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An online integrated programming platform to acquire students' behavior data for immediate feedback teaching

Computer applications in engineering education, 2023-05, Vol.31 (3), p.520-536

2023

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A new phenotype of syndromic retinitis pigmentosa with myopathy is caused by mutations in retinol dehydrogenase 11

Clinical genetics, 2022-04, Vol.101 (4), p.448-453

2022

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Novel mutations in B3GALNT2 gene causing α-dystroglycanopathy in Chinese patients

Chinese medical journal, 2021-06, Vol.134 (12), p.1483-1485

2021

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Comorbidity of chronic fatigue syndrome, postural tachycardia syndrome, and narcolepsy with 5,10-methylenetetrahydrofolate reductase (MTHFR) mutation in an adolescent: a case report

Chinese medical journal, 2021-06, Vol.134 (12), p.1495-1497

2021

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Multisystem involvement in Chinese patients with neuromyopathic phenotype of mitochondrial trifunctional protein deficiency

Chinese medical journal, 2020-06, Vol.133 (11), p.1358-1360

2020

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Phenotype and Genotype Study of Chinese POMT2-Related α-Dystroglycanopathy

Frontiers in genetics, 2021-08, Vol.12, p.692479-692479

2021

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Case report: Muscle involvement in a Chinese patient with TRNT1 -related disorder

Frontiers in pediatrics, 2023-05, Vol.11, p.1160107

2023

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Dynamic evolution of brain structural patterns in liver transplantation recipients: a longitudinal study based on 3D convolutional neuronal network model

European radiology, 2023-09, Vol.33 (9), p.6134-6144

2023

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Novel collagen VI mutations identified in Chinese patients with Ullrich congenital muscular dystrophy

World journal of pediatrics : WJP, 2014-05, Vol.10 (2), p.126-132

2014

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Hot spot mutation screening of RYR1 gene in diagnosis of congenital myopathies

Beijing da xue xue bao. Journal of Peking University. Yi xue ban, 2014-10, Vol.46 (5), p.691

2014

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Febrile seizure, but not hyperthermia alone, induces the expression of heme oxygenase-1 in rat cortex

Chinese medical journal, 2006-02, Vol.119 (3), p.191-196

2006

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Study on text preprocessing and automatic rule learning technology for information extraction

Chang, Xing Zhi Chang Xing Zhi

2008

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Clinical, pathological and molecular biological characteristics of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episode in children

Zhonghua er ke za zhi, 2013-02, Vol.51 (2), p.130

2013

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Successive alterations of hippocampal gamma-aminobutyric acid B receptor subunits in a rat model of febrile seizure

Life sciences (1973), 2006-05, Vol.78 (25), p.2944-2952

2006

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Value of muscle enzyme analysis in differential diagnosis of childhood myopathic hyper-creatine kinase-emia

Beijing da xue xue bao. Journal of Peking University. Yi xue ban, 2014-02, Vol.46 (1), p.130

2014

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Episodic central nervous system symptoms with reversible white matter involvement in Chinese patients with X-linked Charcot-Marie-Tooth disease and literatures review

Zhonghua er ke za zhi, 2013-11, Vol.51 (11), p.813

2013

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Mitochondrial respiratory chain complex I deficiency due to 10191T>C mutation in ND3 gene

Zhongguo dang dai er ke za zhi, 2012-08, Vol.14 (8), p.561

2012

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Detection of vacuolated peripheral blood lymphocytes in screening for and diagnosis of lysosomal storage diseases

Zhonghua er ke za zhi, 2011-02, Vol.49 (2), p.135

2011

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A novel patent technology characterization method based on heterogeneous network message passing algorithm and patent classification system

Expert systems with applications, 2024-12, Vol.256, p.124895, Article 124895

2024

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Value of latex agglutination test in the diagnosis and treatment of cryptococcal meningitis in children

Zhongguo dang dai er ke za zhi, 2011-02, Vol.13 (2), p.115

2011

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Clinical characteristics and follow-up management of 135 children with myasthenia gravis

Beijing da xue xue bao. Journal of Peking University. Yi xue ban, 2011-06, Vol.43 (3), p.455

2011

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Two novel mutations of GJB1 gene associated with typical X-linked Charcot-Marie-Tooth disease

Zhong hua yi xue za zhi, 2009-12, Vol.89 (47), p.3328-3331

2009

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Congenital muscular dystrophy complicated with tetanized spinal column in a case

Zhonghua er ke za zhi, 2008-06, Vol.46 (6), p.477

2008

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Genotype, phenotype analysis and follow-up study on patients with Duchenne/Becker muscular dystrophy

Beijing da xue xue bao. Journal of Peking University. Yi xue ban, 2010-12, Vol.42 (6), p.661

2010

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Study on Text Preprocessing and Automatic Rule Learning Technology for Information Extraction

Chang, Zhi Chang Xing Zhi Xing

2004

Volltextzugriff (PDF)

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An online integrated programming platform to acquire students' behavior data for immediate feedback teaching

A new phenotype of syndromic retinitis pigmentosa with myopathy is caused by mutations in retinol dehydrogenase 11

Novel mutations in B3GALNT2 gene causing α-dystroglycanopathy in Chinese patients

Comorbidity of chronic fatigue syndrome, postural tachycardia syndrome, and narcolepsy with 5,10-methylenetetrahydrofolate reductase (MTHFR) mutation in an adolescent: a case report

Multisystem involvement in Chinese patients with neuromyopathic phenotype of mitochondrial trifunctional protein deficiency

Phenotype and Genotype Study of Chinese POMT2-Related α-Dystroglycanopathy

Case report: Muscle involvement in a Chinese patient with TRNT1 -related disorder

Dynamic evolution of brain structural patterns in liver transplantation recipients: a longitudinal study based on 3D convolutional neuronal network model

Novel collagen VI mutations identified in Chinese patients with Ullrich congenital muscular dystrophy

Hot spot mutation screening of RYR1 gene in diagnosis of congenital myopathies

Febrile seizure, but not hyperthermia alone, induces the expression of heme oxygenase-1 in rat cortex

Study on text preprocessing and automatic rule learning technology for information extraction

Clinical, pathological and molecular biological characteristics of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episode in children

Successive alterations of hippocampal gamma-aminobutyric acid B receptor subunits in a rat model of febrile seizure

Value of muscle enzyme analysis in differential diagnosis of childhood myopathic hyper-creatine kinase-emia

Episodic central nervous system symptoms with reversible white matter involvement in Chinese patients with X-linked Charcot-Marie-Tooth disease and literatures review

Mitochondrial respiratory chain complex I deficiency due to 10191T>C mutation in ND3 gene

Detection of vacuolated peripheral blood lymphocytes in screening for and diagnosis of lysosomal storage diseases

A novel patent technology characterization method based on heterogeneous network message passing algorithm and patent classification system

Value of latex agglutination test in the diagnosis and treatment of cryptococcal meningitis in children

Clinical characteristics and follow-up management of 135 children with myasthenia gravis

Two novel mutations of GJB1 gene associated with typical X-linked Charcot-Marie-Tooth disease

Congenital muscular dystrophy complicated with tetanized spinal column in a case

Genotype, phenotype analysis and follow-up study on patients with Duchenne/Becker muscular dystrophy

Study on Text Preprocessing and Automatic Rule Learning Technology for Information Extraction

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