Found: 26
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Intravenous Mesenchymal Stem Cells Improve Survival and Motor Function in Experimental Amyotrophic Lateral Sclerosis.
- Published in:
- Molecular Medicine, 2012, v. 18, n. 5, p. 794, doi. 10.2119/molmed.2011.00498
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- Publication type:
- Article
Estimating the impact of COVID-19 pandemic on services provided by Italian Neuromuscular Centers: an Italian Association of Myology survey of the acute phase.
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- Acta Myologica, 2020, v. 39, n. 2, p. 57, doi. 10.36185-2532-1900-008
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- Publication type:
- Article
Complexities of Genetic Counseling for ALS: A Case of Two Siblings with Discordant Genetic Test Results.
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- Journal of Genetic Counseling, 2015, v. 24, n. 4, p. 553, doi. 10.1007/s10897-015-9831-y
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- Publication type:
- Article
The unfolded protein response in amyotrophic later sclerosis: results of a phase 2 trial.
- Published in:
- 2021
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- Publication type:
- journal article
Interplay between spinal cord and cerebral cortex metabolism in amyotrophic lateral sclerosis.
- Published in:
- 2018
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- Publication type:
- journal article
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis.
- Published in:
- 2019
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- Publication type:
- journal article
Role of MAPT in Pure Motor Neuron Disease: Report of a Recurrent Mutation in Italian Patients.
- Published in:
- Neurodegenerative Diseases, 2018, v. 18, n. 5/6, p. 310, doi. 10.1159/000497820
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- Publication type:
- Article
A phase I/IIa clinical trial of autologous hematopoietic stem cell transplantation in amyotrophic lateral sclerosis.
- Published in:
- Journal of Neurology, 2022, v. 269, n. 10, p. 5337, doi. 10.1007/s00415-022-11185-w
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- Publication type:
- Article
The Italian multicenter experience with edaravone in amyotrophic lateral sclerosis.
- Published in:
- Journal of Neurology, 2020, v. 267, n. 11, p. 3258, doi. 10.1007/s00415-020-09993-z
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- Publication type:
- Article
Factors predicting survival in ALS: a multicenter Italian study.
- Published in:
- Journal of Neurology, 2017, v. 264, n. 1, p. 54, doi. 10.1007/s00415-016-8313-y
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- Publication type:
- Article
Reply to "Cognition and motor phenotypes in ALS: a retrospective study".
- Published in:
- Neurological Sciences, 2023, v. 44, n. 12, p. 4531, doi. 10.1007/s10072-023-06976-6
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- Publication type:
- Article
Withdrawal of mechanical ventilation in amyotrophic lateral sclerosis patients: a multicenter Italian survey.
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- Neurological Sciences, 2023, v. 44, n. 12, p. 4349, doi. 10.1007/s10072-023-06905-7
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- Publication type:
- Article
Predictors of self-perceived health worsening over COVID-19 emergency in ALS.
- Published in:
- Neurological Sciences, 2021, v. 42, n. 4, p. 1231, doi. 10.1007/s10072-020-04997-z
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- Publication type:
- Article
Myasthenia gravis developing in an HIV-negative patient with Kaposi's sarcoma.
- Published in:
- 2013
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- Publication type:
- Letter
Age at symptom onset influences cortical thinning distribution and survival in amyotrophic lateral sclerosis.
- Published in:
- Neuroradiology, 2021, v. 63, n. 9, p. 1481, doi. 10.1007/s00234-021-02681-3
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- Publication type:
- Article
Cord cross-sectional area at foramen magnum as a correlate of disability in amyotrophic lateral sclerosis.
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- European Radiology Experimental, 2018, v. 2, n. 1, p. N.PAG, doi. 10.1186/s41747-018-0045-6
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- Publication type:
- Article
A PET/CT approach to spinal cord metabolism in amyotrophic lateral sclerosis.
- Published in:
- European Journal of Nuclear Medicine & Molecular Imaging, 2016, v. 43, n. 11, p. 2061, doi. 10.1007/s00259-016-3440-3
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- Publication type:
- Article
The HFE p.H63D (p.His63Asp) Polymorphism Is a Modifier of ALS Outcome in Italian and French Patients with SOD1 Mutations.
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- Biomedicines, 2023, v. 11, n. 3, p. 704, doi. 10.3390/biomedicines11030704
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- Publication type:
- Article
Spinal cord hypermetabolism extends to skeletal muscle in amyotrophic lateral sclerosis: a computational approach to [18F]-fluorodeoxyglucose PET/CT images.
- Published in:
- EJNMMI Research, 2020, v. 10, n. 1, p. 1, doi. 10.1186/s13550-020-0607-5
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- Publication type:
- Article
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72.
- Published in:
- Brain: A Journal of Neurology, 2012, v. 135, n. 3, p. 784
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- Publication type:
- Article
SOD1 mutations in amyotrophic lateral sclerosis.
- Published in:
- Journal of Neurology, 2005, v. 252, n. 7, p. 782, doi. 10.1007/s00415-005-0742-y
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- Publication type:
- Article
MND Phenotypes Differentiation: The Role of Multimodal Characterization at the Time of Diagnosis.
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- Life (2075-1729), 2022, v. 12, n. 10, p. 1506, doi. 10.3390/life12101506
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- Publication type:
- Article
Repeated courses of granulocyte colony-stimulating factor in amyotrophic lateral sclerosis: Clinical and biological results from a prospective multicenter study.
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- Muscle & Nerve, 2011, v. 43, n. 2, p. 189, doi. 10.1002/mus.21851
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- Publication type:
- Article
Correlation between PMP-22 messenger mRNA expression and phenotype in hereditary neuropathy with liability to pressure palsies.
- Published in:
- Annals of Neurology, 1997, v. 42, n. 6, p. 866, doi. 10.1002/ana.410420607
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- Publication type:
- Article
Effect of RNS60 in amyotrophic lateral sclerosis: a phase II multicentre, randomized, double‐blind, placebo‐controlled trial.
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- European Journal of Neurology, 2023, v. 30, n. 1, p. 69, doi. 10.1111/ene.15573
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- Publication type:
- Article
Mild behavioral impairment as a potential marker of predementia risk states in motor neuron diseases.
- Published in:
- European Journal of Neurology, 2023, v. 30, n. 1, p. 47, doi. 10.1111/ene.15570
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- Publication type:
- Article