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Results: 1-3 |
Results: 3
Late-onset ornithine transcarbamylase deficiency in two families with different mutations in the same codon
Authors: Ploechl, E Ploechl, W Stoeckler-Ipsiroglu, S Pokorny, H Wermuth, B
Citation: E. Ploechl et al., Late-onset ornithine transcarbamylase deficiency in two families with different mutations in the same codon, CLIN GENET, 59(2), 2001, pp. 111-114
Budd-Chiari syndrome associated with coagulation abnormalities in a child with carbohydrate deficient glycoprotein syndrome type Ix
Authors: Huemer, M Huber, WD Schima, W Moeslinger, D Holzbach, U Wevers, R Wank, H Stoeckler-Ipsiroglu, S
Citation: M. Huemer et al., Budd-Chiari syndrome associated with coagulation abnormalities in a child with carbohydrate deficient glycoprotein syndrome type Ix, J PEDIAT, 136(5), 2000, pp. 691-695
Cerebral Doppler sonography of the neonate - A resume after 20 years and future aspects
Authors: Ipsiroglu, OS Eichler, F Stoeckler-Ipsiroglu, S
Citation: Os. Ipsiroglu et al., Cerebral Doppler sonography of the neonate - A resume after 20 years and future aspects, CLIN PERIN, 26(4), 1999, pp. 905
Risultati: 1-3 |