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528 results on '"F, Huet"'

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201. Efficient electroabsorption in InGaAsP/InGaAsP MQW optical waveguide

202. Interferometric-type polarisation splitter on Z-propagating LiNbO3:Ti

203. Etude de reactions de protolyse par des organometalliques du groupe II. Mecanisme de la reaction des dialkylcadmiums sur les alcools

204. Comportement nutritionnel du coureur de demi-fond. Aspects qualitatifs et quantitatifs. Rapports avec la dépense énergétique de l'entraînement

205. Formation d'enolates cetoniques par action d'organomagnesiens mixtes dans l'hexamethylphosphorotriamide sur des esters

206. Comparaison entre la protolyse du diméthylcadmium et celle d'un alcoolate mixte. Étude des équilibres et des réactions d'échange

207. L'isomérisation des acétates énoliques en série décalinique

208. Comparison of the limbic route and pars-plana route for phacophagy

209. Subhepatic neonatal appendicitis in premature babies: First case detected by ultrasound

211. [Spontaneous bilateral lens luxation]

218. [Therapeutic indications in Leber's disease]

225. [Heredofamilial megalocornea]

236. [Meyer-Schwickerath syndrome]

239. [The glaucoma of short-sighted young people (author's transl)]

240. [Antibiotic therapy in ophthalmology]

243. V-shaped defects connected to inversion domains in AlGaN layers

244. The microstructure and electrical properties of directly deposited TiN ohmic contacts to gallium nitride

245. Photoconductance measurements and Stokes shift in InGaN alloys

246. Understanding and modeling of thermal runaway events pertaining to new and aged Li-ion batteries

247. Genomic deletions of OFD1 account for 23% of oral-facial-digital type 1 syndrome after negative DNA sequencing

248. Feasibility and Safety of Post-Transcatheter Aortic Valve Replacement Coronary Revascularization Guided by Stress Cardiac Imaging.

249. Motor disorders related to oxaliplatin-induced peripheral neuropathy: long-term severity and impact on quality of life.

250. Further description of two individuals with de novo p.(Glu127Lys) missense variant in the ASCL1 gene.

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