Found: 30
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Pediatric Autoimmune Encephalitis: Case Series From Two Chinese Tertiary Pediatric Neurology Centers.
- Published in:
- Frontiers in Neurology, 2019, p. 1, doi. 10.3389/fneur.2019.00906
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- Article
Saliva microbiomes distinguish caries-active from healthy human populations.
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- ISME Journal: Multidisciplinary Journal of Microbial Ecology, 2012, v. 6, n. 1, p. 1, doi. 10.1038/ismej.2011.71
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- Article
Modeling and analysis of distribution network with photovoltaic cells based on Markov global sensitivity.
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- Frontiers in Energy Research, 2024, p. 1, doi. 10.3389/fenrg.2024.1374467
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- Article
Correlation of Phenotype–Genotype and Protein Structure in RYR1 -Related Myopathy.
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- Frontiers in Neurology, 2022, v. 13, p. 1, doi. 10.3389/fneur.2022.870285
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- Article
Phenotype–Genotype Analysis of Chinese Patients with Early-Onset LMNA-Related Muscular Dystrophy.
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- PLoS ONE, 2015, v. 10, n. 6, p. 1, doi. 10.1371/journal.pone.0129699
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- Article
Saliva Microbiota Carry Caries-Specific Functional Gene Signatures.
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- PLoS ONE, 2014, v. 9, n. 2, p. 1, doi. 10.1371/journal.pone.0076458
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- Article
Nuclear Factor-κB Pathway Mediates the Molecular Pathogenesis of LMNA-Related Muscular Dystrophies.
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- Biochemical Genetics, 2020, v. 58, n. 6, p. 966, doi. 10.1007/s10528-020-09989-4
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- Article
Identification of novel ATP7A mutations and prenatal diagnosis in Chinese patients with Menkes disease.
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- Metabolic Brain Disease, 2017, v. 32, n. 4, p. 1123, doi. 10.1007/s11011-017-9985-4
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- Article
Novel phenotypes of pyridox(am)ine-5'-phosphate oxidase deficiency and high prevalence of c.445_448del mutation in Chinese patients.
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- Metabolic Brain Disease, 2017, v. 32, n. 4, p. 1081, doi. 10.1007/s11011-017-9995-2
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- Article
Fabric Defect Detection Based on Pattern Template Correction.
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- Mathematical Problems in Engineering, 2018, p. 1, doi. 10.1155/2018/3709821
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- Article
Clinical and genetic features of infancy-onset congenital myopathies from a Chinese paediatric centre.
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- 2022
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- journal article
Efficacy of vigabatrin in the treatment of infantile epileptic spasms syndrome: A systematic review and meta‐analysis.
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- Epilepsia Open, 2023, v. 8, n. 2, p. 268, doi. 10.1002/epi4.12703
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- Article
Natural history and genetic study of LAMA2-related muscular dystrophy in a large Chinese cohort.
- Published in:
- 2021
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- journal article
A Novel Power Quality Comprehensive Estimation Model Based on Multi-Factor Variance Analysis for Distribution Network with DG.
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- Processes, 2023, v. 11, n. 8, p. 2385, doi. 10.3390/pr11082385
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- Article
Centronuclear myopathy due to a de novo nonsense variant and a maternally inherited splice‐site variant in TTN: A case report.
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- Clinical Case Reports, 2021, v. 9, n. 7, p. 1, doi. 10.1002/ccr3.4478
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- Article
Analysis of Investment Decision of Coastal Clean Energy Project Based on Market Connection.
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- Journal of Coastal Research, 2020, v. 115, p. 383, doi. 10.2112/JCR-SI115-110.1
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- Article
Analysis of Investment Decision of Coastal Clean Energy Project Based on Market Connection.
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- Journal of Coastal Research, 2020, v. 115, p. 383, doi. 10.2112/JCR-SI115-110.1
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- Article
Identification of Novel ARSA Mutations in Chinese Patients with Metachromatic Leukodystrophy.
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- International Journal of Genomics, 2018, p. 1, doi. 10.1155/2018/2361068
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- Article
Unique genotype-phenotype correlations within LAMA2-related limb girdle muscular dystrophy in Chinese patients.
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- Frontiers in Neurology, 2023, p. 1, doi. 10.3389/fneur.2023.1158094
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- Article
Genetic variations and clinical spectrum of dystroglycanopathy in a large cohort of Chinese patients.
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- Clinical Genetics, 2021, v. 99, n. 3, p. 384, doi. 10.1111/cge.13886
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- Article
Mutational and clinical spectrum in a cohort of Chinese patients with hereditary nemaline myopathy.
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- Clinical Genetics, 2020, v. 97, n. 6, p. 878, doi. 10.1111/cge.13745
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- Article
A splice site mutation c.1251G>A of ISPD gene is a common cause of congenital muscular dystrophy in Chinese patients.
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- Clinical Genetics, 2020, v. 97, n. 5, p. 789, doi. 10.1111/cge.13695
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- Article
Defect inspection research on fabric based on template correction and primitive decomposition.
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- IET Image Processing (Wiley-Blackwell), 2019, v. 13, n. 14, p. 2916, doi. 10.1049/iet-ipr.2018.6626
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- Article
Novel SEPN1 Mutations in Exon 1 Are Common in Rigid Spine With Muscular Dystrophy Type 1 in Chinese Patients.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.825793
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- Article
Clinical Features and Ryanodine Receptor Type 1 Gene Mutation Analysis in a Chinese Family With Central Core Disease.
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- Journal of Child Neurology, 2013, v. 28, n. 3, p. 384, doi. 10.1177/0883073812441251
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- Article
Phaeohyphomycosis of the Central Nervous System Caused by Exophiala dermatitidis in a 3-Year-Old Immunocompetent Host.
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- Journal of Child Neurology, 2009, v. 24, n. 3, p. 342, doi. 10.1177/0883073808323524
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- Article
<i>Nannochloropsis</i> Genomes Reveal Evolution of Microalgal Oleaginous Traits.
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- PLoS Genetics, 2014, v. 10, n. 1, p. 1, doi. 10.1371/journal.pgen.1004094
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- Article
Clinical and genetic analysis of a case with centronuclear myopathy caused by SPEG gene mutation: a case report and literature review.
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- 2021
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- Publication type:
- journal article
Bilayer Markov Random Field Method for Detecting Defects in Patterned Fabric.
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- Journal of Circuits, Systems & Computers, 2022, v. 31, n. 3, p. 1, doi. 10.1142/S021812662250058X
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- Article
Hypomyelinating disorders in China: The clinical and genetic heterogeneity in 119 patients.
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- PLoS ONE, 2018, v. 13, n. 2, p. 1, doi. 10.1371/journal.pone.0188869
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- Article