Retinal and renal complications in patients with a mutation of mitochondrial DNA at position 3,243 (maternally inherited diabetes and deafness). A case-control study (Q46518216)

From Wikidata

Jump to navigation Jump to search

scientific article published on 26 June 2008

Language	Label	Description	Also known as
English	Retinal and renal complications in patients with a mutation of mitochondrial DNA at position 3,243 (maternally inherited diabetes and deafness). A case-control study	scientific article published on 26 June 2008

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

Retinal and renal complications in patients with a mutation of mitochondrial DNA at position 3,243 (maternally inherited diabetes and deafness). A case-control study (English)

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

mitochondrial DNA

0 references

1 reference

based on heuristic

inferred from title

author name string

P Massin

1

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

D Dubois-Laforgue

2

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

T Meas

3

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

M Laloi-Michelin

4

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

H Gin

5

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

B Bauduceau

6

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

C Bellanné-Chantelot

7

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

E Bertin

8

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

J-F Blickle

9

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

B Bouhanick

10

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

J Cahen-Varsaux

11

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

S Casanova

12

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

G Charpentier

13

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

P Chedin

14

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

O Dupuy

15

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

A Grimaldi

16

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

B Guerci

17

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

E Kaloustian

18

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

A Lecleire-Collet

19

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

F Lorenzini

20

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

A Murat

21

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

H Narbonne

22

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

F Olivier

23

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

V Paquis-Flucklinger

24

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

M Virally

25

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

M Vincenot

26

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

B Vialettes

27

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

J Timsit

28

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

P J Guillausseau

29

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

GEDIAM (Mitochondrial Diabetes French Study Group)

30

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

publication date

26 June 2008

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

51

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

9

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

1664-1670

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

Maternally inherited diabetes and deafness: a multicenter study

1 reference

https://api.crossref.org/works/10.1007/S00125-008-1073-1

21 January 2018

Macular pattern dystrophy associated with a mutation of mitochondrial DNA.

1 reference

https://api.crossref.org/works/10.1007/S00125-008-1073-1

21 January 2018

Tight blood pressure control and risk of macrovascular and microvascular complications in type 2 diabetes: UKPDS 38. UK Prospective Diabetes Study Group

1 reference

https://api.crossref.org/works/10.1007/S00125-008-1073-1

21 January 2018

Report of the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus

1 reference

https://api.crossref.org/works/10.1007/S00125-008-1073-1

21 January 2018

A more accurate method to estimate glomerular filtration rate from serum creatinine: a new prediction equation. Modification of Diet in Renal Disease Study Group

1 reference

https://api.crossref.org/works/10.1007/S00125-008-1073-1

21 January 2018

Focal segmental glomerulosclerosis associated with mitochondrial cytopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/18581092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The influence of the photoreceptor-RPE complex on the inner retina. An explanation for the beneficial effects of photocoagulation

1 reference

https://pubmed.ncbi.nlm.nih.gov/18581092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical features of diabetes mellitus with the mitochondrial DNA 3243 (A-G) mutation in Japanese: maternal inheritance and mitochondria-related complications

1 reference

https://pubmed.ncbi.nlm.nih.gov/18581092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heterogeneity of diabetes phenotype in patients with 3243 bp mutation of mitochondrial DNA (Maternally Inherited Diabetes and Deafness or MIDD)

1 reference

https://pubmed.ncbi.nlm.nih.gov/18581092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Renal complications in a patient with A-to-G mutation of mitochondrial DNA at the 3243 position of leucine tRNA.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18581092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incidence of sight-threatening retinopathy in Type 1 diabetes in a systematic screening programme

1 reference

https://pubmed.ncbi.nlm.nih.gov/18581092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The spectrum of systemic involvement in adults presenting with renal lesion and mitochondrial tRNA(Leu) gene mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/18581092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Grading diabetic retinopathy from stereoscopic color fundus photographs--an extension of the modified Airlie House classification. ETDRS report number 10. Early Treatment Diabetic Retinopathy Study Research Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/18581092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial diabetes mellitus: prevalence and clinical characterization of diabetes due to mitochondrial tRNA(Leu(UUR)) gene mutation in Japanese patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/18581092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glycaemic control and development of retinopathy in type 2 diabetes mellitus: a longitudinal study

1 reference

https://pubmed.ncbi.nlm.nih.gov/18581092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Creatinine clearance evaluation in routine diabetes practice

1 reference

https://pubmed.ncbi.nlm.nih.gov/18581092

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/18581092

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/18581092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33). UK Prospective Diabetes Study (UKPDS) Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/18581092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biochemistry and molecular cell biology of diabetic complications

1 reference

https://pubmed.ncbi.nlm.nih.gov/18581092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The sixth report of the Joint National Committee on prevention, detection, evaluation, and treatment of high blood pressure

1 reference

https://pubmed.ncbi.nlm.nih.gov/18581092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ocular clinicopathologic study of the mitochondrial encephalomyopathy overlap syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/18581092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incidence of sight-threatening retinopathy in patients with type 2 diabetes in the Liverpool Diabetic Eye Study: a cohort study.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18581092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Does mitochondrial genome mutation in subjects with maternally inherited diabetes and deafness decrease severity of diabetic retinopathy?

1 reference

https://pubmed.ncbi.nlm.nih.gov/18581092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of A-to-G mutation at nucleotide 3243 of the mitochondrial tRNA(Leu(UUR)) gene in Japanese patients with diabetes mellitus and end stage renal disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18581092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ocular pathology of MELAS syndrome with mitochondrial DNA nucleotide 3243 point mutation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18581092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of macular pattern dystrophy in maternally inherited diabetes and deafness

1 reference

https://pubmed.ncbi.nlm.nih.gov/18581092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prediction of creatinine clearance from serum creatinine

1 reference

https://pubmed.ncbi.nlm.nih.gov/18581092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The effect of intensive treatment of diabetes on the development and progression of long-term complications in insulin-dependent diabetes mellitus. The Diabetes Control and Complications Trial Research Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/18581092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diabetic retinopathy and its relation to errors of refraction

1 reference

https://pubmed.ncbi.nlm.nih.gov/18581092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maternally inherited diabetes and deafness: a new diabetes subtype

1 reference

https://pubmed.ncbi.nlm.nih.gov/18581092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Wisconsin Epidemiologic Study of diabetic retinopathy. XIV. Ten-year incidence and progression of diabetic retinopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/18581092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Extra-pancreatic manifestations in diabetes secondary to mitochondrial DNA point mutation within the tRNALeu(UUR) gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/18581092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/18581092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fundus changes in patients with the mitochondrial DNA point mutation at position 3243

1 reference

https://pubmed.ncbi.nlm.nih.gov/18581092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The absence of diabetic retinopathy in patients with retinitis pigmentosa: implications for pathophysiology and possible treatment

1 reference

https://pubmed.ncbi.nlm.nih.gov/18581092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNALeu A to G mutation11The authors have no proprietary interest in the development or marketing of any device or medica

1 reference

https://pubmed.ncbi.nlm.nih.gov/18581092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Three-year incidence and cumulative prevalence of retinopathy: the atherosclerosis risk in communities study.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18581092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness

1 reference

https://pubmed.ncbi.nlm.nih.gov/18581092

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00125-008-1073-1

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18581092

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q46518216&oldid=2207925355"