Titlebook: Inherited Disorders of Carbohydrate Metabolism; Monograph based upon D. Burman,J. B. Holton,C. A. Pennock Conference proceedings 1980 The S

LITHE

How long should galactosaemia be treated?Numerous recent publications on hereditary galactosaemia indicate that many problems still remain: too many late diagnosed patients; the question of whether population screening is necessary; the atypical cases of galactosaemia; and finally, another major dilemma, should treatment be lifelong or not?

Glossy

责任

buoyant

DAMP

Basic causes of carbohydrate malabsorptional source of metabolic energy. Defects in hydrolysis and/or absorption result in retention of residues within the intestinal tract, and gastrointestinal symptoms, i.e. carbohydrate or sugar ‘intolerance’. Sugar intolerance is a common clinical problem and may have serious consequences, particularly

预定

GEN

Clinical aspects of galactosaemianterdisciplinary approach to the treatment of children with inborn errors of metabolism. Early diagnosis and prompt treatment with a galactose-free diet can lead to excellent immediate results and a favourable long term prognosis. Mass neonatal screening constitutes an essential first step in reduci

Anemia

不自然

AORTA

Clinical and genetic studies of disorders in fructose metabolism has been used widely for clinical purposes as it has been claimed to be of advantage for diabetics, and for parenteral nutrition in adults and children. The latter use has remained controversial as many studies have indicated that for infusion therapy glucose is safest and cheapest.. The clinical a