169 results on '"Yang, Chengqing"'
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2. Aerodynamic performance of a ventilation system for droplet control by coughing in a hospital isolation ward
3. NEW ADVANCES IN THE DIAGNOSIS AND TREATMENT OF PEDIATRIC MIGRAINE
4. The regulation and potential role of interleukin-32 in tuberculous pleural effusion
5. Whole-exome sequencing analysis to identify novel potential pathogenetic NPC1 mutations in two Chinese families with Niemann–Pick disease type C
6. A Novel De Novo TUBB3 Variant Causing Developmental Delay, Epilepsy and Mild Ophthalmological Symptoms in a Chinese Child
7. A heterozygous missense variant in the YWHAG gene causing developmental and epileptic encephalopathy 56 in a Chinese family
8. Clinical study of recurrent mild encephalitis/encephalopathy with a reversible splenial lesion in two cases
9. A rare pediatric patient of anti-IgLON5 encephalitis with epileptic seizures as the first symptom
10. Activation of hypoxia-inducible factor 1 (Hif-1) enhanced bactericidal effects of macrophages to Mycobacterium tuberculosis
11. Association of the Polymorphism of rs1799822 on Carnitine Palmitoyltransferase II Gene with Severe Enterovirus 71 Encephalitis in Chinese Children
12. Clinical Characteristics of Tracheobronchopathia Osteochondroplastica: A Retrospective Study of 33 Patients
13. Two pediatric patients with hemiplegic migraine presenting as acute encephalopathy: case reports and a literature review
14. Oligoadenylate synthetase 3 S381R gene polymorphism is associated with severity of EV71 infection in Chinese children
15. The interaction of NOS1AP, DISC1, DAOA, and GSK3B confers susceptibility of early-onset schizophrenia in Chinese Han population
16. Multidrug-resistant tuberculosis in middle ear: A case report
17. Clinical Characteristics of Tracheobronchopathia Osteochondroplastica: A Retrospective Study of 33 Patients
18. Report of a de novo c.2605C > T (p.Pro869Ser) change in the MED13L gene and review of the literature for MED13L-related intellectual disability
19. Impact of IL-10-1082A/G gene polymorphism on the severity of EV71 infection in Chinese children
20. Effect of a modified regimen on drug-sensitive retreated pulmonary tuberculosis: A multicenter study in China
21. TMEM173 rs7447927 genetic polymorphism and susceptibility to severe enterovirus 71 infection in Chinese children
22. A compromise solution between overlapping and overlooking DSM personality disorders in Chinese psychiatric practice
23. Guillain–Barré syndrome with unilateral peripheral facial paralysis in a Chinese child
24. Aerodynamics performance of a ventilation system for droplets controlling by coughing in a hospital isolation ward
25. Association of the IRAK4 rs4251545 genetic polymorphism with severity of enterovirus‐71 infection in Chinese children
26. A Novel De Novo TUBB3 Variant Causing Developmental Delay, Epilepsy and Mild Ophthalmological Symptoms in a Chinese Child
27. A cohort study of mild encephalitis/encephalopathy with a reversible splenial lesion in children
28. De novo frameshift variants of HNRNPU in patients with early infantile epileptic encephalopathy: Two case reports and literature review
29. Hemiconvulsion–hemiplegia–epilepsy syndrome with 5q33.3q34 microdeletion: Causal or chance association
30. MOG antibody‐positive cerebral cortical encephalitis: Two case reports and literature review
31. Report of a case with ferredoxin reductase ( FDXR ) gene variants in a Chinese boy exhibiting hearing loss, visual impairment, and motor retardation
32. A case of TSC2‐PKD1 contiguous deletion syndrome: Clinical features and effective treatment for epilepsy
33. A Novel Heterozygous Missense Variant in YWHAG Gene Cause Early-Onset Epilepsy in a Chinese Family
34. Genetic Variation Analysis and Treatment Strategy of 20 Patients with Dystrophin Gene Mutations
35. Histopathologic Changes and SARS-CoV-2 Immunostaining in the Lung of a Patient With COVID-19
36. Remdesivir in adults with severe COVID-19: a randomised, double-blind, placebo-controlled, multicentre trial
37. Patient Predisposition at Hospital Admission Indirectly Dictates Disease Severity, Clinical Course and Outcomes of COVID-19 Pneumonia Patients in Wuhan, China
38. Novel compound heterozygous mutations in theWWOXgene cause early infantile epileptic encephalopathy
39. Levodopa is effective in the treatment of three Chinese Tyrosine hydroxylase (TH) deficiency children
40. Different levels of facial expression recognition in patients with first-episode schizophrenia: A functional MRI study
41. Diagnostic efficacy of clinical decision tree and integral model in tuberculous pleurisy.
42. Novel compound heterozygous mutations in the WWOX gene cause early infantile epileptic encephalopathy.
43. The biochemical characterization of a missense mutation m.8914C>T in ATP6 gene associated with mitochondrial encephalomyopathy
44. Gene analysis: A rare gene disease of intellectual deficiency‐Cohen syndrome
45. Synthesis of Sponge‐Like Bi 2 O 3 by Using a Soft/Hard‐Combined Biomembrane Support System for Application as Supercapacitor
46. A case of Pitt‐hopkins Syndrome with de novo mutation in TCF4: Clinical features and treatment for epilepsy
47. Differential gene expression in patients with subsyndromal symptomatic depression and major depressive disorder
48. Changes in event-related potentials in patients with first-episode schizophrenia and their siblings
49. The relationship between facial emotion recognition and executive functions in first-episode patients with schizophrenia and their siblings
50. Synthesis of Sponge‐Like Bi2O3 by Using a Soft/Hard‐Combined Biomembrane Support System for Application as Supercapacitor.
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