(Q50459655)

English

Distal RTA with nerve deafness: clinical spectrum and mutational analysis in five children.

scientific article published on 11 January 2007

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17216496

Distal RTA with nerve deafness: clinical spectrum and mutational analysis in five children. (English)

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17216496

mutational analysis

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

7

object named as

Eliecer Coto

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17216496

author name string

Helena Gil

1

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17216496

Fernando Santos

2

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17216496

Enrique García

3

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17216496

María Victoria Alvarez

4

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17216496

Flor A Ordóñez

5

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17216496

Serafín Málaga

6

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17216496

publication date

11 January 2007

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17216496

Pediatric Nephrology

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17216496

22

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17216496

6

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17216496

825-828

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17216496

https://scigraph.springernature.com/pub.10.1007/s00467-006-0417-7

0 references

Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss

1 reference

https://pubmed.ncbi.nlm.nih.gov/17216496

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Urinary phosphate/creatinine, calcium/creatinine, and magnesium/creatinine ratios in a healthy pediatric population.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17216496

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic investigation of autosomal recessive distal renal tubular acidosis: evidence for early sensorineural hearing loss associated with mutations in the ATP6V0A4 gene.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17216496

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primary distal tubular acidosis in childhood: clinical study and long-term follow-up of 28 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/17216496

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Renal tubular acidosis: developments in our understanding of the molecular basis

1 reference

https://pubmed.ncbi.nlm.nih.gov/17216496

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/17216496

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hearing impairment in association with distal renal tubular acidosis among Saudi children.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17216496

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness

1 reference

https://pubmed.ncbi.nlm.nih.gov/17216496

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The syndrome of renal tubular acidosis and nerve deafness. Discordant manifestations in dizygotic twin brothers

1 reference

https://pubmed.ncbi.nlm.nih.gov/17216496

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ATP6B1 gene mutations associated with distal renal tubular acidosis and deafness in a child.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17216496

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inherited distal renal tubular acidosis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17216496

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Natural history of primary distal renal tubular acidosis treated since infancy

1 reference

https://pubmed.ncbi.nlm.nih.gov/17216496

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Renal tubular acidosis: a new look at an old problem

1 reference

https://pubmed.ncbi.nlm.nih.gov/17216496

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00467-006-0417-7

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17216496

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17216496

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