Search

Your search keyword '"Fan DS"' showing total 276 results

Search Constraints

Start Over You searched for: Author "Fan DS" Remove constraint Author: "Fan DS" Search Limiters Academic (Peer-Reviewed) Journals Remove constraint Search Limiters: Academic (Peer-Reviewed) Journals
276 results on '"Fan DS"'

Search Results

1. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (vol 53, pg 1636, 2021)

2. Gamma Radiation Effects on the Performance of FIR-based Fiber-Optic Temperature Sensors

3. Association of apolipoprotein E polymorphisms with normal tension glaucoma in a Chinese population

4. Sub-Tenon's anesthesia in vitreoretinal surgery: a needleless technique

8. Large expert-curated database for benchmarking document similarity detection in biomedical literature search

9. Author Correction: The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration.

10. [To determine the value of iMAX, a new electrodiagnostic method, and its application in the evaluation of peripheral motor nerve excitability].

11. Penthorum chinense Pursh inhibits ferroptosis in cellular and Caenorhabditis elegans models of Alzheimer's disease.

14. Targeting autophagy to discover the Piper wallichii petroleum ether fraction exhibiting antiaging and anti-Alzheimer's disease effects in Caenorhabditis elegans.

16. The spatial effects of rural toilet retrofitting investment on farmers' medical and health expenditure in China.

17. [Anti-HMGCR immune-mediated necrotizing myopathy: A case report].

19. Promising application of a new ulnar nerve compound muscle action potential measurement montage in amyotrophic lateral sclerosis: a prospective cross-sectional study.

20. [Diagnostic value of F wave changes in patients with Charcot-Marie-Tooth1A and chronic inflammatory demyelinating polyneuropathy].

21. Heterozygous Seryl-tRNA Synthetase 1 Variants Cause Charcot-Marie-Tooth Disease.

23. [Cortical thickness and cognitive impairment in patients with amyotrophic lateral sclerosis].

24. The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration.

25. [Genetic distribution in Chinese patients with hereditary peripheral neuropathy].

28. Ultra-early amplitude decrement after repetitive nerve stimulation supports early neuromuscular junction injury in amyotrophic lateral sclerosis: a prospective cross-sectional study.

29. [Evaluation of vestibular-evoked myogenic potential for functional integrity of the brain stem in Kennedy's disease].

30. Autosomal recessive spinocerebellar ataxia type 4 with a VPS13D mutation: A case report.

31. [Corneal confocal microscopy detects small-fiber neuropathy in patients with amyotrophic lateral sclerosis].

34. Evaluation of chemical similarity among rhizome, pseudo stem and leaf of Musa basjoo by UPLC-ELSD fingerprint combined with chemo metrics methods.

35. [Association between rare UBQLN2 variants and amyotrophic lateral sclerosis in Chinese population].

40. Efficacy of cattle encephalon glycoside and ignotin in patients with acute cerebral infarction: a randomized, double-blind, parallel-group, placebo-controlled study.

41. [Calculation of the prevalence of progressive muscular atrophy among adults in China based on urban medical insurance data from 15 provinces].

42. [The diagnostic value of tremor analysis for defining the Parkinson's disease subtype].

43. [Diagnostic value of tremor analysis in identifying the early Parkinson's syndrome].

44. [Clinical and neuroimaging features in 6 patients with corticobasal syndrome].

45. [Application value of motor unit number index in patients with amyotrophic lateral sclerosis].

46. [Management of severe internal carotid stenosis with unruptured intracranial aneurysm].

47. [Establishment of motor unit number index detection method].

48. Prognostic factors in ALS: a comparison between Germany and China.

49. [Detection of axillary nerve multisegment motor nerve conduction using magnetic stimulation].

50. A novel MYH7 mutation resulting in Laing distal myopathy in a Chinese family.

Catalog

Books, media, physical & digital resources