Search Results - "Stino, Amro"
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Peripheral neuropathy in prediabetes and the metabolic syndrome
Published in Journal of diabetes investigation (01-09-2017)“…Peripheral neuropathy is a major cause of disability worldwide. Diabetes is the most common cause of neuropathy, accounting for 50% of cases. Over half of…”
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Neurological sequela and disruption of neuron-glia homeostasis in SARS-CoV-2 infection
Published in Neurobiology of disease (15-06-2022)“…The coronavirus disease 2019 (COVID-19) pandemic is responsible for 267 million infections and over 5 million deaths globally. COVID-19 is caused by severe…”
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Evolving concepts on the role of dyslipidemia, bioenergetics, and inflammation in the pathogenesis and treatment of diabetic peripheral neuropathy
Published in Journal of the peripheral nervous system (01-06-2020)“…Diabetic peripheral neuropathy (DPN) is one of the most widespread and disabling neurological conditions, accounting for half of all neuropathy cases…”
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Chronic inflammatory demyelinating polyradiculoneuropathy—Diagnostic pitfalls and treatment approach
Published in Muscle & nerve (01-02-2021)“…Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is characterized by progressive weakness and sensory loss, often affecting patientsʼ ability…”
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Intravenous immunoglobulin and plasma exchange prescribing patterns for Guillain‐Barre Syndrome in the United States—2001 to 2018
Published in Muscle & nerve (01-12-2024)“…Introduction/Aims Randomized controlled trials show that repeat intravenous immunoglobulin (IVIG) dosing and plasma exchange (PLEX) followed by IVIG…”
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Fibromyalgia syndrome and small fiber, early or mild sensory polyneuropathy
Published in Muscle & nerve (01-11-2018)“…ABSTRACT Introduction: Pain mechanisms in fibromyalgia syndrome (FMS) are not clearly understood. Growing evidence appears to suggest a role for small fiber…”
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Metabolic syndrome and peripheral neuropathy
Published in Muscle & nerve (01-03-2021)“…Diabetic peripheral neuropathy and metabolic syndrome (MetS) are both global health challenges with well‐established diagnostic criteria and significant…”
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Hypoglossal nerve palsy: 245 cases
Published in Muscle & nerve (01-12-2016)“…ABSTRACT Introduction: Apart from a case series of 100 subjects in 1996 and several small cohorts, there have been no large retrospective series of cranial…”
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Lenalidomide in the treatment of anti‐myelin‐associated glycoprotein neuropathy: A phase 1 study to identify the maximum tolerated dose
Published in European journal of neurology (01-03-2024)“…Background Anti‐myelin‐associated glycoprotein (MAG) neuropathy is a debilitating demyelinating polyneuropathy with no approved therapies. Our primary…”
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Serum Creatine Kinase in Patients with Neuromyelitis Optica Spectrum Disorder
Published in Journal of neuroimmunology (15-05-2019)“…There have been reports of elevated serum creatine kinase (CK) and myopathy in patients with Neuromyelitis Optica Spectrum Disorder (NMOSD). Such findings have…”
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Electrophysiology of Cranial Nerve Testing: Spinal Accessory and Hypoglossal Nerves
Published in Journal of clinical neurophysiology (01-01-2018)“…Multiple techniques have been developed for the electrodiagnostic evaluation of cranial nerves XI and XII. Each of these carries both benefits and limitations,…”
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Defining postoperative C5 palsy and recovery: a systematic review
Published in Journal of neurosurgery. Spine (01-04-2023)“…Postoperative C5 palsy (C5P) is a well-recognized and often-delayed complication of cervical spine surgery. Most patients recover within 6 months of onset, but…”
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Foot measures in patients with pes cavus with and without charcot–marie–tooth disease: A pilot study
Published in Muscle & nerve (01-01-2019)“…ABSTRACT Introduction Pes cavus often signals the presence of Charcot–Marie‐Tooth (CMT) in adult patients, although its prevalence in the general population…”
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Dynamin‐2‐associated myopathy with electrical but not clinical myotonia
Published in Muscle & nerve (01-04-2018)Get full text
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A double-blind, placebo-controlled, randomized trial of PXT3003 for the treatment of Charcot-Marie-Tooth type 1A
Published in Orphanet journal of rare diseases (16-10-2021)“…Charcot-Marie-Tooth disease type 1A (CMT1A) is a rare, orphan, hereditary neuromuscular disorder with no cure and for which only symptomatic treatment is…”
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Lenalidomide‐responsive anti‐myelin‐associated glycoprotein neuropathy
Published in Muscle & nerve (01-10-2017)Get full text
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Patients who meet electrodiagnostic criteria for CIDP rarely present with a sensory predominant DSP phenotype
Published in Muscle & nerve (01-06-2021)“…Introduction It is unknown how often patients with electrodiagnostic evidence of chronic inflammatory demyelinating polyradiculoneuropathy (CIDP), a…”
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Correction to: A double-blind, placebo-controlled, randomized trial of PXT3003 for the treatment of Charcot-Marie-Tooth type 1A
Published in Orphanet journal of rare diseases (01-04-2024)Get full text
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Anti–myelin‐associated glycoprotein neuropathy: Where do we stand?
Published in Muscle & nerve (01-12-2023)“…Myelin‐associated glycoprotein (MAG) is a transmembrane glycoprotein concentrated in periaxonal Schwann cell and oligodendroglial membranes of myelin sheaths…”
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