Found: 9
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Facial Myositis: A Very Rare Syphilitic Symptom.
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- Annals of Military & Health Sciences Research, 2023, v. 21, n. 2, p. 1, doi. 10.5812/amh-140861
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- Article
Multicenter Transversal Two-Phase Study to Determine a National Prevalence of Epilepsy in Algeria.
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- Neuroepidemiology, 2012, v. 39, n. 2, p. 131, doi. 10.1159/000339637
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- Article
Heterozygous EIF2AK2 Variant Causes Adolescence‐Onset Generalized Dystonia Partially Responsive to DBS.
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- Movement Disorders Clinical Practice, 2022, v. 9, n. 2, p. 268, doi. 10.1002/mdc3.13371
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- Article
Validation of a clinical practice-based algorithm for the diagnosis of autosomal recessive cerebellar ataxias based on NGS identified cases.
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- Journal of Neurology, 2016, v. 263, n. 7, p. 1314, doi. 10.1007/s00415-016-8112-5
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- Article
Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia.
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- BMC Medical Genetics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12881-015-0180-3
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- Article
Les syndromes myasthéniques congénitaux avec anomalies cinétiques du récepteur à l'acétylcholine.
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- Médecine Sciences, 2023, v. 39, p. 58, doi. 10.1051/medsci/2023135
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- Article
La grande variabilité phénotypique des mutations du gène RYR1.
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- Médecine Sciences, 2022, v. 38, p. 46, doi. 10.1051/medsci/2022178
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- Article
A recurrent homozygous LMNA missense variant p.Thr528Met causes atypical progeroid syndrome characterized by mandibuloacral dysostosis, severe muscular dystrophy, and skeletal deformities.
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- American Journal of Medical Genetics. Part A, 2023, v. 191, n. 9, p. 2274, doi. 10.1002/ajmg.a.63335
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- Article
Clinical, Biomarker, and Molecular Delineations and Genotype-Phenotype Correlations of Ataxia With Oculomotor Apraxia Type 1.
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- JAMA Neurology, 2018, v. 75, n. 4, p. 495, doi. 10.1001/jamaneurol.2017.4373
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- Article