(Q84965477)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21932010%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

title

A patient with Dent disease and features of Bartter syndrome caused by a novel mutation of CLCN5 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21932010%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21932010%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

author name string

Toshihiro Tajima

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21932010%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

Tomoya Hirayama

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21932010%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

Satoshi Sasaki

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21932010%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

publication date

20 September 2011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21932010%20AND%20SRC:MED&resulttype=core&format=json

European Journal of Pediatrics

13 February 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21932010%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

volume

171

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21932010%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21932010%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

page(s)

401-404

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21932010%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00431-011-1578-3

13 February 2020

exact match

0 references

cites work

Non-steroidal anti-inflammatory drug-associated nephrotoxicity in Bartter syndrome

1 reference

12 December 2020

Growth hormone improves growth rate and preserves renal function in Dent disease.

1 reference

12 December 2020

Atypical phenotype of type I Bartter syndrome accompanied by focal segmental glomerulosclerosis.

1 reference

12 December 2020

Influence of upright activity on plasma renin activity and aldosterone concentration in children.

1 reference

12 December 2020

CLCN5 mutation (R347X) associated with hypokalaemic metabolic alkalosis in a Turkish child: an unusual presentation of Dent's disease

1 reference

12 December 2020

Focal segmental glomerulosclerosis in a boy with Dent-2 disease

1 reference

12 December 2020

Loss of chloride channel ClC-5 impairs endocytosis by defective trafficking of megalin and cubilin in kidney proximal tubules

1 reference

12 December 2020

A novel CLCN5 mutation in a boy with Bartter-like syndrome and partial growth hormone deficiency

1 reference

12 December 2020

Phenotypic and genetic heterogeneity in Dent's disease—the results of an Italian collaborative study

1 reference

12 December 2020

Hypothesis: Dent disease is an underrecognized cause of focal glomerulosclerosis

1 reference

12 December 2020

Bartter syndrome and focal segmental glomerulosclerosis: a possible link between two diseases

1 reference

12 December 2020

Dent's disease: clinical features and molecular basis

1 reference

12 December 2020

A patient with Bartter syndrome accompanying severe growth hormone deficiency and focal segmental glomerulosclerosis

1 reference

12 December 2020