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Authors: STAUDT M WERMUTH B FREISINGER P HASSLER A PONTZ BF
Citation: M. Staudt et al., SYMPTOMATIC ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCY (POINT MUTATIONH202P) WITH NORMAL IN-VITRO ACTIVITY, Journal of inherited metabolic disease, 21(1), 1998, pp. 71-72

Authors: BAX RT HASSLER A LUCK W HEFTER H KRAGELOHMANN I NEUHAUS P EMMRICH P
Citation: Rt. Bax et al., CEREBRAL MANIFESTATION OF WILSONS-DISEASE SUCCESSFULLY TREATED WITH LIVER-TRANSPLANTATION, Neurology, 51(3), 1998, pp. 863-865

Authors: VONWALTER J WERNER R ROSEFELDT H HASSLER A EMMRICH P
Citation: J. Vonwalter et al., ECHOCARDIOGRAPHIC CHANGES IN PATIENTS WIT H ANOREXIA-NERVOSA, Monatsschrift fur Kinderheilkunde, 144(12), 1996, pp. 1342-1351
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