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1. Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings

11. Synapsin autoantibodies during pregnancy are associated with fetal abnormalities

13. Analysis of bihemispheric language function in pediatric neurosurgical patients using repetitive navigated transcranial magnetic stimulation

16. LZTR1 loss-of-function variants associated with café au lait macules with or without freckling.

17. Expression of mGluR5 in Pediatric Hodgkin and Non-Hodgkin lymphoma—A Comparative Analysis of Immunohistochemical and Clinical Findings Regarding the Association between Tumor and Paraneoplastic Neurological Disease.

25. Short- and Long-Delay Consolidation of Memory Accessibility and Precision Across Childhood and Young Adulthood.

28. The clinical-phenotype continuum in DYNC1H1-related disorders—genomic profiling and proposal for a novel classification

29. Cross-sectional Neuromuscular Phenotyping Study of Patients With Arhinia With SMCHD1 Variants

33. Epilepsy surgery in early infancy: A retrospective, multicenter study

36. G protein–coupled receptor kinase 2 and group I metabotropic glutamate receptors mediate inflammation‐induced sensitization to excitotoxic neurodegeneration

39. Next-generation phenotyping integrated in a national framework for patients with ultra-rare disorders improves genetic diagnostics and yields new molecular findings

42. Retrospective Pediatric Cohort Study Validates NEOS Score and Demonstrates Applicability in Children With Anti-NMDAR Encephalitis

44. WWOX developmental and epileptic encephalopathy: Understanding the epileptology and the mortality risk

47. Real‐world data on cannabidiol treatment of various epilepsy subtypes: A retrospective, multicenter study

49. Maternal synapsin autoantibodies are associated with neurodevelopmental delay

50. Gain-of-function variants in the ion channel gene TRPM3 underlie a spectrum of neurodevelopmental disorders

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