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

Year Number of Results
1997 1
1999 1
2001 1
2004 1
2005 4
2006 2
2007 4
2008 4
2009 5
2010 9
2011 7
2012 7
2013 3
2014 1
2015 2
2024 0

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43 results

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Page 1
The TREAT-NMD DMD Global Database: analysis of more than 7,000 Duchenne muscular dystrophy mutations.
Bladen CL, Salgado D, Monges S, Foncuberta ME, Kekou K, Kosma K, Dawkins H, Lamont L, Roy AJ, Chamova T, Guergueltcheva V, Chan S, Korngut L, Campbell C, Dai Y, Wang J, Barišić N, Brabec P, Lahdetie J, Walter MC, Schreiber-Katz O, Karcagi V, Garami M, Viswanathan V, Bayat F, Buccella F, Kimura E, Koeks Z, van den Bergen JC, Rodrigues M, Roxburgh R, Lusakowska A, Kostera-Pruszczyk A, Zimowski J, Santos R, Neagu E, Artemieva S, Rasic VM, Vojinovic D, Posada M, Bloetzer C, Jeannet PY, Joncourt F, Díaz-Manera J, Gallardo E, Karaduman AA, Topaloğlu H, El Sherif R, Stringer A, Shatillo AV, Martin AS, Peay HL, Bellgard MI, Kirschner J, Flanigan KM, Straub V, Bushby K, Verschuuren J, Aartsma-Rus A, Béroud C, Lochmüller H. Bladen CL, et al. Among authors: jeannet py. Hum Mutat. 2015 Apr;36(4):395-402. doi: 10.1002/humu.22758. Epub 2015 Mar 17. Hum Mutat. 2015. PMID: 25604253 Free PMC article.
[Pediatrics].
Fanconi S, Giannoni E, Roth-Kleiner M, Pittet I, Suris JC, Spehrs-Ciaffi V, Jeannet PY, Hafen GM. Fanconi S, et al. Among authors: jeannet py. Rev Med Suisse. 2009 Jan 7;5(185):53-8. Rev Med Suisse. 2009. PMID: 19216326 French.
[Pediatrics].
Fanconi S, Reinberg O, Gapany C, Meyrat BJ, Frey P, Vaudaux B, Di Bernardo S, Boulos T, Sekarski N, Spehrs-Ciaffi V, Jeannet PY. Fanconi S, et al. Among authors: jeannet py. Rev Med Suisse. 2008 Jan 9;4(139):61-6. Rev Med Suisse. 2008. PMID: 18251218 Review. French.
Clinical and histologic findings in autosomal centronuclear myopathy.
Jeannet PY, Bassez G, Eymard B, Laforêt P, Urtizberea JA, Rouche A, Guicheney P, Fardeau M, Romero NB. Jeannet PY, et al. Neurology. 2004 May 11;62(9):1484-90. doi: 10.1212/01.wnl.0000124388.67003.56. Neurology. 2004. PMID: 15136669 Review.
Orofacial dysfunction in Duchenne muscular dystrophy.
Botteron S, Verdebout CM, Jeannet PY, Kiliaridis S. Botteron S, et al. Among authors: jeannet py. Arch Oral Biol. 2009 Jan;54(1):26-31. doi: 10.1016/j.archoralbio.2008.07.012. Epub 2008 Sep 20. Arch Oral Biol. 2009. PMID: 18805518
Cerebral sinus venous thrombosis in Swiss children.
Grunt S, Wingeier K, Wehrli E, Boltshauser E, Capone A, Fluss J, Gubser-Mercati D, Jeannet PY, Keller E, Marcoz JP, Schmitt-Mechelke T, Weber P, Weissert M, Steinlin M; Swiss Neuropaediatric Stroke Registry. Grunt S, et al. Among authors: jeannet py. Dev Med Child Neurol. 2010 Dec;52(12):1145-50. doi: 10.1111/j.1469-8749.2010.03722.x. Dev Med Child Neurol. 2010. PMID: 20573178 Free article.
Sleep disorders in boys with Duchenne muscular dystrophy.
Bloetzer C, Jeannet PY, Lynch B, Newman CJ. Bloetzer C, et al. Among authors: jeannet py. Acta Paediatr. 2012 Dec;101(12):1265-9. doi: 10.1111/apa.12025. Epub 2012 Oct 8. Acta Paediatr. 2012. PMID: 23013479
Acute ischemic stroke in children versus young adults.
Bigi S, Fischer U, Wehrli E, Mattle HP, Boltshauser E, Bürki S, Jeannet PY, Fluss J, Weber P, Nedeltchev K, El-Koussy M, Steinlin M, Arnold M. Bigi S, et al. Among authors: jeannet py. Ann Neurol. 2011 Aug;70(2):245-54. doi: 10.1002/ana.22427. Ann Neurol. 2011. PMID: 21823153
Cerebellar cleft: confirmation of the neuroimaging pattern.
Poretti A, Huisman TA, Cowan FM, Del Giudice E, Jeannet PY, Prayer D, Rutherford MA, du Plessis AJ, Limperopoulos C, Boltshauser E. Poretti A, et al. Among authors: jeannet py. Neuropediatrics. 2009 Oct;40(5):228-33. doi: 10.1055/s-0030-1248265. Epub 2010 Mar 10. Neuropediatrics. 2009. PMID: 20221959
Mutations in dynamin 2 cause dominant centronuclear myopathy.
Bitoun M, Maugenre S, Jeannet PY, Lacène E, Ferrer X, Laforêt P, Martin JJ, Laporte J, Lochmüller H, Beggs AH, Fardeau M, Eymard B, Romero NB, Guicheney P. Bitoun M, et al. Among authors: jeannet py. Nat Genet. 2005 Nov;37(11):1207-9. doi: 10.1038/ng1657. Epub 2005 Oct 16. Nat Genet. 2005. PMID: 16227997 Free article.
43 results