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

Year Number of Results
2001 1
2002 1
2003 2
2004 1
2005 1
2006 3
2007 2
2008 5
2009 5
2010 4
2011 2
2012 2
2013 3
2014 6
2015 4
2016 4
2017 3
2018 3
2019 3
2020 6
2021 1
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50 results
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Page 1
Paediatric-onset neuronal ceroid lipofuscinosis: first symptoms and presentation at diagnosis.
Dozières-Puyravel B, Nasser H, Elmaleh-Bergès M, Lopez Hernandez E, Gelot A, Ilea A, Delanoë C, Puech JP, Caillaud C, Pichard S, Auvin S. Dozières-Puyravel B, et al. Among authors: elmaleh berges m. Dev Med Child Neurol. 2020 Apr;62(4):528-530. doi: 10.1111/dmcn.14346. Epub 2019 Sep 5. Dev Med Child Neurol. 2020. PMID: 31489614 Free article.
Hemiconvulsion-hemiplegia-epilepsy syndrome: current understandings.
Auvin S, Bellavoine V, Merdariu D, Delanoë C, Elmaleh-Bergés M, Gressens P, Boespflug-Tanguy O. Auvin S, et al. Among authors: elmaleh berges m. Eur J Paediatr Neurol. 2012 Sep;16(5):413-21. doi: 10.1016/j.ejpn.2012.01.007. Epub 2012 Feb 14. Eur J Paediatr Neurol. 2012. PMID: 22341151 Review.
Loss of TNR causes a nonprogressive neurodevelopmental disorder with spasticity and transient opisthotonus.
Wagner M, Lévy J, Jung-Klawitter S, Bakhtiari S, Monteiro F, Maroofian R, Bierhals T, Hempel M, Elmaleh-Bergès M, Kitajima JP, Kim CA, Salomao JG, Amor DJ, Cooper MS, Perrin L, Pipiras E, Neu A, Doosti M, Karimiani EG, Toosi MB, Houlden H, Jin SC, Si YC, Rodan LH, Venselaar H, Kruer MC, Kok F, Hoffmann GF, Strom TM, Wortmann SB, Tabet AC, Opladen T. Wagner M, et al. Among authors: elmaleh berges m. Genet Med. 2020 Jun;22(6):1061-1068. doi: 10.1038/s41436-020-0768-7. Epub 2020 Feb 26. Genet Med. 2020. PMID: 32099069
CDK5RAP2 primary microcephaly is associated with hypothalamic, retinal and cochlear developmental defects.
Nasser H, Vera L, Elmaleh-Bergès M, Steindl K, Letard P, Teissier N, Ernault A, Guimiot F, Afenjar A, Moutard ML, Héron D, Alembik Y, Momtchilova M, Milani P, Kubis N, Pouvreau N, Zollino M, Guilmin Crepon S, Kaguelidou F, Gressens P, Verloes A, Rauch A, El Ghouzzi V, Drunat S, Passemard S. Nasser H, et al. Among authors: elmaleh berges m. J Med Genet. 2020 Jun;57(6):389-399. doi: 10.1136/jmedgenet-2019-106474. Epub 2020 Feb 3. J Med Genet. 2020. PMID: 32015000 Clinical Trial.
[Computed tomography of the normal and pathologic temporal bone].
Prades JM, Elmaleh-Berges M, Chatard S, Veyret C, Martin C, Richard C. Prades JM, et al. Among authors: elmaleh berges m. Morphologie. 2011 Dec;95(311):159-69. doi: 10.1016/j.morpho.2011.09.001. Epub 2011 Nov 10. Morphologie. 2011. PMID: 22079599 Review. French.
[Neonatal weight loss with neurological degeneration].
Cardoen L, Schiff M, Lambron J, Rega A, Virlouvet AL, Biran V, Eleni Dit Trolli S, Elmaleh-Bergès M, Alison M. Cardoen L, et al. Among authors: elmaleh berges m. Arch Pediatr. 2016 Dec;23(12):1273-1275. doi: 10.1016/j.arcped.2016.09.012. Epub 2016 Nov 2. Arch Pediatr. 2016. PMID: 27816399 French. No abstract available.
SLC13A3 variants cause acute reversible leukoencephalopathy and α-ketoglutarate accumulation.
Dewulf JP, Wiame E, Dorboz I, Elmaleh-Bergès M, Imbard A, Dumitriu D, Rak M, Bourillon A, Helaers R, Malla A, Renaldo F, Boespflug-Tanguy O, Vincent MF, Benoist JF, Wevers RA, Schlessinger A, Van Schaftingen E, Nassogne MC, Schiff M. Dewulf JP, et al. Among authors: elmaleh berges m. Ann Neurol. 2019 Mar;85(3):385-395. doi: 10.1002/ana.25412. Epub 2019 Jan 29. Ann Neurol. 2019. PMID: 30635937
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