AAAAAA
Results:
1-16
|
Results: 16
Authors:
Garel, L
Dubois, J
Grignon, A
Filiatrault, D
Van Vliet, G
Citation: L. Garel et al., US of the pediatric female pelvis: A clinical perspective, RADIOGRAPHI, 21(6), 2001, pp. 1393-1407
Authors:
Van Vliet, G
Citation: G. Van Vliet, Treatment of congenital hypothyroidism, LANCET, 358(9276), 2001, pp. 86-87
Authors:
Mircescu, H
Wilkin, F
Paquette, J
Oligny, LL
Decaluwe, H
Gaboury, L
Nolet, S
Van Vliet, G
Deal, C
Citation: H. Mircescu et al., Molecular characterization of a pediatric pheochromocytoma with suspected bilateral disease, J PEDIAT, 138(2), 2001, pp. 269-273
Authors:
Heinrichs, C
Parma, J
Scherberg, NH
Delange, F
Van Vliet, G
Duprez, L
Bourdoux, P
Bergmann, P
Vassart, G
Refetoff, S
Citation: C. Heinrichs et al., Congenital central isolated hypothyroidism caused by a homozygous mutationin the TSH-beta subunit gene, THYROID, 10(5), 2000, pp. 387-391
Authors:
Simard, J
Ricketts, AL
Moisan, AM
Tardy, V
Peter, M
Van Vliet, G
Morel, Y
Citation: J. Simard et al., A new insight into the molecular basis of 3 beta-hydroxysteroid dehydrogenase deficiency, ENDOCRINE R, 26(4), 2000, pp. 761-770
Authors:
Mircescu, H
Parma, J
Huot, C
Deal, C
Oligny, LL
Vassart, G
Van Vliet, G
Citation: H. Mircescu et al., Hyperfunctioning malignant thyroid nodule in an 11-year-old girl: Pathologic and molecular studies, J PEDIAT, 137(4), 2000, pp. 585-587
Authors:
Alos, N
Moisan, AM
Ward, L
Desrochers, M
Legault, L
Leboeuf, G
Van Vliet, G
Simard, J
Citation: N. Alos et al., A novel A10E homozygous mutation in the HSD3B2 gene causing severe salt-wasting 3 beta-hydroxysteroid dehydrogenase deficiency in 46,XX and 46,XY French-Canadians: Evaluation of gonadal function after puberty, J CLIN END, 85(5), 2000, pp. 1968-1974
Authors:
Van Vliet, G
Citation: G. Van Vliet, Neonatal hypothyroidism: Treatment and outcome, THYROID, 9(1), 1999, pp. 79-84
Authors:
Van Ginneken, VJT
Van den Thillart, GEEJM
Muller, HJ
Van Deursen, S
Onderwater, M
Visee, J
Hopmans, V
Van Vliet, G
Nicolay, K
Citation: Vjt. Van Ginneken et al., Phosphorylation state of red and white muscle in tilapia during graded hypoxia: an in vivo P-31-NMR study, AM J P-REG, 277(5), 1999, pp. R1501-R1512
Authors:
Ward, L
Huot, C
Lambert, R
Deal, C
Collu, R
Van Vliet, G
Citation: L. Ward et al., Outcome of pediatric Graves' disease after treatment with antithyroid medication and radioiodine, CLIN INV M, 22(4), 1999, pp. 132-139
Authors:
Taback, SP
Guyda, HJ
Van Vliet, G
Citation: Sp. Taback et al., Pharmacological manipulation of height: qualitative review of study populations and designs, CLIN INV M, 22(2), 1999, pp. 53-59
Authors:
Groenendaal, F
De Graaf, RA
Van Vliet, G
Nicolay, K
Citation: F. Groenendaal et al., Effects of hypoxia-ischemia and inhibition of nitric oxide synthase on cerebral energy metabolism in newborn piglets, PEDIAT RES, 45(6), 1999, pp. 827-833
Authors:
Devos, H
Rodd, C
Gagne, N
Laframboise, R
Van Vliet, G
Citation: H. Devos et al., A search for the possible molecular mechanisms of thyroid dysgenesis: Sex ratios and associated malformations, J CLIN END, 84(7), 1999, pp. 2502-2506
Authors:
Taback, SP
Van Vliet, G
Citation: Sp. Taback et G. Van Vliet, Managing the short stature of Turner syndrome: An evidence-based approach to the suggestion of growth hormone supplementation, ENDOCR DEV, 1, 1999, pp. 102-117
Authors:
de Zegher, F
Francois, I
Boehmer, ALM
Saggese, G
Muller, J
Hiort, O
Sultan, C
Clayton, P
Brauner, R
Cacciari, E
Ibanez, L
Van Vliet, G
Tiulpakov, A
Saka, N
Ritzen, M
Sippell, WG
Citation: F. De Zegher et al., Androgens and fetal growth, HORMONE RES, 50(4), 1998, pp. 243-244
Authors:
Van Vliet, G
Deal, C
Citation: G. Van Vliet et C. Deal, Growth hormone supplementation in Turner's syndrome, J PEDIAT, 133(6), 1998, pp. 803-803
Risultati:
1-16
|