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20 documents classés par :  date titre 1er auteur Type de documents Date de dépôt

1 - 2

Cold extends electromyography distinction between ion channel mutations causing myotonia. Fournier E., Viala K., Gervais H., Sternberg D., Arzel-Hézode M., Laforêt P., Eymard B., Tabti N., Willer J.-C., Vial C. et al Annals of Neurology 60, 3 (2006) 356-65 [hal-00272329 - version 1]

Evidence of a 2-day periodicity of striae formation in the tropical scallop Comptopallium radula using calcein marking Thébault J., Chauvaud L., Clavier J., Fichez R., Morize E. Marine Biology 149, 2 (2006) 257-267 [hal-00449282 - version 1]

In vivo and in vitro functional characterization of Andersen's syndrome mutations. Bendahhou S., Fournier E., Sternberg D., Bassez G., Furby A., Sereni C., Donaldson M. R., Larroque M.-M., Fontaine B., Barhanin J. The Journal of Physiology 565, Pt 3 (2005) 731-41 [hal-00272219 - version 1]

A1152D mutation of the Na+ channel causes paramyotonia congenita and emphasizes the role of DIII/S4-S5 linker in fast inactivation. Bouhours M., Luce S., Sternberg D., Willer J. C., Fontaine B., Tabti N. The Journal of Physiology 565, Pt 2 (2005) 415-27 [hal-00272247 - version 1]

First upper molar and mandible shape of wood mice (Apodemus sylvaticus) from northern Germany: ageing, habitat and insularity Renaud S. Mammalian Biology 70, 3 (2005) 157-170 [hal-00180844 - version 1]

Right spatial neglect after left hemisphere stroke: qualitative and quantitative study. Beis J.-M., Keller C., Morin N., Bartolomeo P., Bernati T., Chokron S., Leclercq M., Louis-Dreyfus A., Marchal F., Martin Y. et al Neurology 63, 9 (2004) 1600-5 [hal-00271980 - version 1]

Electromyography guides toward subgroups of mutations in muscle channelopathies. Fournier E., Arzel M., Sternberg D., Vicart S., Laforet P., Eymard B., Willer J.-C., Tabti N., Fontaine B. Annals of Neurology 56, 5 (2004) 650-61 [hal-00272130 - version 1]

Preserved auditory cognitive ERPs in severe akinetic mutism: a case report. Naccache L., Obadia M., Crozier S., Detante O., Guillerm C., Bonneville F., Dormont D., Willer J.-C., Samson Y. Cognitive Brain Researchearch / Brain Researchearch Cognitive Brain Researchearch 19, 2 (2004) 202-5 [hal-00272145 - version 1]

Functional characterization and cold sensitivity of T1313A, a new mutation of the skeletal muscle sodium channel causing paramyotonia congenita in humans. Bouhours M., Sternberg D., Davoine C.-S., Ferrer X., Willer J. C., Fontaine B., Tabti N. The Journal of Physiology 554, Pt 3 (2004) 635-47 [hal-00272125 - version 1]

Jaw transformation with gain of symmetry after Dlx5/Dlx6 inactivation: mirror of the past? Beverdam A., Merlo G. R., Paleari L., Mantero S., Genova F., Barbieri O., Janvier P., Levi G. genesis 34, 4 (2002) 221-7 [hal-00181141 - version 1]