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Name: neurofibromotosis glutathione Neurofibromatosis type I Pediatric low-grade glioma models: advances
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Pediatric low grade glioma models: advances and ongoing challenges Frontiers Neurofibromatosis type 1 Stamford Skin Centre Neurofibromatosis Type 1: Symptoms, Causes, Diagnosis, and Treatment An Update on Neurofibromatosis Type 1: Not Just Caf au Lait Spots, Freckling, and Neurofibromas. An Update. Part I. Dermatological Clinical Criteria Diagnostic of the Disease Actas Dermo Sifiliogrficas Every skin tells a story This brave patient lives with #neurofibromatosis type 1 (NF1), a genetic condition that can cause benign skin growths called neurofibromas. While usually harmless, they can affect confidence Metabolic Features of Neurofibromatosis Type 1 Associated Tumors IntechOpen

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doi:10.1177/1535370218758275 Iftikhar A, Azam H, Ahmed M, et al

Decreased ferritin levels in brain in Parkinsons disease

Nature, 458 (7239), 762765

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The deliberations spanned epidemiology, clinical presentation, diagnosis including autoantibodies, immunoglobulin G (IgG), histology and diagnostic scores, therapeutic strategies, management of difficult-to-treat AIH, long-term monitoring, and special scenarios, such as seronegative AIH (SN-AIH), autoimmune sclerosing cholangitis/overlap syndromes and post-transplant complications like recurrence and de novo-AIH