(Q53857387)

English

A boy with mitochondrial disease: asymptomatic proteinuria without neuromyopathy.

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scholarly article

1 reference

Europe PubMed Central

21 May 2018

http://europepmc.org/abstract/MED/14648337

A boy with mitochondrial disease: asymptomatic proteinuria without neuromyopathy. (English)

1 reference

Europe PubMed Central

21 May 2018

http://europepmc.org/abstract/MED/14648337

mitochondrial disease

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based on heuristic

inferred from title

author name string

Yuka Ueda

1

1 reference

Europe PubMed Central

21 May 2018

http://europepmc.org/abstract/MED/14648337

Atsushi Ando

2

1 reference

Europe PubMed Central

21 May 2018

http://europepmc.org/abstract/MED/14648337

Taeko Nagata

3

1 reference

Europe PubMed Central

21 May 2018

http://europepmc.org/abstract/MED/14648337

Hidehiko Yanagida

4

1 reference

Europe PubMed Central

21 May 2018

http://europepmc.org/abstract/MED/14648337

Kazuro Yagi

5

1 reference

Europe PubMed Central

21 May 2018

http://europepmc.org/abstract/MED/14648337

Keisuke Sugimoto

6

1 reference

Europe PubMed Central

21 May 2018

http://europepmc.org/abstract/MED/14648337

Mitsuru Okada

7

1 reference

Europe PubMed Central

21 May 2018

http://europepmc.org/abstract/MED/14648337

Tsukasa Takemura

8

1 reference

Europe PubMed Central

21 May 2018

http://europepmc.org/abstract/MED/14648337

publication date

25 November 2003

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Europe PubMed Central

21 May 2018

http://europepmc.org/abstract/MED/14648337

Pediatric Nephrology

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Europe PubMed Central

21 May 2018

http://europepmc.org/abstract/MED/14648337

19

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21 May 2018

http://europepmc.org/abstract/MED/14648337

1

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21 May 2018

http://europepmc.org/abstract/MED/14648337

107-110

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Europe PubMed Central

21 May 2018

http://europepmc.org/abstract/MED/14648337

https://scigraph.springernature.com/pub.10.1007/s00467-003-1318-7

0 references

Mitochondrial encephalopathies: molecular genetic diagnosis from blood samples

1 reference

https://pubmed.ncbi.nlm.nih.gov/14648337

12 December 2020

based on heuristic

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Partial deficiency of cytochrome c oxidase with isolated proximal renal tubular acidosis and hypercalciuria

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https://pubmed.ncbi.nlm.nih.gov/14648337

12 December 2020

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Mitochondrial cytopathy. A multisystem disorder with ragged red fibres on muscle biopsy

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https://pubmed.ncbi.nlm.nih.gov/14648337

12 December 2020

based on heuristic

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Retinitis pigmentosa, external ophthalmophegia, and complete heart block: unusual syndrome with histologic study in one of two cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/14648337

12 December 2020

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Migrainous stroke

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https://pubmed.ncbi.nlm.nih.gov/14648337

12 December 2020

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Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome

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https://pubmed.ncbi.nlm.nih.gov/14648337

12 December 2020

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Mutation in mitochondrial tRNA(Leu(UUR)) gene associated with progressive kidney disease.

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https://pubmed.ncbi.nlm.nih.gov/14648337

12 December 2020

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Acute renal failure and the MELAS syndrome, a mitochondrial encephalomyopathy

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https://pubmed.ncbi.nlm.nih.gov/14648337

12 December 2020

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Oxidative phosphorylation diseases. Disorders of two genomes

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https://pubmed.ncbi.nlm.nih.gov/14648337

12 December 2020

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Maternal inheritance of human mitochondrial DNA

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https://pubmed.ncbi.nlm.nih.gov/14648337

12 December 2020

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Deletion of mitochondrial DNA in patient with chronic tubulointerstitial nephritis

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https://pubmed.ncbi.nlm.nih.gov/14648337

12 December 2020

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Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome

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https://pubmed.ncbi.nlm.nih.gov/14648337

12 December 2020

based on heuristic

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mtDNA depletion with variable tissue expression: a novel genetic abnormality in mitochondrial diseases

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https://pubmed.ncbi.nlm.nih.gov/14648337

12 December 2020

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Diseases of the mitochondrial DNA.

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https://pubmed.ncbi.nlm.nih.gov/14648337

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Mitochondrial encephalomyopathies

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https://pubmed.ncbi.nlm.nih.gov/14648337

12 December 2020

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The clinical features of mitochondrial myopathy.

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https://pubmed.ncbi.nlm.nih.gov/14648337

12 December 2020

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Renal involvement in mitochondrial cytopathies

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https://pubmed.ncbi.nlm.nih.gov/14648337

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary glomerulopathy associated with a mitochondrial tRNA(Leu) gene mutation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14648337

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Seminars in medicine of the Beth Israel Hospital, Boston. Mitochondrial DNA and disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/14648337

12 December 2020

based on heuristic

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Mitochondrial disorders. Methods and specimen selection for diagnostic molecular pathology.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14648337

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00467-003-1318-7

1 reference

Europe PubMed Central

21 May 2018

http://europepmc.org/abstract/MED/14648337

1 reference

Europe PubMed Central

21 May 2018

http://europepmc.org/abstract/MED/14648337

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