Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

Motor unit characterization in canine degenerative myelopathy :||a disease model for amyotrophic lateral sclerosis

Morgan-Jack, B. R. (2013) · MOspace Institutional Repository (University of Missouri) · doi:10.32469/10355/44663

Einfluss der Rho-Kinase-Hemmung auf Mikrogliazellen im SOD1-G93A-Mausmodell der Amyotrophen Lateralsklerose

Jansen, J. (2017) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-6353

New cause of death in young adults: Association between illicit drug abuse and amyotrophic lateral sclerosis

Azhari, D. A., Hasanabadi, D. H., & Ardanı, A. R. (2015) · International Journal of Medical Research and Review · doi:10.17511/ijmrr.2015.i7.136

Advances in the Development of Treatments for Amyotrophic Lateral Sclerosis

Aoki, M. (2016) · Nihon Naika Gakkai Zasshi · doi:10.2169/naika.105.2055

Role of astroglial α7 nicotinic acetylcholine receptors in neuroinflammation and oxidative stress

Patel (2017) · doi:10.17760/d20274193

Intra-maxillary Molecular Releasing and its Application in the Assistance of Neurodegenerative Disease Therapeutics

J, L. Y. (2016) · International Journal of Clinical Therapeutics and Diagnosis · doi:10.19070/2332-2926-1600021

Kombinationsbehandlung mit Fasudil und Riluzol im SOD1-G93A-Mausmodell der Amyotrophen Lateralsklerose

Balck, A. (2018) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-6805

Role of nano-biomechanics in brain metastasis formation and amyotrophic lateral sclerosis

Varga, B. (2018) · doi:10.14232/phd.9727

In Silico Determined Properties of Designed Superoxide Dismutase-1 Mutants Predict ALS-like Phenotypes In Vitro and In VivoPreprint

DuVal, M. G., McAlary, L., Habibi, M., Garg, P., Sher, M., Cashman, N. R., Allison, W. T., & Plotkin, S. S. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/474585

Early speech deterioration in amyotrophic lateral sclerosis: A case study of newscaster Donna Britt

Watkins, E. (2018) · doi:10.31390/gradschool_theses.4836

Differenzierung der Pharmakotherapie mit Fasudil und Riluzol im SOD1-G93A Mausmodell der Amyotrophen Lateralsklerose

Scheer, D. (2018) · doi:10.53846/goediss-7164

Endoplasmic Reticulum Stress is Transmissible among Cells of the Central Nervous System

Sprenkle, N. T. (2017) · doi:10.33915/etd.6704

Protective Role of Glial Heat Shock Proteins in Amyotrophic Lateral Sclerosis

Clarke, B. E., Kalmár, B., & Greensmith, L. (2019) · Heat shock proteins · doi:10.1007/978-3-030-24285-5_11

Structural characterization of alpha-synuclein aggregates seeded by patient material

Strohäker, T. (2019) · doi:10.53846/goediss-7768

Exploring the role of lipids in protein modification and amyotrophic lateral sclerosis

Pinto, I. F. D. (2019) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.46.2019.tde-24102019-110456

Versatile Regulator or Integrator RNA-binding Protein TLS/FUS Works for Phase Separation on Regulation of the Human Genome - In Relation to Liposarcoma and ALS

Kurokawa, R. (2020) · Biomedical Sciences · doi:10.11648/j.bs.20200601.12

Therapeutic strategies for the treatment of amyotrophic lateral sclerosis (ALS) with mutations in angiogenin and superoxide dismutase 1

Aluri, K. C. (2020) · doi:10.17760/d20361345

Amyotrophic Lateral Sclerosis

Sreedharan, J., & Brown, R. H. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-410529-4.00087-5

SPEKTR GENETIChESKIKh MUTATsIY V ROSSIYSKOY POPULYaTsII PATsIENTOV, STRADAYuShchIKh BOKOVYM AMIOTROFIChESKIM SKLEROZOM

Lysogorskaya, E. V., Abramycheva, N. Y., Zakharova, M. N., & Illarioshkin, S. N. (2012) · Medical academic journal · doi:10.17816/maj12474-76

Structural and dynamics study of G-rich sequences relevant to genomic disorders

Maity, A. (2020) · doi:10.32657/10356/141701

Untersuchung der Wirkung des antiaggregativen Compounds anle138b auf Löslichkeit und Toxizität von mutierter SOD1

Kleinknecht, A. (2017) · doi:10.53846/goediss-6545

OPTN：a promising target of autophagy to treat autophagy defective diseasesPreprint

Qiu, Y., Wang, J., Wang, J., Yang, B., He, Q., & Weng, Q. (2020) · doi:10.22541/au.158920866.62871852

Estudos genéticos e funcionais sobre os genes VAPB e VRK1 em duas famílias portadoras de Esclerose Lateral Amiotrófica

Oliveira, D. (2020) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.41.2020.tde-15122020-143559

Distribuição celular e função da proteína C9ORF72 em modelos celulares de Esclerose Lateral Amiotrófica

Reis, J. A. (2020) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.41.2020.tde-09112020-111224

Fourier transform ion cyclotron resonance mass spectrometry method development for top-down protein fragmentation and complex organic mixture analysis

Schmitt, N. D. (2020) · Digital Repository Service (Northeastern University) · doi:10.17760/d20398259

Effects of phosphetidyl choline-superoxide dismutase on wobbler mouse motor neuron disease.

Ikeda, K., & Kinoshita, M. (1996) · Ensho · doi:10.2492/jsir1981.16.37

Two Second-site Mutations Alleviate Aggregation of the A4V Variant Human Superoxide Dismutase-1 Associated With Familiar Amyotrophic Lateral Sclerosis

Zhang, S. (2013) · doi:10.18130/v3966f

Semi-rational Protein Engineering Strategies to Reduce Protein Aggregation within Mammalian

Gregoire, S. (2014) · doi:10.18130/v3p520

Electrophysiological and Morphological Studies of SOD1 Transgenic Mice: An Animal Model of ALS

Carpenter, D. O., Hori, N., Tan, Y., Xu, Z., Akaike, N., & Carpenter, D. O. (2021) · Journal of Brain and Nerves · doi:10.31487/j.jbn.2021.01.03

A Molecular View of Amyotrophic Lateral Sclerosis Through the Lens of Interaction Network ModulesPreprint

Jensen, K. H., Stalder, A. K., Wernersson, R., Roloff, T. C., Hansen, D. H., & Groenen, P. M. A. (2021) · Research Square · doi:10.21203/rs.3.rs-656827/v2

Faculty Opinions recommendation of Localization of a toxic form of superoxide dismutase 1 protein to pathologically affected tissues in familial ALS.

Spada, A. R. L., & Bennett, C. L. (2013) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.717970660.793469114

Faculty Opinions recommendation of Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia.

Al‐Chalabi, A., & Jones, A. (2011) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.12946956.14726561

Einfluss des Proteinaggregationshemmstoffs anle138b auf Beginn und Verlauf der Amyotrophen Lateralsklerose im transgenen hSOD1-Mausmodell

Thyssen, S. (2014) · doi:10.53846/goediss-4474

Differentielle Expression und Funktion eines glialen Kaliumkanals (Kir4.1, KCNJ10) im Rückenmark und Bedeutung in einem neurodegenerativen Krankheitsmodell

Kaiser, M. (2008) · doi:10.53846/goediss-265

Charakterisierung von Peroxiredoxin 2 im zentralen Nervensystem bei Multipler Sklerose

Winkler, D. A. (2021) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-8882

Faculty Opinions recommendation of Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS.

Ryder, S. P. (2012) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.13294965.14816061

2013 Spring Padua Muscle Days | Padua and Terme Euganee, March 15-17

Editors, T. M. A. F. C. D. (2013) · European Journal of Translational Myology · doi:10.4081/bam.2013.1.1

Polypyrimidine Tract-binding Protein 2 is a Potential Treated Target in Tg(SOD1*G93A)1Gur MicePreprint

Xiong, Z., Li, X., Yang, D., Xiong, C., & Zhou, Q. (2022) · Research Square · doi:10.21203/rs.3.rs-1470191/v1

Genetic Testing for Rare Diseases

Millán, J. M. (2022) · MDPI eBooks · doi:10.3390/books978-3-0365-3727-6

Nickelhaltige Enzyme: Die steile Karriere eines lange übersehenen Biometalls

Kaim, W., & Schwederski, B. E. (1995) · Teubner-Studienbücher. Chemie · doi:10.1007/978-3-322-91893-2_9

Kupferhaltige Proteine: Die Alternative zu biologischem Eisen

Kaim, W., & Schwederski, B. E. (2005) · Teubner-Studienbücher. Chemie · doi:10.1007/978-3-663-01605-2_10

Faculty Opinions recommendation of Misfolded mutant SOD1 directly inhibits VDAC1 conductance in a mouse model of inherited ALS.

Rouleau, G. A. (2011) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.12801959.14078059

The development of novel cysteine cross-linkers and their application towards neurodegenerative disorders

Donnelly, D. P. (2019) · Digital Repository Service (Northeastern University) · doi:10.17760/d20316343

Doenças do neurônio motor

Chieia, M. A. T. (2019) · Revista Neurociências · doi:10.34024/rnc.2005.v13.8803

A Novel Anti-inflammatory D-peptide Halts Disease Phenotype Progression in an Als Mouse ModelPreprint

Post, J., Kogel, V., Schaffrath, A., Lohmann, P., Shah, N. J., Langen, K., Willbold, D., Willuweit, A., & Kutzsche, J. (2020) · doi:10.21203/rs.3.rs-30893/v1

Faculty Opinions recommendation of Large SOD1 aggregates, unlike trimeric SOD1, do not impact cell viability in a model of amyotrophic lateral sclerosis.

Lapidus, L. J. (2018) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.733074417.793545703

A Molecular View of Amyotrophic Lateral Sclerosis Through the Lens of Interaction Network ModulesPreprint

Jensen, K. H., Stalder, A. K., Wernersson, R., Roloff, T. C., Hansen, D. H., & Groenen, P. M. A. (2021) · Research Square · doi:10.21203/rs.3.rs-656827/v1

The superoxide dismutase 1 (SOD1) is differentially expressed in the brains of patients with psychotic disorders.Preprint

Mamoor, S. (2020) · doi:10.31219/osf.io/ct9sv

Faculty Opinions recommendation of Retromer stabilization results in neuroprotection in a model of Amyotrophic Lateral Sclerosis.

Praticò, D. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.738419431.793580671

Kupferhaltige Proteine: Die Alternative zu biologischem Eisen

Kaim, W., & Schwederski, B. E. (2004) · Teubner-Studienbücher. Chemie · doi:10.1007/978-3-322-92714-9_10

Monitoring Human Copper/Zinc Superoxide Dismutase Misfolding/Aggregation in Mammalian Cells

Gregoire, S. (2012) · doi:10.18130/v38m1c

Preclinical Studies of Induced Pluripotent Stem Cell-Derived Astrocyte Transplantation in ALS

Maragakis, N. J., & Song, H. (2014) · Defense Technical Information Center (DTIC) · doi:10.21236/ada613757

Faculty Opinions recommendation of Antisense oligonucleotide therapies for neurodegenerative diseases.

Disney, M. D. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.736176320.793563807

A Novel Anti-inflammatory D-peptide Halts Disease Phenotype Progression in an ALS Mouse ModelPreprint

Post, J., Kogel, V., Schaffrath, A., Lohmann, P., Shah, N. J., Langen, K., Willbold, D., Willuweit, A., & Kutzsche, J. (2020) · doi:10.21203/rs.3.rs-36091/v1

Faculty Opinions recommendation of Improving mitochondria and ER stability helps eliminate upper motor neuron degeneration that occurs due to mSOD1 toxicity and TDP-43 pathology.

Morgan, B. P. (2021) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.739627914.793583462

Faculty Opinions recommendation of The Role of Insulin-Like Growth Factors and Insulin-Like Growth Factor-Binding Proteins in the Nervous System.

Rosenzweig, S. A. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.737540679.793572319

Structural and functional consequences of cross-linker-mediated stabilization of fA LS-associated SOD1

Sarin, R. (2021) · doi:10.17760/d20413926

Therapeutic interventions of Amyotrophic Lateral Sclerosis (ALS)

Chakraborty, A. K., & Diwan, A. R. (2022) · Neurology and Neuroscience · doi:10.33425/2692-7918.1032

The Impact of Familial ALS-Associated Mutations on Astrocyte Activation under Serum and Serum-Free Conditions

Jones, A. S. (2023) · doi:10.14418/wes01.1.2796

Saccharomyces cerevisiae, a platform for drug discovery

Almeida, L. D. (2022) · doi:10.47749/t/unicamp.2022.1265921

Breaking the amyotrophic lateral sclerosis early diagnostic barrier: the promise of general markers

Lu, Y., He, L., Meng, H., Chen, S., & Zhou, Q. (2023) · Exploration of Neuroprotective Therapy · doi:10.37349/ent.2023.00065

The Role of Stress in the Progression of Motor Neuron Disease: Mechanisms and Implications for Treatment

Lu, C., & Xu, X. (2023) · Stress and Brain · doi:10.26599/sab.2023.9060002

Reviewer #1 (Public Review): EphrinB2 knockdown in cervical spinal cord preserves diaphragm innervation in a mutant SOD1 mouse model of ALS

(2024) · eLife · doi:10.7554/elife.89298.4.sa1

Unraveling the Complex Pathology of Neurodegenerative Diseases: Multiple Prions, Cross-β Networks and Baicalein's ReproFoldPreprint

Chang, H., & Wang, I. (2024) · Preprints.org · doi:10.20944/preprints202402.0790.v1

NRF2 in Neurological Disorders: A Molecular Beacon for Therapeutics

Verma, N. K. (2024) · IntechOpen eBooks · doi:10.5772/intechopen.1004774 · Cited by 2

Mirnômica e proteômica no líquor de doentes com esclerose lateral amiotrófica

Busser, F. D. (2024) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.5.2024.tde-24042024-115026

Técnicas avançadas de neurofisiologia no estudo das doenças do neurônio motor

Martins, M. P. (2023) · doi:10.47749/t/unicamp.2023.1377345

Neuronal glucose metabolism in amyotrophic lateral sclerosis

Dannenberg, J. S. (2024) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-10548

Black chokeberry (×Sorbaronia mitschurinii) fruit extract affects the survival of Drosophila melanogaster with the model of amyotrophic lateral sclerosis depending on the concentration

Zemskaya, N. V., Platonova, E. Y., Ришатовна, П. Н., Shaposhnikov, M. V., & Moskalev, A. (2025) · Proceedings of the Komi Science Centre of the Ural Division of the Russian Academy of Sciences · doi:10.19110/1994-5655-2024-9-84-91

Downregulation of Keratin Proteins in the Neuroendocrine System of Amyotrophic Lateral Sclerosis with PT150 as a Dual NeuroprotectantPreprint

Dunakhe, S., Sharma, A., Das, A., & Kulkarni, P. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.03.18.643927

Other Motor Neuron Diseases of Childhood

Yang, M. L., & Connolly, A. M. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-10944-7.00161-x

Canine Degenerative Myelopathy Caused by Mutations in the Cu2+/Zn2+ Superoxide Dismutase 1 Gene

Kobatake, Y., Kimura, S., & Yokota, S. (2025) · Royal Society of Chemistry eBooks · doi:10.1039/9781837677955-00180

A non-human primate model of Amyotrophic Lateral SclerosisPreprint

Jones, R. H., Saieva, L., Balezeau, F., Schofield, I. S., McCardle, C., Baker, M., & Baker, S. N. (2025) · eLife · doi:10.1101/2025.10.27.684759

Copper ions and Nervous System: From Physiological Functions to Pathological ImplicationsPreprint

Zhang, K., Ma, W., & Ren, S. (2025) · doi:10.22541/au.176433133.38134808/v1

Additional file 7 of A distinct circular DNA profile intersects with proteome changes in the genotoxic stress-related hSOD1G93A model of ALS

Daniela Gerovska, D., Noer, J. B., Qin, Y., Ain, Q., Januzi, D., Schwab, M., Witte, O. W., Araúzo-Bravo, M. J., & Kretz, A. (2023) · Figshare · doi:10.6084/m9.figshare.24136299

Additional file 2 of A distinct circular DNA profile intersects with proteome changes in the genotoxic stress-related hSOD1G93A model of ALS

Daniela Gerovska, D., Noer, J. B., Qin, Y., Ain, Q., Januzi, D., Schwab, M., Witte, O. W., Araúzo-Bravo, M. J., & Kretz, A. (2023) · Figshare · doi:10.6084/m9.figshare.24136278

Additional file 3 of A distinct circular DNA profile intersects with proteome changes in the genotoxic stress-related hSOD1G93A model of ALS

Daniela Gerovska, D., Noer, J. B., Qin, Y., Ain, Q., Januzi, D., Schwab, M., Witte, O. W., Araúzo-Bravo, M. J., & Kretz, A. (2023) · Figshare · doi:10.6084/m9.figshare.24136284

Additional file 6 of A distinct circular DNA profile intersects with proteome changes in the genotoxic stress-related hSOD1G93A model of ALS

Daniela Gerovska, D., Noer, J. B., Qin, Y., Ain, Q., Januzi, D., Schwab, M., Witte, O. W., Araúzo-Bravo, M. J., & Kretz, A. (2023) · Figshare · doi:10.6084/m9.figshare.24136296

Additional file 1 of A distinct circular DNA profile intersects with proteome changes in the genotoxic stress-related hSOD1G93A model of ALS

Daniela Gerovska, D., Noer, J. B., Qin, Y., Ain, Q., Januzi, D., Schwab, M., Witte, O. W., Araúzo-Bravo, M. J., & Kretz, A. (2023) · Figshare · doi:10.6084/m9.figshare.24136275

Additional file 5 of A distinct circular DNA profile intersects with proteome changes in the genotoxic stress-related hSOD1G93A model of ALS

Daniela Gerovska, D., Noer, J. B., Qin, Y., Ain, Q., Januzi, D., Schwab, M., Witte, O. W., Araúzo-Bravo, M. J., & Kretz, A. (2023) · Figshare · doi:10.6084/m9.figshare.24136293

Additional file 4 of A distinct circular DNA profile intersects with proteome changes in the genotoxic stress-related hSOD1G93A model of ALS

Daniela Gerovska, D., Noer, J. B., Qin, Y., Ain, Q., Januzi, D., Schwab, M., Witte, O. W., Araúzo-Bravo, M. J., & Kretz, A. (2023) · Figshare · doi:10.6084/m9.figshare.24136287

Genetic aspects of amyotrophic lateral sclerosis

Nagiev, K. K., Sysoeva, A. Y., Karimullina, E. M., Akhmadieva, L. A., Salafutdinov, I. I., & Mukhamedyarov, M. A. (2025) · Neurology Bulletin · doi:10.17816/nb682224

Polygenic associations with clinical and neuropathological trait heterogeneity across TDP-43 proteinopathies

Spencer, B. E., Irwin, D. J., Deerlin, V. M. V., Suh, E. R., Lee, E. B., Elman, L. B., Quinn, C. C., Amado, D. A., Baer, M., Grossman, M., et al. (2025) · PLoS ONE · doi:10.1371/journal.pone.0338398

A Qualitive Investigation of Geographic Disparities in Genetic Testing and Care Access for Amyotrophic Lateral Sclerosis: Insights From Patient Journey Mapping

Sethi, N., Levy, O. A., Richardson, A., Harari, O., & Sellati, R. (2026) · Patient Preference and Adherence · doi:10.2147/ppa.s566747

Mécanismes de neurodégénérescence associés au processus inflammatoire dans la sclérose latérale amyotrophique

Aebischer, J. (2011) · theses.fr (ABES) · doi:10.70675/7dc30612zb4b4z49a3z864bz8fa2e995aa0e

Développement de nouveaux modèles expérimentaux de la Sclérose Latérale Amyotrophique

Langou, K. (2010) · theses.fr (ABES) · doi:10.70675/b77c5438zccd7z4f8bz935az7ab30698b8a8

Importance du contrôle qualité des mitochondries dans les maladies neurodégénératives : analyse cellulaire et génétique dans des modèles drosophile de la maladie de Huntington et de la sclérose latérale amyotrophique

Khalil, B. (2016) · theses.fr (ABES) · doi:10.70675/4446111fz4182z4737zae76z7f117887a893

Molecular thermodynamic aspects of dissipative structures in oncology, inflammatory and degenerative processes of Central Nervous System diseases

Vallée, A. (2017) · theses.fr (ABES) · doi:10.70675/e07edff7z4f56z4165z8ee2z475c4aafb600

Exploration cérébrale structurelle et morphologique de la posture chez des patients atteints de sclérose latérale amyotrophique

Mseddi, E. (2017) · theses.fr (ABES) · doi:10.70675/98cfe194z89ccz4f25za551ze93a65ceee66

Unravelling the tangle of motor neuron diseases : insights from neuroimaging and neurophysiology

Querin, G. (2019) · theses.fr (ABES) · doi:10.70675/30ad3e2az5051z4364z9ec1z4b8d1f952b7b

Novel FUS and CHCHD10 models to investigate pathogenic mechanisms in Amyotrophic Lateral Sclerosis

Bourefis, A.-R. (2019) · theses.fr (ABES) · doi:10.70675/45ab8515z9859z430fzb472z306dd61206c8

Epidemiological and clinical variability of amyotrophic lateral sclerosis between geographic areas and populations : focus on Africa and Latin America

Luna, J. (2019) · theses.fr (ABES) · doi:10.70675/3d5221e8z35a4z48f5zaeb6z03d61c31c171

Mitochondrial physiology within myelinated axons in health and disease : an energetic interplay between counterparts

van Hameren, G. (2018) · theses.fr (ABES) · doi:10.70675/71c15a42zb6d9z4edazb7c1zd3f51e09c949

Rôle du canal chlorure activé par le calcium TMEM16F dans la motricité et implication dans la sclérose latérale amyotrophique

Soulard, C. (2019) · theses.fr (ABES) · doi:10.70675/ef3970dcz7f20z4693z83d4z1e573317c15c

Study of the involvement of the IRE1α-XBP1 branch of unfolded urotein response in spinal muscular atrophy

D'amico, D. (2020) · theses.fr (ABES) · doi:10.70675/6e54c5b3zdabfz4677z9604zfcce72b7ed92

Etude du continuum mécanistique et physiopathologique entre la Sclérose Latérale Amyotrophique et la Démence FrontoTemporale

Waegaert, R. (2019) · theses.fr (ABES) · doi:10.70675/ff848a6ez0d22z4e0cz9e04z0511c3f18730

Génétique de la Sclérose Latérale Amyotrophique et rôle de la voie de SUMOylation dans l'agrégation de la protéine TDP-43

Maurel, C. (2018) · theses.fr (ABES) · doi:10.70675/06af88a8z908cz41aaz9b6dz8cbea6bde2a8

Étude de la composante neuroinflammatoire dans les DFT/SLA

Smeyers, J. (2020) · theses.fr (ABES) · doi:10.70675/219cfa6fz5b3az4198z9deczdfaad3cd784c

Caractérisation structurale de TDP-43, une protéine de liaison à l’ARN, impliquée dans la Sclérose Latérale Amyotrophique (SLA)

Rengifo-Gonzalez, J. C. (2020) · theses.fr (ABES) · doi:10.70675/e4d4c819zb9c3z4abdza47cz73bc506bbee3

Secretion of neurotoxic vesicles by muscle cells of ALS patients

Gall, L. L. (2019) · theses.fr (ABES) · doi:10.70675/61e48a01z5133z45e6z8569z1b35b4b8fb4f

A novel point mutation in the Cu/Zn superoxide dismutase gene in a patient with familial amyotrophic lateral sclerosis

Ikeda, M., Abe, K., Ogasawara, M., Kameya, T., Watanabe, M., Shoji, M., Hirai, S., & Itoyama, Y. (1995) · Human Molecular Genetics · doi:10.1093/hmg/4.3.491 · Cited by 29

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Identification of a new missense point mutation in exon 4 of the Cu/Zn superoxide dismutase (SOD-1) gene in a family with amyotrophic lateral sclerosis

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Identification of new mutations in the Cu/Zn superoxide dismutase gene of patients with familial amyotrophic lateral sclerosis.

Pramatarova, A., Figlewicz, D. A., Krizus, A., Han, F. Y., Ceballos-Picot, I., Nicole, A., Dib, M., Meininger, V., Brown, R. H., & Rouleau, G. A. (1995) · Europe PMC (PubMed Central) · Cited by 121

A novel two-base mutation in the superoxide dismutase gene associated with familial amyotrophic lateral sclerosis in Japan

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