic dystrophy (CCTG)n expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins: a single shared haplotype indicates an ancestral founder effect.
- Executive dysfunction and avoidant personality trait in myotonic dystrophy type 1 (DM-1) and in proximal myotonic myopathy (PROMM/DM-2).
- Leukocyte CTG repeat length correlates with severity of myotonia in myotonic dystrophy type 1.
- Early predictors of poor outcome in congenital fiber-type disproportion myopathy.
- Myotonic dystrophy type 2 and related myotonic disorders.
- Practice parameter: corticosteroid treatment of Duchenne dystrophy: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society.
- Quantitative analysis of the "warm-up" phenomenon in myotonic dystrophy type 1.
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Practice At 601 Elmwood Ave Box 278984
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