Publications by authors named "Carmel Armon"

ALSUntangled reviews alternate and off-label treatments prompted by patient interest. Here, we review psilocybin, a chemical derived from mushrooms and belonging in the category of drugs known as psychedelics. Psilocybin has plausible mechanisms for slowing ALS progression because of its ability to cross the blood brain barrier and effect neurogenesis and inflammation.

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  • Alzheimer's disease (AD) is a leading cause of dementia, particularly influenced by maternal inheritance but lacking consistent X chromosome risk factors.
  • A new analysis method suggested a 70% risk from the X chromosome in patients with amnestic mild cognitive impairment or early AD but did not confirm this in a larger Utah Population Database study due to methodological issues.
  • Future studies should focus on identifying X chromosome contributions to late-onset Alzheimer's by looking at newly diagnosed patients rather than relying on data from deceased individuals.
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  • - The Wahls diet is a specialized version of the Paleolithic diet, focusing on nutrient-rich foods like leafy greens and omega-3 fatty acids while limiting processed foods and sugars, aiming to reduce inflammation and oxidative stress.
  • - While some studies link components of the Wahls diet, like high carotenoids and omega-3s, to reduced ALS risk, there is no solid evidence proving it slows ALS progression, with conflicting results from animal model research.
  • - Additionally, the Wahls diet has led to significant weight loss in people with multiple sclerosis, raising concerns since weight loss can worsen ALS, leading to the conclusion that the diet shouldn't be endorsed for ALS patients.
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Spurred by patient interest, ALSUntangled herein examines the potential of the Portable Neuromodulation Stimulator (PoNS™) in treating amyotrophic lateral sclerosis (ALS). The PoNS™ device, FDA-approved for the treatment of gait deficits in adult patients with multiple sclerosis, utilizes translingual neurostimulation to stimulate trigeminal and facial nerves via the tongue, aiming to induce neuroplastic changes. While there are early, promising data for PoNS treatment to improve gait and balance in multiple sclerosis, stroke, and traumatic brain injury, no pre-clinical or clinical studies have been performed in ALS.

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  • Several neurological issues can persist in patients who have recovered from COVID-19, and this study focused on their outcomes at the 6-month mark.
  • The research involved over 1,000 patients and found that approximately 52% showed stable or improved functional status, while 46% experienced worse outcomes, with factors like age and hospitalizations influencing these results.
  • Among the neurological symptoms that persisted, fatigue and memory or concentration problems were the most common, highlighting the need for awareness of long-term effects in COVID-19 survivors.
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Lion's Mane ( has historically been used as traditional medicine in Asia and Europe for its potential benefits in fighting infection and cancer. It has gained interest in the neurodegenerative disease field because of its mechanisms of action; these include anti-inflammation, neuroprotection, and promoting neurite growth demonstrated in various cell and animal models. A very small, double-blind, placebo-controlled trial in patients with mild cognitive impairment showed a temporary improvement in cognitive function; this finding has yet to be replicated.

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ALSUntangled reviews alternative and off-label treatments for people living with amyotrophic lateral sclerosis (PALS). Here we review insulin, which has at least one plausible mechanism for slowing ALS progression. However, pre-clinical studies are limited and there have been no trials in PALS yet.

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  • The study aimed to investigate sex-based differences in outcomes for patients with acute ischemic stroke (AIS) who underwent recanalization treatments at a medical center in Israel between 2011 and 2020.
  • Researchers analyzed data from 811 patients, finding that women had higher mean age and more severe conditions compared to men, but both sexes had similar outcomes despite women presenting with more risk factors.
  • The study concluded that while women had more severe symptoms, there were no significant differences in outcomes between sexes, highlighting the importance of managing risk factors to reduce stroke-related issues for both genders.
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ALSUntangled reviews alternative and off-label treatments for people living with amyotrophic lateral sclerosis (PALS). Here we review astaxanthin which has plausible mechanisms for slowing ALS progression including antioxidant, anti-inflammatory, and anti-apoptotic effects. While there are no ALS-specific pre-clinical studies, one verified "ALS reversal" occurred in a person using a combination of alternative therapies which included astaxanthin.

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  • * Data was gathered from a registry created by the European Academy of Neurology, involving 1523 COVID-19 patients across multiple countries, focusing on their demographics, medical history, and neurological issues.
  • * Results showed that 79.6% of patients exhibited neurological symptoms, with cognitive dysfunction, stroke, and sleep disturbances being the most common; findings also indicated variations based on age and existing health conditions.
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ALSUntangled #67: rituximab.

Amyotroph Lateral Scler Frontotemporal Degener

August 2023

ALSUntangled reviews alternative and off-label treatments on behalf of people with ALS who ask about them. Here we review rituximab, a drug which specifically depletes B lymphocytes. We show a current lack of evidence for a role of these cells in ALS progression.

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ALSUntangled #64: butyrates.

Amyotroph Lateral Scler Frontotemporal Degener

November 2022

ALSUntangled reviews alternative and off-label treatments for people living with amyotrophic lateral sclerosis (PALS). Here we review butyrate and its different chemical forms (butyrates). Butyrates have plausible mechanisms for slowing ALS progression and positive pre-clinical studies.

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Background And Purpose: Despite the increasing number of reports on the spectrum of neurological manifestations of COVID-19 (neuro-COVID), few studies have assessed short- and long-term outcome of the disease.

Methods: This is a cohort study enrolling adult patients with neuro-COVID seen in neurological consultation. Data were collected prospectively or retrospectively in the European Academy of Neurology NEuro-covid ReGistrY ((ENERGY).

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Objective: The goal of this study was to analyze the reasons for delayed diagnosis of Guillain-Barre syndrome (GBS).

Methods: We retrospectively reviewed the records of all adult patients with GBS treated at Shamir Medical Center (SMC) from 2006 to 2018. We divided the patients into two groups: those with early initiation of treatment (within 24 h of arrival to ED), and those with later initiation of treatment (>24 h after arrival).

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  • The objective of the study was to update the 2011 AAN guideline on treating painful diabetic neuropathy (PDN), focusing on both topical and oral medications.
  • The authors conducted a systematic review of literature from January 2008 to April 2020 to develop new practice recommendations.
  • The results highlighted that TCAs showed a large effect size for pain relief, while SNRIs and gabapentinoids also demonstrated significant effectiveness, but opioids are not recommended for treating PDN.
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Parental lineage has been shown to increase the risk of Alzheimer's disease (AD) in the offspring, with greater risk attributed to maternal lineage. While 40 genes/loci have been linked to the risk of developing AD, none has been found on the X chromosome. We propose a new method to estimate the risk for developing AD mediated by the X chromosome in a subgroup of late-onset AD (LOAD) patients with amnestic mild cognitive impairment (aMCI) or early AD and unilateral ancestral history of AD or dementia, and pilot-test it on our clinic data.

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  • The study analyzed 100 adult patients with Guillain-Barré syndrome (GBS) from 2006 to 2018, finding that a significant 46.8% exhibited an axonal pattern in their EMG results.
  • A majority (58%) of those who initially presented with mild symptoms experienced a deterioration in their condition, with several losing the ability to walk independently.
  • The research concluded that a higher incidence of axonal GBS was observed in Israel compared to European and North American cohorts, and emphasized the need for prompt treatment following a GBS diagnosis due to the disease's progressive nature.
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To identify factors associated with prior stroke at presentation in patients with cryptogenic stroke (CS) and patent foramen ovale (PFO). We studied cross-sectional data from the International PFO Consortium Study (NCT00859885). Patients with first-ever stroke and those with prior stroke at baseline were analyzed for an association with PFO-related (right-to-left shunt at rest, atrial septal aneurysm, deep venous thrombosis, pulmonary embolism, and Valsalva maneuver) and PFO-unrelated factors (age, gender, BMI, hypertension, diabetes mellitus, hypercholesterolemia, smoking, migraine, coronary artery disease, aortic plaque).

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Introduction: This clinical trial evaluates the efficacy and safety of a 6-week course of daily neuroAD™ therapy.

Methods: 131 subjects between 60 and 90 years old, unmedicated for Alzheimer's disease (AD), or on stable doses of an acetylcholinesterase inhibitor and/or memantine, with Mini-Mental State Examination scores between 18 and 26, clinical dementia rating scale scores of 1 or 2, enrolled for a prospective, randomized, double-blind, sham-controlled, multicenter clinical trial. Structural brain MRIs were obtained for transcranial magnetic stimulation targeting.

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Theme 1 Epidemiology and informatics.

Amyotroph Lateral Scler Frontotemporal Degener

November 2019

Identifying mechanisms of neurodegenerative disease causation has for long seemed to be beyond the pale of traditional epidemiological tools. Elucidating a plausible mechanism for initiation of amyotrophic lateral sclerosis (ALS) has appeared particularly elusive (1). The impression, that environmental risk factors for ALS were not providing consistent direction, meant there was no sturdy epidemiologically-based "handle" to grasp when trying to envisage a biological mechanism for triggering sporadic ALS (2).

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