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53. LATE BREAKING NEWS ORAL PRESENTATION

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

56. Grading of Meningeal Solitary Fibrous Tumors/Hemangiopericytomas: Prognostic Value of the Marseille Grading System in a Cohort of 132 Patients in correlation with molecular data

57. MOESM4 of Mapping actionable pathways and mutations in brain tumours using targeted RNA next generation sequencing

58. Grading of meningeal solitary fibrous tumors/hemangiopericytomas: analysis of the prognostic value of the Marseille Grading System in a cohort of 132 patients

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

62. Grading of meningeal solitary fibrous tumors/hemangiopericytomas: analysis of the prognostic value of the Marseille Grading System in a cohort of 132 patients

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

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

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

72. Clinical aspects of SDHA-related pheochromocytoma and paraganglioma: A nationwide study

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

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

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

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

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

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

84. Prognostic significance of NAB2-STAT6 fusion variants and TERT promotor mutations in solitary fibrous tumors/hemangiopericytomas of the CNS: not (yet) clear.

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

86. The impact of chronic hypertension on small vessel disease – neuroinflammation beyond white matter hyperintensities

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

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

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

92. B3GALNT2 mutations associated with nonsyndromic autosomal recessive intellectual disability reveal a lack of genotype- phenotype associations in the muscular dystrophy-dystroglycanopathies.

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

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

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

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

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