Molecular Diseases. FEBS Federation of European Biochemical Societies: 12th Meeting, Dresden, 1978

Content: 
Proceedings of the 12th FEBS Meeting, Page ii
Front Matter, Page iii
Copyright, Page iv
Erratum, Page vii
PREFACE, Page vii, T. Schewe, S. Rapoport
MOLECULAR BASIS OF THE HEREDITARY DEFECTS OF ENZYME ACTIVITY, Pages 1-12, Axel Kahn, Jean-Claude Dreyfus
HAEMOLYTIC ANAEMIA IN PYRUVATE KINASE DEFICIENCY: POSSIBILITIES OF THERAPY, Pages 13-29, Gisela Jacobasch, Jürgen Schulz, Dimiter Zanev
MEMBRANE DESIALYLATION AND ELIMINATION OF ERYTHROCYTES, Pages 31-40, Roland Schauer
REACTIVE OXYGEN METABOLITES AND HEMOLYSIS, Pages 41-46, S.E. McMahon, A. Stern
RED BLOOD CELL MEMBRANE DEFECTS IN β THALASSEMIA AND THE THERAPEUTIC ROLE OF α-TOCOPHEROL (VITAMIN E), Pages 47-56, E.A. Rachmilewitz, A. Knyszynski, E. Skutelsky, A. Polliack, I. Kahane
HAEMOGLOBIN PRECIPITATION AND RED CELL HAEMOLYSIS, Pages 57-66, Robin W. Carrell, Christine C. Winterbourn
REVERSION OF HGPRT DEFICIENCY OF SKIN FIBROBLASTS FROM LESCH-NYHAN PATIENTS, Pages 67-78, Lieselotte Luebbe, Michael Strauss, Erhard Geissler
SUBSTITUTION THERAPY IN LYSOSOMAL STORAGE DISEASES, Pages 79-88, Brenda E. Ryman, Anne-Marie Seymour
INTRODUCTION OF ENZYMES INTO LIVER CELLS BY MEANS OF LIPOSOMES, Pages 89-98, F.H. ROERDINK, D. HOEKSTRA, J. DAMEN, G.L. SCHERPHOF, E. WISSE
AUTHOR INDEX, Page 99
SUBJECT INDEX, Pages 101-104