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Fits, pyridoxine, and hyperprolinaemia type II

Research output: Contribution to journalArticle

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Fits, pyridoxine, and hyperprolinaemia type II. / Walker, V.; Mills, Graham; Peters, S.; Merton, W.

In: Archives of Disease in Childhood, Vol. 82, No. 3, 03.2000, p. 236-237.

Research output: Contribution to journalArticle

Harvard

Walker, V, Mills, G, Peters, S & Merton, W 2000, 'Fits, pyridoxine, and hyperprolinaemia type II', Archives of Disease in Childhood, vol. 82, no. 3, pp. 236-237. https://doi.org/10.1136/adc.82.3.236

APA

Walker, V., Mills, G., Peters, S., & Merton, W. (2000). Fits, pyridoxine, and hyperprolinaemia type II. Archives of Disease in Childhood, 82(3), 236-237. https://doi.org/10.1136/adc.82.3.236

Vancouver

Walker V, Mills G, Peters S, Merton W. Fits, pyridoxine, and hyperprolinaemia type II. Archives of Disease in Childhood. 2000 Mar;82(3):236-237. https://doi.org/10.1136/adc.82.3.236

Author

Walker, V. ; Mills, Graham ; Peters, S. ; Merton, W. / Fits, pyridoxine, and hyperprolinaemia type II. In: Archives of Disease in Childhood. 2000 ; Vol. 82, No. 3. pp. 236-237.

Bibtex

@article{624e809e65bf47f897481b9c65d652dd,
title = "Fits, pyridoxine, and hyperprolinaemia type II",
abstract = "The rare inherited disorder hyperprolinaemia type II presents with fits in childhood, usually precipitated by infection. A diagnosis of hyperprolinaemia type II and vitamin B6 deficiency was made in a well nourished child with fits. It is thought that pyridoxine deficiency was implicated in her fits and was the result of inactivation of the vitamin by the proline metabolite, pyrroline-5-carboxylate.",
author = "V. Walker and Graham Mills and S. Peters and W. Merton",
year = "2000",
month = "3",
doi = "10.1136/adc.82.3.236",
language = "English",
volume = "82",
pages = "236--237",
journal = "Archives of Disease in Childhood",
issn = "0003-9888",
publisher = "BMJ Publishing Group",
number = "3",

}

RIS

TY - JOUR

T1 - Fits, pyridoxine, and hyperprolinaemia type II

AU - Walker, V.

AU - Mills, Graham

AU - Peters, S.

AU - Merton, W.

PY - 2000/3

Y1 - 2000/3

N2 - The rare inherited disorder hyperprolinaemia type II presents with fits in childhood, usually precipitated by infection. A diagnosis of hyperprolinaemia type II and vitamin B6 deficiency was made in a well nourished child with fits. It is thought that pyridoxine deficiency was implicated in her fits and was the result of inactivation of the vitamin by the proline metabolite, pyrroline-5-carboxylate.

AB - The rare inherited disorder hyperprolinaemia type II presents with fits in childhood, usually precipitated by infection. A diagnosis of hyperprolinaemia type II and vitamin B6 deficiency was made in a well nourished child with fits. It is thought that pyridoxine deficiency was implicated in her fits and was the result of inactivation of the vitamin by the proline metabolite, pyrroline-5-carboxylate.

U2 - 10.1136/adc.82.3.236

DO - 10.1136/adc.82.3.236

M3 - Article

VL - 82

SP - 236

EP - 237

JO - Archives of Disease in Childhood

JF - Archives of Disease in Childhood

SN - 0003-9888

IS - 3

ER -

ID: 246673