Ricardo H Roda

Ricardo H Roda

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Ricardo H Roda

Ricardo H Roda

Publications by authors named "Ricardo H Roda"

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Stopping oral steroid-sparing agents at initiation of rituximab in myasthenia gravis.

Neuromuscul Disord 2019 Jul 6;29(7):554-561. Epub 2019 Jun 6.

Neuromuscular Medicine, Department of Neurology, Johns Hopkins University School of Medicine, Meyer 5-119A, 600N. Wolfe Street, Baltimore, MD 21287, United States.

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http://dx.doi.org/10.1016/j.nmd.2019.06.002DOI Listing
July 2019

Mitochondrial dysfunction in HIV-induced peripheral neuropathy.

Int Rev Neurobiol 2019 14;145:67-82. Epub 2019 May 14.

Solomon H. Snyder Department of Neuroscience and Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, United States.

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http://dx.doi.org/10.1016/bs.irn.2019.04.001DOI Listing
May 2019

Myopathy: Recent Progress, Current Therapies, and Future Directions.

Neurotherapeutics 2018 10;15(4):837-839

Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

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http://link.springer.com/10.1007/s13311-018-00688-y
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http://dx.doi.org/10.1007/s13311-018-00688-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6277290PMC
October 2018

Novel hemizygous nonsense mutation in is associated with inherited neuropathy.

Neurol Genet 2018 Feb 24;4(1):e220. Epub 2018 Jan 24.

Department of Neurology (R.H.R., B.A.M., A.H.), Johns Hopkins University School of Medicine, Baltimore, MD; and Department of Neurology (C.J.K.), Mayo Clinic, Rochester, MN.

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http://dx.doi.org/10.1212/NXG.0000000000000220DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5820600PMC
February 2018

Multigeneration family with dominant SPG30 hereditary spastic paraplegia.

Ann Clin Transl Neurol 2017 11 14;4(11):821-824. Epub 2017 Oct 14.

Neurogenetics Branch National Institute of Neurological Disorders and Stroke National Institutes of Health Bethesda Maryland.

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http://dx.doi.org/10.1002/acn3.452DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5682118PMC
November 2017

SCA8 should not be tested in isolation for ataxia.

Neurol Genet 2017 Jun 21;3(3):e150. Epub 2017 Apr 21.

Neuromuscular Medicine (R.H.R.), Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD; and Neurogenetics Branch (R.H.R., A.B.S., C.B.), National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD.

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http://ng.neurology.org/lookup/doi/10.1212/NXG.0000000000000
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http://dx.doi.org/10.1212/NXG.0000000000000150DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5400807PMC
June 2017

De novo missense mutation in pure hereditary spastic paraplegia.

Ann Clin Transl Neurol 2017 05 11;4(5):347-350. Epub 2017 Apr 11.

Neurogenetics Branch National Institute of Neurological Disorders and Stroke National Institutes of Health Bethesda Maryland.

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http://doi.wiley.com/10.1002/acn3.404
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http://dx.doi.org/10.1002/acn3.404DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5420804PMC
May 2017

Complicated spastic paraplegia in patients with AP5Z1 mutations (SPG48).

Neurol Genet 2016 Oct 25;2(5):e98. Epub 2016 Aug 25.

Cambridge Institute for Medical Research (J.H., J.R.E.), University of Cambridge, Addenbrooke's Hospital, UK; Children's Health Research Center (M.M., A.Y.), Cancer Biology Research Center, Sanford Research, Sioux Falls; Neurogenetics Group (K.S., T.D., J.B., P.D.J.), Department of Molecular Genetics VIB, Antwerp, Belgium; Department of Neurology (K.S., J.B., P.D.J.), Antwerp University Hospital, Belgium; Laboratories of Neurogenetics and Neuropathology (K.S., T.D., J.B., P.D.J.), Institute Born-Bunge, University of Antwerp, Belgium; Department of Neurology (L.S., J. Liepert), Hertie Institute for Clinical Brain Research, Tübingen, Germany; German Center for Neurodegenerative Diseases (DZNE) (L.S.), Tübingen, Germany; Department of Neurology (J. Li), Vanderbilt University, Nashville, TN; Department of Ophthalmology (E.V.A.), Department of Neurology (J.D.B.), Ghent University Hospital, Belgium; National Eye Institute (M.B.D.), National Institutes of Health, Bethesda, MD; Cell Biology Section (R.H.R., C.B.), Neurogenetics Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD; Department of Neurology (R.H.R.), Johns Hopkins University School of Medicine, Baltimore, MD; Department of Neurorehabilitation (J. Liepert), Kliniken Schmieder, Allensbach, Germany; Department of Human Genetics and Hussman Institute for Human Genomics (S.Z.), Miller School of Medicine, University of Miami, FL; Genetics of Neurodegenerative and Metabolic Diseases Unit (C.M.), IRCCS-Fondazione Istituto Neurologico Carlo Besta, Milan, Italy; Departments of Child Health, Neurology & Genetics (M.C.K.), University of Arizona College of Medicine, Phoenix; Program in Neuroscience (M.C.K.), Arizona State University, Tempe; and Pediatric Movement Disorders Program and Neurogenetics Research Program (M.C.K.), Barrow Neurological Institute, Phoenix Children's Hospital, AZ.

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http://dx.doi.org/10.1212/NXG.0000000000000098DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5001803PMC
October 2016

Neurologic syndrome associated with homozygous mutation at MAG sialic acid binding site.

Ann Clin Transl Neurol 2016 08 23;3(8):650-4. Epub 2016 Jun 23.

Neurogenetics Branch National Institute of Neurological Disorders and Stroke National Institutes of Health Bethesda Maryland.

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http://dx.doi.org/10.1002/acn3.329DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4999596PMC
August 2016

Fragile X Tremor Ataxia Syndrome With Rapidly Progressive Myopathy.

JAMA Neurol 2015 Aug;72(8):946-8

Department of Neurology, NYU School of Medicine, New York.

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http://archneur.jamanetwork.com/article.aspx?doi=10.1001/jam
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http://dx.doi.org/10.1001/jamaneurol.2015.0812DOI Listing
August 2015

Laing distal myopathy pathologically resembling inclusion body myositis.

Ann Clin Transl Neurol 2014 Dec 6;1(12):1053-8. Epub 2014 Nov 6.

Department of Neurology, Johns Hopkins University School of Medicine Baltimore, Maryland ; Department of Neuroscience, Johns Hopkins University School of Medicine Baltimore, Maryland.

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http://dx.doi.org/10.1002/acn3.140DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4284131PMC
December 2014

Ataxia with oculomotor apraxia type 2 fibroblasts exhibit increased susceptibility to oxidative DNA damage.

J Clin Neurosci 2014 Sep 6;21(9):1627-31. Epub 2014 May 6.

Cell Biology Section, Neurogenetics Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Building 35, Room 2C-911, 9000 Rockville Pike, Bethesda, MD 20892-3738, USA.

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https://linkinghub.elsevier.com/retrieve/pii/S09675868140011
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http://dx.doi.org/10.1016/j.jocn.2013.11.048DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4127342PMC
September 2014

Role of the Reverse Transcriptase, Nucleocapsid Protein, and Template Structure in the Two-step Transfer Mechanism in Retroviral Recombination.

J Biol Chem 2003 Aug 11;278(34):31536-46. Epub 2003 Jun 11.

Department of Biochemistry and Biophysics, University of Rochester, Rochester, New York 14642, USA.

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http://dx.doi.org/10.1074/jbc.M304608200DOI Listing
August 2003

Strand transfer occurs in retroviruses by a pause-initiated two-step mechanism.

J Biol Chem 2002 Dec 4;277(49):46900-11. Epub 2002 Oct 4.

Department of Biochemistry and Biophysics, University of Rochester Medical Center, Rochester, New York 14642, USA.

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http://www.jbc.org/lookup/doi/10.1074/jbc.M208638200
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http://dx.doi.org/10.1074/jbc.M208638200DOI Listing
December 2002