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

Year Number of Results
1987 1
1988 1
1990 1
1994 1
2000 1
2001 1
2002 1
2003 1
2004 1
2005 4
2006 1
2007 1
2008 4
2009 3
2010 1
2011 1
2012 2
2013 2
2014 2
2015 1
2016 1
2017 1
2018 1
2019 4
2020 2
2021 3
2023 2
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44 results

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Page 1
PRRT2 mutations cause hemiplegic migraine.
Riant F, Roze E, Barbance C, Méneret A, Guyant-Maréchal L, Lucas C, Sabouraud P, Trébuchon A, Depienne C, Tournier-Lasserve E. Riant F, et al. Among authors: sabouraud p. Neurology. 2012 Nov 20;79(21):2122-4. doi: 10.1212/WNL.0b013e3182752cb8. Epub 2012 Oct 17. Neurology. 2012. PMID: 23077016
Spectrum of Phenotypes in SMA Patients With 4 SMN2 Copies in the French Population: Registre SMA France.
Gerin L, Ropars J, Garcia-Uzquiano R, Gómez-García De la Banda M, Saugier-Veber P, Desguerre I, Salort-Campana E, Espil C, Barnerias C, Laugel V, Cances C, Audic F, Cintas P, Le Goff L, Mallaret M, Nouguès MC, Drunat S, Tard C, Grimaldi L, Quijano-Roy S; R-SMA Study Group (FILNEMUS). Gerin L, et al. Neurol Genet. 2025 Apr 1;11(2):e200222. doi: 10.1212/NXG.0000000000200222. eCollection 2025 Apr. Neurol Genet. 2025. PMID: 40212804 Free PMC article.
[Ifosfamide induced encephalopathy: 15 observations].
Dufour C, Grill J, Sabouraud P, Behar C, Munzer M, Motte J, Oberlin O, Paci A, Hartmann O. Dufour C, et al. Among authors: sabouraud p. Arch Pediatr. 2006 Feb;13(2):140-5. doi: 10.1016/j.arcped.2005.10.021. Epub 2005 Dec 20. Arch Pediatr. 2006. PMID: 16364615 French.
Novel SPEG Mutations in Congenital Myopathy without Centralized Nuclei.
Lornage X, Sabouraud P, Lannes B, Gaillard D, Schneider R, Deleuze JF, Boland A, Thompson J, Böhm J, Biancalana V, Laporte J. Lornage X, et al. Among authors: sabouraud p. J Neuromuscul Dis. 2018;5(2):257-260. doi: 10.3233/JND-170265. J Neuromuscul Dis. 2018. PMID: 29614691 Free article.
Moyamoya disease associated with hereditary spherocytosis.
Vo Van P, Sabouraud P, Mac G, Abely M, Bednarek N. Vo Van P, et al. Among authors: sabouraud p. Pediatr Neurol. 2011 Jan;44(1):69-71. doi: 10.1016/j.pediatrneurol.2010.08.002. Pediatr Neurol. 2011. PMID: 21147392
Uncommon nucleotide excision repair phenotypes revealed by targeted high-throughput sequencing.
Calmels N, Greff G, Obringer C, Kempf N, Gasnier C, Tarabeux J, Miguet M, Baujat G, Bessis D, Bretones P, Cavau A, Digeon B, Doco-Fenzy M, Doray B, Feillet F, Gardeazabal J, Gener B, Julia S, Llano-Rivas I, Mazur A, Michot C, Renaldo-Robin F, Rossi M, Sabouraud P, Keren B, Depienne C, Muller J, Mandel JL, Laugel V. Calmels N, et al. Among authors: sabouraud p. Orphanet J Rare Dis. 2016 Mar 22;11:26. doi: 10.1186/s13023-016-0408-0. Orphanet J Rare Dis. 2016. PMID: 27004399 Free PMC article.
High-Throughput Digital Image Analysis Reveals Distinct Patterns of Dystrophin Expression in Dystrophinopathy Patients.
Torelli S, Scaglioni D, Sardone V, Ellis MJ, Domingos J, Jones A, Feng L, Chambers D, Eastwood DM, Leturcq F, Yaou RB, Urtizberea A, Sabouraud P, Barnerias C, Stojkovic T, Ricci E, Beuvin M, Bonne G, Sewry CA, Willis T, Kulshrestha R, Tasca G, Phadke R, Morgan JE, Muntoni F. Torelli S, et al. Among authors: sabouraud p. J Neuropathol Exp Neurol. 2021 Oct 26;80(10):955-965. doi: 10.1093/jnen/nlab088. J Neuropathol Exp Neurol. 2021. PMID: 34498054 Free PMC article.
Hereditary sensory neuropathy with spastic paraplegia.
Kherbaoui-Redouani L, Ploton D, Abely M, Bednarek N, Stourbe A, Sabouraud P, Motte J. Kherbaoui-Redouani L, et al. Among authors: sabouraud p. Eur J Paediatr Neurol. 2004;8(2):95-9. doi: 10.1016/j.ejpn.2003.12.006. Eur J Paediatr Neurol. 2004. PMID: 15253057
44 results