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

Year Number of Results
1995 1
2002 1
2003 1
2005 1
2007 2
2008 1
2009 1
2010 1
2011 1
2012 1
2016 2
2018 2
2019 1
2021 1
2023 0

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16 results

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Page 1
Lymphangioleiomyomatosis: A review.
Hohman DW, Noghrehkar D, Ratnayake S. Hohman DW, et al. Eur J Intern Med. 2008 Jul;19(5):319-24. doi: 10.1016/j.ejim.2007.10.015. Epub 2007 Dec 26. Eur J Intern Med. 2008. PMID: 18549932 Review.
LAM can occur without evidence of other disease (sporadic LAM) or in conjunction with tuberous sclerosis complex (TSC). TSC is an autosomal dominant tumor suppressor gene syndrome characterized by seizures, mental retardation, and tumors in the brain, heart, skin, a …
LAM can occur without evidence of other disease (sporadic LAM) or in conjunction with tuberous sclerosis complex (TSC). TSC is an aut …
Pathogenesis and Molecular Mechanisms of Zika Virus.
Nayak S, Lei J, Pekosz A, Klein S, Burd I. Nayak S, et al. Semin Reprod Med. 2016 Sep;34(5):266-272. doi: 10.1055/s-0036-1592071. Epub 2016 Sep 9. Semin Reprod Med. 2016. PMID: 27612156 Review.
A developing outbreak in the Americas has demonstrated an association between the virus and serious clinical manifestations, such as Guillain-Barre syndrome in adults and congenital malformations in infants born to infected mothers. Pathogenesis and mechanisms of ne …
A developing outbreak in the Americas has demonstrated an association between the virus and serious clinical manifestations, such as Guillai …
Cutaneous Manifestations of Tuberous Sclerosis.
Bakić M, Ratković M, Gledović B, Vujović B, Radunović D, Babić V, Prelević V. Bakić M, et al. Acta Dermatovenerol Croat. 2018 Apr;26(1):73-74. Acta Dermatovenerol Croat. 2018. PMID: 29782307 Review.
Polycystic kidney changes were verified by ultrasound when the patient was three years old, with the presence of several calcified nodules in lateral ventricles and supraventricularly in the brain as well as the existence of several hypopigmented maculae on the skin. Durin …
Polycystic kidney changes were verified by ultrasound when the patient was three years old, with the presence of several calcified nodules i …
Pathophysiology of neurodevelopmental mTOR pathway-associated epileptic conditions: Current status of biomedical research.
Gruber V, Scholl T, Samueli S, Gröppel G, Mühlebner A, Hainfellner JA, Feucht M. Gruber V, et al. Clin Neuropathol. 2019 Sep/Oct;38(5):210-224. doi: 10.5414/NP301214. Clin Neuropathol. 2019. PMID: 31347492 Review.
In this review, special focus is put on the prototypes of "mTORpathies": tuberous sclerosis complex (TSC) and focal cortical dysplasia (FCD) type IIb. We review recent research data on mTORpathies, with emphasis on cortical tubers and FCD-like lesions …
In this review, special focus is put on the prototypes of "mTORpathies": tuberous sclerosis complex (TSC) and focal cortical
Tuberous sclerosis complex: genetics to pathogenesis.
Narayanan V. Narayanan V. Pediatr Neurol. 2003 Nov;29(5):404-9. doi: 10.1016/j.pediatrneurol.2003.09.002. Pediatr Neurol. 2003. PMID: 14684235 Review.
This disorder is characterized by multiple hamartomas in several organs, particularly the brain. Commonly recognized clinical features include hypomelanotic skin macules, facial angiofibromas, periungual fibromas, delayed development, and seizures. Abnormalities
This disorder is characterized by multiple hamartomas in several organs, particularly the brain. Commonly recognized clinical feature …
Emerging treatments in the management of tuberous sclerosis complex.
Kohrman MH. Kohrman MH. Pediatr Neurol. 2012 May;46(5):267-75. doi: 10.1016/j.pediatrneurol.2012.02.015. Pediatr Neurol. 2012. PMID: 22520346 Review.
Tuberous sclerosis complex is a genetic disorder characterized by the formation of nonmalignant hamartomas in the brain, heart, skin, kidney, lung, and other organs. ...The tuberous sclerosis complex 1/tuberous sclerosis complex 2 protein dimer comp
Tuberous sclerosis complex is a genetic disorder characterized by the formation of nonmalignant hamartomas in the brain, heart …
The neurobiology of the dystrophin-associated glycoprotein complex.
Waite A, Tinsley CL, Locke M, Blake DJ. Waite A, et al. Ann Med. 2009;41(5):344-59. doi: 10.1080/07853890802668522. Ann Med. 2009. PMID: 19172427 Review.
Accordingly, dystrophin and members of the dystrophin-associated glycoprotein complex (DGC) are found in the brain where they participate in macromolecular assemblies that anchor receptors to specialized sites within the membrane. ...Several types of congenital
Accordingly, dystrophin and members of the dystrophin-associated glycoprotein complex (DGC) are found in the brain where they …
Rapamycin and rapalogs for tuberous sclerosis complex.
Sasongko TH, Ismail NF, Zabidi-Hussin Z. Sasongko TH, et al. Cochrane Database Syst Rev. 2016 Jul 13;7(7):CD011272. doi: 10.1002/14651858.CD011272.pub2. Cochrane Database Syst Rev. 2016. PMID: 27409709 Free PMC article. Updated. Review.
BACKGROUND: Previous studies have shown potential benefits of rapamycin or rapalogs for treating people with tuberous sclerosis complex. Although everolimus (a rapalog) is currently approved by the FDA (U.S. Food and Drug Administration) and the EMA (European Medici …
BACKGROUND: Previous studies have shown potential benefits of rapamycin or rapalogs for treating people with tuberous sclerosis complex
Tuberous sclerosis complex: neurological, renal and pulmonary manifestations.
Franz DN, Bissler JJ, McCormack FX. Franz DN, et al. Neuropediatrics. 2010 Oct;41(5):199-208. doi: 10.1055/s-0030-1269906. Epub 2011 Jan 5. Neuropediatrics. 2010. PMID: 21210335 Free PMC article. Review.
Tuberous sclerosis complex (TSC) is an important cause of epilepsy and autism, as well as renal and pulmonary disease in adults and children. ...
Tuberous sclerosis complex (TSC) is an important cause of epilepsy and autism, as well as renal and pulmonary disease in adults and c …
Direct and indirect costs and cost-driving factors in adults with tuberous sclerosis complex: a multicenter cohort study and a review of the literature.
Zöllner JP, Grau J, Rosenow F, Sauter M, Knuf M, Kurlemann G, Mayer T, Hertzberg C, Bertsche A, Immisch I, Klein KM, Knake S, Marquard K, Meyer S, Noda AH, von Podewils F, Schäfer H, Thiels C, Willems LM, Zukunft B, Schubert-Bast S, Strzelczyk A. Zöllner JP, et al. Orphanet J Rare Dis. 2021 Jun 2;16(1):250. doi: 10.1186/s13023-021-01838-w. Orphanet J Rare Dis. 2021. PMID: 34078440 Free PMC article. Review.
BACKGROUND: Tuberous sclerosis complex (TSC) is a monogenetic, multisystem disorder characterized by benign growths due to TSC1 or TSC2 mutations. ...Reported TSC disease manifestations included skin (94.8%) and kidney and urinary tract (74%) disorders, epilepsy (72.9%), s …
BACKGROUND: Tuberous sclerosis complex (TSC) is a monogenetic, multisystem disorder characterized by benign growths due to TSC1 or TS …
16 results