(Q67543711)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1383603%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

title

Mitochondrial abnormalities in the DIDMOAD syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1383603%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

S Bundey

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1383603%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

K Poulton

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1383603%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

H Whitwell

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1383603%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

E Curtis

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1383603%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

I A Brown

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1383603%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

A R Fielder

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1383603%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

publication date

1 January 1992

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1383603%20AND%20SRC:MED&resulttype=core&format=json

Journal of Inherited Metabolic Disease

14 September 2019

published in

1 reference

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14 September 2019

volume

1 reference

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14 September 2019

issue

1 reference

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14 September 2019

page(s)

315-319

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1383603%20AND%20SRC:MED&resulttype=core&format=json

Glutamate dehydrogenase in olivopontocerebellar atrophies: leukocytes, fibroblasts, and muscle mitochondria

14 September 2019

cites work

1 reference

12 December 2020

Diabetes mellitus, diabetes insipidus, and optic atrophy. An autosomal recessive syndrome?

1 reference

12 December 2020

Juvenile diabetes mellitus, optic atrophy, hearing loss, diabetes insipidus, atonia of the urinary tract and bladder, and other abnormalities (Wolfram syndrome). A review of 88 cases from the literature with personal observations on 3 new patients

1 reference

12 December 2020

Simultaneous occurrence of diabetes mellitus, diabetes insipidus, and optic atrophy in a brother and sister

1 reference

12 December 2020

Optic atrophy in Wolfram syndrome

1 reference

12 December 2020

Psychiatric findings in Wolfram syndrome homozygotes

1 reference

12 December 2020

Thiamine-responsive anemia in DIDMOAD syndrome

1 reference

12 December 2020