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82 results

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Page 1
[Experimental and pathological changes of the neuromuscular junction].
Koenig J, Bauché S, Ben Ammar A, Nicolle D, Rigoard P, Eymard B, Hantaï D. Koenig J, et al. Among authors: hantai d. Neurochirurgie. 2009 Mar;55 Suppl 1:S104-9. doi: 10.1016/j.neuchi.2008.05.008. Epub 2009 Feb 10. Neurochirurgie. 2009. PMID: 19211115 Review. French.
[Tools and techniques dedicated to neuromuscular junction observation].
Rigoard P, Buffenoir K, Bauche S, Fares M, Koenig J, Hantaï D, Giot JP, Seguin F, Huze C, Schaeffer L, Maixent JM. Rigoard P, et al. Among authors: hantai d. Neurochirurgie. 2009 Mar;55 Suppl 1:S43-8. doi: 10.1016/j.neuchi.2008.03.013. Epub 2009 Feb 18. Neurochirurgie. 2009. PMID: 19232651 Review. French.
[Morphological study of CNS lesions and the consequences on rat neuromuscular junction and peripheral nerve using confocal laser scanning microscopy and Koelle's technique].
Rigoard P, Buffenoir K, Chaillou M, Fares M, Da Costa L, Boildieu N, Seguin F, Lapierre F, Maixent JM, Bauche S, Koenig J, Hantaï D. Rigoard P, et al. Among authors: hantai d. Neurochirurgie. 2009 Mar;55 Suppl 1:S110-23. doi: 10.1016/j.neuchi.2008.05.009. Epub 2009 Feb 23. Neurochirurgie. 2009. PMID: 19233439 French.
Electrophysiological and morphological characterization of a case of autosomal recessive congenital myasthenic syndrome with acetylcholine receptor deficiency due to a N88K rapsyn homozygous mutation.
Yasaki E, Prioleau C, Barbier J, Richard P, Andreux F, Leroy JP, Dartevelle P, Koenig J, Molgó J, Fardeau M, Eymard B, Hantaï D. Yasaki E, et al. Among authors: hantai d. Neuromuscul Disord. 2004 Jan;14(1):24-32. doi: 10.1016/j.nmd.2003.07.002. Neuromuscul Disord. 2004. PMID: 14659409
Congenital myasthenic syndromes.
Hantaï D, Richard P, Koenig J, Eymard B. Hantaï D, et al. Curr Opin Neurol. 2004 Oct;17(5):539-51. doi: 10.1097/00019052-200410000-00004. Curr Opin Neurol. 2004. PMID: 15367858 Review.
[Pathophysiological characterization of congenital myasthenic syndromes: the example of mutations in the MUSK gene].
Chevessier F, Faraut B, Ravel-Chapuis A, Richard P, Gaudon K, Bauché S, Prioleau C, Herbst R, Goillot E, Ioos C, Azulay JP, Attarian S, Leroy JP, Fournier E, Legay C, Schaeffer L, Koenig J, Fardeau M, Eymard B, Pouget J, Hantaï D. Chevessier F, et al. Among authors: hantai d. J Soc Biol. 2005;199(1):61-77. doi: 10.1051/jbio:2005008. J Soc Biol. 2005. PMID: 16114265 French.
A mutation causes MuSK reduced sensitivity to agrin and congenital myasthenia.
Ben Ammar A, Soltanzadeh P, Bauché S, Richard P, Goillot E, Herbst R, Gaudon K, Huzé C, Schaeffer L, Yamanashi Y, Higuchi O, Taly A, Koenig J, Leroy JP, Hentati F, Najmabadi H, Kahrizi K, Ilkhani M, Fardeau M, Eymard B, Hantaï D. Ben Ammar A, et al. Among authors: hantai d. PLoS One. 2013;8(1):e53826. doi: 10.1371/journal.pone.0053826. Epub 2013 Jan 9. PLoS One. 2013. PMID: 23326516 Free PMC article.
Congenital myasthenic syndromes.
Eymard B, Hantaï D, Estournet B. Eymard B, et al. Among authors: hantai d. Handb Clin Neurol. 2013;113:1469-80. doi: 10.1016/B978-0-444-59565-2.00016-2. Handb Clin Neurol. 2013. PMID: 23622369 Review.
82 results