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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1973 1
1976 2
1977 1
1978 1
1983 1
1984 2
1985 3
1986 1
1988 4
1989 3
1990 1
1991 5
1992 5
1993 1
1994 2
1995 3
1996 9
1997 4
1998 8
1999 4
2000 3
2001 3
2002 7
2003 6
2004 2
2005 2
2006 4
2007 5
2008 2
2009 6
2010 7
2011 4
2012 7
2013 7
2014 3
2015 10
2016 2
2017 6
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2019 8
2020 5
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2022 8
2023 5
2024 4

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169 results

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Page 1
Familial spinal neurofibromatosis.
Pascual-Castroviejo I, Pascual-Pascual SI, Velazquez-Fragua R, Botella P, Viaño J. Pascual-Castroviejo I, et al. Neuropediatrics. 2007 Apr;38(2):105-8. doi: 10.1055/s-2007-985136. Neuropediatrics. 2007. PMID: 17712740
Familial spinal neurofibromatosis (FSNF) is a rare localized subtype of NF1 which shows neurological symptomatology during adult life. Only a few families have been reported to date. We describe a family in which three members in two generations
Familial spinal neurofibromatosis (FSNF) is a rare localized subtype of NF1 which shows neurological symptomatology dur
An update on the CNS manifestations of neurofibromatosis type 2.
Coy S, Rashid R, Stemmer-Rachamimov A, Santagata S. Coy S, et al. Acta Neuropathol. 2020 Apr;139(4):643-665. doi: 10.1007/s00401-019-02029-5. Epub 2019 Jun 4. Acta Neuropathol. 2020. PMID: 31161239 Free PMC article. Review.
Neurofibromatosis type II (NF2) is a tumor predisposition syndrome characterized by the development of distinctive nervous system lesions. ...NF2 is most commonly associated with the development of bilateral vestibular schwannomas; however, patients also have a predisposit
Neurofibromatosis type II (NF2) is a tumor predisposition syndrome characterized by the development of distinctive nervous system les
Meningioma.
Alruwaili AA, De Jesus O. Alruwaili AA, et al. 2023 Aug 23. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. 2023 Aug 23. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. PMID: 32809373 Free Books & Documents.
Meningioma originates from the meningeal layers of either the brain or the spinal cord. These tumors are classified into three grades, according to the World Health Organization (WHO). ...Several predisposing factors increase the risk of occurrence, including genetic disor …
Meningioma originates from the meningeal layers of either the brain or the spinal cord. These tumors are classified into three grades …
Familial spinal neurofibromatosis due to a multiexonic NF1 gene deletion.
Pizzuti A, Bottillo I, Inzana F, Lanari V, Buttarelli F, Torrente I, Giallonardo AT, De Luca A, Dallapiccola B. Pizzuti A, et al. Neurogenetics. 2011 Aug;12(3):233-40. doi: 10.1007/s10048-011-0278-5. Epub 2011 Mar 2. Neurogenetics. 2011. PMID: 21365283
We report the detailed clinical presentation and molecular features of a spinal neurofibromatosis familial case where a 40-year-old woman, presenting with multiple bilateral spinal neurofibromas and no other clinical feature of neurofibromatosis
We report the detailed clinical presentation and molecular features of a spinal neurofibromatosis familial case where a …
[Neurofibromatosis].
Matthies C, Rampeltshammer E, Breun M. Matthies C, et al. Fortschr Neurol Psychiatr. 2023 May;91(5):213-232. doi: 10.1055/a-2000-3713. Epub 2023 May 16. Fortschr Neurol Psychiatr. 2023. PMID: 37192611 German.
BACKGROUND & FOCUS: While the Neurofibromatoses have been observed and classified by their phenotypes for several centuries, their great variability constitutes a considerable challenge in diagnostics and therapy selection. ...Major features are tumors of the periphera …
BACKGROUND & FOCUS: While the Neurofibromatoses have been observed and classified by their phenotypes for several centuries, thei …
The natural history of spinal neurofibromatosis: a critical review of clinical and genetic features.
Ruggieri M, Polizzi A, Spalice A, Salpietro V, Caltabiano R, D'Orazi V, Pavone P, Pirrone C, Magro G, Platania N, Cavallaro S, Muglia M, Nicita F. Ruggieri M, et al. Clin Genet. 2015 May;87(5):401-10. doi: 10.1111/cge.12498. Epub 2014 Nov 22. Clin Genet. 2015. PMID: 25211147 Review.
Spinal neurofibromatosis (SNF) is a related form of neurofibromatosis 1 (NF1), characterized by bilateral neurofibromas (histologically proven) of all spinal roots (and, eventually, of all the major peripheral nerve branches) with or without other mani
Spinal neurofibromatosis (SNF) is a related form of neurofibromatosis 1 (NF1), characterized by bilateral neurofibromas
Familial spinal neurofibromatosis: clinical and DNA linkage analysis.
Pulst SM, Riccardi VM, Fain P, Korenberg JR. Pulst SM, et al. Neurology. 1991 Dec;41(12):1923-7. doi: 10.1212/wnl.41.12.1923. Neurology. 1991. PMID: 1745350
We studied two families with an unusual variant of neurofibromatosis (NF). The first family had spinal neurofibromas and cafe au lait spots (CLS), the second spinal neurofibromas without CLS. ...Using genetic linkage analysis with DNA markers ti …
We studied two families with an unusual variant of neurofibromatosis (NF). The first family had spinal neurofibr …
A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort.
Paterra R, Bettinaglio P, Borghi A, Mangano E, Tritto V, Cesaretti C, Schettino C, Bordoni R, Santoro C, Avignone S, Moscatelli M, Melone MAB, Saletti V, Piluso G, Natacci F, Riva P, Eoli M. Paterra R, et al. Cancers (Basel). 2022 Dec 22;15(1):59. doi: 10.3390/cancers15010059. Cancers (Basel). 2022. PMID: 36612057 Free PMC article.
Spinal neurofibromatosis (SNF), a phenotypic subclass of neurofibromatosis 1 (NF1), is characterized by bilateral neurofibromas involving all spinal roots. In order to deepen the understanding of SNF's clinical and genetic features, we identified 81 pa
Spinal neurofibromatosis (SNF), a phenotypic subclass of neurofibromatosis 1 (NF1), is characterized by bilateral neuro
Meningiomas and neurofibromatosis.
Goutagny S, Kalamarides M. Goutagny S, et al. J Neurooncol. 2010 Sep;99(3):341-7. doi: 10.1007/s11060-010-0339-x. Epub 2010 Aug 17. J Neurooncol. 2010. PMID: 20714782 Review.
Neurofibromatosis type 2 (NF2) is a rare genetic disorder predisposing to multiple benign tumors of the nervous system. ...Patients harboring seemingly isolated multiple meningiomas should be investigated to diagnose NF2 by careful familial history collection, detai
Neurofibromatosis type 2 (NF2) is a rare genetic disorder predisposing to multiple benign tumors of the nervous system. ...Patients h
Cellular mechanisms of heterogeneity in NF2-mutant schwannoma.
Chiasson-MacKenzie C, Vitte J, Liu CH, Wright EA, Flynn EA, Stott SL, Giovannini M, McClatchey AI. Chiasson-MacKenzie C, et al. Nat Commun. 2023 Mar 21;14(1):1559. doi: 10.1038/s41467-023-37226-0. Nat Commun. 2023. PMID: 36944680 Free PMC article.
Schwannomas are common sporadic tumors and hallmarks of familial neurofibromatosis type 2 (NF2) that develop predominantly on cranial and spinal nerves. ...
Schwannomas are common sporadic tumors and hallmarks of familial neurofibromatosis type 2 (NF2) that develop predominantly on …
169 results