S-sulphocysteine, monosodium salt

 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1963-2015
02419632015

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2015
2015
BACKGROUND Molybdenum cofactor deficiency (MoCD) is characterised by early, rapidly progressive postnatal encephalopathy and… (More)
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2005
2005
We report a newborn with exaggerated startle reactions and stiffness of neonatal onset, the prototypical signs of hyperekplexia… (More)
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2005
2005
Molybdenum cofactor and isolated sulphite oxidase deficiencies are two related rare autosomal recessive diseases characterized by… (More)
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2005
2005
Isolated sulphite oxidase deficiency (ISOD) is a rare autosomal recessive inborn error of metabolism, which may present at birth… (More)
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Review
2002
Review
2002
Isolated sulphite oxidase deficiency (ISOD) is a very rare hereditary metabolic disorder. Imaging findings of the neonatal form… (More)
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2000
2000
We report an attempt at dietetic therapy in two unrelated patients with isolated sulphite oxidase deficiency, with a mild… (More)
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1998
1998
Comparison of the pharmacological effects of a range of sulphur-containing amino acids on human mGluR1alpha and mGluR5a has been… (More)
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1995
1995
Sulphite oxidase deficiency occurs in man in two forms, as the isolated deficiency and as a syndrome of combined molybdoenzyme… (More)
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1978
1978
A child is described who presented in the neonatal period with feeding difficulties, severe neurological abnormalities, lens… (More)
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1971
1971
Four components of O-acetylserine (OAS) sulphhydrylase with different molecular weights have been detected in extracts of… (More)
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