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2. Retour d’expérience sur le pilotage des Réacteurs à Neutrons Rapides

3. Modélisation de l'amplification d'une impulsion laser UV nanoseconde dans un milieu à excimères

4. Deformed Core Reactivity Evaluation with Mesh Projection–Based Method

5. Développement d'un système laser XeCl nanoseconde de forte énergie (Résultats préliminaires)

6. SMALL VOLUME LONG PULSE X RAY PREIONISED XeCl LASER WITH DOUBLE DISCHARGE AND FAST FERRITE MAGNETIC SWITCH

7. RECENT PROGRESS AT IMFM ON EXCIMER LASERS AND THEIR APPLICATIONS

8. Excimer lasers in France

11. Interpretation of the Control Rod Withdrawal Test in the Sodium-Cooled Fast Reactor Phénix

12. Methodology for Designing a Sodium-Cooled Fast Reactor with Inherent Safety

13. Banded geckos, Gekko vittatus(Reptilia, Gekkonidae), as the main prey of barn owls (Tyto alba) on the Torres Islands (northern Vanuatu)

14. Neuromyelitis optica and pregnancy

17. Long-term follow-up of neuromyelitis optica with a pediatric onset(CME)

19. Neuromyelitis optica in France

21. The primary periodic paralyses: diagnosis, pathogenesis and treatment

22. Canaux ioniques dépendants du voltage et maladies neuromusculaires

24. A preliminary study on the social relationships in a semi-free ranging colony of sun-tailed monkeys (Cercopithecus solatus), a species recently discovered in gabon

25. Correlating multiple MRI parameters with clinical features: an attempt to define a new strategy in multiple sclerosis

26. Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A.

31. The humanCDC42gene: genomic organization, evidence for the existence of a putative pseudogene and exclusion as a SJS1 candidate gene

33. The human CDC42 gene: genomic organization, evidence for the existence of a putative pseudogene and exclusion as a SJS1 candidate gene

34. Coupled ocean-atmosphere surface variability and its climate impacts in the tropical Atlantic region

35. Familial factors influence disability in MS multiplex families

37. Novel mutations in the muscle chloride channel CLCN1gene causing myotonia congenita in Spanish families

38. Capillary zone electrophoresis: An additional technique for the identification of hemoglobin variants

39. Detection of the nicotinic acetylcholine receptor alpha‐subunit mRNA by in situ hybridization at neuromuscular junctions of 15‐day‐old chick striated muscles.

40. High repetition rate spiker-sustainer XeCl laser

42. Paramyotonia congenita: genotype to phenotype correlations in two families and report of a new mutation in the sodium channel gene

43. Quality assessment of whole genome mapping data in the refined familial spastic paraplegia interval on chromosome 14q.

44. A systematic study of oligodendrocyte growth factors as candidates for genetic susceptibility to MS

46. Recessive Schwartz-Jampel syndrome (SJS): confirmation of linkage to chromosome 1p, evidence of genetic homogeneity and reduction of the SJS locus to a 3-cM interval

48. Fourth meeting of the European Neurological Society 25–29 June 1994 Barcelona, Spain

49. Evolution of the relationship between near global and Atlantic SST modes and the rainy season in West Africa: statistical analyses and sensitivity experiments

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