Authors:
Moslinger, D
Stockler-Ipsiroglu, S
Scheibenreiter, S
Tiefenthaler, M
Muhl, A
Seidl, R
Strobl, W
Plecko, B
Suormala, T
Baumgartner, ER
Citation: D. Moslinger et al., Clinical and neuropsychological outcome in 33 patients with biotinidase deficiency ascertained by nationwide newborn screening and family studies in Austria, EUR J PED, 160(5), 2001, pp. 277-282
Authors:
Ipsiroglu, OS
Stromberger, C
Ilas, J
Hoger, H
Muhl, A
Stockler-Ipsiroglu, S
Citation: Os. Ipsiroglu et al., Changes of tissue creatine concentrations upon oral supplementation of creatine-monohydrate in various animal species, LIFE SCI, 69(15), 2001, pp. 1805-1815
Authors:
Item, CB
Stockler-Ipsiroglu, S
Stromberger, C
Muhl, A
Alessandri, MG
Bianchi, MC
Tosetti, M
Fornai, F
Cioni, G
Citation: Cb. Item et al., Arginine : glycine amidinotransferase deficiency: The third inborn error of creatine metabolism in humans, AM J HU GEN, 69(5), 2001, pp. 1127-1133
Citation: J. Ilas et al., Guanidinoacetate methyltransferase (GAMT) deficiency: non-invasive enzymatic diagnosis of a newly recognized inborn error of metabolism, CLIN CHIM A, 290(2), 2000, pp. 179-188
Authors:
Knoblauch, H
Muller-Myhsok, B
Busjahn, A
Ben Avi, L
Bahring, S
Baron, H
Heath, SC
Uhlmann, R
Faulhaber, HD
Shpitzen, S
Aydin, A
Reshef, A
Rosenthal, M
Eliav, O
Muhl, A
Lowe, A
Schurr, D
Harats, D
Jeschke, E
Friedlander, Y
Schuster, H
Luft, FC
Leitersdorf, E
Citation: H. Knoblauch et al., A cholesterol-lowering gene maps to chromosome 13q, AM J HU GEN, 66(1), 2000, pp. 157-166