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204 results on '"Miltenberger‐Miltenyi, Gabriel"'

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1. Serum Phospholipid Profile Changes in Gaucher Disease and Parkinson’s Disease

9. An Autopsy Series of Seven Cases of VPS13A Disease (Chorea‐Acanthocytosis)

10. Serum lipid alterations in GBA-associated Parkinson's disease

11. Language impairment in the genetic forms of behavioural variant frontotemporal dementia

12. Neurodevelopmental effects of genetic frontotemporal dementia in young adult mutation carriers

14. Sphingolipid and Phospholipid Levels Are Altered in Human Brain in Chorea‐Acanthocytosis.

16. Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia

22. Further evidence for genetic heterogeneity of distal HMN type V, CMT2 with predominant hand involvement and Silver syndrome

25. A Pan-European Study of the C9orf72 Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats

28. C9orf72 expansion is associated with accelerated decline of respiratory function and decreased survival in amyotrophic lateral sclerosis

30. Phosphatidylethanolamines are the Main Lipid Class Altered in Red Blood Cells from Patients with VPS13A Disease/Chorea‐Acanthocytosis.

33. Rastreio de doença de Fabry em doentes com não compactação do ventrículo esquerdo

34. Parkinson’s Disease and Fabry Disease: Clinical, Biochemical and Neuroimaging Analysis of Three Pedigrees

36. C9orf72 expansion is associated with accelerated decline of respiratory function and decreased survival in amyotrophic lateral sclerosis

37. p.G360R Is a Pathogenic GLA Gene Mutation Responsible for a Classic Phenotype of Fabry Disease

38. Increased monohexosylceramide levels in the serum of established rheumatoid arthritis patients.

39. Mild Left Ventricular Hypertrophy Unravels a Novel Nonsense Mutation of the GLA Gene Associated with the Classical Phenotype of Fabry Disease

40. Gene Expression Differences in Peripheral Blood of Parkinson's Disease Patients with Distinct Progression Profiles

42. International Survey of ALS Experts about Critical Questions for Assessing Patients with ALS

43. TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

47. No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients

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