57 results on '"Kusters, Benno"'
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2. Tissue inhibitor of matrix metalloproteinases 4: a novel marker associated with CAA
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
8. Superior preservation of capillaries, myofibrils and mitochondria after long-term extracorporeal perfusion of free muscle flaps – A descriptive electron microscopy study
9. Subacute parkinsonism due to systemic lupus erythematosus and catastrophic antiphospholipid syndrome
10. Facioscapulohumeral muscular dystrophy myopathologic dissection in 22 patients shows highly variable morphologic findings (P14-13.009)
11. Early Restrictive Fluid Strategy Impairs the Diaphragm Force in Lambs with Acute Respiratory Distress Syndrome
12. Clinical, genetic, and histological features of centronuclear myopathy in the Netherlands
13. Rectus Abdominis Flap Replantation after 18 h Hypothermic Extracorporeal Perfusion—A Porcine Model
14. Accuracy of Machine Learning Algorithms for the Classification of Molecular Features of Gliomas on MRI: A Systematic Literature Review and Meta-Analysis
15. Pathogenic variants in TNNC2 cause congenital myopathy due to an impaired force response to calcium
16. Genotype-specific Differences in the Expression of Markers of Warburg Effect in Pheochromocytoma and Paraganglioma
17. Prognostic and Predictive Value of Integrated Qualitative and Quantitative Magnetic Resonance Imaging Analysis in Glioblastoma
18. LATE BREAKING NEWS ORAL PRESENTATION
19. Recurrence of paraproteinemic crystalline keratopathy after corneal transplantation: A case of monoclonal gammopathy of ocular significance
20. Clinical, morphological and genetic characterization of Brody disease: an international study of 40 patients
21. Preserved single muscle fiber specific force in facioscapulohumeral muscular dystrophy
22. Mapping actionable pathways and mutations in brain tumours using targeted RNA next generation sequencing
23. 1st ENMC European meeting: The EURO-NMD pathology working group Recommended Standards for Muscle Pathology Amsterdam, The Netherlands, 7 December 2018
24. Panel-Based Exome Sequencing for Neuromuscular Disorders as a Diagnostic Service
25. New perioperative imaging techniques, immunohistochemistry and genetic analysis to investigate the suitability of laparoscopic partial adrenalectomy in primary aldosteronism
26. Structural changes in the zona glomerulosa of normal aging adrenals
27. Aberrant regulation of epigenetic modifiers contributes to the pathogenesis in patients with selenoprotein N ‐ related myopathies
28. SUN-381 Somatic PRKACA Mutations In Patients With Transition From Pituitary-dependent To Adrenal-dependent Cushing’S Syndrome
29. Targeted RNA NextGenSeq profiling in oncology using single molecule molecular inversion probes
30. Isocitrate dehydrogenase 1–mutated human gliomas depend on lactate and glutamate to alleviate metabolic stress
31. Pathogenesis of Idiopathic Ventral Herniation of Spinal Cord: Neuropathologic Analysis
32. A pedunculated aldosterone-producing adenoma drained by an extra vein causing puzzling results of adrenal vein sampling
33. Development of Nerve Fibre Diameter in Young Infants With Hirschsprung Disease
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
40. Widening the spectrum of filamin-C myopathy: Predominantly proximal myopathy due to the p.A193T mutation in the actin-binding domain of FLNC
41. Fatal Complications after Pediatric Surgical Interventions: Lessons Learned
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
44. Intradural prepontine chordoma in an 11-year-old boy. A case report
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
47. P2-117: MICRO-RNAS AS NOVEL BIOMARKERS IN AD: DIFFERENTIAL EXPRESSION IN HIPPOCAMPUS AND IN CELL-FREE CEREBROSPINAL FLUID
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
50. Response to: Morphological distinction of cortisol‐producing and aldosterone‐producing adrenal cortical adenomas: not only possible but a critical clinical responsibility
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