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HCL hairy-cell leukemia; human cultured lymphoblasts
HCl hydrogen chloride
B6 pyridoxine
PDD pervasive developmental disorder; platinum diamminodichloride [cisplatin]; primary degenerative deme...
PNK polynucleotide kinase; pyridoxine kinase
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PN Pyridoxine
Apo Apomorphine HCl
HCL Hairy Cell Leukaemia
DPPE N,N-Diethyl-2-[4-(phenylmethyl) phenoxy]ethanamine.HCl
Gu.HCl guanidinium chloride
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pyridoxine <biochemistry> Member of the water soluble B vitamin group. Vitamin B6 or pyridoxine, is active in the metabolism of proteins, carbohydrates and fats. It is also a necessary part of haemoglobin synthesis. B6 deficiency results in retarded growth and a peripheral neuropathy.
(27 Sep 1997)
pyridoxine 4-dehydrogenase <enzyme> Chemical name: dehydrogenase, pyridoxol 4-
Registry number: EC 1.1.1.65
Synonym: pyridoxine phosphate dehydrogenase, pyridoxal reductase
(26 Jun 1999)
pyridoxine deficiency A nutritional condition produced by a deficiency of pyridoxine in the diet, characterised by dermatitis, glossitis, cheilosis, and stomatitis. Marked deficiency causes irritability, weakness, depression, dizziness, peripheral neuropathy, and seizures. In infants and children typical manifestations are diarrhoea, anaemia, and seizures. Increasingly recognised as a cause is prolonged therapy with certain medications, among them isoniazid, cycloserine, and l-dopa.
(12 Dec 1998)
pyridoxine dependency with seizure An inherited disorder (autosomal recessive) apparently associated with deficient brain type I glutamate decarboxylase; seizures can be controlled with vitamin B6.
(05 Mar 2000)
pyridoxine phosphate phosphatase <enzyme> Involved in metabolism of vitamin b(6)
Registry number: EC 3.1.3.-
Synonym: pyridoxal phosphate phosphatase, pyridoxamine phosphate phosphatase, pyridoxal-p hydrolase, pyridoxamine-p hydrolase, vitamin b(6)-phosphate phosphatase
(26 Jun 1999)
familial pyridoxine-responsive anaemia A rare autosomal recessive hereditary hypochromic anaemia; autosomal trait, responsive to pyridoxine.
(05 Mar 2000)
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