(Q46361960)

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Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes syndrome with hypothyroidism and focal segmental glomerulosclerosis in a paediatric patient

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scholarly article

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Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/17294289

Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes syndrome with hypothyroidism and focal segmental glomerulosclerosis in a paediatric patient (English)

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/17294289

1 reference

based on heuristic

inferred from title

focal segmental glomerulosclerosis

1 reference

based on heuristic

inferred from title

lactic acidosis

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based on heuristic

inferred from title

author name string

Keith K Lau

1

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/17294289

Samuel P Yang

2

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/17294289

Maha N Haddad

3

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/17294289

Lavjay Butani

4

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/17294289

Sudesh P Makker

5

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/17294289

publication date

10 February 2007

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/17294289

International Urology and Nephrology

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/17294289

39

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/17294289

3

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/17294289

941-946

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/17294289

Organismal effects of mitochondrial dysfunction

1 reference

https://api.crossref.org/works/10.1007%2FS11255-006-9172-8

21 January 2018

Mitochondria: beyond oxidative phosphorylation

1 reference

https://api.crossref.org/works/10.1007%2FS11255-006-9172-8

21 January 2018

The neurology of mitochondrial DNA disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294289

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hearing loss with a mitochondrial gene mutation is highly prevalent in Japan.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294289

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial diseases in man and mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294289

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complexes of sequential metabolic enzymes

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294289

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mechanical stretch induces podocyte hypertrophy in vitro.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294289

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial encephalomyopathies preceded by de-Toni-Debré-Fanconi syndrome or focal segmental glomerulosclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294289

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial encephalopathies: molecular genetic diagnosis from blood samples

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294289

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An autopsy case of mitochondrial encephalomyopathy (MELAS) with special reference to extra-neuromuscular abnormalities

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294289

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294289

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial respiratory chain disorders II: neurodegenerative disorders and nuclear gene defects

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294289

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Renal complications in patients with diabetes mellitus associated with an A to G mutation of mitochondrial DNA at the 3243 position of leucine tRNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294289

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and pathologic features of focal segmental glomerulosclerosis with mitochondrial tRNALeu(UUR) gene mutation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294289

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and genetic features in two families with MELAS and the T3271C mutation in mitochondrial DNA.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294289

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial myopathies and encephalomyopathies

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294289

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An autopsy case of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome with chronic renal failure

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294289

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA mutations in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294289

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MELAS syndrome associated with diabetes mellitus and hyperthyroidism: a case report from Taiwan

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294289

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Endocrine disorders in two sisters affected by MELAS syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294289

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Successful cochlear implantation in a patient with MELAS syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294289

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pleiotropic molecular defects in energy-transducing complexes in mitochondrial encephalomyopathy (MELAS).

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294289

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA deletion in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes (MELAS) and Fanconi's syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17294289

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S11255-006-9172-8

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/17294289

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/17294289

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