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Osteofibroma in type I neurofibromatosis.
Background: Neurofibromatosis type 1 is an autosomal dominant genetic disorder caused by a mutation in the NF1 gene on chromosome 17q11.2. There is insufficient evidence in the literature regarding the prevalence and incidence of neurofibromatosis type 1 in Hispanic populations, including Mexico. However, globally, the prevalence is estimated at 1 in 3,Daniela Isabel Ramírez Jiménez M.D. +4 more
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Dural ectasia in neurofibromatosis type I
2020Clinical History: A 12-year-old female patient is brought to the emergency room due to a fall. She is referred for further evaluation due to some findings in his clinical examination in the emergency and orthopedic evaluation.
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Neurofibromatosis type 1 I. General overview
Journal of Neuroscience Research, 2000M M, Lakkis, G I, Tennekoon
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Ulnar hypoplasia and neurofibromatosis type I
The Journal of Pediatrics, 2004Euthymia, Vargiami +2 more
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Neurofibromatosis Type I: case report
Introduction: neurofibromatosis comprises three dominant inherited disorders, type I being the most common, relatively frequent, with a prevalence of 1 in 3500, with defining features and diverse manifestations, including a 5-10 times increased risk of cancer, with a cumulative risk of 40% at 50 years of age.León Bermeo, Cristina Martha +2 more
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Lisch nodules in neurofibromatosis type I
Medicina Clínica (English Edition), 2019Antonio, Ramos Suárez +2 more
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Neurofibromatosis type I and Arnold–Chiari malformation
Journal of the European Academy of Dermatology and Venereology, 2002GIUSTINI, Sandra +7 more
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Neurofibromatosis Type I and Neurofibromatosis Type II
Rebecca Ronsley +2 moreopenaire +1 more source