Melatonin use in managing insomnia in children with autism and other neurogenetic disorders - An assessment by the international pediatric sleep association (IPSA)

Autor: Kotagal, Suresh, Malow, Beth, Spruyt, Karen, Wang, Guanghai, Bolaños Almeida, Carlos Ernest, Tavera Saldaña, Lina Marcela, Blunden, Sarah, Narang, Indra, Ipsiroglu, Osman S., Bruni, Oliviero, Strazisar, Barbara Gnidovec, Simakajornboon, Narong, Nunes, Magda Lahorgue, Cortese, Samuele

Publikováno v: In Sleep Medicine July 2024 119:222-228

Daylight Saving Time: Pros and Cons

Autor: Stražišar, Barbara Gnidovec, Stražišar, Lea

Publikováno v: In Sleep Medicine Clinics September 2021 16(3):523-531

TBC1D24 genotype-phenotype correlation: Epilepsies and other neurologic features

Autor: Balestrini, Simona, Milh, Mathieu, Castiglioni, Claudia, Lüthy, Kevin, Finelli, Mattea J, Verstreken, Patrik, Cardon, Aaron, Stražišar, Barbara Gnidovec, Holder, J Lloyd, Lesca, Gaetan, Mancardi, Maria M, Poulat, Anne L, Repetto, Gabriela M, Banka, Siddharth, Bilo, Leonilda, Birkeland, Laura E, Bosch, Friedrich, Brockmann, Knut, Cross, J Helen, Doummar, Diane, Félix, Temis M, Giuliano, Fabienne, Hori, Mutsuki, Hüning, Irina, Kayserili, Hulia, Kini, Usha, Lees, Melissa M, Meenakshi, Girish, Mewasingh, Leena, Pagnamenta, Alistair T, Peluso, Silvio, Mey, Antje, Rice, Gregory M, Rosenfeld, Jill A, Taylor, Jenny C, Troester, Matthew M, Stanley, Christine M, Ville, Dorothee, Walkiewicz, Magdalena, Falace, Antonio, Fassio, Anna, Lemke, Johannes R, Biskup, Saskia, Tardif, Jessica, Ajeawung, Norbert F, Tolun, Aslihan, Corbett, Mark, Gecz, Jozef, Afawi, Zaid, Howell, Katherine B, Oliver, Karen L, Berkovic, Samuel F, Scheffer, Ingrid E, de Falco, Fabrizio A, Oliver, Peter L, Striano, Pasquale, Zara, Federico, Campeau, Phillipe M, Sisodiya, S M

Publikováno v: Neurology
Neurology, American Academy of Neurology, 2016, 87 (1), pp.77-85. ⟨10.1212/WNL.0000000000002807⟩
Neurology, 2016, 87 (1), pp.77-85. ⟨10.1212/WNL.0000000000002807⟩
Balestrini, S, Milh, M, Castiglioni, C, Lüthy, K, Finelli, M J, Verstreken, P, Cardon, A, Stražišar, B G, Holder, J L, Lesca, G, Mancardi, M M, Poulat, A L, Repetto, G M, Banka, S, Bilo, L, Birkeland, L E, Bosch, F, Brockmann, K, Cross, J H, Doummar, D, Félix, T M, Giuliano, F, Hori, M, Hüning, I, Kayserili, H, Kini, U, Lees, M M, Meenakshi, G, Mewasingh, L, Pagnamenta, A T, Peluso, S, Mey, A, Rice, G M, Rosenfeld, J A, Taylor, J C, Troester, M M, Stanley, C M, Ville, D, Walkiewicz, M, Falace, A, Fassio, A, Lemke, J R, Biskup, S, Tardif, J, Ajeawung, N F, Tolun, A, Corbett, M, Gecz, J, Afawi, Z, Howell, K B, Oliver, K L, Berkovic, S F, Scheffer, I E, de Falco, F A, Oliver, P L, Striano, P, Zara, F, Campeau, P M & Sisodiya, S M 2016, ' TBC1D24 genotype-phenotype correlation : Epilepsies and other neurologic features ', Neurology, vol. 87, no. 1, pp. 77-85 . https://doi.org/10.1212/WNL.0000000000002807

OBJECTIVE: To evaluate the phenotypic spectrum associated with mutations in TBC1D24.METHODS: We acquired new clinical, EEG, and neuroimaging data of 11 previously unreported and 37 published patients. TBC1D24 mutations, identified through various seq

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::bb68a978dbabbb1ae3c124a31067618c
https://lirias.kuleuven.be/handle/123456789/544682

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