BREATH GAS ANALYSIS IN PATIENTS SUFFERING FROM PROPIONIC ACIDAEMIA

[1]  T. Suormala,et al.  Propionic acidaemia: clinical, biochemical and therapeutic aspects , 2005, European Journal of Pediatrics.

[2]  T. Suormala,et al.  The gene coding for the α-chain of human propionyl-CoA carboxylase maps to chromosome band 13q32 , 1990, Human Genetics.

[3]  R. Urbanek,et al.  Excretion of 2-methyl-3-oxovaleric acid in propionic acidemia , 1978, European Journal of Pediatrics.

[4]  J. Müller,et al.  Perzentile für den Body-mass-Index für das Kindes- und Jugendalter unter Heranziehung verschiedener deutscher Stichproben , 2001, Monatsschrift Kinderheilkunde.

[5]  H. Doderer Die Merowinger oder Die totale Familie. , 2000 .

[6]  P R Evans,et al.  Conformational changes on substrate binding to methylmalonyl CoA mutase and new insights into the free radical mechanism. , 1998, Structure.

[7]  J. Leonard Stable isotope studies in propionic and methylmalonic acidaemia , 1997, European Journal of Pediatrics.

[8]  W. Sperl,et al.  [Metabolic disorders of branched-chain amino acids: most common forms of organic aciduria in the neonatal period]. , 1990, Klinische Padiatrie.

[9]  H. Willard,et al.  Isolation of cDNA clones coding for the alpha and beta chains of human propionyl-CoA carboxylase: chromosomal assignments and DNA polymorphisms associated with PCCA and PCCB genes. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[10]  J. Rétey,et al.  On the mechanism of action of methylmalonyl-CoA mutase. Change of the steric course on isotope substitution. , 1986, European journal of biochemistry.

[11]  U. Francke,et al.  Cloning and screening with nanogram amounts of immunopurified mRNAs: cDNA cloning and chromosomal mapping of cystathionine beta-synthase and the beta subunit of propionyl-CoA carboxylase. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[12]  D. Harris,et al.  Propionic acidemia: a clinical update. , 1981, The Journal of pediatrics.

[13]  J. Menkes Idiopathic hyperglycinemia: isolation and identification of three previously undescribed urinary ketones. , 1966, The Journal of pediatrics.