Long-term results of selective screening for inborn errors of metabolism

Author:

Lehnert Willy

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Reference8 articles.

1. Coulombe JT, Shih VE, Levy HL (1981) Massachusetts metabolic disorders screening program. II. Methylmalonic aciduria. Pediatrics 67:26–31

2. Hayasaka K, Tada K, Fueki N, Aikawa J (1990) Prenatal diagnosis of nonketotic hyperglycinemia: Enzymatic analysis of the glycine cleavage system in chorionic villi. J Pediatr 116: 444–445

3. Kolvraa S, Gregersen N, Christensen E, Lundemose JB, Blakemore AIF, Curtis D, Bolund L (1991) Studies of the association between a specific genetic background and the most common mutation causing MCAD deficiency (G985). Second International Symposium on Clinical, Biochemical, and Molecular Aspects of Fatty Acid Oxidation. Philadelphia, Pennsylvania

4. Lehnert W, Niederhoff H (1984) Seven years of experience with selective screening for organic acidurias. Eur J Pediatr 142:208–210

5. Lehnert W, Schuchmann L, Urbánek R, Niederhoff H, Böhm N (1978) Excretion of 2-methyl-3-oxovaleric acid in propionic acidemia. Eur J Pediatr 128:197–205

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