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

Year Number of Results
1968 1
1970 1
1971 2
1972 3
1973 2
1974 1
1978 1
1980 1
1981 1
1983 1
1984 3
1985 6
1988 6
1989 2
1990 5
1991 4
1992 5
1993 1
1994 4
1995 1
1996 4
1997 11
1998 4
1999 5
2000 9
2001 2
2002 5
2003 5
2004 7
2005 3
2006 10
2007 6
2008 4
2009 6
2010 3
2011 4
2012 6
2013 13
2014 9
2015 10
2016 8
2017 14
2018 12
2019 6
2020 4
2021 6
2022 6
2023 4

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217 results

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Page 1
Neurofibromatosis type 1.
Gutmann DH, Ferner RE, Listernick RH, Korf BR, Wolters PL, Johnson KJ. Gutmann DH, et al. Nat Rev Dis Primers. 2017 Feb 23;3:17004. doi: 10.1038/nrdp.2017.4. Nat Rev Dis Primers. 2017. PMID: 28230061 Review.
Some individuals develop skeletal abnormalities (scoliosis, tibial pseudarthrosis and orbital dysplasia), brain tumours (optic pathway gliomas and glioblastoma), peripheral nerve tumours (spinal neurofibromas, plexiform neurofibromas and malignant peripheral nerv …
Some individuals develop skeletal abnormalities (scoliosis, tibial pseudarthrosis and orbital dysplasia), brain tumours (optic pathwa …
Current treatment of optic nerve gliomas.
Farazdaghi MK, Katowitz WR, Avery RA. Farazdaghi MK, et al. Curr Opin Ophthalmol. 2019 Sep;30(5):356-363. doi: 10.1097/ICU.0000000000000587. Curr Opin Ophthalmol. 2019. PMID: 31246635 Free PMC article. Review.
They can affect the optic nerve, optic chiasm, optic tracts and radiations and can either be sporadic or associated with neurofibromatosis type one. Gliomas isolated to the optic nerve (ONG) represent a subgroup of optic pathway gl …
They can affect the optic nerve, optic chiasm, optic tracts and radiations and can either be sporadic or associa …
Neurofibromatosis type 1 (NF1): diagnosis and management.
Ferner RE, Gutmann DH. Ferner RE, et al. Handb Clin Neurol. 2013;115:939-55. doi: 10.1016/B978-0-444-52902-2.00053-9. Handb Clin Neurol. 2013. PMID: 23931823 Review.
Individuals with NF1 have a predisposition to benign and malignant tumor formation and the hallmark lesion is the neurofibroma, a benign peripheral nerve sheath tumor. The gene for NF1 was cloned on chromosome 17q11.2 and neurofibromin, the NF1 protein, controls cell growt …
Individuals with NF1 have a predisposition to benign and malignant tumor formation and the hallmark lesion is the neurofibroma, a benign per …
Pediatric Suprasellar Tumors.
McCrea HJ, George E, Settler A, Schwartz TH, Greenfield JP. McCrea HJ, et al. J Child Neurol. 2016 Oct;31(12):1367-76. doi: 10.1177/0883073815620671. Epub 2015 Dec 15. J Child Neurol. 2016. PMID: 26676303 Review.
The various childhood suprasellar tumors, while pathologically distinct, present similar clinical and surgical challenges as a result of their common anatomic location. These lesions are in close proximity to or may invade the optic nerve and chiasm, pituitary gland …
The various childhood suprasellar tumors, while pathologically distinct, present similar clinical and surgical challenges as a result of the …
Neurofibromatosis Type 1: Review and Update on Emerging Therapies.
Karaconji T, Whist E, Jamieson RV, Flaherty MP, Grigg JRB. Karaconji T, et al. Asia Pac J Ophthalmol (Phila). 2019 Jan-Feb;8(1):62-72. doi: 10.22608/APO.2018182. Epub 2018 Nov 2. Asia Pac J Ophthalmol (Phila). 2019. PMID: 30387339 Review.
Early diagnosis and management led by a multidisciplinary team remains the standard of care, particularly in the management of optic pathway glioma. Emerging concepts in the genetic patterns of this condition have led to the introduction of new treatment modalities …
Early diagnosis and management led by a multidisciplinary team remains the standard of care, particularly in the management of optic …
Neurofibromatosis type 1.
Anderson JL, Gutmann DH. Anderson JL, et al. Handb Clin Neurol. 2015;132:75-86. doi: 10.1016/B978-0-444-62702-5.00004-4. Handb Clin Neurol. 2015. PMID: 26564071 Review.
Optic nerve glioma: an update.
Nair AG, Pathak RS, Iyer VR, Gandhi RA. Nair AG, et al. Int Ophthalmol. 2014 Aug;34(4):999-1005. doi: 10.1007/s10792-014-9942-8. Epub 2014 Apr 16. Int Ophthalmol. 2014. PMID: 24736941 Review.
Optic nerve glioma is the most common optic nerve tumour. However, it has an unpredictable natural history. ...The aim of this review article is to present current diagnostic and treatment protocols for optic nerve glioma... …
Optic nerve glioma is the most common optic nerve tumour. However, it has an unpredictable natural histor …
Diagnosis and management of optic nerve glioma.
Shapey J, Danesh-Meyer HV, Kaye AH. Shapey J, et al. J Clin Neurosci. 2011 Dec;18(12):1585-91. doi: 10.1016/j.jocn.2011.09.003. Epub 2011 Nov 8. J Clin Neurosci. 2011. PMID: 22071462 Review.
Optic nerve gliomas are highly variable tumours with an unpredictable clinical course. ...Our aim is to clarify current best practice in the management of optic nerve gliomas....
Optic nerve gliomas are highly variable tumours with an unpredictable clinical course. ...Our aim is to clarify current best p …
The optic chiasm.
Kidd D. Kidd D. Handb Clin Neurol. 2011;102:185-203. doi: 10.1016/B978-0-444-52903-9.00013-3. Handb Clin Neurol. 2011. PMID: 21601067 Review.
The neuro-ophthalmic signs, including the pattern of visual field defects, appearance of the optic disc, and various uncommon clinical accompaniments, are described. ...These are divided into inflammatory disorders, including sarcoidosis, multiple sclerosis, and idiopathic …
The neuro-ophthalmic signs, including the pattern of visual field defects, appearance of the optic disc, and various uncommon clinica …
[Clinical diagnosis and treatment of optic nerve glioma: a review].
Ren TT, Ma JM. Ren TT, et al. Zhonghua Yan Ke Za Zhi. 2023 May 11;59(5):415-419. doi: 10.3760/cma.j.cn112142-20221230-00664. Zhonghua Yan Ke Za Zhi. 2023. PMID: 37151013 Review. Chinese.
Optic nerve glioma (ONG) is a relatively rare central nervous system tumor that mainly affects children and adolescents. ...
Optic nerve glioma (ONG) is a relatively rare central nervous system tumor that mainly affects children and adolescents …
217 results