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

Year Number of Results
1984 1
1994 1
2001 1
2002 1
2006 1
2008 1
2009 1
2011 1
2014 2
2016 1
2017 1
2018 1
2019 3
2020 1
2022 2
2023 2
2024 0

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19 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.
Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental condition.
Palmer EE, Pusch M, Picollo A, Forwood C, Nguyen MH, Suckow V, Gibbons J, Hoff A, Sigfrid L, Megarbane A, Nizon M, Cogné B, Beneteau C, Alkuraya FS, Chedrawi A, Hashem MO, Stamberger H, Weckhuysen S, Vanlander A, Ceulemans B, Rajagopalan S, Nunn K, Arpin S, Raynaud M, Motter CS, Ward-Melver C, Janssens K, Meuwissen M, Beysen D, Dikow N, Grimmel M, Haack TB, Clement E, McTague A, Hunt D, Townshend S, Ward M, Richards LJ, Simons C, Costain G, Dupuis L, Mendoza-Londono R, Dudding-Byth T, Boyle J, Saunders C, Fleming E, El Chehadeh S, Spitz MA, Piton A, Gerard B, Abi Warde MT, Rea G, McKenna C, Douzgou S, Banka S, Akman C, Bain JM, Sands TT, Wilson GN, Silvertooth EJ, Miller L, Lederer D, Sachdev R, Macintosh R, Monestier O, Karadurmus D, Collins F, Carter M, Rohena L, Willemsen MH, Ockeloen CW, Pfundt R, Kroft SD, Field M, Laranjeira FER, Fortuna AM, Soares AR, Michaud V, Naudion S, Golla S, Weaver DD, Bird LM, Friedman J, Clowes V, Joss S, Pölsler L, Campeau PM, Blazo M, Bijlsma EK, Rosenfeld JA, Beetz C, Powis Z, McWalter K, Brandt T, Torti E, Mathot M, Mohammad SS, Armstrong R, Kalscheuer VM. Palmer EE, et al. Among authors: mathot m. Mol Psychiatry. 2023 Feb;28(2):668-697. doi: 10.1038/s41380-022-01852-9. Epub 2022 Nov 16. Mol Psychiatry. 2023. PMID: 36385166 Free PMC article.
[PRRT2 mutation and infantile convulsions].
Mathot M, Lederer D, Gerard S, Gueulette E, Deprez M. Mathot M, et al. Arch Pediatr. 2017 Oct;24(10):1010-1012. doi: 10.1016/j.arcped.2017.08.004. Epub 2017 Sep 1. Arch Pediatr. 2017. PMID: 28870817 French.
Quantification of methane emitted by ruminants: a review of methods.
Tedeschi LO, Abdalla AL, Álvarez C, Anuga SW, Arango J, Beauchemin KA, Becquet P, Berndt A, Burns R, De Camillis C, Chará J, Echazarreta JM, Hassouna M, Kenny D, Mathot M, Mauricio RM, McClelland SC, Niu M, Onyango AA, Parajuli R, Pereira LGR, Del Prado A, Paz Tieri M, Uwizeye A, Kebreab E. Tedeschi LO, et al. Among authors: mathot m. J Anim Sci. 2022 Jul 1;100(7):skac197. doi: 10.1093/jas/skac197. J Anim Sci. 2022. PMID: 35657151 Free PMC article. Review.
Hypomyelination and congenital cataract: broadening the clinical phenotype.
Biancheri R, Zara F, Rossi A, Mathot M, Nassogne MC, Yalcinkaya C, Erturk O, Tuysuz B, Di Rocco M, Gazzerro E, Bugiani M, van Spaendonk R, Sistermans EA, Minetti C, van der Knaap MS, Wolf NI. Biancheri R, et al. Among authors: mathot m. Arch Neurol. 2011 Sep;68(9):1191-4. doi: 10.1001/archneurol.2011.201. Arch Neurol. 2011. PMID: 21911699 Review.
Early skin sensitization to aeroallergens.
de Bilderling G, Mathot M, Agustsson S, Tuerlinckx D, Jamart J, Bodart E. de Bilderling G, et al. Among authors: mathot m. Clin Exp Allergy. 2008 Apr;38(4):643-8. doi: 10.1111/j.1365-2222.2008.02938.x. Clin Exp Allergy. 2008. PMID: 18352977
[Intervision for nurses - a recommendable matter].
Cox D, Iedema Y, Mathôt M, van Zelst W. Cox D, et al. Among authors: mathot m. Tijdschr Ziekenverpl. 1984 Jan 17;37(2):50-2. Tijdschr Ziekenverpl. 1984. PMID: 6560936 Dutch. No abstract available.
19 results