Search Results - "Kennelly, Kathleen D."

Occurrence of Crohn's disease with Parkinson’s disease by Fujioka, Shinsuke, MD, Curry, Sadie E., DS, Kennelly, Kathleen D., MD, PhD, Tacik, Pawel, MD, Heckman, Michael G., MS, Tsuboi, Yoshio, MD, PhD, Strongosky, Audrey J, van Gerpen, Jay A., MD, Uitti, Ryan J., MD, Ross, Owen A., PhD, Ikezu, Tsuneya, MD, PhD, Wszolek, Zbigniew K., MD

“…Abstract We retrospectively investigated the co-occurrence of Crohn's disease in a cohort of 876 patients with Parkinson’s disease, based on the observation…”
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Electrodiagnostic Approach to Cranial Neuropathies by Kennelly, Kathleen D., MD, PhD

“…This article is a general review of cranial nerve conduction studies, including techniques as well as interpretation of data. The needle examination of various…”
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Patient Experience Contributing to Outcomes of Laryngeal Botulinum Toxin Injection by Rutt, Amy, Kennelly, Kathleen D., Martinez-Paredes, Jhon F.

“…Laryngeal Botulinum Toxin injection (LBTX) in the adductor musculature is the current therapy for Adductor Spasmodic Dysphonia. This study explores…”
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Clinical neurophysiology of cranial nerve disorders by Kennelly, Kathleen D

“…Electrophysiologic techniques are available to measure many of the cranial nerves. The procedures can be done using equipment available in standard clinical…”
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Improving referring physicians' understanding of electromyography reports when qualifying radiculopathies: A need for standardized terminology by Mauricio, Elizabeth A., Dimberg, Elliot L., Kennelly, Kathleen D., Rubin, Devon I.

“…ABSTRACT Electromyographic (EMG) reporting of radiculopathies is not standardized, and the terminology used in reports can be misinterpreted by referring…”
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Whole‐exome sequencing for variant discovery in blepharospasm by Tian, Jun, Vemula, Satya R., Xiao, Jianfeng, Valente, Enza Maria, Defazio, Giovanni, Petrucci, Simona, Gigante, Angelo Fabio, Rudzińska‐Bar, Monika, Wszolek, Zbigniew K., Kennelly, Kathleen D., Uitti, Ryan J., van Gerpen, Jay A., Hedera, Peter, Trimble, Elizabeth J., LeDoux, Mark S.

“…Background Blepharospasm (BSP) is a type of focal dystonia characterized by involuntary orbicularis oculi spasms that are usually bilateral, synchronous, and…”
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The effect of paired stimuli on blink reflex latencies in normal subjects by Rubin, Devon I., Dimberg, Elliot L., Kennelly, Kathleen D.

“…Introduction: In this study we assessed the effect of paired stimuli on the latencies and amplitudes of the blink reflex. Methods: Blink reflexes were…”
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Cryoglobulinemic vasculitis in a patient with CREST syndrome by Hurst, Rebecca L, Berianu, Florentina, Ginsburg, William W, Klein, Christopher J, Englestad, Janean K, Kennelly, Kathleen D

“…Abstract Cryoglobulinemic vasculitis is a rare entity. Although it has been reported in diffuse systemic sclerosis, it has not been reported in calcinosis,…”
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Electrophysiological Evaluation of Cranial Neuropathies by Kennelly, Kathleen D.

“…BACKGROUND:Cranial nerve abnormalities occur frequently in both focal and diffuse neurologic disorders and can be evaluated by electrophysiological techniques…”
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Popliteus muscle hemorrhage as a rare cause of a proximal tibial neuropathy by Dimberg, Elliot L, Rubin, Devon I, Ortiguera, Cedric J, Kennelly, Kathleen D

“…Abstract Proximal tibial neuropathy is an uncommon focal mononeuropathy that is most often caused by trauma, ischemia, or neoplastic infiltration or…”
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Whole exome sequencing of a patient with suspected mitochondrial myopathy reveals novel compound heterozygous variants in RYR1 by Blackburn, Patrick R., Selcen, Duygu, Gass, Jennifer M., Jackson, Jessica L., Macklin, Sarah, Cousin, Margot A., Boczek, Nicole J., Klee, Eric W., Dimberg, Elliot L., Kennelly, Kathleen D., Atwal, Paldeep S.

“…Background Pathogenic variants in ryanodine receptor 1 (RYR1, MIM# 180901) are the cause of congenital myopathy with fiber‐type disproportion, malignant…”
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Whole exome sequencing of a patient with suspected mitochondrial myopathy reveals novel compound heterozygous variants in RYR 1 by Blackburn, Patrick R., Selcen, Duygu, Gass, Jennifer M., Jackson, Jessica L., Macklin, Sarah, Cousin, Margot A., Boczek, Nicole J., Klee, Eric W., Dimberg, Elliot L., Kennelly, Kathleen D., Atwal, Paldeep S.

“…Abstract Background Pathogenic variants in ryanodine receptor 1 ( RYR 1, MIM # 180901) are the cause of congenital myopathy with fiber‐type disproportion,…”
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Defining Normal Duration for Afterdischarges With Repetitive Nerve Stimulation: A Pilot Study by Bodkin, Cynthia L, Kennelly, Kathleen D, Boylan, Kevin B, Crook, Julia E, Heckman, Michael G, Rubin, Devon I

“…The presence of afterdischarges on repetitive nerve stimulation may be useful to diagnose cramp fasciculation syndrome, however, the presence and normal…”
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Reply by Mauricio, Elizabeth A., Dimberg, Elliot L., Kennelly, Kathleen D., Rubin, Devon I.

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Reply by Mauricio, Elizabeth A., Dimberg, Elliot L., Kennelly, Kathleen D., Rubin, Devon I.

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Reply by Mauricio, Elizabeth A., Dimberg, Elliot L., Kennelly, Kathleen D., Rubin, Devon I.

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Reply by Mauricio, Elizabeth A, Dimberg, Elliot L, Kennelly, Kathleen D, Rubin, Devon I

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Improving referring physicians' understanding of electromyography reports when qualifying radiculopathies: A need for standardized terminology: Short Reports by Mauricio, Elizabeth A., Dimberg, Elliot L., Kennelly, Kathleen D., Rubin, Devon I.

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Editorial by concerned physicians: Unintended effect of the orphan drug act on the potential cost of 3,4-diaminopyridine by Burns, Ted M., Smith, Gordon A., Allen, Jeffrey A., Arnold, W. David, Barohn, Richard, Benatar, Michael, Bird, Shawn J., Bromberg, Mark, Chahin, Nizar, Ciafaloni, Emma, Cohen, Jeffrey A., Corse, Andrea, Crum, Brian A., David, William S., Dimberg, Elliot, Sousa, Eduardo A. De, Donofrio, Peter D., Engel, Andrew G., Ensrud, Erik R., Ferrante, Mark, Freimer, Miriam, Gable, Karissa L., Gibson, Summer, Gilchrist, James M., Goldstein, Jonathan M., Gooch, Clifton L., Goodman, Brent P., Gorelov, Dmitri, Gospe Jr, Sidney M., Goyal, Namita A., Guidon, Amanda C., Guptill, Jeffrey T., Gutmann, Laurie, Gutmann, Ludwig, Gwathmey, Kelly, Harati, Yadollah, Harper Jr, C. Michel, Hehir, Michael K., Hobson-Webb, Lisa D., Howard Jr, James F., Jackson, Carlayne E., Johnson, Nicholas, Jones, Sarah M., Juel, Vern C., Kaminski, Henry J., Karam, Chafic, Kennelly, Kathleen D., Khella, Sami, Khoury, Julie, Kincaid, John C., Kissel, John T., Kolb, Noah, Lacomis, David, Ladha, Shafeeq, Larriviere, Daniel, Lewis, Richard A., Li, Yuebing, Logigian, Eric, Lou, Jau-Shin, MacGowen, Daniel J.L., Maselli, Ricardo, Massey, Janice M., Mauermann, Michelle L., Mathews, Katherine D., Meriggioli, Matthew N., Miller, Robert G., Moon, Joon-Shik, Mozaffar, Tahseen, Nations, Sharon P., Nowak, Richard J., Pascuzzi, Robert M., Peltier, Amanda, Ruzhansky, Katherine, Richman, David P., Ross, Mark A., Rubin, DEVON I., Russell, James A., Sachs, George M., Salajegheh, Mohammad Kian, Saperstein, David S., Scelsa, Stephen, Selcen, Duygu, Shieh, Perry B., Silvestri, Nicholas J., Singleton, J. Rob, Smith, Benn E., So, Yuen T., Solorzano, Guillermo, Sorenson, Eric J., Srinivasen, Jayashri, Tavee, Jinny, Tawil, Rabi, Thornton, Charles, Trivedi, Jaya, Vernino, Steven, Wang, Annabel K., Webb, Tyler A., Weiss, Michael D., Windebank, Anthony J., Wolfe, Gil I.

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Robotic-assisted rehabilitation for Parsonage-Turner syndrome by Duret, Christophe, Lehenaff, Laurent, Hutin, Emilie, Aghasaryan, Manvel, Gracies, Jean-Michel

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