Found: 14
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Neurological Characteristics of Allgrove Syndrome: A Case Series.
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- Annals of Child Neurology, 2024, v. 32, n. 2, p. 130, doi. 10.26815/acn.2024.00458
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- Article
Guillain-Barré syndrome following the first dose of Pfizer-BioNTech COVID-19 vaccine: case report and review of reported cases.
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- Neurological Sciences, 2022, v. 43, n. 2, p. 755, doi. 10.1007/s10072-021-05733-x
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- Article
PTPA variants and impaired PP2A activity in early-onset parkinsonism with intellectual disability.
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- Brain: A Journal of Neurology, 2023, v. 146, n. 4, p. 1496, doi. 10.1093/brain/awac326
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- Article
Intrathecal B cell-related markers for an optimized biological investigation of multiple sclerosis patients.
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- Scientific Reports, 2022, v. 11, n. 1, p. 1, doi. 10.1038/s41598-022-19811-3
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- Article
Novel Missense CAPN3 Mutation Responsible for Adult-Onset Limb Girdle Muscular Dystrophy with Calves Hypertrophy.
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- Journal of Molecular Neuroscience, 2019, v. 69, n. 4, p. 563, doi. 10.1007/s12031-019-01383-z
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- Article
A Novel SYNJ1 Mutation in a Tunisian Family with Juvenile Parkinson’s Disease Associated with Epilepsy.
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- Journal of Molecular Neuroscience, 2018, v. 66, n. 2, p. 273, doi. 10.1007/s12031-018-1167-2
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- Article
Acute-onset chronic inflammatory demyelinating polyneuropathy following AstraZeneca COVID-19 vaccine: a case report.
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- Pan African Medical Journal, 2024, v. 47, p. 1, doi. 10.11604/pamj.2024.47.46.42455
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- Article
Facteurs pronostiques de mortalité par accident vasculaire cérébral artériel à la phase aiguë dans une population nord-africaine.
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- Pan African Medical Journal, 2020, v. 35, p. 1, doi. 10.11604/pamj.2020.35.50.16287
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- Article
Étalonnage du test des cinq mots dans une population tunisienne de sujets sains.
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- Pan African Medical Journal, 2019, v. 34, p. 1, doi. 10.11604/pamj.2019.34.58.14472
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- Article
Novel splicing dysferlin mutation causing myopathy with intra-familial heterogeneity.
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- Molecular Biology Reports, 2020, v. 47, n. 8, p. 5755, doi. 10.1007/s11033-020-05643-9
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- Article
Rickettsial infection‐related encephalitis/encephalopathy with reversible splenial lesion of the corpus callosum.
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- Neurology & Clinical Neuroscience, 2023, v. 11, n. 2, p. 100, doi. 10.1111/ncn3.12697
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- Article
MTHFR (C677T, A1298C), FV Leiden polymorphisms, and the prothrombin G20210A mutation in arterial ischemic stroke among young tunisian adults.
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- Metabolic Brain Disease, 2021, v. 36, n. 3, p. 421, doi. 10.1007/s11011-020-00663-7
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- Article
Mild limb girdle muscular dystrophy R9 phenotype caused by novel compound heterozygous FKRP gene mutation.
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- Acta Myologica, 2023, v. 42, n. 4, p. 106, doi. 10.36185/2532-1900-391
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- Article
VITAMIN D DEFICIENCY IN RELATION WITH THE SYSTEMIC AND CENTRAL INFLAMMATION DURING MULTIPLE SCLEROSIS.
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- Journal of Medical Biochemistry, 2023, v. 42, n. 3, p. 364, doi. 10.5937/jomb0-37676
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- Article