PubMed (OMIM) for id: 75658

Year	Number of Results
1963	1
1965	1
1967	1
1968	1
1969	1
1970	2
1971	1
1972	1
1973	1
1979	1
1980	1
1981	1
1982	1
1983	1
1984	1
1985	2
1986	2
1988	2
1989	1
1990	4
1991	4
1992	2
1993	2
1994	1
1996	1
1997	2
1998	1
1999	3
2002	1
2003	1
2004	1
2024	0

1

Diet and the frequency of the alanine:glyoxylate aminotransferase Pro11Leu polymorphism in different human populations.

Caldwell EF, Mayor LR, Thomas MG, Danpure CJ. Caldwell EF, et al. Hum Genet. 2004 Nov;115(6):504-9. doi: 10.1007/s00439-004-1191-x. Epub 2004 Oct 5. Hum Genet. 2004. PMID: 15480793

2

STUDIES ON PRIMARY HYPEROXALURIA. I. IN VIVO DEMONSTRATION OF A DEFECT IN GLYOXYLATE METABOLISM.

FREDERICK EW, RABKIN MT, RICHIE RH Jr, SMITH LH Jr. FREDERICK EW, et al. N Engl J Med. 1963 Oct 17;269:821-9. doi: 10.1056/NEJM196310172691601. N Engl J Med. 1963. PMID: 14052264 No abstract available.

3

Primary hyperoxaluria type 1 in the Canary Islands: a conformational disease due to I244T mutation in the P11L-containing alanine:glyoxylate aminotransferase.

Santana A, Salido E, Torres A, Shapiro LJ. Santana A, et al. Proc Natl Acad Sci U S A. 2003 Jun 10;100(12):7277-82. doi: 10.1073/pnas.1131968100. Epub 2003 May 30. Proc Natl Acad Sci U S A. 2003. PMID: 12777626 Free PMC article.

4

Choroidal neovascularization in primary hyperoxaluria.

Theodossiadis PG, Friberg TR, Panagiotidis DN, Gogas PS, Pantelia EM, Moschos MN. Theodossiadis PG, et al. Am J Ophthalmol. 2002 Jul;134(1):134-7. doi: 10.1016/s0002-9394(02)01458-7. Am J Ophthalmol. 2002. PMID: 12095827

5

Primary hyperoxaluria in infants: medical, ethical, and economic issues.

Cochat P, Koch Nogueira PC, Mahmoud MA, Jamieson NV, Scheinman JI, Rolland MO. Cochat P, et al. J Pediatr. 1999 Dec;135(6):746-50. doi: 10.1016/s0022-3476(99)70095-8. J Pediatr. 1999. PMID: 10586179

6

Primary hyperoxaluria 1: catch up growth and normalization of oxaluria 6 years after hepatorenal transplantation in a prepubertal boy.

Walden U, Böswald M, Dörr HG, Ruder H. Walden U, et al. Eur J Pediatr. 1999 Sep;158(9):727-9. doi: 10.1007/s004310051188. Eur J Pediatr. 1999. PMID: 10485304

7

Molecular analysis of hyperoxaluria type 1 in Italian patients reveals eight new mutations in the alanine: glyoxylate aminotransferase gene.

Pirulli D, Puzzer D, Ferri L, Crovella S, Amoroso A, Ferrettini C, Marangella M, Mazzola G, Florian F. Pirulli D, et al. Hum Genet. 1999 Jun;104(6):523-5. doi: 10.1007/s004390050998. Hum Genet. 1999. PMID: 10453743

8

Preemptive liver transplantation from a living related donor for primary hyperoxaluria type I.

Gruessner RW. Gruessner RW. N Engl J Med. 1998 Jun 25;338(26):1924. doi: 10.1056/NEJM199806253382615. N Engl J Med. 1998. PMID: 9643991 No abstract available.

9

Primary hyperoxaluria type 1: a cluster of new mutations in exon 7 of the AGXT gene.

von Schnakenburg C, Rumsby G. von Schnakenburg C, et al. J Med Genet. 1997 Jun;34(6):489-92. doi: 10.1136/jmg.34.6.489. J Med Genet. 1997. PMID: 9192270 Free PMC article.

10

Variable peroxisomal and mitochondrial targeting of alanine: glyoxylate aminotransferase in mammalian evolution and disease.

Danpure CJ. Danpure CJ. Bioessays. 1997 Apr;19(4):317-26. doi: 10.1002/bies.950190409. Bioessays. 1997. PMID: 9136629 Review.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Results by year

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

46 results

Results by year

Filters

My Custom Filters

Results by year

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

PubMed (OMIM) for id: 75658

46 results

Results by year