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

Year Number of Results
1965 1
1967 1
1977 1
1978 1
1985 1
1991 2
1992 4
1994 3
1995 1
1996 1
1997 1
1998 2
2000 1
2001 1
2002 3
2003 2
2005 1
2006 3
2007 3
2008 2
2009 1
2010 3
2011 2
2012 6
2013 7
2014 5
2015 4
2016 4
2017 6
2018 5
2019 6
2020 8
2021 12
2022 16
2023 9
2024 3

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118 results

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Page 1
Updated International Tuberous Sclerosis Complex Diagnostic Criteria and Surveillance and Management Recommendations.
Northrup H, Aronow ME, Bebin EM, Bissler J, Darling TN, de Vries PJ, Frost MD, Fuchs Z, Gosnell ES, Gupta N, Jansen AC, Jóźwiak S, Kingswood JC, Knilans TK, McCormack FX, Pounders A, Roberds SL, Rodriguez-Buritica DF, Roth J, Sampson JR, Sparagana S, Thiele EA, Weiner HL, Wheless JW, Towbin AJ, Krueger DA; International Tuberous Sclerosis Complex Consensus Group. Northrup H, et al. Pediatr Neurol. 2021 Oct;123:50-66. doi: 10.1016/j.pediatrneurol.2021.07.011. Epub 2021 Jul 24. Pediatr Neurol. 2021. PMID: 34399110 Free article.
Changes to surveillance and management criteria largely reflected increased emphasis on early screening for electroencephalographic abnormalities, enhanced surveillance and management of TSC-associated neuropsychiatric disorders, and new medication approvals. CONCLUSIONS: …
Changes to surveillance and management criteria largely reflected increased emphasis on early screening for electroencephalographic abnor
Coats disease: An overview of classification, management and outcomes.
Sen M, Shields CL, Honavar SG, Shields JA. Sen M, et al. Indian J Ophthalmol. 2019 Jun;67(6):763-771. doi: 10.4103/ijo.IJO_841_19. Indian J Ophthalmol. 2019. PMID: 31124484 Free PMC article. Review.
Coats disease is an idiopathic retinal vascular disorder with retinal telangiectasia with intraretinal and/or subretinal exudation without appreciable retinal or vitreal traction. The condition is sporadic with no associated systemic abnormalities. Unilateral involvement i …
Coats disease is an idiopathic retinal vascular disorder with retinal telangiectasia with intraretinal and/or subretinal exudation without a …
Joubert syndrome: Molecular basis and treatment.
Spahiu L, Behluli E, Grajçevci-Uka V, Liehr T, Temaj G. Spahiu L, et al. J Mother Child. 2023 Feb 22;26(1):118-123. doi: 10.34763/jmotherandchild.20222601.d-22-00034. eCollection 2022 Mar 1. J Mother Child. 2023. PMID: 36803942 Free PMC article. Review.
Joubert syndrome (JS; MIM PS213300) is a rare genetic autosomal recessive disease characterized by cerebellar vermis hypoplasia, a distinctive malformation of the cerebellum and the so-called "molar tooth sign." ...This review will describe some characteristics of JS assoc …
Joubert syndrome (JS; MIM PS213300) is a rare genetic autosomal recessive disease characterized by cerebellar vermis hypoplasia, a di …
Genotype-phenotype correlates in Joubert syndrome: A review.
Gana S, Serpieri V, Valente EM. Gana S, et al. Am J Med Genet C Semin Med Genet. 2022 Mar;190(1):72-88. doi: 10.1002/ajmg.c.31963. Epub 2022 Mar 3. Am J Med Genet C Semin Med Genet. 2022. PMID: 35238134 Free PMC article. Review.
To date, gene-phenotype correlates have been delineated only for a handful of genes, directly translating into improved counseling and clinical care. For instance, JS individuals harboring pathogenic variants in TMEM67 have a significantly higher risk of liver fibrosis, wh …
To date, gene-phenotype correlates have been delineated only for a handful of genes, directly translating into improved counseling and clini …
Current and Novel Therapeutic Approaches for Treatment of Diabetic Macular Edema.
Chauhan MZ, Rather PA, Samarah SM, Elhusseiny AM, Sallam AB. Chauhan MZ, et al. Cells. 2022 Jun 17;11(12):1950. doi: 10.3390/cells11121950. Cells. 2022. PMID: 35741079 Free PMC article. Review.
Treatment for DME generally involves primary management of DM, laser photocoagulation, and pharmacotherapeutics targeting mediators, namely, the anti-VEGF pathway. The emergence of anti-VEGF therapies has resulted in significant clinical improvements compared to laser t
Treatment for DME generally involves primary management of DM, laser photocoagulation, and pharmacotherapeutics targeting mediators, namely, …
The Utility of Universal Newborn Eye Screening: A Review.
Azad AD, Al-Moujahed A, Ludwig CA, Vail D, Callaway NF, Rosenblatt TR, Kumm J, Moshfeghi DM. Azad AD, et al. Ophthalmic Surg Lasers Imaging Retina. 2021 Dec;52(S2):S6-S16. doi: 10.3928/23258160-20211115-02. Epub 2021 Dec 1. Ophthalmic Surg Lasers Imaging Retina. 2021. PMID: 34908491 Review.
Universal newborn eye screening can identify ocular abnormalities early and help mitigate long-term visual impairment. Traditional neonatal and infant eye screening is administered by neonatologists and pediatricians using the red reflex test. ...In this review, the author …
Universal newborn eye screening can identify ocular abnormalities early and help mitigate long-term visual impairment. Traditional ne …
Clinical characteristics and current treatment of glaucoma.
Cohen LP, Pasquale LR. Cohen LP, et al. Cold Spring Harb Perspect Med. 2014 Jun 2;4(6):a017236. doi: 10.1101/cshperspect.a017236. Cold Spring Harb Perspect Med. 2014. PMID: 24890835 Free PMC article. Review.
Clinically, glaucoma refers to an array of conditions associated with variably elevated intraocular pressure (IOP) that contributes to RGC loss via mechanical stress, vascular abnormalities, and other mechanisms, such as immune phenomena. The clinical diagnosis of glaucoma …
Clinically, glaucoma refers to an array of conditions associated with variably elevated intraocular pressure (IOP) that contributes to RGC l …
The use of emergency apheresis in the management of plasma cell disorders.
Kalayoglu-Besisik S. Kalayoglu-Besisik S. Transfus Apher Sci. 2018 Feb;57(1):35-39. doi: 10.1016/j.transci.2018.02.014. Epub 2018 Feb 20. Transfus Apher Sci. 2018. PMID: 29477943 Review.
Hyperviscosity syndrome (HVS) develops most commonly in Waldenstrom's macroglobulinemia (WM) and multiple myeloma (MM). Plasmapheresis is the immediate therapy and very effective at relieving symptoms by removing paraprotein. The most commonly used replacement fluid is 4%- …
Hyperviscosity syndrome (HVS) develops most commonly in Waldenstrom's macroglobulinemia (WM) and multiple myeloma (MM). Plasmapheresis is th …
118 results