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Genetics and genotype-phenotype correlations in early onset epileptic encephalopathy with burst suppression.
Olson HE, Kelly M, LaCoursiere CM, Pinsky R, Tambunan D, Shain C, Ramgopal S, Takeoka M, Libenson MH, Julich K, Loddenkemper T, Marsh ED, Segal D, Koh S, Salman MS, Paciorkowski AR, Yang E, Bergin AM, Sheidley BR, Poduri A. Olson HE, et al. Among authors: julich k. Ann Neurol. 2017 Mar;81(3):419-429. doi: 10.1002/ana.24883. Epub 2017 Feb 14. Ann Neurol. 2017. PMID: 28133863 Free PMC article.
CDKL5 deficiency disorder and other infantile-onset genetic epilepsies.
Daniels C, Greene C, Smith L, Pestana-Knight E, Demarest S, Zhang B, Benke TA, Poduri A, Olson HE; CDKL5 Study Group. Daniels C, et al. Dev Med Child Neurol. 2024 Apr;66(4):456-468. doi: 10.1111/dmcn.15747. Epub 2023 Sep 28. Dev Med Child Neurol. 2024. PMID: 37771170
Mechanism-based treatment in tuberous sclerosis complex.
Jülich K, Sahin M. Jülich K, et al. Pediatr Neurol. 2014 Apr;50(4):290-6. doi: 10.1016/j.pediatrneurol.2013.12.002. Epub 2013 Dec 5. Pediatr Neurol. 2014. PMID: 24486221 Free PMC article. Review.
SKAR is a specific target of S6 kinase 1 in cell growth control.
Richardson CJ, Bröenstrup M, Fingar DC, Jülich K, Ballif BA, Gygi S, Blenis J. Richardson CJ, et al. Among authors: julich k. Curr Biol. 2004 Sep 7;14(17):1540-9. doi: 10.1016/j.cub.2004.08.061. Curr Biol. 2004. PMID: 15341740 Free article.
Vitamin-Dependent Genetic Disorders of Childhood.
Ramirez EL, Gibson JB, Jülich K. Ramirez EL, et al. Among authors: julich k. Pediatr Rev. 2023 Nov 1;44(11):618-631. doi: 10.1542/pir.2022-005637. Pediatr Rev. 2023. PMID: 37907415 No abstract available.
15 results