The Roots of Neurofibromas in Neurofibromatosis 1 — A Question of Multipotency, Differentiation and Hiding [PDF]
Neurofibromatosis type 1 (NF1) is an autosomal dominant cancer predisposition syndrome that affects about 1 in 3500 individuals worldwide. NF1 is caused by mutations in the NF1 gene that encodes the tumor suppressor protein neurofibromin, an ...
Jouhilahti, Eeva-Mari
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Neurofibromatose de von Recklinghausen.
Neurofibromatosis is a multisystemic disease in which the multiple possible clinical manifestations may have important diagnostic and prognostic implications; if arterial hypertension coexists, many pathogenic mechanisms justify that the possible secondary etiology must be considered.
Ventura, A +4 more
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The impact of a virtual mind-body program on resilience factors among international English-speaking adults with neurofibromatoses: secondary analysis of a randomized clinical trial. [PDF]
Presciutti AM +7 more
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Neurofibromatosis type 1: natural history and impact on quality of life [PDF]
Neurofibromatosis Type 1 (NF1, von Recklinghausen’s disease) is among the more common autosomal dominant genetic disorders, with a worldwide incidence of approximately 1 in 3000 live births. NF1 can occur as either an inherited defect or as a spontaneous
Obagi, Zaidal
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Correction to: Surgical management of peripheral nerve sheath tumours in children, with special consideration of neurofibromatoses. [PDF]
Zipfel J +9 more
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Orbito-facial plexiform neurofibromatosis: a rare clinical image. [PDF]
Sharma A, Daigavane S.
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The riddle of multinucleated “floret-like” giant cells and their detection in an extensive gluteal neurofibroma: a case report [PDF]
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Clinical trials targeting neurofibromatoses-associated tumors: a systematic review. [PDF]
Roman Souza G, Abdalla A, Mahadevan D.
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Evaluating overweight and obesity prevalence in survivors of childhood brain tumors: a systematic review protocol [PDF]
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