Research Topics
| Chad HeatwoleSummaryAffiliation: University of Rochester Country: USA Publications
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Detail Information
Publications
Patient-reported impact of symptoms in myotonic dystrophy type 1 (PRISM-1)Chad Heatwole
University of Rochester, Rochester, NY, USA
Neurology 79:348-57. 2012..To determine the most critical symptoms in a national myotonic dystrophy type 1 (DM1) population and to identify the modifying factors that have the greatest effect on the severity of these symptoms...
Plasma exchange versus intravenous immunoglobulin for myasthenia gravis crisis: an acute hospital cost comparison studyChad Heatwole
Department of Neurology, University of Rochester, Rochester, NY 14642, USA
J Clin Neuromuscul Dis 13:85-94. 2011..To compare the short-term financial costs of treating a patient in myasthenia gravis crisis with intravenous immunoglobulin (IVIG) versus plasma exchange...
Extreme spindles: a distinctive EEG pattern in Mycoplasma pneumoniae encephalitisChad R Heatwole
University of Rochester, NY, USA
Neurology 64:1096-7. 2005
Laboratory abnormalities in patients with myotonic dystrophy type 2Chad Heatwole
Neuromuscular Division, Department of Neurology, University of Rochester Medical Center, Rochester, NY 14642, USA
Arch Neurol 68:1180-4. 2011..Similar to DM1, this disease causes progressive debilitating weakness, clinical myotonia, and early cataracts and is thought to cause widespread physiologic dysfunction of multiple organ systems...
Open-label trial of recombinant human insulin-like growth factor 1/recombinant human insulin-like growth factor binding protein 3 in myotonic dystrophy type 1Chad R Heatwole
University of Rochester Medical Center, Rochester, NY 14642, USA
Arch Neurol 68:37-44. 2011..To evaluate the safety and tolerability of recombinant human insulin-like growth factor 1 (rhIGF-1) complexed with IGF binding protein 3 (rhIGF-1/rhIGFBP-3) in patients with myotonic dystrophy type 1 (DM1)...
International Education Issues: practicing and teaching international neurology: the Krakow experienceChad Heatwole
The University of Rochester, 174 Edgemont Rd, Rochester, NY 14620, USA
Neurology 69:1721-3. 2007
Laboratory abnormalities in ambulatory patients with myotonic dystrophy type 1Chad R Heatwole
Neuromuscular Disease Center, Strong Memorial Hospital, University of Rochester, 601 Elmwood Avenue, Rochester, NY 14642, USA
Arch Neurol 63:1149-53. 2006..Myotonic dystrophy type 1 (DM1) is the most prevalent form of adult muscular dystrophy worldwide. Although well known for the classic manifestations of myotonia, weakness, and early cataracts, it has broad effects on multiple organ systems...
The nondystrophic myotoniasChad R Heatwole
Department of Neurology, University of Rochester, Rochester, New York, USA
Neurotherapeutics 4:238-51. 2007....
Reevaluating measures of disease progression in facioscapulohumeral muscular dystrophyJeffrey M Statland
Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA
Neuromuscul Disord 23:306-12. 2013....
Evoked myotonia can be "dialed-up" by increasing stimulus train length in myotonic dystrophy type 1Eric L Logigian
Department of Neurology, University of Rochester Medical Center, Box 673, 601 Elmwood Avenue, Rochester, New York, USA
Muscle Nerve 41:191-6. 2010..Evoked myotonia testing utilizing a stimulus paradigm of at least 20 stimuli at 30-50 HZ may be useful in antimyotonic drug trials, particularly when grip RT is normal or equivocal...
