(Q37928429)

25 August 2017

1 reference

title

Primary hyperoxaluria type I. (English)

1 reference

25 August 2017

primary hyperoxaluria

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K Latta

1

1 reference

PubMed ID

2189732

25 August 2017

J Brodehl

series ordinal

2

1 reference

25 August 2017

1 May 1990

1 reference

European Journal of Pediatrics

25 August 2017

1 reference

25 August 2017

149

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25 August 2017

8

1 reference

25 August 2017

518-522

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https://scigraph.springernature.com/pub.10.1007/bf01957682

25 August 2017

0 references

cites work

Mitochondrial damage and the subcellular distribution of 2-oxoglutarate:glyoxylate carboligase in normal human and rat liver and in the liver of a patient with primary hyperoxaluria type I.

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF01957682

Ultrasound demonstration of diffuse cortical nephrocalcinosis in a case of primary hyperoxaluria

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF01957682

L-glyceric aciduria. A new genetic variant of primary hyperoxaluria

21 January 2018

1 reference

12 December 2020

Studies on some possible biochemical treatments of primary hyperoxaluria

1 reference

12 December 2020

L-Glyceric aciduria (primary hyperoxaluria type 2) in siblings in two unrelated families

1 reference

12 December 2020

Renal failure in children with hepatic failure undergoing liver transplantation

1 reference

12 December 2020

Heredity of familial oxalosis

1 reference

12 December 2020

Deficiency of 2-oxo-glutarate: glyoxylate carboligase activity in primary hyperoxaluria

1 reference

12 December 2020

Primary hyperoxaluria (type I): attempted treatment by combined hepatic and renal transplantation.

1 reference

12 December 2020

Primary oxalosis of the heart: a cause of heart block

1 reference

12 December 2020

Successful strategies for renal transplantation in primary oxalosis

1 reference

12 December 2020

Hyperoxaluria and hyperoxalemia: one more concern for the nephrologist.

1 reference

12 December 2020

Enzymological diagnosis of primary hyperoxaluria type 1 by measurement of hepatic alanine: glyoxylate aminotransferase activity

1 reference

12 December 2020

Children with chronic renal failure in the Federal Republic of Germany: I. Epidemiology, modes of treatment, survival. Arbeits- gemeinschaft für Pädiatrische Nephrologie

1 reference

12 December 2020

Primary hyperoxaluria type I: ultrastructural observations in liver biopsies

1 reference

12 December 2020

Ultrasonic diagnosis of primary hyperoxaluria in infancy

1 reference

12 December 2020

Primary hyperoxaluria: an important cause of renal failure in infancy

1 reference

12 December 2020

Immunological heterogeneity of hepatic alanine:glyoxylate aminotransferase in primary hyperoxaluria type 1

1 reference

12 December 2020

Primary hyperoxaluria with normal alpha-ketoglutarate: glyoxylate carboligase activity. Treatment with isocarboxazid

1 reference

12 December 2020

Renal homotransplantation in a patient with primary familial oxalosis

1 reference

12 December 2020

Radiological aspects of primary hyperoxaluria

1 reference

12 December 2020

Combined report on regular dialysis and transplantation of children in Europe, XIII, 1983

1 reference

12 December 2020

Enzymatic heterogeneity in primary hyperoxaluria type 1 (hepatic peroxisomal alanine: glyoxylate aminotransferase deficiency)

1 reference

12 December 2020

Severe vascular complications in oxalosis after successful cadaveric kidney transplantation

1 reference

12 December 2020

Capillary gas chromatography measurement of oxalate in plasma and urine

1 reference

12 December 2020

Peroxisomal localization of alanine: Glyoxylate aminotransferase in human liver

1 reference

12 December 2020

Children with chronic renal failure in the Federal Republic of Germany: II. Primary renal diseases, age and intervals from early renal failure to renal death. Arbeitsgemeinschaft für Pädiatrische Nephrologie.

1 reference

12 December 2020

[Kidney transplantation in childhood]

1 reference

12 December 2020

Primary hyperoxaluria type I: oxalate and glycolate unsuitable for prenatal diagnosis

1 reference

12 December 2020

Progressive peripheral neuropathy in patient with primary hyperoxaluria

1 reference

12 December 2020

Primary oxalosis. report of a case with radiologic-pathologic-anatomical correlation and review of the literature (author's transl)

1 reference

12 December 2020

Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type I

1 reference

12 December 2020

Oxalosis-induced bone disease: a complication of transplantation and prolonged survival in primary hyperoxaluria

1 reference

12 December 2020

Plasma concentration and peritoneal clearance of oxalate in patients on continuous ambulatory peritoneal dialysis (CAPD)

1 reference

12 December 2020

Biochemical studies on the treatment of primary hyperoxaluria

1 reference

12 December 2020

Enzymatic prenatal diagnosis of primary hyperoxaluria type 1: potential and limitations

1 reference

12 December 2020

Timing of renal transplantation in the management of pyridoxine-resistant type I primary hyperoxaluria.

1 reference

12 December 2020

Pyridoxine treatment of type 1 hyperoxaluria

1 reference

12 December 2020

Bone changes in end-stage oxalosis

1 reference

12 December 2020

Reversal by liver transplantation of the complications of primary hyperoxaluria as well as the metabolic defect

1 reference

12 December 2020

Pancytopenia and hepatosplenomegaly in oxalosis

1 reference

12 December 2020

Peroxisomal disorders in neurology

1 reference

12 December 2020

Primary bone oxalosis: the roles of oxalate deposits and renal osteodystrophy

1 reference

12 December 2020

PRIMARY HYPEROXALURIA

1 reference

12 December 2020

Use of Magnesium Oxide in Management of Familial Hyperoxaluria

1 reference

12 December 2020

Primary hyperoxaluria

1 reference

12 December 2020

Oxalosis with peripheral gangrene

1 reference

12 December 2020

Response to a physiologic dose of pyridoxine in type I primary hyperoxaluria

1 reference

12 December 2020

Further observations on the genetic basis of primary hyperoxaluria

1 reference

12 December 2020

Oxalate dynamics and removal rates during haemodialysis and peritoneal dialysis in patients with primary hyperoxaluria and severe renal failure

1 reference

12 December 2020

Indications and results of liver transplantation in childhood

1 reference

12 December 2020

Calcium-oxalate-crystal-induced bone disease

1 reference

12 December 2020

Ophthalmic manifestations of primary oxalosis

1 reference

12 December 2020

Heart disease in primary oxalosis

1 reference

12 December 2020

Oxalate dynamics in chronic renal failure. Comparison with normal subjects and patients with primary hyperoxaluria

1 reference

12 December 2020

Successful treatment of primary hyperoxaluria type I by combined hepatic and renal transplantation

1 reference

12 December 2020

Diversity in residual alanine glyoxylate aminotransferase activity in hyperoxaluria type I: correlation with pyridoxine responsiveness

1 reference

12 December 2020

Successful treatment of infantile type I primary hyperoxaluria complicated by pyridoxine toxicity

1 reference

12 December 2020

End stage renal failure: 14 years' experience of dialysis and renal transplantation

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01957682

1 reference

25 August 2017

1 reference

PubMed ID

2189732