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Constitutive opening of the Kv7.2 pore activation gate causes KCNQ2-developmental encephalopathy.
Nappi M, Alberini G, Berselli A, Roscioni A, Soldovieri MV, Servettini I, Barrese V, Weckhuysen S, Chiu TA, Scheffer IE, Benfenati F, Maragliano L, Miceli F, Taglialatela M. Nappi M, et al. Among authors: scheffer ie. Proc Natl Acad Sci U S A. 2024 Dec 3;121(49):e2412388121. doi: 10.1073/pnas.2412388121. Epub 2024 Nov 27. Proc Natl Acad Sci U S A. 2024. PMID: 39602259
Early mortality in STXBP1-related disorders.
Furia F, Rigby CS, Scheffer IE, Allen N, Baker K, Hengsbach C, Kegele J, Goss J, Gorman K, Mala MI, Nicita F, Allan T, Spalice A, Weber Y; European STXBP1 consortium (ESCO); STXBP1 foundation; Rubboli G, Møller RS, Gardella E. Furia F, et al. Among authors: scheffer ie. Neurol Sci. 2024 Oct 11. doi: 10.1007/s10072-024-07783-3. Online ahead of print. Neurol Sci. 2024. PMID: 39392525
Developmental and epileptic encephalopathies.
Scheffer IE, Zuberi S, Mefford HC, Guerrini R, McTague A. Scheffer IE, et al. Nat Rev Dis Primers. 2024 Sep 5;10(1):61. doi: 10.1038/s41572-024-00546-6. Nat Rev Dis Primers. 2024. PMID: 39237642 Review.
Epilepsies.
McTague A, Scheffer IE, Kullmann DM, Sisodiya S. McTague A, et al. Among authors: scheffer ie. Handb Clin Neurol. 2024;203:157-184. doi: 10.1016/B978-0-323-90820-7.00016-1. Handb Clin Neurol. 2024. PMID: 39174247 Review.
Inherited PURA Pathogenic Variant Associated With a Mild Neurodevelopmental Disorder.
Hildebrand MS, Braden RO, Lauretta ML, Kaspi A, Leventer RJ, Anderson M, Goel H, Bahlo M, Scheffer IE, Amor DJ, Janowski R, Niessing D, Morgan AT. Hildebrand MS, et al. Among authors: scheffer ie. Neurol Genet. 2024 Aug 6;10(5):e200181. doi: 10.1212/NXG.0000000000200181. eCollection 2024 Oct. Neurol Genet. 2024. PMID: 39131487 Free PMC article.
642 results