Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 38

Related Articles by Review for PubMed (Select 16602095)

1.

The genetic tyrosinemias.

Scott CR.

Am J Med Genet C Semin Med Genet. 2006 May 15;142C(2):121-6. Review.

PMID:
16602095
2.

Tyrosinemia Type I.

Sniderman King L, Trahms C, Scott CR.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Dolan CR, Fong CT, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2015.
2006 Jul 24 [updated 2014 Jul 17].

3.

Hereditary tyrosinemia type I--an overview.

Kvittingen EA.

Scand J Clin Lab Invest Suppl. 1986;184:27-34. Review.

PMID:
3296130
4.

The pathophysiology and treatment of hereditary tyrosinemia type 1.

Grompe M.

Semin Liver Dis. 2001 Nov;21(4):563-71. Review.

PMID:
11745044
5.

Animal models reveal pathophysiologies of tyrosinemias.

Endo F, Tanaka Y, Tomoeda K, Tanoue A, Tsujimoto G, Nakamura K.

J Nutr. 2003 Jun;133(6 Suppl 1):2063S-2067S. Review.

6.

Hepatorenal tyrosinemia.

Kitagawa T.

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

7.

Hereditary tyrosinaemia type I: from basics to progress in treatment.

Pitkänen ST, Salo MK, Heikinheimo M.

Ann Med. 2000 Nov;32(8):530-8. Review.

PMID:
11127930
8.

Animal models of tyrosinemia.

Nakamura K, Tanaka Y, Mitsubuchi H, Endo F.

J Nutr. 2007 Jun;137(6 Suppl 1):1556S-1560S; discussion 1573S-1575S. Review.

9.

Tyrosinemia: the Quebec experience.

Paradis K.

Clin Invest Med. 1996 Oct;19(5):311-6. Review.

PMID:
8889268
10.

Tyrosinemia II: lessons in molecular pathophysiology.

Goldsmith LA.

Pediatr Dermatol. 1983 Jul;1(1):25-34. Review.

PMID:
6149527
11.

Richner-Hanhart syndrome (tyrosinemia type II). Case report and literature review.

al-Hemidan AI, al-Hazzaa SA.

Ophthalmic Genet. 1995 Mar;16(1):21-6. Review.

PMID:
7648039
12.

Current strategies for the treatment of hereditary tyrosinemia type I.

Ashorn M, Pitkänen S, Salo MK, Heikinheimo M.

Paediatr Drugs. 2006;8(1):47-54. Review.

PMID:
16494511
13.

Painful keratoderma and photophobia: hallmarks of tyrosinemia type II.

Rabinowitz LG, Williams LR, Anderson CE, Mazur A, Kaplan P.

J Pediatr. 1995 Feb;126(2):266-9. Review.

PMID:
7844676
14.

Diagnosis and management of tyrosinemia type I.

Holme E, Lindstedt S.

Curr Opin Pediatr. 1995 Dec;7(6):726-32. Review.

PMID:
8776026
15.

Tyrosinemia: a review.

Russo PA, Mitchell GA, Tanguay RM.

Pediatr Dev Pathol. 2001 May-Jun;4(3):212-21. Review.

PMID:
11370259
16.

[Hereditary tyrosinemia: an endoplasmic reticulum stress disorder?].

Bergeron A, Jorquera R, Tanguay RM.

Med Sci (Paris). 2003 Oct;19(10):976-80. Review. French.

17.

Tyrosine and its catabolites: from disease to cancer.

Tanguay RM, Jorquera R, Poudrier J, St-Louis M.

Acta Biochim Pol. 1996;43(1):209-16. Review.

18.

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
19.
20.

Tyrosinaemia type I and NTBC (2-(2-nitro-4-trifluoromethylbenzoyl)-1,3-cyclohexanedione).

Holme E, Lindstedt S.

J Inherit Metab Dis. 1998 Aug;21(5):507-17. Review.

PMID:
9728331
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk