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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1999 2
2000 3
2001 2
2002 5
2004 2
2005 6
2006 2
2007 2
2008 3
2009 7
2010 10
2011 12
2012 8
2013 4
2014 5
2015 7
2016 9
2017 5
2018 9
2019 8
2020 14
2021 18
2022 10
2023 12
2024 2

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138 results

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Page 1
GRIN2A-related disorders: genotype and functional consequence predict phenotype.
Strehlow V, Heyne HO, Vlaskamp DRM, Marwick KFM, Rudolf G, de Bellescize J, Biskup S, Brilstra EH, Brouwer OF, Callenbach PMC, Hentschel J, Hirsch E, Kind PC, Mignot C, Platzer K, Rump P, Skehel PA, Wyllie DJA, Hardingham GE, van Ravenswaaij-Arts CMA, Lesca G, Lemke JR; GRIN2A study group. Strehlow V, et al. Brain. 2019 Jan 1;142(1):80-92. doi: 10.1093/brain/awy304. Brain. 2019. PMID: 30544257 Free PMC article.
Neurosurgical aspects of Noonan syndrome.
Saragosti E, Fattal-Valevski A, Levin D, Hausman-Kedem M, Constantini S, Mecica N, Zarour S, Roth J. Saragosti E, et al. Childs Nerv Syst. 2023 Apr;39(4):849-856. doi: 10.1007/s00381-023-05888-2. Epub 2023 Feb 27. Childs Nerv Syst. 2023. PMID: 36847963 Review.
Medical treatment of tuberous sclerosis-related epilepsy.
Uliel-Sibony S, Chernuha V, Meirson H, Fattal-Valevski A. Uliel-Sibony S, et al. Childs Nerv Syst. 2020 Oct;36(10):2511-2517. doi: 10.1007/s00381-020-04772-7. Epub 2020 Aug 22. Childs Nerv Syst. 2020. PMID: 32829444 Review.
Efficacy and safety of abobotulinumtoxinA for upper limb spasticity in children with cerebral palsy: a randomized repeat-treatment study.
Delgado MR, Tilton A, Carranza-Del Río J, Dursun N, Bonikowski M, Aydin R, Maciag-Tymecka I, Oleszek J, Dabrowski E, Grandoulier AS, Picaut P; Dysport in PUL study group. Delgado MR, et al. Dev Med Child Neurol. 2021 May;63(5):592-600. doi: 10.1111/dmcn.14733. Epub 2020 Nov 18. Dev Med Child Neurol. 2021. PMID: 33206382 Free PMC article. Clinical Trial.
Hereditary orotic aciduria identified by newborn screening.
Staretz-Chacham O, Damseh NS, Daas S, Abu Salah N, Anikster Y, Barel O, Dumin E, Fattal-Valevski A, Falik-Zaccai TC, Hershkovitz E, Josefsberg S, Landau Y, Lerman-Sagie T, Mandel H, Rock R, Rostami N, Saraf-Levy T, Shaul Lotan N, Spiegel R, Tal G, Ulanovsky I, Wilnai Y, Korman SH, Almashanu S. Staretz-Chacham O, et al. Front Genet. 2023 Mar 14;14:1135267. doi: 10.3389/fgene.2023.1135267. eCollection 2023. Front Genet. 2023. PMID: 36999056 Free PMC article.
Molecular diagnosis of 405 individuals with autism spectrum disorder.
Miyake N, Tsurusaki Y, Fukai R, Kushima I, Okamoto N, Ohashi K, Nakamura K, Hashimoto R, Hiraki Y, Son S, Kato M, Sakai Y, Osaka H, Deguchi K, Matsuishi T, Takeshita S, Fattal-Valevski A, Ekhilevitch N, Tohyama J, Yap P, Keng WT, Kobayashi H, Takubo K, Okada T, Saitoh S, Yasuda Y, Murai T, Nakamura K, Ohga S, Matsumoto A, Inoue K, Saikusa T, Hershkovitz T, Kobayashi Y, Morikawa M, Ito A, Hara T, Uno Y, Seiwa C, Ishizuka K, Shirahata E, Fujita A, Koshimizu E, Miyatake S, Takata A, Mizuguchi T, Ozaki N, Matsumoto N. Miyake N, et al. Eur J Hum Genet. 2023 Mar 27. doi: 10.1038/s41431-023-01335-7. Online ahead of print. Eur J Hum Genet. 2023. PMID: 36973392
Controlled amnioreduction for twin-to-twin transfusion syndrome.
Gordon Z, Fattal-Valevski A, Elad D, Jaffa AJ. Gordon Z, et al. Ther Adv Reprod Health. 2022 Mar 29;16:26334941221080727. doi: 10.1177/26334941221080727. eCollection 2022 Jan-Dec. Ther Adv Reprod Health. 2022. PMID: 35369393 Free PMC article.
Leukodystrophies: clinical and genetic aspects.
Lyon G, Fattal-Valevski A, Kolodny EH. Lyon G, et al. Top Magn Reson Imaging. 2006 Aug;17(4):219-42. doi: 10.1097/RMR.0b013e31804c99d4. Top Magn Reson Imaging. 2006. PMID: 17414998 Review.
138 results