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Gyula Acsadi, MD, PhD

Division Head, Neurology


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Practice Name: Connecticut Children's Specialty Group
Education

Education:
MD, Medical School of Pecs, 1981
PhD, Molecular Genetics, Hungarian Academy of Sciences, 1993
Residency:
Pediatrics/Neurology, Medical School of Pecs, 1983-1987
Pediatrics/Neurology, Children’s Hospital of Michigan, 1995-1999
Fellowship:
Neurophysiology and Behavioral Sciences, Medical School of Pecs, 1981-1983
Molecular Genetic Research, Waisman Center, University of Wisconsin, Madison, 1989-1991
Neuromuscular Research, Montreal Neurological Institute, McGill University, 1992-1995

Board Certifications
  • Neuromuscular Medicine
  • Pediatric Neurology
  • Faculty Appointment

    Professor of Pediatrics and Neurology, University of Connecticut School of Medicine

    Clinical Expertise
    • Spinal Muscular Atrophy
    • Muscular Dystrophies
    • Charcot-Marie-Tooth Disease
    • Genetic Treatments
    Selected Publications
    • Kim J, Liao Y-H, Ionita C, Bale AE, Darras B, Acsadi G: Mitochondrial Membrane Protein-Associated Neurodegeneration Mimicking Juvenile Amyotrophic Lateral Sclerosis. Ped Neur. 2016;64:83-86

    • Jani-Acsadi A; Ounpuu S; Pierz K, Acsadi G: Pediatric Charcot-Marie-Tooth Disease. Ped Clin North Am. 2015 2015 Jun;62(3):767-786.

    • Rossor AM, Oates EC, Salter HK, Liu Y, Murphy SM, Schule R, Gonzalez MA, Scoto M, Phadke R, Sewry CA, Houlden H, Jordanova A, Tournev I, Chamova T, Litvinenko I, Zuchner S, Herrmann DN, Blake J, Sowden JE, Acsadi G, Rodriguez ML, Menezes MP, Clarke NF, Auer Grumbach M, Bullock SL, Muntoni F, Reilly MM, North KN. Phenotypic and molecular insights into spinal muscular atrophy due to mutations in BICD2. Brain. 2015 Feb;138(Pt 2):293-310.

    • Ounpuu S, Garibay E, Solomito M, Bell K, Pierz K, Thomson J, Acsadi G, Deluca P. A comprehensive evaluation of the variation in ankle function during gait in children and youth with Charcot-Marie-tooth disease. Gait Posture. 2013 Sep;38(4):900-6

    • Acsadi G, Moore SA, Chéron A, Delalande O, Bennett L, Kupsky W, El-Baba M, Le Rumeur E, Hubert JF. Novel mutation in spectrin-like repeat 1 of dystrophin central domain causes protein misfolding and mild Becker muscular dystrophy. J Biol Chem 2012 May 25;287(22):18153-62.

    • Burns J, Finkel R, de Laura M, Estilow T, Shy R, pallant J, Lel M, Montoni F, Reilly M, Pareyson D, Acsadi G, Ouvrier R, Shy M.:Validation of the CMT Pediatric Scale as an outcome measure of disability. Ann Neurol 2012 May;71(5):642-52.

    Additional Information

    Dr. Acsadi is a member of the Scientific Review Committee of the Child Neurology Society, a Fellow of the American Academy of Neurology, a member of the International Child Neurology Association, and serves on the editorial board of Pediatric Neurology.

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