Nusinersen Induces Disease-Severity-Specific Neurometabolic Effects in Spinal Muscular Atrophy
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A. Usiello | T. Mazza | A. D’Amico | M. Grimaldi | A. D'Ursi | C. Bruno | L. Pellizzoni | E. Bertini | V. Valsecchi | M. Carta | F. Errico | V. Bassareo | Carmen Marino | E. Di Schiavi | Tommaso Nuzzo | C. Panicucci
[1] R. Finkel,et al. Motor function in type 2 and 3 SMA patients treated with Nusinersen: a critical review and meta-analysis , 2021, Orphanet Journal of Rare Diseases.
[2] S. Corti,et al. Onasemnogene abeparvovec gene therapy for symptomatic infantile-onset spinal muscular atrophy type 1 (STR1VE-EU): an open-label, single-arm, multicentre, phase 3 trial , 2021, The Lancet Neurology.
[3] J. Vissing,et al. Prolonged fasting‐induced hyperketosis, hypoglycaemia and impaired fat oxidation in child and adult patients with spinal muscular atrophy type II , 2021, Acta paediatrica.
[4] S. Kolb,et al. Update on Biomarkers in Spinal Muscular Atrophy , 2021, Biomarker insights.
[5] P. Fontoura,et al. Risdiplam-Treated Infants with Type 1 Spinal Muscular Atrophy versus Historical Controls. , 2021, The New England journal of medicine.
[6] T. Gillingwater,et al. Spinal muscular atrophy: From approved therapies to future therapeutic targets for personalized medicine , 2021, Cell reports. Medicine.
[7] R. Finkel,et al. Treatment of infantile-onset spinal muscular atrophy with nusinersen: final report of a phase 2, open-label, multicentre, dose-escalation study. , 2021, The Lancet. Child & adolescent health.
[8] R. Kothary,et al. Metabolic Dysfunction in Spinal Muscular Atrophy , 2021, International journal of molecular sciences.
[9] R. Finkel,et al. Onasemnogene abeparvovec gene therapy for symptomatic infantile-onset spinal muscular atrophy in patients with two copies of SMN2 (STR1VE): an open-label, single-arm, multicentre, phase 3 trial , 2021, The Lancet Neurology.
[10] J. Plavec,et al. Spinal Muscular Atrophy after Nusinersen Therapy: Improved Physiology in Pediatric Patients with No Significant Change in Urine, Serum, and Liquor 1H-NMR Metabolomes in Comparison to an Age-Matched, Healthy Cohort , 2021, Metabolites.
[11] E. Mercuri,et al. Risdiplam in Type 1 Spinal Muscular Atrophy. , 2021, The New England journal of medicine.
[12] T. Crawford,et al. Impaired prenatal motor axon development necessitates early therapeutic intervention in severe SMA , 2021, Science Translational Medicine.
[13] C. Sumner,et al. Gene-Targeting Therapeutics for Neurological Disease: Lessons Learned from Spinal Muscular Atrophy. , 2021, Annual review of medicine.
[14] B. Wirth. Spinal Muscular Atrophy: In the Challenge Lies a Solution , 2021, Trends in Neurosciences.
[15] J. Rungby,et al. Effects of Ketone Bodies on Brain Metabolism and Function in Neurodegenerative Diseases , 2020, International journal of molecular sciences.
[16] R. Finkel,et al. Spinal muscular atrophy — insights and challenges in the treatment era , 2020, Nature Reviews Neurology.
[17] Zhenhong Ye,et al. Coordinated Modulation of Energy Metabolism and Inflammation by Branched-Chain Amino Acids and Fatty Acids , 2020, Frontiers in Endocrinology.
[18] Ewout J. N. Groen,et al. Pre-natal manifestation of systemic developmental abnormalities in spinal muscular atrophy , 2020, Human molecular genetics.
[19] B. Wirth,et al. Twenty-Five Years of Spinal Muscular Atrophy Research: From Phenotype to Genotype to Therapy, and What Comes Next. , 2020, Annual review of genomics and human genetics.
[20] K. Swoboda,et al. Serum creatinine is a biomarker of progressive denervation in spinal muscular atrophy , 2019, Neurology.
[21] T. Crawford,et al. Age-dependent SMN expression in disease-relevant tissue and implications for SMA treatment. , 2019, The Journal of clinical investigation.
[22] M. Roden,et al. Hungry for your alanine: when liver depends on muscle proteolysis. , 2019, The Journal of clinical investigation.
[23] R. Finkel,et al. Nusinersen initiated in infants during the presymptomatic stage of spinal muscular atrophy: Interim efficacy and safety results from the Phase 2 NURTURE study , 2019, Neuromuscular Disorders.
[24] E. Bertini,et al. Nusinersen in type 1 spinal muscular atrophy: Twelve‐month real‐world data , 2019, Annals of neurology.
[25] M. Bowerman,et al. Abnormal fatty acid metabolism is a core component of spinal muscular atrophy , 2019, Annals of clinical and translational neurology.
[26] K. Blennow,et al. NFL is a marker of treatment response in children with SMA treated with nusinersen , 2019, Journal of Neurology.
[27] R. Finkel,et al. Neurofilament as a potential biomarker for spinal muscular atrophy , 2019, Annals of clinical and translational neurology.
[28] L. Servais,et al. Nusinersen in patients older than 7 months with spinal muscular atrophy type 1 , 2018, Neurology.
[29] E. Bertini,et al. An observational study of functional abilities in infants, children, and adults with type 1 SMA , 2018, Neurology.
[30] Jana G Hashash,et al. Severe ketoacidosis in a patient with spinal muscular atrophy , 2018, CEN Case Reports.
[31] R. Finkel,et al. Evaluator Training and Reliability for SMA Global Nusinersen Trials1 , 2018, Journal of neuromuscular diseases.
[32] David S. Wishart,et al. MetaboAnalyst 4.0: towards more transparent and integrative metabolomics analysis , 2018, Nucleic Acids Res..
[33] M. Onofrj,et al. Enhanced release of acid sphingomyelinase-enriched exosomes generates a lipidomics signature in CSF of Multiple Sclerosis patients , 2018, Scientific Reports.
[34] R. Finkel,et al. Nusinersen versus Sham Control in Later‐Onset Spinal Muscular Atrophy , 2018, The New England journal of medicine.
[35] R. J. Ramamurthi,et al. Nusinersen versus Sham Control in Infantile‐Onset Spinal Muscular Atrophy , 2017, The New England journal of medicine.
[36] Brian K. Kaspar,et al. Single‐Dose Gene‐Replacement Therapy for Spinal Muscular Atrophy , 2017, The New England journal of medicine.
[37] Hans Morreau,et al. Quantitative NMR analysis of intra- and extracellular metabolism of mammalian cells: A tutorial. , 2017, Analytica chimica acta.
[38] Alexander Lex,et al. UpSetR: an R package for the visualization of intersecting sets and their properties , 2017, bioRxiv.
[39] P. Puchalska,et al. Multi-dimensional Roles of Ketone Bodies in Fuel Metabolism, Signaling, and Therapeutics. , 2017, Cell metabolism.
[40] R. Finkel,et al. Treatment of infantile-onset spinal muscular atrophy with nusinersen: a phase 2, open-label, dose-escalation study , 2016, The Lancet.
[41] L. Hubert,et al. Llllll Iii Ill Ii Ill1 Lllllll Lllllllll Ill1 Illi Swp 25/88 Issues to Be Addressed Prior to Undertaking Hierarchical Cluster Analysis A-prtort Weighting of Attributes? , 2000 .
[42] Thomas M. Smith,et al. SMN2 splice modulators enhance U1-pre-mRNA association and rescue SMA mice. , 2015, Nature chemical biology.
[43] L. Pellizzoni,et al. Disease Mechanisms and Therapeutic Approaches in Spinal Muscular Atrophy , 2015, The Journal of Neuroscience.
[44] Chris Henderson. Faculty Opinions recommendation of Peripheral SMN restoration is essential for long-term rescue of a severe spinal muscular atrophy mouse model. , 2014 .
[45] David S. Wishart,et al. Accurate, Fully-Automated NMR Spectral Profiling for Metabolomics , 2014, PloS one.
[46] Philippe Bardou,et al. jvenn: an interactive Venn diagram viewer , 2014, BMC Bioinformatics.
[47] Kidakan Saithanu,et al. CUTOFF THRESHOLD OF VARIABLE IMPORTANCE IN PROJECTION FOR VARIABLE SELECTION , 2014 .
[48] M. Dashty,et al. A quick look at biochemistry: carbohydrate metabolism. , 2013, Clinical biochemistry.
[49] W. Chung,et al. SMA-MAP: A Plasma Protein Panel for Spinal Muscular Atrophy , 2013, PloS one.
[50] Robert Powers,et al. Utilities for quantifying separation in PCA/PLS-DA scores plots. , 2013, Analytical biochemistry.
[51] Lawrence J. Clos,et al. NMRbot: Python scripts enable high-throughput data collection on current Bruker BioSpin NMR spectrometers , 2013, Metabolomics.
[52] M. Adeva,et al. Ammonium metabolism in humans. , 2012, Metabolism: clinical and experimental.
[53] M. Bowerman,et al. Glucose metabolism and pancreatic defects in spinal muscular atrophy , 2012, Annals of neurology.
[54] R. Finkel,et al. Candidate Proteins, Metabolites and Transcripts in the Biomarkers for Spinal Muscular Atrophy (BforSMA) Clinical Study , 2012, PloS one.
[55] T. Soni Madhulatha,et al. An Overview on Clustering Methods , 2012, ArXiv.
[56] R. McKay. How the 1D‐NOESY suppresses solvent signal in metabonomics NMR spectroscopy: An examination of the pulse sequence components and evolution , 2011 .
[57] A. Smilde,et al. Double-check: validation of diagnostic statistics for PLS-DA models in metabolomics studies , 2011, Metabolomics.
[58] R. Finkel,et al. The Children’s Hospital of Philadelphia Infant Test of Neuromuscular Disorders (CHOP INTEND): Test development and reliability , 2010, Neuromuscular Disorders.
[59] Guoyao Wu,et al. Amino acids: metabolism, functions, and nutrition , 2009, Amino Acids.
[60] R. Finkel,et al. An expanded version of the Hammersmith Functional Motor Scale for SMA II and III patients , 2007, Neuromuscular Disorders.
[61] J. Rho,et al. Ketone bodies are protective against oxidative stress in neocortical neurons , 2007, Journal of neurochemistry.
[62] Erik J. Saude,et al. Optimization of NMR analysis of biological fluids for quantitative accuracy , 2006, Metabolomics.
[63] J. Vissing,et al. Patients with severe muscle wasting are prone to develop hypoglycemia during fasting , 2003, Neurology.
[64] J. Vion-Dury,et al. Experimental protocol for clinical analysis of cerebrospinal fluid by high resolution proton magnetic resonance spectroscopy. , 1998, Brain research. Brain research protocols.
[65] J. Melki,et al. Spinal muscular atrophy. , 1997, Current opinion in neurology.
[66] Wei-Hao Wang,et al. Studies , 1926 .
[67] W. Chung,et al. Validation of the Children's Hospital of Philadelphia Infant Test of Neuromuscular Disorders (CHOP INTEND) , 2011, Pediatric physical therapy : the official publication of the Section on Pediatrics of the American Physical Therapy Association.
[68] in in Humans. , 2021 .