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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2014 | 1 |
2015 | 1 |
2017 | 2 |
2018 | 1 |
2020 | 1 |
2024 | 0 |
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Page 1
Large-scale discovery of novel genetic causes of developmental disorders.
Nature. 2015 Mar 12;519(7542):223-8. doi: 10.1038/nature14135. Epub 2014 Dec 24.
Nature. 2015.
PMID: 25533962
Free PMC article.
GNAO1 encephalopathy: Broadening the phenotype and evaluating treatment and outcome.
Danti FR, Galosi S, Romani M, Montomoli M, Carss KJ, Raymond FL, Parrini E, Bianchini C, McShane T, Dale RC, Mohammad SS, Shah U, Mahant N, Ng J, McTague A, Samanta R, Vadlamani G, Valente EM, Leuzzi V, Kurian MA, Guerrini R.
Danti FR, et al.
Neurol Genet. 2017 Mar 21;3(2):e143. doi: 10.1212/NXG.0000000000000143. eCollection 2017 Apr.
Neurol Genet. 2017.
PMID: 28357411
Free PMC article.
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Movement disorder in GNAO1 encephalopathy associated with gain-of-function mutations.
Feng H, Sjögren B, Karaj B, Shaw V, Gezer A, Neubig RR.
Feng H, et al.
Neurology. 2017 Aug 22;89(8):762-770. doi: 10.1212/WNL.0000000000004262. Epub 2017 Jul 26.
Neurology. 2017.
PMID: 28747448
Free PMC article.
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Deep brain stimulation is effective in pediatric patients with GNAO1 associated severe hyperkinesia.
Koy A, Cirak S, Gonzalez V, Becker K, Roujeau T, Milesi C, Baleine J, Cambonie G, Boularan A, Greco F, Perrigault PF, Cances C, Dorison N, Doummar D, Roubertie A, Beroud C, Körber F, Stüve B, Waltz S, Mignot C, Nava C, Maarouf M, Coubes P, Cif L.
Koy A, et al.
J Neurol Sci. 2018 Aug 15;391:31-39. doi: 10.1016/j.jns.2018.05.018. Epub 2018 May 22.
J Neurol Sci. 2018.
PMID: 30103967
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Genetic basis of neurodevelopmental disorders in 103 Jordanian families.
Froukh T, Nafie O, Al Hait SAS, Laugwitz L, Sommerfeld J, Sturm M, Baraghiti A, Issa T, Al-Nazer A, Koch PA, Hanselmann J, Kootz B, Bauer P, Al-Ameri W, Abou Jamra R, Alfrook AJ, Hamadallah M, Sofan L, Riess A, Haack TB, Riess O, Buchert R.
Froukh T, et al.
Clin Genet. 2020 Apr;97(4):621-627. doi: 10.1111/cge.13720. Epub 2020 Mar 1.
Clin Genet. 2020.
PMID: 32056211
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