(Q72318333)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7783407%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

title

Renal amino acid transport in adults with oxidative phosphorylation diseases (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7783407%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

author name string

J M Shoffner

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7783407%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

A S Voljavec

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7783407%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

J Dixon

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7783407%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

A Kaufman

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7783407%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

D C Wallace

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7783407%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

W E Mitch

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7783407%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

language of work or name

English

0 references

publication date

1 April 1995

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7783407%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7783407%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

volume

47

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7783407%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7783407%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

page(s)

1101-1107

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7783407%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/ki.1995.157

25 October 2019

exact match

0 references

cites work

Fatal infhntile mitochondrial myopathy and renal dysfunction due to cytochrome-c-oxidase deficiency

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

Abnormal mitochondria on a renal biopsy from a case of mitochondrial myopathy.

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

Mitochondrial cytopathy with lactic acidosis, carnitine deficiency and DeToni-Fanconi-Debré syndrome

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

de Toni-Fanconi-Debré syndrome with Leigh syndrome revealing severe muscle cytochrome c oxidase deficiency

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

Kearns-Sayre syndrome presenting as renal tubular acidosis

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

Renal tubular involvement mimicking Bartter syndrome in a patient with Kearns-Sayre syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

Renal and skin involvement in a patient with complete Kearns-Sayre syndrome

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

Mitochondrial DNA deletion: a cause of chronic tubulointerstitial nephropathy

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

Maternally inherited mitochondrial myopathy and myoclonic epilepsy.

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

Familial mitochondrial encephalomyopathy (MERRF): genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA disease

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

Clinical spectrum of mitochondrial DNA mutation at base pair 8344

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

Evaluation of procedures for assaying oxidative phosphorylation enzyme activities in mitochondrial myopathy muscle biopsies

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

DECLINE IN SKELETAL MUSCLE MITOCHONDRIAL RESPIRATORY CHAIN FUNCTION: POSSIBLE FACTOR IN AGEING

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

A T-->C mutation at nt 8993 of mitochondrial DNA in a child with Leigh syndrome

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

A MERRF/MELAS overlap syndrome associated with a new point mutation in the mitochondrial DNA tRNA(Lys) gene

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

A new mtDNA mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNALeu(UUR)

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): a correlative study of the clinical features and mitochondrial DNA mutation

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

Subacute necrotizing encephalopathy: oxidative phosphorylation defects and the ATPase 6 point mutation

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

Utility of radioisotopic filtration markers in chronic renal insufficiency: simultaneous comparison of 125I-iothalamate, 169Yb-DTPA, 99mTc-DTPA, and inulin. The Modification of Diet in Renal Disease Study

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNA.

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

The Fanconi syndrome and mechanisms of tubular transport dysfunction

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

Fatal infantile mitochondrial myopathy due to cytochrome c oxidase deficiency

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

Fatal lipid storage myopathy with deficiency of cytochrome-c-oxidase and carnitine. A contribution to the combined cytochemical-finestructural identification of cytochrome-c-oxidase in longterm frozen muscle

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

Fatal infantile mitochondrial myopathy and renal dysfunction caused by cytochrome c oxidase deficiency: immunological studies in a new patient

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

Mitochondrial cytochrome deficiency presenting as a myopathy with hypotonia, external ophthalmoplegia, and lactic acidosis in an infant and as fatal hepatopathy in a second cousin.

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

Defects of the mitochondrial respiratory chain complexes in three pediatric cases with hypotonia and cardiac involvement

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

Fatal cytochrome c oxidase-deficient myopathy of infancy associated with mtDNA depletion. Differential involvement of skeletal muscle and cultured fibroblasts

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

Mitochondrial myopathy of childhood associated with depletion of mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

The renal handling of amino acids and oligopeptides

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

Renal Clearance of Amino Acids in Patients with Severe Chronic Renal Failure

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

Renal metabolism of amino acids and ammonia in subjects with normal renal function and in patients with chronic renal insufficiency.

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

Evaluation of Amino Acid and Protein Requirements in Chronic Uremia

1 reference

https://api.crossref.org/works/10.1038%2FKI.1995.157

7 January 2021

Identifiers

DOI

10.1038/KI.1995.157

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7783407%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

1 reference