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INHERITED METABOLIC DISORDERS

INHERITED METABOLIC DISORDERS
遗传性代谢紊乱
批准号:
3849080
负责人:
J NEVIN ISENBERG
金额:
$0.0万
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:

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中文摘要
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英文摘要
Studies of infants who have a positive newborn screen of phenylalanine, methionine and galactose help identify classical and variant forms. This allows early identification and treatment. This protocol is to study the effect of early identification and treatment on the growth and development of these infants. Sibling and parents growth and cognitive development serve as controls.
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PANCREATIC REPLACEMENT THERAPY IN MALDIGESTION OF CYSTIC FIBROSIS--CIMETIDINE
INTRALUMINAL DIGESTIVE EVENTS IN CYSTIC FIBROSIS
PRONE REFLUX SLING TREATMENT EVALUATION FOR GASTROESOPHAGEAL REFLUX
VITAMIN E LIVER DISEASE