(Q43065156)

English

Mitochondrial cytopathy presenting with focal segmental glomerulosclerosis, hypoparathyroidism, sensorineural deafness, and progressive neurological disease

scientific article published in August 2001

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

13 November 2017

Mitochondrial cytopathy presenting with focal segmental glomerulosclerosis, hypoparathyroidism, sensorineural deafness, and progressive neurological disease (English)

1 reference

Europe PubMed Central

PMC publication ID

13 November 2017

focal segmental glomerulosclerosis

1 reference

based on heuristic

hypoparathyroidism

1 reference

based on heuristic

mitochondrial myopathy

1 reference

based on heuristic

1 reference

based on heuristic

author name string

Hameed R

1

1 reference

Europe PubMed Central

PMC publication ID

13 November 2017

Raafat F

2

1 reference

Europe PubMed Central

PMC publication ID

13 November 2017

Ramani P

3

1 reference

Europe PubMed Central

PMC publication ID

13 November 2017

Gray G

4

1 reference

Europe PubMed Central

PMC publication ID

13 November 2017

Roper HP

5

1 reference

Europe PubMed Central

PMC publication ID

13 November 2017

Milford DV

6

1 reference

Europe PubMed Central

PMC publication ID

13 November 2017

language of work or name

0 references

publication date

1 August 2001

1 reference

Europe PubMed Central

PMC publication ID

13 November 2017

Postgraduate Medical Journal

1 reference

Europe PubMed Central

PMC publication ID

13 November 2017

77

1 reference

Europe PubMed Central

PMC publication ID

13 November 2017

910

1 reference

Europe PubMed Central

PMC publication ID

13 November 2017

523-526

1 reference

Europe PubMed Central

PMC publication ID

13 November 2017

HDR syndrome (hypoparathyroidism, sensorineural deafness, renal dysplasia) associated with del(10)(p13).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1742114

26 May 2018

Autosomal recessive hypoparathyroidism with renal insufficiency and developmental delay

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1742114

26 May 2018

Familial nephrosis, nerve deafness, and hypoparathyroidism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1742114

26 May 2018

Successful cochlear implantation in a patient with MELAS syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1742114

15 August 2018

A case of mitochondrial cytopathy with a typical point mutation for MELAS, presenting with severe focal-segmental glomerulosclerosis as main clinical manifestation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1742114

15 August 2018

Bilateral sensorineural hearing loss associated with the point mutation in mitochondrial genome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1742114

15 August 2018

Autosomal Dominant Familial Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1742114

1 December 2018

Identifiers

10.1136/PMJ.77.910.523

1 reference

Europe PubMed Central

PMC publication ID

13 November 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 November 2017

ResearchGate publication ID

0 references

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