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Page 1
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.
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.
Blockade of ActRIIB signaling triggers muscle fatigability and metabolic myopathy.
Relizani K, Mouisel E, Giannesini B, Hourdé C, Patel K, Morales Gonzalez S, Jülich K, Vignaud A, Piétri-Rouxel F, Fortin D, Garcia L, Blot S, Ritvos O, Bendahan D, Ferry A, Ventura-Clapier R, Schuelke M, Amthor H. Relizani K, et al. Among authors: julich k. Mol Ther. 2014 Aug;22(8):1423-1433. doi: 10.1038/mt.2014.90. Epub 2014 May 27. Mol Ther. 2014. PMID: 24861054 Free PMC article.
18 results