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Maximum lingual pressure impacts both swallowing safety and efficiency in individuals with amyotrophic lateral sclerosis

Neurogastroenterology and motility, 2023-04, Vol.35 (4), p.e14521-n/a

2023

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Defining SOD1 ALS natural history to guide therapeutic clinical trial design

Journal of neurology, neurosurgery and psychiatry, 2017-02, Vol.88 (2), p.99-105

2017

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The evolution and multi-molecular properties of NF1 cutaneous neurofibromas originating from C-fiber sensory endings and terminal Schwann cells at normal sites of sensory terminations in the skin

PloS one, 2019-05, Vol.14 (5), p.e0216527-e0216527

2019

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Relationship between pulmonary, cough, and swallowing functions in individuals with amyotrophic lateral sclerosis

Muscle & nerve, 2024-07, Vol.70 (1), p.140-147

2024

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Keratinocyte Biomarkers Distinguish Painful Diabetic Peripheral Neuropathy Patients and Correlate With Topical Lidocaine Responsiveness

Frontiers in pain research (Lausanne, Switzerland), 2021-12, Vol.2, p.790524-790524

2021

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Functional Lingual Pressure Thresholds for Swallowing Safety and Efficiency Impairments in Amyotrophic Lateral Sclerosis

Dysphagia, 2023-04, Vol.38 (2), p.676-685

2023

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Swallowing Safety and Efficiency Impairment Profiles in Individuals with Amyotrophic Lateral Sclerosis

Dysphagia, 2022-06, Vol.37 (3), p.644-654

2022

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Combined respiratory training in an individual with C9orf72 amyotrophic lateral sclerosis

Annals of clinical and translational neurology, 2018-09, Vol.5 (9), p.1134-1138

2018

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Respiratory Strength Training in Amyotrophic Lateral Sclerosis: A Double-Blind, Randomized, Multicenter, Sham-Controlled Trial

Neurology, 2023-04, Vol.100 (15), p.e1634

2023

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Sleep disorders in myotonic dystrophies

Muscle & nerve, 2020-09, Vol.62 (3), p.309-320

2020

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Profiling Number of Swallows per Bolus and Residue in Individuals With Amyotrophic Lateral Sclerosis

Journal of speech, language, and hearing research, 2023-10, Vol.66 (10), p.3763-3772

2023

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Acute intermittent hypoxia and respiratory muscle recruitment in people with amyotrophic lateral sclerosis: A preliminary study

Experimental neurology, 2022-01, Vol.347, p.113890-113890, Article 113890

2022

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Maximum Phonation Time as a Surrogate Marker for Airway Clearance Physiologic Capacity and Pulmonary Function in Individuals With Amyotrophic Lateral Sclerosis

Journal of speech, language, and hearing research, 2023-04, Vol.66 (4), p.1165-1172

2023

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Discriminant Ability of the Eating Assessment Tool‐10 to Detect Swallowing Safety and Efficiency Impairments

The Laryngoscope, 2022-12, Vol.132 (12), p.2319-2326

2022

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Profiles of Dysarthria and Dysphagia in Individuals with Amyotrophic Lateral Sclerosis

Journal of speech, language, and hearing research, 2023-01, Vol.66 (1), p.154-162

2023

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Sensitivity and specificity of the Amyotrophic Lateral Sclerosis Functional Rating Scale—Revised to detect dysarthria in individuals with amyotrophic lateral sclerosis

Muscle & nerve, 2023-09, Vol.68 (3), p.296-302

2023

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Discriminant ability of the 3‐ounce water swallow test to detect aspiration in amyotrophic lateral sclerosis

Neurogastroenterology and motility, 2022-07, Vol.34 (7), p.e14310-n/a

2022

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Respiratory therapies for Amyotrophic Lateral Sclerosis: A state of the art review

Chronic Respiratory Disease, 2023-01, Vol.20, p.14799731231175915

2023

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Excessive Peptidergic Sensory Innervation of Cutaneous Arteriole–Venule Shunts (AVS) in the Palmar Glabrous Skin of Fibromyalgia Patients: Implications for Widespread Deep Tissue Pain and Fatigue

Pain medicine (Malden, Mass.), 2013-06, Vol.14 (6), p.895-915

2013

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Efficacy and Safety of Lacosamide in Diabetic Neuropathic Pain: An 18-week Double-blind Placebo-controlled Trial of Fixed-dose Regimens

The Clinical journal of pain, 2009-06, Vol.25 (5), p.376-385

2009

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Expansion of the myotonic dystrophy CTG repeat reduces expression of the flanking DMAHP gene

Nature genetics, 1997-08, Vol.16 (4), p.407-409

1997

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Voltage-gated sodium channel expression in rat and human epidermal keratinocytes: Evidence for a role in pain

Pain (Amsterdam), 2008-09, Vol.139 (1), p.90-105

2008

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Increased levels of hyper-stable protein aggregates in plasma of older adults

AGE, 2016-06, Vol.38 (3), p.56-56, Article 56

2016

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Randomized, controlled trial of dextromethorphan/quinidine for pseudobulbar affect in multiple sclerosis

Annals of neurology, 2006-05, Vol.59 (5), p.780-787

2006

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An open-label multicenter study to assess the safety of dextromethorphan/quinidine in patients with pseudobulbar affect associated with a range of underlying neurological conditions

Current medical research and opinion, 2014-11, Vol.30 (11), p.2255-2265

2014

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Maximum lingual pressure impacts both swallowing safety and efficiency in individuals with amyotrophic lateral sclerosis

Defining SOD1 ALS natural history to guide therapeutic clinical trial design

The evolution and multi-molecular properties of NF1 cutaneous neurofibromas originating from C-fiber sensory endings and terminal Schwann cells at normal sites of sensory terminations in the skin

Relationship between pulmonary, cough, and swallowing functions in individuals with amyotrophic lateral sclerosis

Keratinocyte Biomarkers Distinguish Painful Diabetic Peripheral Neuropathy Patients and Correlate With Topical Lidocaine Responsiveness

Functional Lingual Pressure Thresholds for Swallowing Safety and Efficiency Impairments in Amyotrophic Lateral Sclerosis

Swallowing Safety and Efficiency Impairment Profiles in Individuals with Amyotrophic Lateral Sclerosis

Combined respiratory training in an individual with C9orf72 amyotrophic lateral sclerosis

Respiratory Strength Training in Amyotrophic Lateral Sclerosis: A Double-Blind, Randomized, Multicenter, Sham-Controlled Trial

Sleep disorders in myotonic dystrophies

Profiling Number of Swallows per Bolus and Residue in Individuals With Amyotrophic Lateral Sclerosis

Acute intermittent hypoxia and respiratory muscle recruitment in people with amyotrophic lateral sclerosis: A preliminary study

Maximum Phonation Time as a Surrogate Marker for Airway Clearance Physiologic Capacity and Pulmonary Function in Individuals With Amyotrophic Lateral Sclerosis

Discriminant Ability of the Eating Assessment Tool‐10 to Detect Swallowing Safety and Efficiency Impairments

Profiles of Dysarthria and Dysphagia in Individuals with Amyotrophic Lateral Sclerosis

Sensitivity and specificity of the Amyotrophic Lateral Sclerosis Functional Rating Scale—Revised to detect dysarthria in individuals with amyotrophic lateral sclerosis

Discriminant ability of the 3‐ounce water swallow test to detect aspiration in amyotrophic lateral sclerosis

Respiratory therapies for Amyotrophic Lateral Sclerosis: A state of the art review

Excessive Peptidergic Sensory Innervation of Cutaneous Arteriole–Venule Shunts (AVS) in the Palmar Glabrous Skin of Fibromyalgia Patients: Implications for Widespread Deep Tissue Pain and Fatigue

Efficacy and Safety of Lacosamide in Diabetic Neuropathic Pain: An 18-week Double-blind Placebo-controlled Trial of Fixed-dose Regimens

Expansion of the myotonic dystrophy CTG repeat reduces expression of the flanking DMAHP gene

Voltage-gated sodium channel expression in rat and human epidermal keratinocytes: Evidence for a role in pain

Increased levels of hyper-stable protein aggregates in plasma of older adults

Randomized, controlled trial of dextromethorphan/quinidine for pseudobulbar affect in multiple sclerosis

An open-label multicenter study to assess the safety of dextromethorphan/quinidine in patients with pseudobulbar affect associated with a range of underlying neurological conditions

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