AAAAAA
Results:
1-11
|
Results: 11
Authors:
Chigot, V
De Lonlay, P
Nassogne, MC
Laborde, K
Delagne, V
Fournet, JC
Nihoul-Fekete, C
Saudubray, JM
Brunelle, F
Citation: V. Chigot et al., Pancreatic arterial calcium stimulation in the diagnosis and localisation of persistent hyperinsulinemic hypoglycaemia of infancy, PEDIAT RAD, 31(9), 2001, pp. 650-655
Authors:
Nassogne, MC
Henrot, B
Aubert, G
Bonnier, C
Marie, S
Saint-Martin, C
Van den Berghe, G
Sebire, G
Vincent, MF
Citation: Mc. Nassogne et al., Adenylosuccinase deficiency: an unusual cause of early-onset epilepsy associated with acquired microcephaly, BRAIN DEVEL, 22(6), 2000, pp. 383-386
Authors:
Nassogne, MC
Henrot, B
Saint-Martin, C
Kadhim, H
Dobyns, WB
Sebire, G
Citation: Mc. Nassogne et al., Polymicrogyria and motor neuropathy in micro syndrome, NEUROPEDIAT, 31(4), 2000, pp. 218-221
Authors:
De Lonlay, P
Nassogne, MC
van Gennip, AH
van Cruchten, AC
de Villemeur, TB
Cretz, M
Stoll, C
Launay, JM
Steenberger-Spante, GCV
van den Heuvel, LPW
Wevers, RA
Saudubray, JM
Abeling, NGGM
Citation: P. De Lonlay et al., Tyrosine hydroxylase deficiency unresponsive to L-dopa treatment with unusual clinical and biochemical presentation, J INH MET D, 23(8), 2000, pp. 819-825
Authors:
Saudubray, JM
De Lonlay, P
Touati, G
Martin, D
Nassogne, MC
Castelnau, P
Sevin, C
Laborde, C
Baussan, C
Brivet, M
Vassault, A
Rabier, D
Bonnefont, JP
Kamoun, P
Citation: Jm. Saudubray et al., Genetic hypoglycaemia in infancy and childhood: Pathophysiology and diagnosis, J INH MET D, 23(3), 2000, pp. 197-214
Authors:
Libert, R
Van Hoof, F
Thillaye, M
Vincent, MF
Nassogne, MC
de Hoffmann, E
Schanck, A
Citation: R. Libert et al., Identification of undescribed medium-chain acylcarnitines present in urineof patients with propionic and methylmalonic acidemias, CLIN CHIM A, 295(1-2), 2000, pp. 87-96
Authors:
De Caluwe, D
Nassogne, MC
Reding, R
de Goyet, JD
Clapuyt, P
Otte, JB
Citation: D. De Caluwe et al., Cricopharyngeal achalasia: Case reports and review of the literature, EUR J PED S, 9(2), 1999, pp. 109-112
Authors:
Nassogne, MC
Baudhuin, P
Courtoy, PJ
Citation: Mc. Nassogne et al., Comparison of antigen contents in co-cultures by an in situ immunoradiometric assay, BIO CELL, 91(8), 1999, pp. 629-636
Authors:
del Campo, M
Hall, BD
Aeby, A
Nassogne, MC
Verloes, A
Roche, C
Gonzalez, C
Sanchez, H
Garcia-Alix, A
Cabanas, F
Escudero, RM
Hernandez, R
Quero, J
Citation: M. Del Campo et al., Albinism and agenesis of the corpus callosum with profound developmental delay: Vici syndrome, evidence for autosomal recessive inheritance, AM J MED G, 85(5), 1999, pp. 479-485
Authors:
Libert, R
Van Hoof, F
Thillaye, M
Vincent, MF
Nassogne, MC
Stroobant, V
de Hoffmann, E
Schanck, A
Citation: R. Libert et al., Identification of new medium-chain acylcarnitines present in urine of a patient with medium-chain acyl-CoA dehydrogenase deficiency, J INH MET D, 22(1), 1999, pp. 9-18
Authors:
Bonnier, C
Nassogne, MC
Evrard, P
Citation: C. Bonnier et al., Ketanserin treatment of Tourette's syndrome in children, AM J PSYCHI, 156(7), 1999, pp. 1122-1123
Risultati:
1-11
|