(Q39611386)

English

Alport's syndrome and achalasia

scientific article published on July 1988

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

1 reference

Europe PubMed Central

Alport's syndrome and achalasia (English)

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

Alport syndrome

1 reference

based on heuristic

inferred from title

author name string

H E Leichter

1

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

J Vargas

2

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

A H Cohen

3

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

M Ament

4

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

I B Salusky

5

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

1 July 1988

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

Pediatric Nephrology

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

312-314

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

https://scigraph.springernature.com/pub.10.1007/bf00858684

0 references

Hyperprolinemia: clinical and biochemical family study

1 reference

https://pubmed.ncbi.nlm.nih.gov/3153032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary nephritis with associated defects in proximal renal tubular function

1 reference

https://pubmed.ncbi.nlm.nih.gov/3153032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alport's syndrome. A report of 58 cases and a review of the literature

1 reference

https://pubmed.ncbi.nlm.nih.gov/3153032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Familial esophageal leiomyomatosis associated with Alport's syndrome in a 9-year-old boy]

1 reference

https://pubmed.ncbi.nlm.nih.gov/3153032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary interstitial nephritis associated with polyneuropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/3153032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Antithyroid antibodies in Alport's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3153032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary macrothrombocytopathia, nephritis and deafness

1 reference

https://pubmed.ncbi.nlm.nih.gov/3153032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HEREDITARY RENAL DYSFUNCTION AND DEAFNESS

1 reference

https://pubmed.ncbi.nlm.nih.gov/3153032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lenticonus anterior and Alport's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3153032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Leiomyomatosis of the esophagus, tracheo-bronchi and genitals associated with Alport type hereditary nephropathy: a new syndrome]

1 reference

https://pubmed.ncbi.nlm.nih.gov/3153032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HEREDITARY FAMILIAL CONGENITAL HAEMORRHAGIC NEPHRITIS.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3153032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00858684

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

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