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| Open AccessEvidence for disrupted copper availability in human spinal cord supports CuII(atsm) as a treatment option for sporadic cases of ALS
- James B. W. Hilton
- , Kai Kysenius
- & Peter J. Crouch
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Article
| Open AccessReconstitution of C9orf72 GGGGCC repeat-associated non-AUG translation with purified human translation factors
- Hayato Ito
- , Kodai Machida
- & Hideki Taguchi
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| Open AccessAI-assisted quantification of hypothalamic atrophy in amyotrophic lateral sclerosis by convolutional neural network-based automatic segmentation
- Ina Vernikouskaya
- , Hans-Peter Müller
- & Volker Rasche
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| Open AccessAccurate personalized survival prediction for amyotrophic lateral sclerosis patients
- Li-Hao Kuan
- , Pedram Parnianpour
- & Russell Greiner
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| Open AccessCystatin C based estimation of chronic kidney disease and amyotrophic lateral sclerosis in the ALS registry Swabia: associated risk and prognostic value
- Gabriele Nagel
- , Deborah Kurz
- & Dietrich Rothenbacher
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| Open AccessmiRNA profiling as a complementary diagnostic tool for amyotrophic lateral sclerosis
- Jack Cheng
- , Wen-Kuang Ho
- & Wei-Yong Lin
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| Open AccessProspective study to evaluate quality of life in amyotrophic lateral sclerosis
- Candela Caballero-Eraso
- , Carlos Carrera-Cueva
- & Luis Jara-Palomares
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Article
| Open AccessImpaired ATF3 signaling involves SNAP25 in SOD1 mutant ALS patients
- Volkan Yazar
- , Julia K. Kühlwein
- & Karin M. Danzer
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| Open AccessCortical glia in SOD1(G93A) mice are subtly affected by ALS-like pathology
- Tereza Filipi
- , Zuzana Matusova
- & Miroslava Anderova
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| Open AccessMutant and curli-producing E. coli enhance the disease phenotype in a hSOD1-G93A mouse model of ALS
- Zimple Kurlawala
- , Joseph D. McMillan
- & Robert P. Friedland
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| Open AccessMotor unit number index (MUNIX) loss of 50% occurs in half the time of 50% functional loss according to the D50 disease progression model of ALS
- Theresa Ebersbach
- , Annekathrin Roediger
- & Julian Grosskreutz
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| Open AccessNOTCH2NLC GGC repeats are not expanded in Italian amyotrophic lateral sclerosis patients
- Arianna Manini
- , Delia Gagliardi
- & Dario Ronchi
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| Open AccessMolecular basis of C9orf72 poly-PR interference with the β-karyopherin family of nuclear transport receptors
- Hamidreza Jafarinia
- , Erik Van der Giessen
- & Patrick R. Onck
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| Open AccessA novel assessment of fine-motor function reveals early hindlimb and detectable forelimb deficits in an experimental model of ALS
- C. Sahara Khademullah
- & Yves De Koninck
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| Open AccessOptimized multi-echo gradient-echo magnetic resonance imaging for gray and white matter segmentation in the lumbosacral cord at 3 T
- Silvan Büeler
- , Marios C. Yiannakas
- & Gergely David
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| Open AccessMotor unit number index (MUNIX) in the D50 disease progression model reflects disease accumulation independently of disease aggressiveness in ALS
- Theresa Ebersbach
- , Annekathrin Roediger
- & Julian Grosskreutz
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| Open AccessImportance of the Q/N-rich segment for protein stability of endogenous mouse TDP-43
- Toshiya Sato
- , Kanako Oda
- & Minesuke Yokoyama
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| Open AccessA new method for estimating under-recruitment of a patient registry: a case study with the Ohio Registry of Amyotrophic Lateral Sclerosis
- Meifang Li
- , Xun Shi
- & Walter G. Bradley
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| Open AccessAmyotrophic lateral sclerosis and cerebellum
- Renata Kabiljo
- , Alfredo Iacoangeli
- & Ivana Rosenzweig
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| Open AccessHyperexcitability in young iPSC-derived C9ORF72 mutant motor neurons is associated with increased intracellular calcium release
- Sarah Burley
- , Dayne A. Beccano-Kelly
- & Richard Wade-Martins
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| Open AccessDual-gRNA approach with limited off-target effect corrects C9ORF72 repeat expansion in vivo
- Xuejiao Piao
- , Dawei Meng
- & Yichang Jia
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| Open AccessBody fat compartment determination by encoder–decoder convolutional neural network: application to amyotrophic lateral sclerosis
- Ina Vernikouskaya
- , Hans-Peter Müller
- & Volker Rasche
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| Open AccessArgonaute 2 is lost from neuromuscular junctions affected with amyotrophic lateral sclerosis in SOD1G93A mice
- Dillon Shapiro
- , Ryan Massopust
- & Gregorio Valdez
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| Open AccessMitochondrial dysregulation occurs early in ALS motor cortex with TDP-43 pathology and suggests maintaining NAD+ balance as a therapeutic strategy
- Mukesh Gautam
- , Aksu Gunay
- & P. Hande Ozdinler
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| Open AccessSOD1 mutations associated with amyotrophic lateral sclerosis analysis of variant severity
- Mariusz Berdyński
- , Przemysław Miszta
- & Magdalena Kuźma-Kozakiewicz
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| Open AccessA selectable all-in-one CRISPR prime editing piggyBac transposon allows for highly efficient gene editing in human cell lines
- Reto Eggenschwiler
- , Thomas Gschwendtberger
- & Tobias Cantz
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| Open AccessNeurofilaments can differentiate ALS subgroups and ALS from common diagnostic mimics
- Arvin Behzadi
- , Fani Pujol-Calderón
- & Peter Munch Andersen
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| Open AccessCuATSM improves motor function and extends survival but is not tolerated at a high dose in SOD1G93A mice with a C57BL/6 background
- Jeremy S. Lum
- , Mikayla L. Brown
- & Justin J. Yerbury
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| Open AccessNeuronal mitochondrial dysfunction in sporadic amyotrophic lateral sclerosis is developmentally regulated
- Tanisha Singh
- , Yuanyuan Jiao
- & Diane L. Carlisle
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| Open AccessPrognostic prediction by hypermetabolism varies depending on the nutritional status in early amyotrophic lateral sclerosis
- Ryutaro Nakamura
- , Mika Kurihara
- & Makoto Urushitani
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| Open AccessProtein disulphide isomerase (PDI) is protective against amyotrophic lateral sclerosis (ALS)-related mutant Fused in Sarcoma (FUS) in in vitro models
- S. Parakh
- , E. R. Perri
- & J. D. Atkin
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| Open AccessClearance of peripheral nerve misfolded mutant protein by infiltrated macrophages correlates with motor neuron disease progression
- Wataru Shiraishi
- , Ryo Yamasaki
- & Jun-ichi Kira
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| Open AccessLipidomics study of plasma from patients suggest that ALS and PLS are part of a continuum of motor neuron disorders
- Estela Area-Gomez
- , D. Larrea
- & H. Mitsumoto
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| Open AccessNMJ-Analyser identifies subtle early changes in mouse models of neuromuscular disease
- Alan Mejia Maza
- , Seth Jarvis
- & Carole H. Sudre
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| Open AccessFGF23, a novel muscle biomarker detected in the early stages of ALS
- Ying Si
- , Mohamed Kazamel
- & Peter H. King
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| Open AccessResidential exposure to electromagnetic fields and risk of amyotrophic lateral sclerosis: a dose–response meta-analysis
- Tommaso Filippini
- , Elizabeth E. Hatch
- & Marco Vinceti
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| Open AccessOxaloacetate treatment preserves motor function in SOD1G93A mice and normalizes select neuroinflammation-related parameters in the spinal cord
- Sudheer K. Tungtur
- , Heather M. Wilkins
- & Hiroshi Nishimune
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| Open AccessCharacterization of the human TARDBP gene promoter
- Marco Baralle
- & Maurizio Romano
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| Open AccessMotor cortical excitability predicts cognitive phenotypes in amyotrophic lateral sclerosis
- Smriti Agarwal
- , Elizabeth Highton-Williamson
- & Matthew C. Kiernan
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| Open AccessIL-10 based immunomodulation initiated at birth extends lifespan in a familial mouse model of amyotrophic lateral sclerosis
- Michael R. Strickland
- , Kristen R. Ibanez
- & Paramita Chakrabarty
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| Open AccessPremature termination codons in SOD1 causing Amyotrophic Lateral Sclerosis are predicted to escape the nonsense-mediated mRNA decay
- Claire Guissart
- , Kevin Mouzat
- & Serge Lumbroso
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| Open AccessFemale sex mitigates motor and behavioural phenotypes in TDP-43Q331K knock-in mice
- Jodie Watkins
- , Anshua Ghosh
- & Jemeen Sreedharan
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| Open AccessWnt antagonist FRZB is a muscle biomarker of denervation atrophy in amyotrophic lateral sclerosis
- Thaddaeus Kwan
- , Mohamed Kazamel
- & Peter H. King
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| Open AccessInducible EphA4 knockout causes motor deficits in young mice and is not protective in the SOD1G93A mouse model of ALS
- Sara L. Dominguez
- , Timothy Earr
- & Jesse E. Hanson
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| Open AccessThe 6-min walk test as a new outcome measure in Amyotrophic lateral sclerosis
- Massimo Russo
- , Christian Lunetta
- & Sonia Messina
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| Open AccessPredictive factors for prognosis after gastrostomy placement in routine non-invasive ventilation users ALS patients
- Adèle Hesters
- , Maria del Mar Amador
- & Gaëlle Bruneteau
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| Open AccessFunctional fine-mapping of noncoding risk variants in amyotrophic lateral sclerosis utilizing convolutional neural network
- Ali Yousefian-Jazi
- , Min Kyung Sung
- & Jinwook Choi
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| Open AccessStimulus modality influences session-to-session transfer of training effects in auditory and tactile streaming-based P300 brain–computer interfaces
- P. Ziebell
- , J. Stümpfig
- & S. Halder
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| Open AccessProteomics analysis of FUS mutant human motoneurons reveals altered regulation of cytoskeleton and other ALS-linked proteins via 3′UTR binding
- Maria Giovanna Garone
- , Vincenzo Alfano
- & Alessandro Rosa