Goorden SM - Search Results

1

Oncogenes on my mind: ERK and MTOR signaling in cognitive diseases.

Krab LC, Goorden SM, Elgersma Y. Krab LC, et al. Among authors: goorden sm. Trends Genet. 2008 Oct;24(10):498-510. doi: 10.1016/j.tig.2008.07.005. Epub 2008 Sep 4. Trends Genet. 2008. PMID: 18774199 Review.

2

Cognitive deficits in Tsc1+/- mice in the absence of cerebral lesions and seizures.

Goorden SM, van Woerden GM, van der Weerd L, Cheadle JP, Elgersma Y. Goorden SM, et al. Ann Neurol. 2007 Dec;62(6):648-55. doi: 10.1002/ana.21317. Ann Neurol. 2007. PMID: 18067135

3

Rheb is essential for murine development.

Goorden SM, Hoogeveen-Westerveld M, Cheng C, van Woerden GM, Mozaffari M, Post L, Duckers HJ, Nellist M, Elgersma Y. Goorden SM, et al. Mol Cell Biol. 2011 Apr;31(8):1672-8. doi: 10.1128/MCB.00985-10. Epub 2011 Feb 14. Mol Cell Biol. 2011. PMID: 21321084 Free PMC article.

4

TORC1-dependent epilepsy caused by acute biallelic Tsc1 deletion in adult mice.

Abs E, Goorden SM, Schreiber J, Overwater IE, Hoogeveen-Westerveld M, Bruinsma CF, Aganović E, Borgesius NZ, Nellist M, Elgersma Y. Abs E, et al. Among authors: goorden sm. Ann Neurol. 2013 Oct;74(4):569-79. doi: 10.1002/ana.23943. Epub 2013 Sep 10. Ann Neurol. 2013. PMID: 23720219

5

Intact neuronal function in Rheb1 mutant mice: implications for TORC1-based treatments.

Goorden SM, Abs E, Bruinsma CF, Riemslagh FW, van Woerden GM, Elgersma Y. Goorden SM, et al. Hum Mol Genet. 2015 Jun 15;24(12):3390-8. doi: 10.1093/hmg/ddv087. Epub 2015 Mar 10. Hum Mol Genet. 2015. PMID: 25759467

6

Temporal and region-specific requirements of αCaMKII in spatial and contextual learning.

Achterberg KG, Buitendijk GH, Kool MJ, Goorden SM, Post L, Slump DE, Silva AJ, van Woerden GM, Kushner SA, Elgersma Y. Achterberg KG, et al. Among authors: goorden sm. J Neurosci. 2014 Aug 20;34(34):11180-7. doi: 10.1523/JNEUROSCI.0640-14.2014. J Neurosci. 2014. PMID: 25143599 Free PMC article.

7

Rheb: enrichment beyond the brain.

Goorden SM, Elgersma Y. Goorden SM, et al. Cell Cycle. 2011 Aug 1;10(15):2412-3. doi: 10.4161/cc.10.15.16385. Epub 2011 Aug 1. Cell Cycle. 2011. PMID: 21670600 No abstract available.

8

Successful Treatment of Hereditary Folate Malabsorption With Intramuscular Folinic Acid.

Lubout CMA, Goorden SMI, van den Hurk K, Jaeger B, Jager NGL, van Koningsbruggen S, Chegary M, van Karnebeek CDM. Lubout CMA, et al. Pediatr Neurol. 2020 Jan;102:62-66. doi: 10.1016/j.pediatrneurol.2019.06.009. Epub 2019 Jun 22. Pediatr Neurol. 2020. PMID: 31371121

9

Hereditary folate malabsorption due to a mutation in the external gate of the proton-coupled folate transporter SLC46A1.

Aluri S, Zhao R, Lubout C, Goorden SMI, Fiser A, Goldman ID. Aluri S, et al. Blood Adv. 2018 Jan 5;2(1):61-68. doi: 10.1182/bloodadvances.2017012690. eCollection 2018 Jan 9. Blood Adv. 2018. PMID: 29344585 Free PMC article.

10

Biochemical Screening of Intellectually Disabled Patients: A Stepping Stone to Initiate a Newborn Screening Program in Pakistan.

Wasim M, Khan HN, Ayesha H, Goorden SMI, Vaz FM, van Karnebeek CDM, Awan FR. Wasim M, et al. Front Neurol. 2019 Jul 17;10:762. doi: 10.3389/fneur.2019.00762. eCollection 2019. Front Neurol. 2019. PMID: 31379716 Free PMC article.

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