Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Jeanne Dekdebrun"'
Autor:
Chad Heatwole, Elizabeth Luebbe, Johanna Hamel, Philip Mongiovi, Emma Ciafaloni, Nuran Dilek, William Martens, David Weber, Rashid Hani, Jamie Allen, Claire Smith, Samantha Howell, Spencer Rosero, Katy Eichinger, Linday Baker, Jeanne Dekdebrun, Jim Hilbert, Anika Varma, Michael McDermott, Charles Thornton, Richard Moxley
Publikováno v:
Thursday, April 27.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::afd63fdd53d8a52e822a84008710698e
https://doi.org/10.1212/wnl.0000000000202958
https://doi.org/10.1212/wnl.0000000000202958
Publikováno v:
Muscle & Nerve. 66:336-339
Remote study visits (RSVs) are emerging as important tools for clinical research. We tested the feasibility of using RSVs to evaluate patients with myotonic dystrophy type 1 (DM1), including remote quantitative assessment of muscle function, and we a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e71e9580ef38bae8ab4db91d5792aa38
https://doi.org/10.1002/mus.27559
https://doi.org/10.1002/mus.27559
Autor:
Gayle K, Deutsch, Katharine A, Hagerman, Jacinda, Sampson, Gersham, Dent, Jeanne, Dekdebrun, Dana M, Parker, Charles A, Thornton, Chad R, Heatwole, Sub H, Subramony, Ami K, Mankodi, Tetsuo, Ashizawa, Jeffrey M, Statland, W David, Arnold, Richard T, Moxley, John W, Day
Publikováno v:
Muscle Nerve
Myotonic dystrophy type 1 (DM1) is known to affect cognitive function, but the best methods to assess central nervous system involvement in multicenter studies have not been determined. In this study our primary aim was to evaluate the potential of c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de9e6a103276407a2bfbbf964cbe5a08
https://doi.org/10.1002/mus.27520
https://doi.org/10.1002/mus.27520
Autor:
Wojciech Zareba, Jeanne Dekdebrun, Nicholas E. Johnson, James E. Hilbert, Christopher A. Beck, Araya Puwanant, William B. Martens, Charles A. Thornton, Michael P. McDermott, Chad Heatwole, Katy Eichinger, Richard T. Moxley, Elizabeth Luebbe, Christine Zizzi, Spencer Rosero, Nuran Dilek, Giovanni Schifitto, Rabi Tawil, J. Franklin Richeson
Publikováno v:
Neurology
ObjectiveTo assess mexiletine's long-term safety and effect on 6-minute walk distance in a well-defined cohort of patients with myotonic dystrophy type 1 (DM1).MethodsWe performed a randomized, double-blind, placebo-controlled trial of mexiletine (15
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::052924b7c00134145a0aabd091edbfbf
https://doi.org/10.1212/wnl.0000000000011002
https://doi.org/10.1212/wnl.0000000000011002
Autor:
Elizabeth Luebbe, James E. Hilbert, Charles A. Thornton, Nicholas E. Johnson, Rita K. Bode, Jeanne Dekdebrun, Eric L. Logigian, Nuran Dilek, Nan E. Rothrock, Araya Puwanant, Michael P. McDermott, David Victorson, William B. Martens, Katy Eichinger, Chad Heatwole, Richard T. Moxley, Shree Pandya, Barbara G. Vickrey
Publikováno v:
Muscle & Nerve. 53:183-190
Introduction The Myotonic Dystrophy Health Index (MDHI) is a disease-specific patient-reported outcome measure. Here, we examine the associations between the MDHI and other measures of disease burden in a cohort of individuals with myotonic dystrophy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::039e742f90156273cb5f123932fa9d93
https://doi.org/10.1002/mus.24725
https://doi.org/10.1002/mus.24725
Autor:
Chad, Heatwole, Nicholas, Johnson, Jeanne, Dekdebrun, Nuran, Dilek, Kate, Eichinger, James, Hilbert, Elizabeth, Luebbe, William, Martens, Michael P, Mcdermott, Charles, Thornton, Richard, Moxley
Publikováno v:
Musclenerve.
When preparing for clinical trials in myotonic dystrophy type-1 (DM1), it is important that researchers develop and identify patient-reported outcome measures with good measurement properties.Fifty-two DM1 patients enrolled in 2 clinical studies comp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::27357b6eddc8f92dc83c12291aa8662a
https://pubmed.ncbi.nlm.nih.gov/29328504
https://pubmed.ncbi.nlm.nih.gov/29328504
Autor:
Chad Heatwole, Nicholas E. Johnson, Richard T. Moxley, Mark Heatwole, William B. Martens, Jeanne Dekdebrun, Rita K. Bode, Nan E. Rothrock, Charles A. Thornton, Michael P. McDermott, Elizabeth Luebbe, James E. Hilbert, Nuran Dilek, Barbara G. Vickrey, David Victorson
Publikováno v:
Muscle & Nerve. 49:906-914
Introduction: In preparation for clinical trials we examine the validity, reliability, and patient understanding of the Myotonic Dystrophy Health Index (MDHI). Methods: Initially we partnered with 278 myotonic dystrophy type-1 (DM1) patients and iden
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e40cf1117efa2fbc69ff5e386d89220
https://doi.org/10.1002/mus.24097
https://doi.org/10.1002/mus.24097
Autor:
Michael P. McDermott, Nicholas E. Johnson, David Victorson, Charles A. Thornton, Jeanne Dekdebrun, Christine Quinn, Rita K. Bode, William B. Martens, Nuran Dilek, Nan E. Rothrock, Elizabeth Luebbe, Chad Heatwole, Richard T. Moxley, Barbara G. Vickrey, James E. Hilbert
Publikováno v:
Neurology. 85(24)
To determine the frequency and relative importance of the most life-affecting symptoms in myotonic dystrophy type 2 (DM2) and to identify the factors that have the strongest association with these symptoms.We conducted a cross-sectional study of adul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7afa18591dc97ed27a67bae597f8705
https://pubmed.ncbi.nlm.nih.gov/26581301
https://pubmed.ncbi.nlm.nih.gov/26581301
Publikováno v:
Neuromuscular Disorders. 23:833
Individuals with myotonic dystrophy (DM) type 1 are less active than healthy individuals, which may result in secondary complications and decreased functional abilities. Therefore, the purpose of this study was to document the physical activity profi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8897004d4324083530b649a30867c61f
https://doi.org/10.1016/j.nmd.2013.06.673
https://doi.org/10.1016/j.nmd.2013.06.673
Autor:
W. Martens, Chad Heatwole, Richard T. Moxley, Jeanne Dekdebrun, Nuran Dilek, Charles A. Thornton, Katy Eichinger, Shree Pandya
Publikováno v:
Neuromuscular Disorders. 23:833
Patients with myotonic dystrophy (DM1) have distal upper extremity weakness which initially focuses on the long finger flexors. Grip strength using a Jamar dynamometer with the handle in the second position has provided reliable measurement of hand s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::35b8ce3e098553184c846caef01b1d74
https://doi.org/10.1016/j.nmd.2013.06.672
https://doi.org/10.1016/j.nmd.2013.06.672