The clinical course of methylmalonic aciduria (MMA) is fulminant in neonates and emergency management is necessary to save lives. It is therefore very important to differentiate affected from unaffected neonates immediately when there are abnormal results regarding MMA in newborn screening. Methods: Between January 2002 and December 2008, 598,522 newborns were screened for MMA by 2 neonatal screening centers: the Chinese Foundation of Health and the Taipei Institute of Pathology. A total of 22 newborns were referred to confirmatory medical centers, and 7 were confirmed as having MMA. The initial propionylcarnitine (C3) level, C3/acetylcarnitine (C2) ratio, plasma ammonia, liver function tests, blood pH and bicarbonate were compared between ...
Methylmalonic acidemia caused by all L-Methylinalonyl-CoA mutase deficiency. The mut(0) type is asso...
Evidence for effectiveness of newborn screening (NBS) for propionic acidemia (PA) and isolated methy...
Background: Medium Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency is an autosomal recessive disorder...
BackgroundThe clinical course of methylmalonic aciduria (MMA) is fulminant in neonates and emergency...
Background: The clinical course of methylmalonic aciduria ( MMA) is fulminant in neonates and emerge...
A newborn screening pilot study using tandem mass spectrometry has been set up since 2003. To date m...
In Taiwan, during the period March 2000 to June 2009, 1,495, 132 neonates were screened for phenylke...
Background/Purpose: Neonatal screening using tandem mass spectrometry (MS /MS) started in Taiwan in ...
Methylmalonic aciduria is the most common disorder of organic acidurias in the mainland of China. It...
Background: Methylmalonic acidemia (MMA) incidence was evaluated based on newborn screening in Xuzho...
Methylmalonic acidemias, a group of heterogeneous dis-orders, are characterized by accumulation of m...
Neonatal screening using tandem mass spectrometry (MS/MS) started in Taiwan in 2000. We evaluated th...
Background: The expansion of newborn screening pro-grams has increased the number of newborns diag-n...
Background/PurposeNeonatal screening using tandem mass spectrometry (MS/MS) started in Taiwan in 200...
Background: The expansion of newborn screening pro-grams has increased the number of newborns diag-n...
Methylmalonic acidemia caused by all L-Methylinalonyl-CoA mutase deficiency. The mut(0) type is asso...
Evidence for effectiveness of newborn screening (NBS) for propionic acidemia (PA) and isolated methy...
Background: Medium Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency is an autosomal recessive disorder...
BackgroundThe clinical course of methylmalonic aciduria (MMA) is fulminant in neonates and emergency...
Background: The clinical course of methylmalonic aciduria ( MMA) is fulminant in neonates and emerge...
A newborn screening pilot study using tandem mass spectrometry has been set up since 2003. To date m...
In Taiwan, during the period March 2000 to June 2009, 1,495, 132 neonates were screened for phenylke...
Background/Purpose: Neonatal screening using tandem mass spectrometry (MS /MS) started in Taiwan in ...
Methylmalonic aciduria is the most common disorder of organic acidurias in the mainland of China. It...
Background: Methylmalonic acidemia (MMA) incidence was evaluated based on newborn screening in Xuzho...
Methylmalonic acidemias, a group of heterogeneous dis-orders, are characterized by accumulation of m...
Neonatal screening using tandem mass spectrometry (MS/MS) started in Taiwan in 2000. We evaluated th...
Background: The expansion of newborn screening pro-grams has increased the number of newborns diag-n...
Background/PurposeNeonatal screening using tandem mass spectrometry (MS/MS) started in Taiwan in 200...
Background: The expansion of newborn screening pro-grams has increased the number of newborns diag-n...
Methylmalonic acidemia caused by all L-Methylinalonyl-CoA mutase deficiency. The mut(0) type is asso...
Evidence for effectiveness of newborn screening (NBS) for propionic acidemia (PA) and isolated methy...
Background: Medium Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency is an autosomal recessive disorder...