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

Year Number of Results
1985 1
1996 1
1998 2
2000 1
2001 1
2002 3
2003 2
2004 3
2005 3
2006 2
2007 2
2008 2
2009 1
2010 1
2011 2
2012 3
2013 4
2014 2
2015 3
2016 1
2017 1
2018 4
2019 1
2020 3
2021 1
2022 1
2024 2

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49 results

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Page 1
Tuberous Sclerosis Complex: A Review.
Randle SC. Randle SC. Pediatr Ann. 2017 Apr 1;46(4):e166-e171. doi: 10.3928/19382359-20170320-01. Pediatr Ann. 2017. PMID: 28414398 Review.
Neurocutaneous melanosis.
Islam MP. Islam MP. Handb Clin Neurol. 2015;132:111-7. doi: 10.1016/B978-0-444-62702-5.00007-X. Handb Clin Neurol. 2015. PMID: 26564074 Review.
Treatment is symptomatic and death occurs in many within 3 years of onset of neurologic symptoms. This prognosis may limit the extent to which extensive procedures or interventions are undertaken....
Treatment is symptomatic and death occurs in many within 3 years of onset of neurologic symptoms. This prognosis may limit the extent …
Sturge-Weber syndrome.
Nabbout R, Juhász C. Nabbout R, et al. Handb Clin Neurol. 2013;111:315-21. doi: 10.1016/B978-0-444-52891-9.00037-3. Handb Clin Neurol. 2013. PMID: 23622182 Review.
MRI with gadolinium enhancement and pondered T1, T2, FLAIR and diffusion sequences is today the technique of choice to visualize the leptomeningeal angioma or to suspect it by indirect signs, even before the development of neurological signs, from the first months of life. The …
MRI with gadolinium enhancement and pondered T1, T2, FLAIR and diffusion sequences is today the technique of choice to visualize the leptome …
Sturge-Weber syndrome: from the past to the present.
Sudarsanam A, Ardern-Holmes SL. Sudarsanam A, et al. Eur J Paediatr Neurol. 2014 May;18(3):257-66. doi: 10.1016/j.ejpn.2013.10.003. Epub 2013 Nov 7. Eur J Paediatr Neurol. 2014. PMID: 24275166 Review.
Sturge-Weber syndrome is marked by a variable but usually progressive course in early childhood characterised by seizures, stroke-like episodes, headaches, neurological and cognitive deterioration, hemiparesis, glaucoma and visual field defects. ...
Sturge-Weber syndrome is marked by a variable but usually progressive course in early childhood characterised by seizures, stroke-lik …
Melanoma on congenital melanocytic nevi.
Alos L, Carrasco A, Teixidó C, Szumera-Ciećkiewicz A, Vicente A, Massi D, Carrera C. Alos L, et al. Pathol Res Pract. 2024 Apr;256:155262. doi: 10.1016/j.prp.2024.155262. Epub 2024 Mar 11. Pathol Res Pract. 2024. PMID: 38518732 Review.
Most CMNi harbour an NRAS mutation, but other genes are rarely involved, and gene translocations have recently been described. However, no prognostic implications have been associated with the CMN genotype. Melanomas developed on CMNi harbour additional molecular alteratio …
Most CMNi harbour an NRAS mutation, but other genes are rarely involved, and gene translocations have recently been described. However, no …
Encephalocraniocutaneous lipomatosis.
Gawel J, Schwartz RA, Józwiak S. Gawel J, et al. J Cutan Med Surg. 2003 Jan-Feb;7(1):61-5. doi: 10.1007/s10227-002-1142-x. Epub 2002 Oct 9. J Cutan Med Surg. 2003. PMID: 12362260 Review.
Periodic neurologic and cardiologic assessment with echocardiography and electrocardiography should be carried out in all patients with ECCL because of a possible progressive disease course....
Periodic neurologic and cardiologic assessment with echocardiography and electrocardiography should be carried out in all patients with ECCL …
Epigenetics and survivorship in pediatric brain tumor patients.
Bhattacharya D, Pomeroy SL, Pomeranz Krummel DA, Sengupta S. Bhattacharya D, et al. J Neurooncol. 2020 Oct;150(1):77-83. doi: 10.1007/s11060-020-03535-3. Epub 2020 May 25. J Neurooncol. 2020. PMID: 32451770 Review.
We focus on glioblastoma, medulloblastoma, and the neurocutaneous syndrome neurofibromatosis type-1 to highlight epigenetic biomarkers that can potentially serve not only as prognostic indicators of overall patient survival, but hopefully as indicators to the response to t …
We focus on glioblastoma, medulloblastoma, and the neurocutaneous syndrome neurofibromatosis type-1 to highlight epigenetic biomarkers that …
Tuberous sclerosis complex.
Rodrigues DA, Gomes CM, Costa IM. Rodrigues DA, et al. An Bras Dermatol. 2012 Mar-Apr;87(2):184-96. doi: 10.1590/s0365-05962012000200001. An Bras Dermatol. 2012. PMID: 22570021
The dermatologist plays an essential role in the history of the disease, since skin manifestations represent the most prevalent clinical features, enabling early diagnosis and intervention in its natural course. This article aims to inform the scientific community about ad …
The dermatologist plays an essential role in the history of the disease, since skin manifestations represent the most prevalent clinical fea …
Pictorial review of tuberous sclerosis in various organs.
Umeoka S, Koyama T, Miki Y, Akai M, Tsutsui K, Togashi K. Umeoka S, et al. Radiographics. 2008 Nov-Dec;28(7):e32. doi: 10.1148/rg.e32. Epub 2008 Sep 4. Radiographics. 2008. PMID: 18772274 Review.
Moreover, tuberous sclerosis can involve bone, liver, and the alimentary tract. The clinical course and patient prognosis depend on the sites of manifestations. ...
Moreover, tuberous sclerosis can involve bone, liver, and the alimentary tract. The clinical course and patient prognosis depe …
49 results