(Q39611906)

English

Variants of Alport's syndrome

scientific article published on July 1987

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

1 reference

Europe PubMed Central

Variants of Alport's syndrome (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

J P Grünfeld

1

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

G Grateau

2

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

L H Noel

3

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

R Charbonneau

4

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

M C Gubler

5

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

C O Savage

6

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

C M Lockwood

7

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

publication date

1 July 1987

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

Pediatric Nephrology

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

419-421

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

https://scigraph.springernature.com/pub.10.1007/bf00849247

0 references

Hereditary Thrombocytopenia, Deafness, and Renal Disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/3153311

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Goodpasture antigen in Alport's syndrome: studies with a monoclonal antibody

1 reference

https://pubmed.ncbi.nlm.nih.gov/3153311

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Use of a monoclonal antibody in differential diagnosis of children with haematuria and hereditary nephritis

1 reference

https://pubmed.ncbi.nlm.nih.gov/3153311

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alport's syndrome: experience at Hôpital Necker

1 reference

https://pubmed.ncbi.nlm.nih.gov/3153311

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fechtner syndrome--a variant of Alport's syndrome with leukocyte inclusions and macrothrombocytopenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/3153311

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Smooth-muscle tumours of the oesophagus

1 reference

https://pubmed.ncbi.nlm.nih.gov/3153311

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thrombocytopenia, macrothrombocytopathia, nephritis and deafness

1 reference

https://pubmed.ncbi.nlm.nih.gov/3153311

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary Nephritis Associated with May-Hegglin Anomaly

1 reference

https://pubmed.ncbi.nlm.nih.gov/3153311

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nephritogenic antigen determinants in epidermal and renal basement membranes of kindreds with Alport-type familial nephritis

1 reference

https://pubmed.ncbi.nlm.nih.gov/3153311

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/3153311

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic heterogeneity of Alport syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3153311

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biochemical and molecular genetic characterization of a new variant prealbumin associated with hereditary amyloidosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/3153311

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/3153311

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The clinical spectrum of hereditary nephritis

1 reference

https://pubmed.ncbi.nlm.nih.gov/3153311

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00849247

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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