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Glutamate formiminotransferase deficiency

Known as: FIGLU-Uria, FORMIMINOGLUTAMIC ACIDURIA, Formiminotransferase Deficiency 
 
National Institutes of Health

Papers overview

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2006
2006
Methylmalonic aciduria (MMA‐uria) is an autosomal recessive inborn error of amino acid metabolism, involving valine, threonine… Expand
Highly Cited
2004
Highly Cited
2004
The Common Guillemot Uria aalge is one of the most abundant seabird species in the North Atlantic. The diet delivered to the… Expand
2003
2003
Abstract Background : Orally administered betaine (Bet) is regarded as an effective and safe therapy for homocystinuria. However… Expand
1995
1995
A 49-year-old Woman was referred to the Renal Unit because of azotemia and fatigue. Two months earlier she had herpes zoster… Expand
1994
1994
Dicarboxylic aciduria (DCA‐uria) is a relatively common finding in the screening of organic acidemias by gas chromatography/mass… Expand
1987
1987
The effect of one single injection of two new bisphosphonates, 4-amino-1-hydroxybutylidene-1,1-bisphosphonate and 2-(2-pyridyl… Expand
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1966
1966
Summary Thirty-day-old rats were fed a magnesium-deficient diet for up to 34 days. There was a decrease in serum alkaline phos… Expand
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1966
1966
  • T. Arakawa, Y. Wada
  • The Tohoku journal of experimental medicine
  • 1966
  • Corpus ID: 19419584
Urinary excretion of AICA (4-amino-5-imidazolecarboxamide) following an oral dose of AICA was greater in amount in two cases with… Expand