Komrower Lecture: Abnormal cholesterol biosynthesis in sitosterolaemia and the Smith-Lemli-Opitz syndrome;
G. Salen, et al.
Genetic screening, testing and treatment: how far can we go?
C.R.
Scriver.
Somatic gene therapy for phenylketonuria and other hepatic deficiencies;
R.C. Eisensmith, S.L.C. Woo.
Ethical reflections concerning genetic services. A paradigm for the future?
C. Alonso.
Metabolic fuel utilization and pyruvate oxidation during the postnatal period;
J.M. Medina, et al.
Regulation and function of the mitochondrial genome;
S. Jeong-Yu, D.A. Clayton.
Disorders of pyruvate carboxylase and the pyruvate dehydrogenase complex;
B.H. Robinson, et
al.
Disorders of the electron transport chain;
P.L. Adams, D.M.
Turnbull.
Disorders of gluconeogenesis;
G. van den Berghe.
Metabolic intermediates in lactic acidosis: compounds, samples and interpretation;
F. Poggi-Travert, et al.
Mitochondrial encephalomyopathies: what next?
S. DiMauro.
Neurological presentations of mitochondrial diseases;
M. Zeviani, et al.
Clinical presentation of mitochondrial disorders in childhood;
A. Munnich, et al.
Morphological studies of skeletal muscle in lactic acidosis;
N.B. Romero, et al.
Magnetic resonance imaging in lactic acidosis;
M.S. van der Knaap, et
al.
The role of magnetic resonance spectroscopy in the investigation of lactic acidosis and inborn errors of energy metabolism;
D.G.
Gadian, J.V. Leonard.
Neuropathology and pathogenesis of mitochondrial diseases;
G.K. Brown, M.V. Squier.
The treatment of congenital lactic acidosis;
A.A.M. Morris, J.V. Leonard.
Genetic counselling and prenatal diagnosis in disorders of the mitochondrial energy metabolism;
W. Ruitenbeek, et al.
