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1. Genome-Wide Association Study Points to Novel Locus for Gilles de la Tourette Syndrome

2. Safety and efficacy of givinostat in boys with Duchenne muscular dystrophy (EPIDYS): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial

3. Investigation of gene-environment interactions in relation to tic severity.

4. Validation of a Set of Instruments to Assess Patient- and Caregiver-Oriented Measurements in Spinal Muscular Atrophy: Results of the SMA-TOOL Study

5. Safety and efficacy of tamoxifen in boys with Duchenne muscular dystrophy (TAMDMD): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial

6. Safety and efficacy of once-daily risdiplam in type 2 and non-ambulant type 3 spinal muscular atrophy (SUNFISH part 2): a phase 3, double-blind, randomised, placebo-controlled trial

7. Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach

9. Pre- and perinatal complications in relation to Tourette syndrome and co-occurring obsessive-compulsive disorder and attention-deficit/hyperactivity disorder

11. Assessment of comorbidity and social anxiety in adolescents with attention deficit hyperactivity disorder: The SELFIE study

12. Evaluación de la comorbilidad y la ansiedad social en adolescentes con trastorno por déficit de atención con hiperactividad: Estudio SELFIE

13. Biallelic variants inHMGCS1are a novel cause of rare rigid spine syndrome

14. Safety and efficacy of tamoxifen in boys with Duchenne muscular dystrophy (TAMDMD): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial

17. Growth Differentiation Factor 15 is a potential biomarker of therapeutic response for TK2 deficient myopathy

18. Pain in Children and Adolescents with Spinal Muscular Atrophy: A Longitudinal Study from a Patient Registry.

19. Genome-wide Association Study Points to Novel Locus for Gilles de la Tourette Syndrome

20. Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndrome

21. Validation of a Set of Instruments to Assess Patient- and Caregiver-Oriented Measurements in Spinal Muscular Atrophy: Results of the SMA-TOOL Study

22. Treatment of spinal muscular atrophy in European countries: A call to action

23. Tic disorders in children and adolescents:does the clinical presentation differ in males and females? A report by the EMTICS group

24. Safety and efficacy of once-daily risdiplam in type 2 and non-ambulant type 3 spinal muscular atrophy (SUNFISH part 2): a phase 3, double-blind, randomised, placebo-controlled trial

26. GDNF gene is associated with tourette syndrome in a family study

28. Investigation of gene-environment interactions in relation to tic severity

29. Synaptic processes and immune-related pathways implicated in Tourette syndrome

30. Collaborative model for diagnosis and treatment of very rare diseases: experience in Spain with thymidine kinase 2 deficiency

31. Synaptic processes and immune-related pathways implicated in Tourette syndrome

32. Support of the histaminergic hypothesis in Tourette Syndrome: association of the histamine decarboxylase gene in a large sample of families

33. The Premonitory Urge for Tics Scale in a large sample of children and adolescents:psychometric properties in a developmental context. An EMTICS study

34. Anti-dopamine D2 receptor antibodies in chronic tic disorders

36. Detailed Clinical and Psychological Phenotype of the X-linked HNRNPH2-Related Neurodevelopmental Disorder

37. Antibodies to neuronal surface proteins in Tourette Syndrome: Lack of evidence in a European paediatric cohort

38. Targeted Next-Generation Sequencing in a Large Cohort of Genetically Undiagnosed Patients with Neuromuscular Disorders in Spain

39. Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders

40. Analysis of shared heritability in common disorders of the brain

42. Antibodies to neuronal surface proteins in Tourette Syndrome: Lack of evidence in a European paediatric cohort

43. Deoxynucleoside Therapy for Thymidine Kinase 2–Deficient Myopathy

44. Assessment of comorbidity and social anxiety in adolescents with attention deficit hyperactivity disorder: The SELFIE study

45. Evaluación de la comorbilidad y la ansiedad social en adolescentes con trastorno por déficit de atención con hiperactividad: Estudio SELFIE

46. Analysis of shared heritability in common disorders of the brain

47. Analysis of shared heritability in common disorders of the brain

48. De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis

49. Retrospective natural history of thymidine kinase 2 deficiency

50. Targeted next generation sequencing in patients with infantile bilateral striatal necrosis

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