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Did you mean neurofibromatosis type ii (2,689 results)?
Treatment decisions and the use of MEK inhibitors for children with neurofibromatosis type 1-related plexiform neurofibromas.
Armstrong AE, Belzberg AJ, Crawford JR, Hirbe AC, Wang ZJ. Armstrong AE, et al. BMC Cancer. 2023 Jun 16;23(1):553. doi: 10.1186/s12885-023-10996-y. BMC Cancer. 2023. PMID: 37328781 Free PMC article. Review.
Neurofibromatosis type 1 (NF1), the most common tumor predisposition syndrome, occurs when NF1 gene variants result in loss of neurofibromin, a negative regulator of RAS activity. ...
Neurofibromatosis type 1 (NF1), the most common tumor predisposition syndrome, occurs when NF1 gene variants result in loss of
Macrodactyly.
Dell PC. Dell PC. Hand Clin. 1985 Aug;1(3):511-24. Hand Clin. 1985. PMID: 3938454
There seem to be three variants that overlap somewhat in clinical presentation. They are type I digital gigantism with lipofibromatous hamartoma of a peripheral nerve, type II digital gigantism associated with neurofibromatosis, and type III hyp …
There seem to be three variants that overlap somewhat in clinical presentation. They are type I digital gigantism with lipofibromatou …
Constipation in adults with neurofibromatosis type 1.
Ejerskov C, Krogh K, Ostergaard JR, Fassov JL, Haagerup A. Ejerskov C, et al. Orphanet J Rare Dis. 2017 Aug 16;12(1):139. doi: 10.1186/s13023-017-0691-4. Orphanet J Rare Dis. 2017. PMID: 28814319 Free PMC article.
BACKGROUND: Neurofibromatosis type 1 (NF1) is an autosomal-dominant disease characterised by symptoms of the skin, eyes, nervous system and bones. ...Gastrointestinal symptoms were assessed with a web-based, self-administered, validated, Rome III diagnostic q …
BACKGROUND: Neurofibromatosis type 1 (NF1) is an autosomal-dominant disease characterised by symptoms of the skin, eyes, nervo …
Oral manifestations in patients with neurofibromatosis type-1: a comprehensive literature review.
Javed F, Ramalingam S, Ahmed HB, Gupta B, Sundar C, Qadri T, Al-Hezaimi K, Romanos GE. Javed F, et al. Crit Rev Oncol Hematol. 2014 Aug;91(2):123-9. doi: 10.1016/j.critrevonc.2014.02.007. Epub 2014 Mar 12. Crit Rev Oncol Hematol. 2014. PMID: 24679902 Review.
Oral health status is jeopardized in patients with neurofibromatosis (NF) type-1 (NF-1). The aim of the present study was to comprehensively review the oral manifestations in NF-1 patients. ...RESULTS: Neurofibromas of oral and perioral soft tissues with subsequent …
Oral health status is jeopardized in patients with neurofibromatosis (NF) type-1 (NF-1). The aim of the present study was to c …
Meningioma: A Pathology Perspective.
Toland A, Huntoon K, Dahiya SM. Toland A, et al. Neurosurgery. 2021 Jun 15;89(1):11-21. doi: 10.1093/neuros/nyab001. Neurosurgery. 2021. PMID: 33588439
The World Health Organization classifies meningiomas into 3 grades based on increased risk of recurrence and associated mortality in grade III tumors. Although most tumors are categorized as low-grade, up to 15%-20% demonstrate more aggressive behavior. With the long-recog …
The World Health Organization classifies meningiomas into 3 grades based on increased risk of recurrence and associated mortality in grade …
Improved renal function in neurofibromatosis type 1 patients.
Yasuda KI, Nobeyama Y, Asahina A. Yasuda KI, et al. Skin Health Dis. 2022 May 2;2(2):e119. doi: 10.1002/ski2.119. eCollection 2022 Jun. Skin Health Dis. 2022. PMID: 35677927 Free PMC article.
Neurofibromatosis type 1 (NF1), or von Recklinghausen disease, is an autosomal dominant disease that presents with various symptoms, including cafe-au-lait spots and neurofibromas. ...For both sexes, i) the mean creatinine value was significantly lower in the NF1 pa
Neurofibromatosis type 1 (NF1), or von Recklinghausen disease, is an autosomal dominant disease that presents with various sym
Sporadic and neurofibromatosis type 2-associated meningioma in children and adolescents.
Wagener K, Beckhaus J, Boekhoff S, Friedrich C, Müller HL. Wagener K, et al. J Neurooncol. 2023 Jul;163(3):555-563. doi: 10.1007/s11060-023-04344-0. Epub 2023 Jul 4. J Neurooncol. 2023. PMID: 37402092
Multiple meningiomas were detected in 69% of NF2 patients and in 9% of sporadic meningiomas. 50% of the meningiomas were WHO grade I, 37% WHO grade II and 6% WHO grade III. Progressions or recurrences occurred after a median interval of 1.9 years. ...
Multiple meningiomas were detected in 69% of NF2 patients and in 9% of sporadic meningiomas. 50% of the meningiomas were WHO grade I, 37% WH …
Biomarkers in Vestibular Schwannoma-Associated Hearing Loss.
Lassaletta L, Calvino M, Morales-Puebla JM, Lapunzina P, Rodriguez-de la Rosa L, Varela-Nieto I, Martinez-Glez V. Lassaletta L, et al. Front Neurol. 2019 Sep 18;10:978. doi: 10.3389/fneur.2019.00978. eCollection 2019. Front Neurol. 2019. PMID: 31620068 Free PMC article. Review.
They can be classified into two groups: sporadic VS and those associated with neurofibromatosis type 2 (NF2). VSs usually grow slowly, initially causing unilateral sensorineural hearing loss (HL) and tinnitus. ...
They can be classified into two groups: sporadic VS and those associated with neurofibromatosis type 2 (NF2). VSs usually grow …
Losartan prevents tumor-induced hearing loss and augments radiation efficacy in NF2 schwannoma rodent models.
Wu L, Vasilijic S, Sun Y, Chen J, Landegger LD, Zhang Y, Zhou W, Ren J, Early S, Yin Z, Ho WW, Zhang N, Gao X, Lee GY, Datta M, Sagers JE, Brown A, Muzikansky A, Stemmer-Rachamimov A, Zhang L, Plotkin SR, Jain RK, Stankovic KM, Xu L. Wu L, et al. Sci Transl Med. 2021 Jul 14;13(602):eabd4816. doi: 10.1126/scitranslmed.abd4816. Sci Transl Med. 2021. PMID: 34261799 Free PMC article.
Hearing loss is one of the most common symptoms of neurofibromatosis type 2 (NF2) caused by vestibular schwannomas (VSs). ...Using NF2 mouse models, we found that losartan treatment normalized the TME by (i) reducing neuroinflammatory IL-6/STAT3 signaling and preven …
Hearing loss is one of the most common symptoms of neurofibromatosis type 2 (NF2) caused by vestibular schwannomas (VSs). ...U …
207 results