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ALS (amyotrophic lateral sclerosis)
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Publications and studies (2470)
- Prognostic value of geriatric nutritional risk index in patients with amyotrophic lateral sclerosis. (2024/04/01) ♡
- Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Use of Muscle Ultrasonography in Morphofunctional Assessment of Amyotrophic Lateral Sclerosis (ALS). (2024/03/31) ♡
- Timing and impact of percutaneous endoscopic gastrostomy insertion in patients with amyotrophic lateral sclerosis: a comprehensive analysis. (2024/03/26) ♡
- Percutaneous Gastrostomies: Associated Complications in PUSH vs. PULL Techniques over 12 Years in a Referral Centre. (2024/03/22) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Disruption of Neuromuscular Junction Following Spinal Cord Injury and Motor Neuron Diseases. (2024/03/20) ♡
- Randomized researchiParticipants were divided into groups by lottery and compared with each other. This reduces the chance that a difference is due to something other than the treatment. Sunitinib for metastatic progressive phaeochromocytomas and paragangliomas: results from FIRSTMAPPP, an academic, multicentre, international, randomised, placebo-controlled, double-blind, phase 2 trial. (2024/03/16) ♡
- Constipation in patients with motor neuron disease: A retrospective longitudinal study. (2024/03/13) ♡
- Analysis of C9orf72 repeat expansions in Georgian patients with Amyotrophic lateral sclerosis (ALS). (2024/03/06) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. The role of artificial intelligence in electrodiagnostic and neuromuscular medicine: Current state and future directions. (2024/03/01) ♡
- Nuclear pore pathology underlying multisystem proteinopathy type 3-related inclusion body myopathy. (2024/03/01) ♡
- Healthcare Utilization and Supportive Care Timing in South Korean People Living With Amyotrophic Lateral Sclerosis: A Single-Center Retrospective Study. (2024/03/01) ♡
- Commentary or editorialiAn expert's opinion or commentary, not new research. Heterozygous SPTLC1 p.Leu39del is a major cause of slow-progressing juvenile ALS. (2024/02/14) ♡
- Impact of the COVID-19 Pandemic on People Living With Rare Diseases and Their Families: Results of a National Survey. (2024/02/14) ♡
- Right Brain: The Strangeness of a Good Diagnosis. (2024/02/13) ♡
- Laboratory or animal researchiNo research in humans yet. Promising in a test tube or in mice unfortunately means nothing for patients. Generation of a human induced pluripotent stem cell line (SMUSHi002-A) from an ALS patient carrying a heterozygous mutation c.1562G > A in the FUS gene. (2024/02/01) ♡
- A neurophysiological approach to mirror movements in amyotrophic lateral sclerosis. (2024/02/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Generation of two induced pluripotent stem cell lines from two sporadic amyotrophic lateral sclerosis patients. (2024/02/01) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Novel approaches to motoneuron disease/ALS treatment using non-invasive brain and spinal stimulation: IFCN handbook chapter. (2024/02/01) ♡
- Describing and characterising variability in ALS disease progression. (2024/02/01) ♡
- The value of routine blood work-up in clinical stratification and prognosis of patients with amyotrophic lateral sclerosis. (2024/02/01) ♡
- Sound-based cough peak flow estimation in patients with neuromuscular disorders. (2024/02/01) ♡
- Racial disparities in ALS diagnostic delay: a single center's experience and review of potential contributing factors. (2024/02/01) ♡
- Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Higher Glycemic Index and Glycemic Load Diet Is Associated with Slower Disease Progression in Amyotrophic Lateral Sclerosis. (2024/02/01) ♡
- Leptin haploinsufficiency exerts sex-dependent partial protection in SOD1(G93A) mice by reducing inflammatory pathways in the adipose tissue. (2024/02/01) ♡
- MATR3 pathogenic variants differentially impair its cryptic splicing repression function. (2024/02/01) ♡
- Carbon disulfide induces accumulation of TDP-43 in the cytoplasm and mitochondrial dysfunction in rat spinal cords. (2024/01/31) ♡
- Pro-Brain-Derived Neurotrophic Factor (BDNF), but Not Mature BDNF, Is Expressed in Human Skeletal Muscle: Implications for Exercise-Induced Neuroplasticity. (2024/01/27) ♡
- Nutritional, Clinical and Sociodemographic Profiles of Spanish Patients with Amyotrophic Lateral Sclerosis. (2024/01/25) ♡
- Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Structural and Functional Brain Network Connectivity at Different King's Stages in Patients With Amyotrophic Lateral Sclerosis. (2024/01/23) ♡
- Observing Patterns in MRI With QSM in Patients With SOD1 Genetic ALS (5047). (2024/01/23) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Superoxide dismutase and neurological disorders. (2024/01/23) ♡
- Analyzing the ER stress response in ALS patient derived motor neurons identifies druggable neuroprotective targets. (2024/01/19) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Time-restricted ketogenic diet in amyotrophic lateral sclerosis: a case study. (2024/01/18) ♡
- Reduction of inflammation and mitochondrial degeneration in mutant SOD1 mice through inhibition of voltage-gated potassium channel Kv1.3. (2024/01/16) ♡
- Biochemical parameters as a tool to assess the nutritional status of patients with amyotrophic lateral sclerosis. (2024/01/15) ♡
- Genetic analyses identify brain imaging-derived phenotypes associated with the risk of amyotrophic lateral sclerosis. (2024/01/14) ♡
- Alzheimer and Parkinson diseases, frontotemporal lobar degeneration and amyotrophic lateral sclerosis overlapping neuropathology start in the first two decades of life in pollution exposed urbanites and brain ultrafine particulate matter and industrial nanoparticles, including Fe, Ti, Al, V, Ni, Hg, Co, Cu, Zn, Ag, Pt, Ce, La, Pr and W are key players. Metropolitan Mexico City health crisis is in progress. (2024/01/12) ♡
- Towards a Machine Learning Empowered Prognostic Model for Predicting Disease Progression for Amyotrophic Lateral Sclerosis. (2024/01/11) ♡
- Elevation of inositol pyrophosphate IP(7) in the mammalian spinal cord of amyotrophic lateral sclerosis. (2024/01/11) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Autophagy in spinal muscular atrophy: from pathogenic mechanisms to therapeutic approaches. (2024/01/08) ♡
- Commentary or editorialiAn expert's opinion or commentary, not new research. Editorial: Molecular mechanisms underlying C9orf72 neurodegeneration, volume II. (2024/01/08) ♡
- Commentary or editorialiAn expert's opinion or commentary, not new research. Is there evidence of a ketogenic effect of coconut oil? Commentary: Effect of the Mediterranean diet supplemented with nicotinamide riboside and pterostilbene and/or coconut oil on anthropometric variables in amyotrophic lateral sclerosis. A pilot study. (2024/01/08) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Diagnostic utility of transcranial magnetic stimulation for neurodegenerative disease: a critical review. (2024/01/05) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Emerging perspectives of synaptic biomarkers in ALS and FTD. (2024/01/05) ♡
- Cystatin C is associated with poor survival in amyotrophic lateral sclerosis patients. (2024/01/05) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. ATP13A2 (PARK9) and basal ganglia function. (2024/01/05) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Simple models to understand complex disease: 10 years of progress from Caenorhabditis elegans models of amyotrophic lateral sclerosis and frontotemporal lobar degeneration. (2024/01/04) ♡
- Commentary or editorialiAn expert's opinion or commentary, not new research. Editorial: The role of glial cells in neurodegeneration. (2024/01/04) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Pathogenesis of Neurodegenerative Diseases and the Protective Role of Natural Bioactive Components. (2024/01/01) ♡
- Remote respiratory resistance exercise training improves respiratory function in individuals with VCP multisystem proteinopathy. (2024/01/01) ♡
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