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Understanding the Biological Activities of Vitamin D in Type 1 Neurofibromatosis: New Insights into Disease Pathogenesis and Therapeutic Design PMC Neurofibromatosis Type 1 (Von Recklinghausen Disease) MD Searchlight Loss of neurofibromin induces inflammatory macrophage phenotypic switch and retinal neovascularization via GLUT1 activation ScienceDirect What is neurofibromatosis type 1 diagnosis? Born with BODY TUMORS Neurofibromatosis Type 1 (NF1) is a genetic condition marked by caf au lait spots, skin neurofibromas, and sometimes bone or nerve complications. Early recognition and
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