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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
2024 1
2025 0

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42 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
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
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.
International retrospective natural history study of LMNA-related congenital muscular dystrophy.
Ben Yaou R, Yun P, Dabaj I, Norato G, Donkervoort S, Xiong H, Nascimento A, Maggi L, Sarkozy A, Monges S, Bertoli M, Komaki H, Mayer M, Mercuri E, Zanoteli E, Castiglioni C, Marini-Bettolo C, D'Amico A, Deconinck N, Desguerre I, Erazo-Torricelli R, Gurgel-Giannetti J, Ishiyama A, Kleinsteuber KS, Lagrue E, Laugel V, Mercier S, Messina S, Politano L, Ryan MM, Sabouraud P, Schara U, Siciliano G, Vercelli L, Voit T, Yoon G, Alvarez R, Muntoni F, Pierson TM, Gómez-Andrés D, Reghan Foley A, Quijano-Roy S, Bönnemann CG, Bonne G. Ben Yaou R, et al. Among authors: sabouraud p. Brain Commun. 2021 Apr 11;3(3):fcab075. doi: 10.1093/braincomms/fcab075. eCollection 2021 Jul. Brain Commun. 2021. PMID: 34240052 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.
[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.
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
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.
42 results