Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 6

1.

Epilepsy in biotinidase deficiency after biotin treatment.

Micó SI, Jiménez RD, Salcedo EM, Martínez HA, Mira AP, Fernández CC.

JIMD Rep. 2012;4:75-8. doi: 10.1007/8904_2011_74. Epub 2011 Nov 4.

2.

Multiple carboxylase deficiency: inherited and acquired disorders of biotin metabolism.

Baumgartner ER, Suormala T.

Int J Vitam Nutr Res. 1997;67(5):377-84. Review.

PMID:
9350481
3.

The neurology of biotinidase deficiency.

Wolf B.

Mol Genet Metab. 2011 Sep-Oct;104(1-2):27-34. doi: 10.1016/j.ymgme.2011.06.001. Epub 2011 Jun 12. Review.

PMID:
21696988
4.

Biotinidase deficiency: "if you have to have an inherited metabolic disease, this is the one to have".

Wolf B.

Genet Med. 2012 Jun;14(6):565-75. doi: 10.1038/gim.2011.6. Epub 2012 Jan 5. Review.

PMID:
22241090
5.

[Multiple carboxylase deficiency].

Andersen JB, Haagerup A, Christensen E.

Ugeskr Laeger. 1998 Feb 16;160(8):1151-7. Review. Danish.

PMID:
9492625
6.

Adolescence/adult onset MTHFR deficiency may manifest as isolated and treatable distinct neuro-psychiatric syndromes.

Gales A, Masingue M, Millecamps S, Giraudier S, Grosliere L, Adam C, Salim C, Navarro V, Nadjar Y.

Orphanet J Rare Dis. 2018 Feb 1;13(1):29. doi: 10.1186/s13023-018-0767-9. Review.

Supplemental Content

Support Center