15 results on '"Chong, Peter Siao Tick"'
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2. Phosphoglycerate mutase deficiency with tubular aggregates in a patient from panama
- Author
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Salameh, Johnny, Goyal, Namita, Choudry, Rabia, Camelo-Piragua, Sandra, and Chong, Peter Siao Tick
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- 2013
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3. Cervical nerve root stimulation. Part I: Technical aspects and normal data
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Vucic, Steve, Cairns, Kevin D., Black, Kristin R., Chong, Peter Siao Tick, and Cros, Didier
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- 2006
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4. PATIENT WITH AMYLOIDOMA OF THE ULNAR NERVE AND SALIVARY GLANDS
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Salameh, Johnny, Baran, Johanna L., and Chong, Peter Siao Tick
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- 2009
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5. Natural history of vocal fold paralysis in Arnold-Chiari malformation
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King, Ericka F., Zwienenberg-Lee, Marike, Maturo, Steve, Chong, Peter Siao Tick, Hartnick, Christopher, and Brown, David J.
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- 2011
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6. Relapsing Guillain Barré Syndrome and nephrotic syndrome secondary to focal segmental glomerulosclerosis
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Souayah, Nizar, Cros, Didier, Stein, T.D., and Chong, Peter Siao Tick
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- 2008
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7. Acute sensory neuronopathy as the presenting symptom of Sjögren’s syndrome
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Souayah, Nizar, Chong, Peter Siao Tick, and Cros, Didier
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- 2006
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8. Serial Electromyography of the Thyroarytenoid Muscles Using the NIM-Response System in a Canine Model of Vocal Fold Paralysis.
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Scott, Andrew R., Chong, Peter Siao Tick, Brigger, Matthew T., Randolph, Gregory W., and Hartnick, Christopher J.
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LARYNGECTOMY , *ELECTROMYOGRAPHY , *IATROGENIC diseases , *VENTRICULAR fibrillation ,VOCAL cord diseases - Abstract
Objectives: We sought to determine whether serial intraoperative laryngeal electromyography (L-EMG) or evoked L-EMG predicts vocal fold (VF) recovery following iatrogenic injury. Methods: Six beagles were sedated, and bipolar needle electrodes were inserted into each thyroarytenoid (TA) muscle. Endotracheal tube surface electrodes were also placed. As the sedation lightened. L-EMG activity was recorded from all electrodes with an intraoperative nerve monitoring system. The neck was opened, and direct recurrent laryngeal nerve (RLN) stimulation was performed. Subsequently, 4 animals underwent crush injury of the left RLN, and 2 animals underwent nerve transection. The L-EMG procedures were repeated every 1 to 2 weeks until left VF motion was observed in the dogs that suffered RLN crush injury. At each time point, the neck was opened and both RLNs were stimulated. Results: Fibrillation potentials were detected in ail animals after RLN injury. A change to electrical silence was seen in the animals in the crush injury group that were evaluated during the week preceding VF recovery. Fibrillation potentials and VF immobility persisted in the transection group throughout the complete time course of these experiments. The first appearance of an evoked response coincided with occurred after the return of left VF motion in the crush injury group. The threshold, latency, and amplitude differed from those of the controls and approached normal values over time. No response was detected in the transected nerves. Conclusions: The disappearance of fibrillations on intraoperative L-EMG was noted in the animals tested the week before the return of VF motion, and the return of motor unit action potentials was seen along with return of VF function. Evoked L-EMG was not helpful in predicting the return of VF mobility, but it may help quantify degrees of RLN injury and predict the speed of recovery. [ABSTRACT FROM AUTHOR]
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- 2009
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9. Intraoperative laryngeal electromyography in children with vocal fold immobility: results of a multicenter longitudinal study.
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Maturo SC, Braun N, Brown DJ, Chong PS, Kerschner JE, and Hartnick CJ
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- Brain Diseases surgery, Child, Child, Preschool, Ductus Arteriosus, Patent surgery, Evoked Potentials, Motor physiology, Female, Heart Defects, Congenital surgery, Humans, Infant, Infant, Newborn, Laryngeal Muscles innervation, Laryngoscopy, Longitudinal Studies, Male, Postoperative Complications etiology, Postoperative Complications physiopathology, Postoperative Complications surgery, Predictive Value of Tests, Prognosis, Recurrent Laryngeal Nerve physiopathology, Tracheoesophageal Fistula surgery, Vocal Cord Paralysis etiology, Vocal Cord Paralysis physiopathology, Electromyography methods, Monitoring, Intraoperative methods, Vocal Cord Paralysis diagnosis
- Abstract
Objectives: To determine whether laryngeal electromyography (LEMG) can predict recurrent laryngeal nerve function return in children and whether LEMG can aid in the management of vocal fold immobility (VFI)., Design: Prospective case series., Setting: Tertiary pediatric aerodigestive centers., Patients: Twenty-five children aged 14 days to 7 years at the time of first LEMG (mean age, 21.4 months) with VFI who underwent flexible fiberoptic laryngeal examination, intraoperative LEMG of the thyroarytenoid muscles, and 12-month follow-up., Main Outcome Measures: To compare results of LEMG with flexible fiberoptic laryngeal examination in children with vocal fold paresis and to determine if LEMG can predict vocal fold return., Results: In children who had a patent ductus arteriosus ligation, the LEMG data suggest that if there is no activity 6 months after injury, then the nerve is unlikely to regain function. In 3 of 3 children with central causes of VFI, normal LEMG findings predicted return of nerve function 2 to 7 months before vocal fold movement on fiberoptic examination. Finally, in 3 of 3 children with idiopathic VFI, LEMG predicted return within 2 to 14 months of vocal folds with normal findings., Conclusions: Intraoperative LEMG is a safe, easy-to-use method for determining the likelihood of recurrent laryngeal nerve function return in children who have undergone patent ductus arteriosus ligation, in children with centrally correctable lesions, and in children with idiopathic VFI. More work is needed in the area of pediatric LEMG, but it is possible that LEMG data can be used to aid in management strategies and provide families with more information to make better informed decisions regarding their child's care.
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- 2011
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10. Spontaneous and evoked laryngeal electromyography of the thyroarytenoid muscles: a canine model for intraoperative recurrent laryngeal nerve monitoring.
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Scott AR, Chong PS, Hartnick CJ, and Randolph GW
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- Action Potentials, Animals, Dogs, Electrodes, Electromyography, Feasibility Studies, Intraoperative Complications physiopathology, Models, Animal, Monitoring, Intraoperative, Recurrent Laryngeal Nerve Injuries, Intraoperative Complications diagnosis, Laryngeal Muscles physiology, Recurrent Laryngeal Nerve physiology
- Abstract
Objectives: We sought to determine the feasibility of performing spontaneous and evoked intraoperative laryngeal electromyography (L-EMG) using nerve monitoring equipment and to compare recording electrode configurations and methods of recurrent laryngeal nerve (RLN) stimulation in dogs., Methods: Four beagles underwent crush injury of the left RLN, and 2 beagles underwent left RLN transection. Serial spontaneous and evoked L-EMG was recorded with the NIM-Response nerve monitoring system under sedation. Transesophageal, percutaneous, and direct open RLN stimulation was performed. Recordings of spontaneous and evoked responses were made with endotracheal tube surface electrodes and bipolar vocal fold needle electrodes. The L-EMG procedures were repeated every 1 to 2 weeks after injury, and intersubject and intertrial differences were evaluated., Results: Low-amplitude motor unit action potentials, polyphasic potentials, fasciculations, and fibrillations were detected in injured animals with bipolar needle recording electrodes with this system of spontaneous L-EMG. The surface recording electrodes did not detect pathologic waveforms. Percutaneous needle stimulation of the RLN is possible at currents slightly higher than those used for direct stimulation. Consistent, discrete, transesophageal stimulation of the RLN could not be reliably performed. Recording evoked responses with needle electrodes generated sharper waveforms, facilitating calculation of latency and wave duration. Evoked L-EMG utilizing surface recording electrodes limited the intertrial and intersubject variability of evoked amplitude., Conclusions: Typical patterns of nerve injury can be detected with this system of intraoperative L-EMG in a canine model. Quantitative measures of amplitude, latency, and wave duration in healthy and injured canine RLNs may be determined with this system.
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- 2010
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11. Multifocal motor neuropathy with conduction block: Distribution of demyelination and axonal degeneration.
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Vucic S, Black K, Chong PS, and Cros D
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- Action Potentials physiology, Adult, Aged, Demyelinating Diseases pathology, Electric Stimulation methods, Female, Humans, Male, Middle Aged, Motor Neuron Disease pathology, Muscle, Skeletal physiopathology, Neural Conduction physiology, Reaction Time physiology, Demyelinating Diseases physiopathology, Electrophysiology, Motor Neuron Disease physiopathology, Nerve Degeneration physiopathology
- Abstract
Objective: Multifocal motor neuropathy with conduction block (MMN) is an immune-mediated neuropathy, characterized by progressive muscle weakness. Although demyelination is regarded as the underlying pathophysiologic mechanism of MMN, recently, it was reported that different pathophysiologic mechanisms were responsible for disease in the upper and lower limbs. Specifically, demyelination in the upper limbs and axonal loss in the lower limbs. Consequently, the aim of the present study was to assess, through clinical neurophysiology studies, whether different pathophysiologic mechanisms were occurring in the upper and lower extremities. Furthermore, we wanted to investigate whether the presence of conduction block (CB) correlated with axonal degeneration (AD), and to determine the electrophysiological abnormalities that correlate with muscle weakness., Methods: We reviewed medical records of 18 patients with MMN for clinical features (using the Medical Research Council score and Guys Neurology Disability Scale) and neurophysiologic abnormalities (CB, AD prolongation of distal motor and F-wave latencies, and reduction of conduction velocity in the demyelinating range)., Results: Electrophysiological abnormalities deemed specific of demyelination were non-significantly different in the upper and lower extremities. The presence of axonal degeneration correlated significantly with conduction block (odds ratio 10.4, 95% CI 4.2-25.6), and both parameters correlated with muscle weakness (P<0.01)., Conclusion: Our study suggests that the same pathophysiologic process occurs in the upper and lower extremity nerves. Moreover, one pathophysiologic process may be responsible for the development of CB and AD, and therefore muscle weakness., Significance: The present study has established that both AD and CB occur in MMN, irrespective of extremity, and both correlate with muscle weakness.
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- 2007
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12. Multifocal motor neuropathy: decrease in conduction blocks and reinnervation with long-term IVIg.
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Vucic S, Black KR, Chong PS, and Cros D
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- Action Potentials drug effects, Adult, Axons drug effects, Axons physiology, Drug Administration Schedule, Female, Follow-Up Studies, Humans, Immunoglobulins, Intravenous administration & dosage, Male, Middle Aged, Motor Neuron Disease physiopathology, Muscle Weakness physiopathology, Muscle Weakness therapy, Muscles drug effects, Muscles physiopathology, Nerve Degeneration physiopathology, Polyneuropathies physiopathology, Immunoglobulins, Intravenous therapeutic use, Motor Neuron Disease therapy, Neural Conduction drug effects, Polyneuropathies therapy
- Abstract
Background: Multifocal motor neuropathy with conduction blocks (MMNCB) is an immune-mediated motor neuropathy. Previous long-term IV immunoglobulin (IVIg) treatment studies have documented improvement in muscle strength and functional disability but revealed a concomitant increase in acute axonal degeneration (AD) and conduction block (CB)., Objective: To determine the long-term effects of IVIg therapy on clinical and neurophysiologic outcome measures in MMNCB patients responsive to IVIg., Methods: The authors reviewed medical records of 10 patients with MMNCB for outcomes in muscle strength (Medical Research Council score), functional disability (Modified Rankin Disability score), CB, and AD. All patients had received IVIg (2g/kg in 5 days for 3 consecutive months), followed by monthly maintenance therapy., Results: Patients were followed for an average of 7.25 years (range, 3.5 to 12 years). There was significant and sustained improvement in muscle strength and functional disability while on IVIg therapy. Furthermore, the authors found significant improvement in CB, decrease in AD, and evidence of reinnervation by the end of the follow-up period., Conclusion: Long-term IV immunoglobulin therapy improves muscle strength and functional disability, decreases the number of conduction blocks and the extent of axonal degeneration, and promotes reinnervation. These findings differ from previous reports of deterioration in neurophysiologic outcome measures. Comparison of the IV immunoglobulin regimen in those reports and this study shows that the authors' patients were treated with significantly higher IV immunoglobulin maintenance doses. These findings have implications for the long-term treatment of patients with multifocal motor neuropathy with conduction blocks.
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- 2004
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13. Neurophysiologic findings in early acute inflammatory demyelinating polyradiculoneuropathy.
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Vucic S, Cairns KD, Black KR, Chong PS, and Cros D
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- Adolescent, Adult, Aged, Aged, 80 and over, Blinking physiology, Child, Child, Preschool, Disease Progression, Electric Stimulation, Electromyography, Evoked Potentials physiology, Female, H-Reflex physiology, Humans, Male, Middle Aged, Neural Conduction, Neurologic Examination, Retrospective Studies, Guillain-Barre Syndrome physiopathology
- Abstract
Background: Patients with early acute inflammatory demyelinating polyradiculoneuropathy (AIDP) may not meet the current neurophysiologic criteria., Objective: To document neurophysiologic findings in early AIDP., Methods: Clinical and neurophysiologic data from 38 AIDP patients, assessed within 10 days of symptom onset were reviewed., Results: In addition to absent H reflexes and abnormal F-wave responses in the acute stage of AIDP, abnormalities of blink reflexes, upper limb sensory responses abnormalities with spared sural responses, presence of distal CMAP dispersion, and A-waves were frequently observed. Established demyelinating neurophysiologic parameters were infrequently seen., Conclusions: Abnormalities of H reflexes and F responses were most frequently noted in early AIDP. Additionally, distal temporal dispersion, prolonged or absent blink reflexes, and A-waves were often present in the acute stage of AIDP when classic diagnostic criteria of AIDP were not satisfied., Significance: Neurophysiologic studies in early AIDP frequently reveal abnormalities that are not specific of primary demyelinating neuropathy.
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- 2004
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14. Technology literature review: quantitative sensory testing.
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Chong PS and Cros DP
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- Humans, Neural Conduction physiology, Peripheral Nervous System Diseases diagnosis, Peripheral Nervous System Diseases physiopathology, Practice Guidelines as Topic, Reproducibility of Results, Sensation Disorders physiopathology, Electrodiagnosis methods, Electrodiagnosis standards, Neurologic Examination methods, Neurologic Examination standards, Sensation Disorders diagnosis, Sensory Thresholds physiology
- Abstract
The development of the personal computer has simplified the process of quantitating sensory thresholds using various testing algorithms. We reviewed the technical aspects and reproducibility of different methods to determine threshold for light touch-pressure, vibration, thermal, and pain stimuli. Clinical uses and limitations of quantitative sensory testing (QST) were also reviewed. QST is a reliable psychophysical test of large- and small-fiber sensory modalities. The results of QST are highly dependent on methodology and the full cooperation of the subject. QST has been shown to be reasonably reproducible over a period of days or weeks in normal subjects. The use of QST in research and patient care should be limited to instruments and their corresponding methodologies that have been shown to be reproducible. Literature data do not allow conclusions regarding the relative merits of individual QST instruments.
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- 2004
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15. Atypical presentations of primary amyloid neuropathy.
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Vucic S, Chong PS, and Cros D
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- Action Potentials physiology, Adipose Tissue pathology, Aged, Amyloid Neuropathies pathology, Demyelinating Diseases pathology, Electromyography, Female, Humans, Lymph Nodes pathology, Male, Middle Aged, Neural Conduction physiology, Neurologic Examination, Peripheral Nervous System Diseases pathology, Sural Nerve pathology, Amyloid Neuropathies diagnosis
- Abstract
Primary amyloidosis (AL) may be complicated by peripheral neuropathy in 15-35% of cases. We report on four patients with atypical neurological presentations of AL neuropathy, whose diagnoses were delayed due to varied clinical presentations. The clinical presentation included painful sensory neuropathy (two patients), mononeuropathy multiplex (one patient), and primary demyelinating polyneuropathy (one patient). The latter two types of presentation have not been reported previously. The diagnosis was established by fat pad biopsy in two patients, lymph node biopsy in one, and sural nerve biopsy in one. Two patients were treated with high-dose melphalan followed by stem cell rescue, and one was treated with oral melphalan and prednisone. All three cases experienced stabilization of neuropathic symptoms. We report these cases in order to raise awareness of the varied clinical presentation of AL neuropathy.
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- 2003
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