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Results: 9

1.

The role of nitisinone in tyrosine pathway disorders.

Lock E, Ranganath LR, Timmis O.

Curr Rheumatol Rep. 2014 Nov;16(11):457. doi: 10.1007/s11926-014-0457-0. Review.

PMID:
25266991
2.

Tyrosinemia type 1: an overview of nursing care.

Barnby E.

Pediatr Nurs. 2014 Mar-Apr;40(2):61-8, 90. Review.

PMID:
24941508
3.

Recommendations for the management of tyrosinaemia type 1.

de Laet C, Dionisi-Vici C, Leonard JV, McKiernan P, Mitchell G, Monti L, de Baulny HO, Pintos-Morell G, Spiekerk├Âtter U.

Orphanet J Rare Dis. 2013 Jan 11;8:8. doi: 10.1186/1750-1172-8-8. Review.

4.

Hepatorenal tyrosinemia.

Kitagawa T.

Proc Jpn Acad Ser B Phys Biol Sci. 2012;88(5):192-200. Review.

5.

[Tandem mass spectrometry as screening for inborn errors of metabolism].

Campos H D.

Rev Med Chil. 2011 Oct;139(10):1356-64. doi: /S0034-98872011001000017. Epub 2012 Jan 3. Review. Spanish.

6.

Acute liver failure in children.

Devictor D, Tissieres P, Afanetti M, Debray D.

Clin Res Hepatol Gastroenterol. 2011 Jun;35(6-7):430-7. doi: 10.1016/j.clinre.2011.03.005. Epub 2011 Apr 30. Review.

PMID:
21531191
7.

Novel techniques and newer markers for the evaluation of "proximal tubular dysfunction".

Ludwig M, Sethi SK.

Int Urol Nephrol. 2011 Dec;43(4):1107-15. doi: 10.1007/s11255-011-9914-0. Epub 2011 Mar 1. Review.

PMID:
21360162
8.

Hypermethioninemias of genetic and non-genetic origin: A review.

Mudd SH.

Am J Med Genet C Semin Med Genet. 2011 Feb 15;157C(1):3-32. doi: 10.1002/ajmg.c.30293. Epub 2011 Feb 9. Review.

PMID:
21308989
9.

Liver transplantation for inherited metabolic disorders of the liver.

Moini M, Mistry P, Schilsky ML.

Curr Opin Organ Transplant. 2010 Jun;15(3):269-76. doi: 10.1097/MOT.0b013e3283399dbd. Review.

PMID:
20489626
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