(Q46871391)

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14 January 2020

title

"Bartter-like" phenotype in Kearns-Sayre syndrome (English)

1 reference

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14 January 2020

7

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14 January 2020

Andrea Onetti Muda

5

1 reference

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14 January 2020

Filippo Maria Santorelli

6

object named as

Filippo M Santorelli

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14 January 2020

author name string

Francesco Emma

1

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14 January 2020

Carla Pizzini

2

1 reference

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14 January 2020

Alessandra Tessa

3

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14 January 2020

Silvia Di Giandomenico

4

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14 January 2020

Gianfranco Rizzoni

8

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14 January 2020

publication date

29 December 2005

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14 January 2020

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14 January 2020

volume

21

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14 January 2020

issue

3

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14 January 2020

page(s)

355-360

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https://scigraph.springernature.com/pub.10.1007/s00467-005-2092-5

14 January 2020

exact match

0 references

cites work

Mitochondrial respiratory-chain diseases

1 reference

12 December 2020

Renal disease and mitochondrial genetics.

1 reference

12 December 2020

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

1 reference

12 December 2020

Distribution of wild-type and common deletion forms of mtDNA in normal and respiration-deficient muscle fibers from patients with mitochondrial myopathy

1 reference

12 December 2020

Renal Sodium Handling Study in an Atypical Case of Bartter's Syndrome Associated with Mitochondriopathy and Sensorineural Blindness

1 reference

12 December 2020

Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome

1 reference

12 December 2020

Endocrine dysfunction in Kearns-Sayre syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Detection of deleted mitochondrial DNA in Kearns-Sayre syndrome using laser capture microdissection.

1 reference

12 December 2020

Cytochemistry and immunocytochemistry of mitochondria in tissue sections

1 reference

12 December 2020

Severe hypomagnesemia and hypoparathyroidism in Kearns-Sayre syndrome.

1 reference

12 December 2020

Neurodegenerative disorders and hyperaldosteronism.

1 reference

12 December 2020

Kearns-Sayre syndrome presenting as renal tubular acidosis

1 reference

12 December 2020

Response of the collecting duct to disturbances of acid-base and potassium balance.

1 reference

12 December 2020

Mitochondrial DNA deletion: a cause of chronic tubulointerstitial nephropathy

1 reference

12 December 2020

Dietary NaCl modulates Na(+)-H+ antiporter activity in renal cortical apical membrane vesicles

1 reference

12 December 2020

Congenital hypoplastic anemia, diabetes, and severe renal tubular dysfunction associated with a mitochondrial DNA deletion

1 reference

12 December 2020

Renal manifestations of congenital lactic acidosis

1 reference

12 December 2020

Mineralocorticoid effects on Na-K-ATPase in individual nephron segments

1 reference

12 December 2020

The kidney in mitochondrial cytopathies

1 reference

12 December 2020

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

1 reference

12 December 2020

Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: a study of 56 patients

1 reference

12 December 2020

Genetic features of mitochondrial respiratory chain disorders

1 reference

12 December 2020

10.1007/S00467-005-2092-5

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16382326%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

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