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	1.	Early diagnosis of vertebral osteomyelitis due to a rare pathogen: Haemophilus parainfluenzae. [electronic resource] by Beauvais, C Berenbaum, F Spentchian, M Prier, A Kaplan, G Producer: 19920610 In: The Journal of rheumatology vol. 19 Availability: No items available. Save to lists Add to cart (remove)
	2.	Time course of troponin I, myoglobulin, and cardiac enzyme release after electrical cardioversion. [electronic resource] by Georges, J L Spentchian, M Caubel, C Collignon, I Schwob, J Livarek, B Normand, J P Producer: 19961127 In: The American journal of cardiology vol. 78 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Molecular study of three cases of odontohypophosphatasia resulting from heterozygosity for mutations in the tissue non-specific alkaline phosphatase gene. [electronic resource] by Herasse, M Spentchian, M Taillandier, A Keppler-Noreuil, K Fliorito, A N M Bergoffen, J Wallerstein, R Muti, C Simon-Bouy, B Mornet, E Producer: 20031103 In: Journal of medical genetics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Rapid clinical improvement of peripheral artery occlusive disease symptoms after nilotinib discontinuation despite persisting vascular occlusion. [electronic resource] by Maurizot, A Beressi, J-P Manéglier, B de la Marre, N H Spentchian, M Soury, P Solvet-Sebire, P Collet-Gaudillat, C Baud, J-M Livarek, B Guilhot, F Rousselot, P Producer: 20150916 In: Blood cancer journal vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Trisomy 4, a new chromosomal abnormality in Waldenström's macroglobulinemia: a study of 39 cases. [electronic resource] by Terré, C Nguyen-Khac, F Barin, C Mozziconacci, M J Eclache, V Léonard, C Chapiro, E Farhat, H Bouyon, A Rousselot, P Choquet, S Spentchian, M Dubreuil, P Leblond, V Castaigne, S Producer: 20060927 In: Leukemia vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	High prevalence of ventricular repolarization abnormalities in people carrying TGFβR2 mutations. [electronic resource] by Extramiana, F Milleron, O Elbitar, S Uccellini, A Langeois, M Spentchian, M Delorme, G Arnoult, F Denjoy, I Bouleti, C Fressart, V Iserin, F Maison-Blanche, P Abifadel, M Leenhardt, A Boileau, C Jondeau, G Producer: 20191104 In: Scientific reports vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Severe hypophosphatasia: characterization of fifteen novel mutations in the ALPL gene. [electronic resource] by Spentchian, M Merrien, Y Herasse, M Dobbie, Z Gläser, D Holder, S E Ivarsson, S-A Kostiner, D Mansour, S Norman, A Roth, J Stipoljev, F Taillemite, J-L van der Smagt, J J Serre, J-L Simon-Bouy, B Taillandier, A Mornet, E Producer: 20030811 In: Human mutation vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)