Neurofibromatosis type 1 with concomitant Peutz-Jeghers syndrome in a child: a case report. [PDF]
Liu Q, Long Y.
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Case Report: Primary sciatic leiomyosarcoma in a patient with neurofibromatosis type 1. [PDF]
Chen L +5 more
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From genes to therapy: navigating the complex landscape of neurofibromatosis management in Canada through advanced diagnostic, targeted therapies, and holistic care. [PDF]
Zhao VSC.
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Ocular manifestations in pediatric tumor suppressor gene mutations: a case series and literature review of RB1, NF1, NF2, VHL, and TSC. [PDF]
Wang A +5 more
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A novel synonymous variant in the NF1 gene disrupting splicing contributes to neurofibromatosis pathogenesis. [PDF]
Lin T +23 more
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Lambdoid Suture Defect in a 12-year-old Neurofibromatosis Patient. [PDF]
Almahmood H, Al-Sayed S, Agab W.
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Analysis of visual evoked potentials in patients with neurofibromatosis type 1: new concepts. [PDF]
Jancic J +5 more
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Internal carotid artery sympathetic plexus neurofibroma - A case report. [PDF]
Maleknia PD +8 more
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CONCURRENT OCCURRENCE OF NEUROFIBROMATOSIS TYPE 1 AND TURNER SYNDROME: A PEDIATRIC CASE REPORT WITH COMPREHENSIVE LITERATURE REVIEW. [PDF]
Singin B +5 more
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