AAAAAA
Results:
1-8
|
Results: 8
Authors:
Biebermann, H
Schoneberg, T
Krude, H
Gudermann, T
Gruters, A
Citation: H. Biebermann et al., Constitutively activating TSH-receptor mutations as a molecular cause of non-autoimmune hyperthyroidism in childhood, LANG ARCH S, 385(6), 2000, pp. 390-392
Authors:
Netchine, I
Sobrier, ML
Krude, H
Schnabel, D
Maghnie, M
Marcos, E
Duriez, B
Cacheux, V
von Moers, A
Goossens, M
Gruters, A
Amselem, S
Citation: I. Netchine et al., Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency, NAT GENET, 25(2), 2000, pp. 182-186
Authors:
Krude, H
Gruters, A
Citation: H. Krude et A. Gruters, Implications of proopiomelanocortin (POMC) mutations in humans: The POMC deficiency syndrome, TRENDS ENDO, 11(1), 2000, pp. 15-22
Authors:
Kreissig, R
Amthauer, H
Krude, H
Steinmueller, P
Stroszczynski, C
Hosten, N
Grueters, A
Felix, R
Citation: R. Kreissig et al., The use of FDG-PET and CT for the staging of adrenocortical carcinoma in children, PEDIAT RAD, 30(5), 2000, pp. 306-306
Authors:
Krude, H
Biebermann, H
Schnabel, D
Ambrugger, P
Gruters, A
Citation: H. Krude et al., Molecular pathogenesis of neonatal hypothyroidism, HORMONE RES, 53, 2000, pp. 12-18
Authors:
Schnabel, D
L'Allemand, D
Krude, H
Keller, E
Gruters, A
Citation: D. Schnabel et al., Results of the newborn screening program for congenital adrenal hyperplasia in Berlin (1992-1999), MONATS KIND, 148(11), 2000, pp. 1006-1011
Authors:
L'Allemand, D
Tardy, V
Gruters, A
Schnabel, D
Krude, H
Morel, Y
Citation: D. L'Allemand et al., How a patient homozygous for a 30-kb deletion of the C4-CYP 21 genomic region can have a nonclassic form of 21-hydroxylase deficiency, J CLIN END, 85(12), 2000, pp. 4562-4567
Authors:
Gruters, A
Krude, H
Biebermann, H
Liesenkotter, K
Schoneberg, T
Gudermann, T
Citation: A. Gruters et al., Alterations of neonatal thyroid function, ACT PAEDIAT, 88, 1999, pp. 17-22
Risultati:
1-8
|