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1. Serum vitamin D, vitamin D receptor and binding protein genes polymorphisms in restless legs syndrome

3. Association between endothelial nitric oxide synthase (NOS3) rs2070744 and the risk for migraine

4. Gamma-aminobutyric acid (GABA) receptors genes polymorphisms and risk for restless legs syndrome

5. Vitamin D receptor and binding protein genes variants in patients with migraine

6. Correction to: Serum vitamin D, vitamin D receptor and binding protein genes polymorphisms in restless legs syndrome

7. Thr105Ile (rs11558538) polymorphism in the histamine-1-methyl-transferase (HNMT) gene and risk for restless legs syndrome

8. Lack of Association between Common LAG3/CD4 Variants and Risk of Migraine

9. Association between LAG3/CD4 Genes Variants and Risk for Multiple Sclerosis

10. Association Between the rs1229984 Polymorphism in the Alcohol Dehydrogenase 1B Gene and Risk for Restless Legs Syndrome

11. LAG3/CD4 Genes Variants and the Risk for Restless Legs Syndrome

13. Neuronal nitric oxide synthase (nNOS, NOS1) rs693534 and rs7977109 variants and risk for restless legs syndrome

16. Increased serum diamine oxidase activity in nonallergic patients with migraine

17. Serum Trace Elements Concentrations in Patients with Restless Legs Syndrome

18. MAPT1 gene rs1052553 variant is unrelated with the risk for restless legs syndrome

19. Common Endothelial Nitric Oxide Synthase Single Nucleotide Polymorphisms are not Related With the Risk for Restless Legs Syndrome

20. Serum vitamin D, vitamin D receptor and binding protein genes polymorphisms in restless legs syndrome

22. Association between endothelial nitric oxide synthase (NOS3) rs2070744 and the risk for migraine

23. The solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene, SLC1A2, rs3794087 variant and assessment risk for restless legs syndrome

24. Dopamine receptor D3 (DRD3) gene rs6280 variant and risk for restless legs syndrome

25. Thr105Ile (rs11558538) polymorphism in the histamine-1-methyl-transferase (HNMT) gene and risk for restless legs syndrome

27. Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Multiple Sclerosis

28. Association Between Vitamin D Receptor rs731236 (Taq1) Polymorphism and Risk for Restless Legs Syndrome in the Spanish Caucasian Population

29. Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Restless Legs Syndrome

30. Actividad asistencial neurológica en un hospital comarcal de reciente creación: modelo de alta eficiencia

31. NQO1 gene rs1800566 variant is not associated with risk for multiple sclerosis

32. The GSTP1 gene variant rs1695 is not associated with an increased risk of multiple sclerosis

33. Neuronal nitric oxide synthase (nNOS, NOS1) rs693534 and rs7977109 variants and risk for restless legs syndrome

34. NQO1gene rs1800566 variant is not associated with risk for multiple sclerosis

35. MAPT gene rs1052553 variant is not associated with the risk for multiple sclerosis

36. LINGO1 rs9652490 and rs11856808 polymorphisms are not associated with risk for multiple sclerosis

38. Vitamin D3 Receptor (VDR) Gene rs2228570 (Fok1) and rs731236 (Taq1) Variants Are Not Associated with the Risk for Multiple Sclerosis: Results of a New Study and a Meta-Analysis

39. LINGO1 rs9652490 and rs11856808 polymorphisms are not associated with risk for multiple sclerosis

40. MAPT1 gene rs1052553 variant is unrelated with the risk for restless legs syndrome

42. Tratamiento del bruxismo grave con toxina botulínica tipo A

44. NQO1 gene rs1800566 variant is not associated with risk for multiple sclerosis.

46. Vitamin D3 Receptor(VDR) Gene rs2228570 (Fok1) and rs731236 (Taq1) Variants Are Not Associated with the Risk for Multiple Sclerosis: Results of a New Study and a Meta-Analysis.

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