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1. Brody Disease, an Early-Onset Myopathy With Delayed Relaxation and Abnormal Gait

3. Heparin-resistance in AL amyloidosis: a case report

4. Supplementary figures 1 to 3 from Genotype-Specific Abnormalities in Mitochondrial Function Associate with Distinct Profiles of Energy Metabolism and Catecholamine Content in Pheochromocytoma and Paraganglioma

5. Supplementary legend from Genotype-Specific Abnormalities in Mitochondrial Function Associate with Distinct Profiles of Energy Metabolism and Catecholamine Content in Pheochromocytoma and Paraganglioma

6. Supplementary figures 1 to 3 from Genotype-Specific Abnormalities in Mitochondrial Function Associate with Distinct Profiles of Energy Metabolism and Catecholamine Content in Pheochromocytoma and Paraganglioma

7. The double homeodomain protein DUX4c is associated with regenerating muscle fibers and RNA-binding proteins

12. Clinical, genetic, and histological features of centronuclear myopathy in the Netherlands

15. Pathogenic variants in TNNC2 cause congenital myopathy due to an impaired force response to calcium

17. Prognostic and Predictive Value of Integrated Qualitative and Quantitative Magnetic Resonance Imaging Analysis in Glioblastoma

18. LATE BREAKING NEWS ORAL PRESENTATION

20. Clinical, morphological and genetic characterization of Brody disease: an international study of 40 patients

22. Mapping actionable pathways and mutations in brain tumours using targeted RNA next generation sequencing

24. Panel-Based Exome Sequencing for Neuromuscular Disorders as a Diagnostic Service

27. Aberrant regulation of epigenetic modifiers contributes to the pathogenesis in patients with selenoprotein N ‐ related myopathies

30. Isocitrate dehydrogenase 1–mutated human gliomas depend on lactate and glutamate to alleviate metabolic stress

34. Somatic USP8 mutations are frequent events in corticotroph tumor progression causing Nelson’s tumor

35. B3GALNT2 mutations associated with non-syndromic autosomal recessive intellectual disability reveal a lack of genotype–phenotype associations in the muscular dystrophy-dystroglycanopathies

36. Clinical Aspects of SDHA-Related Pheochromocytoma and Paraganglioma: A Nationwide Study

37. Dominant Centronuclear Myopathy with Early Childhood Onset due to a Novel Mutation in BIN1

38. Somatic mutations in USP8 are frequent events in pituitary tumors causing Nelson's syndrome

39. A novel Ile1455Thr variant in the skeletal muscle sodium channel alpha-subunit in a patient with a severe adult-onset proximal myopathy with electrical myotonia and a patient with mild paramyotonia phenotype

42. Complex immunometabolic pathways mediate the interaction between thyroid carcinoma cells and tumor-associated macrophages

43. Autophagy activity is associated with membranous sodium iodide symporter expression and clinical response to radioiodine therapy in non-medullary thyroid cancer

45. Semiquantitative 123I-Metaiodobenzylguanidine Scintigraphy to Distinguish Pheochromocytoma and Paraganglioma from Physiologic Adrenal Uptake and Its Correlation with Genotype-Dependent Expression of Catecholamine Transporters

46. Predictive value of nerve trunk size in the neonate

48. Correlation Between In Vivo 18F-FDG PET and Immunohistochemical Markers of Glucose Uptake and Metabolism in Pheochromocytoma and Paraganglioma

49. Genotype-Specific Abnormalities in Mitochondrial Function Associate with Distinct Profiles of Energy Metabolism and Catecholamine Content in Pheochromocytoma and Paraganglioma

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