(Q46551819)

23 December 2017

title

Primary hyperoxaluria type 1 in Japan. (English)

1 reference

23 December 2017

primary hyperoxaluria type I

main subject

primary hyperoxaluria

1 reference

based on heuristic

inferred from title

1 reference

Tatsuya Takayama

1

1 reference

23 December 2017

Masao Nagata

series ordinal

2

1 reference

23 December 2017

Arata Ichiyama

series ordinal

3

1 reference

23 December 2017

Seiichiro Ozono

series ordinal

4

1 reference

23 December 2017

publication date

1 May 2005

1 reference

23 December 2017

American Journal of Nephrology

published in

1 reference

23 December 2017

volume

25

1 reference

23 December 2017

issue

3

1 reference

23 December 2017

page(s)

297-302

1 reference

23 December 2017

Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type I

cites work

1 reference

Control of oxalate formation from L-hydroxyproline in liver mitochondria

21 January 2018

1 reference

Primary hyperoxaluria type 1 in The Netherlands: prevalence and outcome

21 January 2018

1 reference

A glycine-to-glutamate substitution abolishes alanine:glyoxylate aminotransferase catalytic activity in a subset of patients with primary hyperoxaluria type 1

21 January 2018

1 reference

Functional synergism between the most common polymorphism in human alanine:glyoxylate aminotransferase and four of the most common disease-causing mutations

21 January 2018

1 reference

Primary hyperoxaluria type I due to a point mutation of T to C in the coding region of the serine:pyruvate aminotransferase gene

21 January 2018

1 reference

ATP-dependent degradation of a mutant serine: pyruvate/alanine:glyoxylate aminotransferase in a primary hyperoxaluria type 1 case

21 January 2018

1 reference

An enzyme trafficking defect in two patients with primary hyperoxaluria type 1: peroxisomal alanine/glyoxylate aminotransferase rerouted to mitochondria

21 January 2018

1 reference

Calcinosis cutis in a patient with primary hyperoxaluria due to hepatic enzyme deficiency

21 January 2018

1 reference

Sequential liver-kidney transplantation from a living-related donor in primary hyperoxaluria type 1 (oxalosis).

21 January 2018

1 reference

Pyridoxal 5'-phosphate binding of a recombinant rat serine: pyruvate/alanine:glyoxylate aminotransferase.

21 January 2018

1 reference

Bone Biopsy to Diagnose Hyperoxaluria in Patients with Renal Failure

21 January 2018

1 reference

Evaluation of mutation screening as a first line test for the diagnosis of the primary hyperoxalurias.

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1159/000086361

1 reference

23 December 2017

1 reference

23 December 2017