Your search returned 237 results.

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	161.	Primary hyperoxaluria type 1: the therapeutic dilemma. [electronic resource] by Cochat, P Deloraine, A Olive, F Rolland, M O Gillet, Y Divry, P Schärer, K Producer: 19951107 In: Advances in nephrology from the Necker Hospital vol. 24 Availability: No items available. Save to lists Add to cart (remove)
	162.	A 300 year history of lead contamination in northern French Alps reconstructed from distant lake sediment records. [electronic resource] by Arnaud, F Revel-Rolland, M Bosch, D Winiarski, T Desmet, M Tribovillard, N Givelet, N Producer: 20040920 In: Journal of environmental monitoring : JEM vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	163.	Comparison of red cell transfusion and polyethylene glycol-modified adenosine deaminase therapy in an adenosine deaminase-deficient child: measurement of erythrocyte deoxyadenosine triphosphate as a useful tool. [electronic resource] by Bory, C Boulieu, R Souillet, G Chantin, C Rolland, M O Mathieu, M Hershfield, M Producer: 19901011 In: Pediatric research vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	164.	[Partial monosomy 20q: a new syndrome. Regional assignment of the adenosine deaminase (ADA) locus on 20q132 (author's transl)]. [electronic resource] by Fraisse, J Bertheas, M F Frère, F Lauras, B Rolland, M O Brizard, C P Producer: 19820412 In: Annales de genetique vol. 24 Availability: No items available. Save to lists Add to cart (remove)
	165.	An intestinal obstruction in an eight-month-old child suffering from mevalonic aciduria. [electronic resource] by Nimubona, L Laloum, D Rolland, M O Read, M H Guillois, B Duhamel, J F Producer: 20030116 In: Acta paediatrica (Oslo, Norway : 1992) vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	166.	22q11 deletion in DGS/VCFS monozygotic twins with discordant phenotypes. [electronic resource] by Vincent, M C Heitz, F Tricoire, J Bourrouillou, G Kuhlein, E Rolland, M Calvas, P Producer: 19990804 In: Genetic counseling (Geneva, Switzerland) vol. 10 Availability: No items available. Save to lists Add to cart (remove)
	167.	Common resistance mechanisms to nucleoside analogues in variants of the human erythroleukemic line K562. [electronic resource] by Dumontet, C Bauchu, E C Fabianowska, K Lepoivre, M Wyczechowska, D Bodin, F Rolland, M O Producer: 19991104 In: Advances in experimental medicine and biology vol. 457 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	168.	Structure-directing weak phosphoryl XH...O=P (X = C, N) hydrogen bonds in cyclic oxazaphospholidines and oxazaphosphinanes. [electronic resource] by van der Lee, A Rolland, M Marat, X Virieux, D Volle, J N Pirat, J L Producer: 20080612 In: Acta crystallographica. Section B, Structural science vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	169.	Early prenatal diagnosis of propionic acidaemia with simultaneous sampling of chorionic villus and amniotic fluid. [electronic resource] by Rolland, M O Divry, P Mandon, G Guibaud, P Mathieu, M Sournies, G Thoulon, J M Producer: 19901212 In: Journal of inherited metabolic disease vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	170.	Synthesis and biological activity of 2-phenylethyl ester analogues of C-terminal heptapeptide of cholecystokinin modified in Trp 30 region. [electronic resource] by Rolland, M Rodriguez, M Lignon, M F Galas, M C Laur, J Aumelas, A Martinez, J Producer: 19920317 In: International journal of peptide and protein research vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	171.	[Systematic screening for congenital hypothyroidism by determination of TSH in dried blood samples: results of experience during a 21-month period]. [electronic resource] by David, M Dorche, C Rolland, M O Feit, J P Chopard, A Cotte, J Jeune, M Producer: 19790223 In: Pediatrie vol. 33 Availability: No items available. Save to lists Add to cart (remove)
	172.	[Neonatal intestinal obstruction due to congenital hypothyroidism (author's transl)]. [electronic resource] by Fries, F Lelong-Tissier, M C Rolland, M Robert, A Cau, D Rochiccioli, P Régnier, C Producer: 19801218 In: Archives francaises de pediatrie vol. 37 Availability: No items available. Save to lists Add to cart (remove)
	173.	[Congenital erythropoietic porphyria. Apropos of a fatal case in the neonatal period due to acute hemolysis with hepatic failure]. [electronic resource] by de Verneuil, H Moreau-Gaudry, F Ged, C Bensidhoum, M Hombrados, I Tricoire, J Rolland, M Producer: 19951031 In: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	174.	A new patient with 4-hydroxybutyric aciduria, a possible defect of 4-aminobutyrate metabolism. [electronic resource] by Divry, P Baltassat, P Rolland, M O Cotte, J Hermier, M Duran, M Wadman, S K Producer: 19830715 In: Clinica chimica acta; international journal of clinical chemistry vol. 129 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	175.	Synthesis and biological activities of some cholecystokinin analogues substituted in position 29 by a beta-alanine. [electronic resource] by Rodriguez, M Rolland, M Lignon, M F Galas, M C Laur, J Aumelas, A Martinez, J Producer: 19900306 In: International journal of peptide and protein research vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	176.	Isolated 3-methylcrotonyl-CoA carboxylase deficiency in a 16-month-old child. [electronic resource] by Rolland, M O Divry, P Zabot, M T Guibaud, P Gomez, S Lachaux, A Loras, I Producer: 19920310 In: Journal of inherited metabolic disease vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	177.	Recombinant human granulocyte colony-stimulating factor therapy for patients with neutropenia and/or neutrophil dysfunction secondary to glycogen storage disease type 1b. [electronic resource] by Calderwood, S Kilpatrick, L Douglas, S D Freedman, M Smith-Whitley, K Rolland, M Kurtzberg, J Producer: 20010315 In: Blood vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	178.	Neonatal hyperphenylalaninaemia presumably caused by a new variant of biopterin synthetase deficiency. [electronic resource] by Dhondt, J L Guibaud, P Rolland, M O Dorche, C Andre, S Forzy, G Hayte, J M Producer: 19880614 In: European journal of pediatrics vol. 147 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	179.	[Biotidinase deficiency: a disease with neurologic and cutaneous expression susceptible to biotin]. [electronic resource] by de Parscau, L Beaufrère, B Vianey-Liaud, C Rolland, M O Langue, J Divry, P Guibaud, P Producer: 19891128 In: Pediatrie vol. 44 Availability: No items available. Save to lists Add to cart (remove)
	180.	Juxta-centromeric region of human chromosome 21 is enriched for pseudogenes and gene fragments. [electronic resource] by Ruault, M Trichet, V Gimenez, S Boyle, S Gardiner, K Rolland, M Roizès, G De Sario, A Producer: 19991210 In: Gene vol. 239 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 237 results.