CARRIE MOHILA to Mutation
This is a "connection" page, showing publications CARRIE MOHILA has written about Mutation.
Connection Strength
0.149
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The use of BRAF V600E mutation-specific immunohistochemistry in pediatric Langerhans cell histiocytosis. Hematol Oncol. 2018 Feb; 36(1):307-315.
Score: 0.053
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Intracranial calcifications simulating Aicardi-Gouti?res syndrome in PARS2-related mitochondrial disease. Am J Med Genet A. 2024 07; 194(7):e63589.
Score: 0.022
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Circulating tumor DNA sequencing of pediatric solid and brain tumor patients: An institutional feasibility study. Pediatr Hematol Oncol. 2023; 40(8):719-738.
Score: 0.020
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In vivo functional characterization of EGFR variants identifies novel drivers of glioblastoma. Neuro Oncol. 2023 03 14; 25(3):471-481.
Score: 0.020
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Pediatric spinal cord diffuse midline glioma, H3 K27-altered with intracranial and spinal leptomeningeal spread: A case report. Neuroradiol J. 2022 Oct; 35(5):634-639.
Score: 0.018
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ATRX protein loss and deregulation of PI3K/AKT pathway is frequent in pilocytic astrocytoma with anaplastic features. Clin Neuropathol. 2019 Mar/Apr; 38(2):59-73.
Score: 0.015