Year |
Citation |
Score |
2020 |
Ottenhoff MJ, Krab LC, Elgersma Y. Considerations for clinical therapeutic development of statins for neurodevelopmental disorders. Eneuro. PMID 32071072 DOI: 10.1523/ENEURO.0392-19.2020 |
0.501 |
|
2017 |
Rietman AB, van der Vaart T, Plasschaert E, Nicholson BA, Oostenbrink R, Krab LC, Descheemaeker MJ, Wit MY, Moll HA, Legius E, Nijs PFA. Emotional and behavioral problems in children and adolescents with neurofibromatosis type 1. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 29243874 DOI: 10.1002/ajmg.b.32612 |
0.591 |
|
2012 |
van Beveren NJ, Krab LC, Swagemakers S, Buitendijk G, Buitendijk GH, Boot E, van der Spek P, Elgersma Y, van Amelsvoort TA. Functional gene-expression analysis shows involvement of schizophrenia-relevant pathways in patients with 22q11 deletion syndrome. Plos One. 7: e33473. PMID 22457764 DOI: 10.1371/journal.pone.0033473 |
0.506 |
|
2012 |
van Beveren NJ, Buitendijk GH, Swagemakers S, Krab LC, Röder C, de Haan L, van der Spek P, Elgersma Y. Marked reduction of AKT1 expression and deregulation of AKT1-associated pathways in peripheral blood mononuclear cells of schizophrenia patients. Plos One. 7: e32618. PMID 22393424 DOI: 10.1371/journal.pone.0032618 |
0.494 |
|
2012 |
Beveren NJMv, Krab LC, Swagemakers S, Buitendijk GHS, Boot E, Spek Pvd, Elgersma Y, Amelsvoort TAMJv. Correction: Functional Gene-Expression Analysis Shows Involvement of Schizophrenia-Relevant Pathways in Patients with 22q11 Deletion Syndrome Plos One. 7. DOI: 10.1371/Annotation/D80F4E7D-5E96-41Da-9Dae-717B0D0D3C60 |
0.481 |
|
2011 |
Krab LC, de Goede-Bolder A, Aarsen FK, Moll HA, De Zeeuw CI, Elgersma Y, van der Geest JN. Motor learning in children with neurofibromatosis type I. Cerebellum (London, England). 10: 14-21. PMID 20927664 DOI: 10.1007/s12311-010-0217-2 |
0.498 |
|
2009 |
Krab LC, Oostenbrink R, de Goede-Bolder A, Aarsen FK, Elgersma Y, Moll HA. Health-related quality of life in children with neurofibromatosis type 1: contribution of demographic factors, disease-related factors, and behavior. The Journal of Pediatrics. 154: 420-5, 425.e1. PMID 18950800 DOI: 10.1016/j.jpeds.2008.08.045 |
0.522 |
|
2008 |
Krab LC, Aarsen FK, de Goede-Bolder A, Catsman-Berrevoets CE, Arts WF, Moll HA, Elgersma Y. Impact of neurofibromatosis type 1 on school performance. Journal of Child Neurology. 23: 1002-10. PMID 18827266 DOI: 10.1177/0883073808316366 |
0.535 |
|
2008 |
Krab LC, Goorden SM, Elgersma Y. Oncogenes on my mind: ERK and MTOR signaling in cognitive diseases. Trends in Genetics : Tig. 24: 498-510. PMID 18774199 DOI: 10.1016/j.tig.2008.07.005 |
0.612 |
|
2008 |
Krab LC, de Goede-Bolder A, Aarsen FK, Pluijm SM, Bouman MJ, van der Geest JN, Lequin M, Catsman CE, Arts WF, Kushner SA, Silva AJ, de Zeeuw CI, Moll HA, Elgersma Y. Effect of simvastatin on cognitive functioning in children with neurofibromatosis type 1: a randomized controlled trial. Jama. 300: 287-94. PMID 18632543 DOI: 10.1001/Jama.300.3.287 |
0.576 |
|
2008 |
van Engelen SJ, Krab LC, Moll HA, de Goede-Bolder A, Pluijm SM, Catsman-Berrevoets CE, Elgersma Y, Lequin MH. Quantitative differentiation between healthy and disordered brain matter in patients with neurofibromatosis type I using diffusion tensor imaging. Ajnr. American Journal of Neuroradiology. 29: 816-22. PMID 18339726 DOI: 10.3174/ajnr.A0921 |
0.476 |
|
2008 |
Shilyansky C, Li W, Acosta M, Elgersma Y, Hannan F, Hardt M, Hunter-Schaedle K, Krab LC, Legius E, Wiltgen B, J Silva A. Molecular and cellular mechanisms of learning disabilities: A focus on neurofibromatosis type I Animal and Translational Models For Cns Drug Discovery. 2: 77-92. DOI: 10.1016/B978-0-12-373861-5.00015-1 |
0.463 |
|
2008 |
Elgersma Y, Krab LC, Moll HA. Statin therapy and cognitive deficits associated with neurofibromatosis type 1: Reply Jama - Journal of the American Medical Association. 300: 2369-2370. DOI: 10.1001/jama.2008.688 |
0.504 |
|
Low-probability matches (unlikely to be authored by this person) |
2020 |
Krab LC, Marcos-Alcalde I, Assaf M, Balasubramanian M, Andersen JB, Bisgaard AM, Fitzpatrick DR, Gudmundsson S, Huisman SA, Kalayci T, Maas SM, Martinez F, McKee S, Menke LA, Mulder PA, et al. Delineation of phenotypes and genotypes related to cohesin structural protein RAD21. Human Genetics. PMID 32193685 DOI: 10.1007/s00439-020-02138-2 |
0.133 |
|
2009 |
Oostenbrink R, Krab LC, de Goede-Bolder A, Moll HA. Reply Journal of Pediatrics. 155: 454. DOI: 10.1016/j.jpeds.2009.06.022 |
0.01 |
|
Hide low-probability matches. |