Zobrazeno 1 - 10 of 189 pro vyhledávání: '"D. Hantaï"'
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[Congenital myasthenic syndromes: difficulties in the diagnosis, course and prognosis, and therapy--The French National Congenital Myasthenic Syndrome Network experience]
Autor: B, Eymard, T, Stojkovic, D, Sternberg, P, Richard, S, Nicole, E, Fournier, A, Béhin, P, Laforêt, L, Servais, N, Romero, M, Fardeau, D, Hantaï, C, Mignard
Publikováno v: Revue neurologique. 169
Congenital myasthenic syndromes (CMS) are a heterogeneous group of disorders caused by genetic defects affecting neuromuscular transmission and leading to muscle weakness accentuated by exertion. Three different aspects have been investigated by memb
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::010bdbfbc6fd8e95ff577204a31846ee
https://pubmed.ncbi.nlm.nih.gov/23452772
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3
[Morphological study of CNS lesions and the consequences on rat neuromuscular junction and peripheral nerve using confocal laser scanning microscopy and Koelle's technique]
Autor: P, Rigoard, K, Buffenoir, M, Chaillou, M, Fares, L, Da Costa, N, Boildieu, F, Seguin, F, Lapierre, J-M, Maixent, S, Bauche, J, Koenig, D, Hantaï
Publikováno v: Neuro-Chirurgie. 55
In humans, it is currently believed that peripheral nerves remain intact after central nervous system (CNS) injuries. This should lead us to observe a lack of amyotrophy in the peripheral projection areas of CNS damage. Nevertheless, the appearance o
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b2a5590aff2ab3e325c332f626728ab0
https://pubmed.ncbi.nlm.nih.gov/19233439
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4
[Experimental and pathological changes of the neuromuscular junction]
Autor: J, Koenig, S, Bauché, A, Ben Ammar, D, Nicolle, P, Rigoard, B, Eymard, D, Hantaï
Publikováno v: Neuro-Chirurgie. 55
The objective of our study was to investigate the cellular communication between the axon and its postsynaptic targets in the synapse. We used the neuromuscular junction (NMJ) model, which is a highly specialized structure between the nerve, the musc
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::c2699782334267a607e681c1d42055b4
https://pubmed.ncbi.nlm.nih.gov/19211115
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5
[Tools and techniques dedicated to neuromuscular junction observation]
Autor: P, Rigoard, K, Buffenoir, S, Bauche, M, Fares, J, Koenig, D, Hantaï, J-P, Giot, F, Seguin, C, Huze, L, Schaeffer, J-M, Maixent
Publikováno v: Neuro-Chirurgie. 55
A few decades ago, the neuromuscular junction (NMJ) concept was reduced to two elements: the nerve ending and the facing muscular zone. This description has since changed substantially based on recent studies conducted on the molecular aspects of neu
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::4474c53d11c456bf83bce87b38b7c6a1
https://pubmed.ncbi.nlm.nih.gov/19232651
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6
[Structural and molecular organization, development and maturation of the neuromuscular junction]
Autor: P, Rigoard, K, Buffenoir, S, Bauche, J-P, Giot, J, Koenig, D, Hantaï, F, Lapierre, M, Wager
Publikováno v: Neuro-Chirurgie. 55
The neuromuscular junction is made up of the apposition of highly differentiated domains of three types of cell: the motor neuronal ending, the terminal Schwann cell and the muscle postsynaptic membrane. These three components are surrounded by a bas
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::72e106079dafe4c7e3edc4b858b9f26a
https://pubmed.ncbi.nlm.nih.gov/19233436
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7
[Congenital myasthenic syndromes due to mutations in the rapsyn gene]
Autor: B, Eymard, C, Ioos, A, Barois, B, Estournet, M, Mayer, E, Fournier, E, Yasaki, C, Prioleau, S, Bauché, K, Gaudon, J P, Leroy, J, Koenig, P, Richard, D, Hantaï
Publikováno v: Revue neurologique. 160(5 Pt 2)
Congenital myasthenic syndromes (CMS) are genetic diseases characterized by dysfunctional neuromuscular transmission and usually start during the neonatal period. Most are due to postsynaptic abnormalities, specifically to mutations in the acetylchol
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::37f2bf7527b13bbff6e3f4756695fc07
https://pubmed.ncbi.nlm.nih.gov/15269664
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8
[Congenital myasthenic syndromes: phenotypic expression and pathophysiological characterisation]
Autor: F, Andreux, D, Hantaï, B, Eymard
Publikováno v: Revue neurologique. 160(2)
Congenital Myasthenic Syndromes (CMS) are a heterogeneous group of diseases caused by genetic defects affecting neuromuscular transmission. The twenty five past Years saw major advances in identifying different types of CMS due to abnormal presynapti
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::c609362860597820e72400203a88bda6
https://pubmed.ncbi.nlm.nih.gov/15034473
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10
Protease nexin I expression is up-regulated in human skeletal muscle by injury-related factors
Autor: C, Mbebi, D, Hantaï, M, Jandrot-Perrus, M A, Doyennette, M, Verdière-Sahuqué
Publikováno v: Journal of cellular physiology. 179(3)
Protease nexin I is a 43-50 kDa glycoprotein capable of inhibiting a number of serine proteases. In cultured differentiated human skeletal muscle (myotubes), we previously found that protease nexin I was localized in patches at their surface where it
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ae63a03ab8f7a83d74b35010c67ef387
https://pubmed.ncbi.nlm.nih.gov/10228949
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