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Items: 5


Maple syrup urine disease: mechanisms and management.

Blackburn PR, Gass JM, Vairo FPE, Farnham KM, Atwal HK, Macklin S, Klee EW, Atwal PS.

Appl Clin Genet. 2017 Sep 6;10:57-66. doi: 10.2147/TACG.S125962. eCollection 2017. Review.


A Review of Selected Genes with Known Effects on Performance and Health of Cattle.

Casas E, Kehrli ME Jr.

Front Vet Sci. 2016 Dec 15;3:113. doi: 10.3389/fvets.2016.00113. eCollection 2016. Review.


Quality of life, psychological adjustment, and adaptive functioning of patients with intoxication-type inborn errors of metabolism - a systematic review.

Zeltner NA, Huemer M, Baumgartner MR, Landolt MA.

Orphanet J Rare Dis. 2014 Oct 25;9:159. doi: 10.1186/s13023-014-0159-8. Review.


Branched-chain amino acid metabolism: from rare Mendelian diseases to more common disorders.

Burrage LC, Nagamani SC, Campeau PM, Lee BH.

Hum Mol Genet. 2014 Sep 15;23(R1):R1-8. doi: 10.1093/hmg/ddu123. Epub 2014 Mar 20. Review.


Maple Syrup Urine Disease.

Strauss KA, Puffenberger EG, Morton DH.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Mefford HC, Stephens K, Amemiya A, Ledbetter N, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2017.
2006 Jan 30 [updated 2013 May 9].

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