(Q58620406)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24033287%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

title

Unbiased next generation sequencing analysis confirms the existence of autosomal dominant Alport syndrome in a relevant fraction of cases (English)

1 reference

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21 February 2020

1 reference

1 reference

autosomal dominant Alport syndrome

1 reference

11

1 reference

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21 February 2020

Gian Marco Ghiggeri

12

1 reference

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21 February 2020

Daniela Giachino

21

1 reference

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21 February 2020

Francesca Mari

23

1 reference

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21 February 2020

Alessandra Renieri

25

1 reference

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21 February 2020

Francesca Ariani

26

1 reference

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21 February 2020

author name string

C Fallerini

1

1 reference

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21 February 2020

L Dosa

2

1 reference

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21 February 2020

R Tita

3

1 reference

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21 February 2020

D Del Prete

4

1 reference

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21 February 2020

S Feriozzi

5

1 reference

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21 February 2020

G Gai

6

1 reference

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21 February 2020

M Clementi

7

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21 February 2020

A La Manna

8

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21 February 2020

N Miglietti

9

1 reference

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21 February 2020

R Mancini

10

1 reference

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21 February 2020

G Piaggio

13

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21 February 2020

F Brancati

14

1 reference

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21 February 2020

L Diano

15

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21 February 2020

E Frate

16

1 reference

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21 February 2020

A R Pinciaroli

17

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21 February 2020

M Giani

18

1 reference

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21 February 2020

P Castorina

19

1 reference

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21 February 2020

E Bresin

20

1 reference

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21 February 2020

M De Marchi

22

1 reference

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21 February 2020

M Bruttini

24

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21 February 2020

publication date

17 October 2013

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21 February 2020

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21 February 2020

volume

86

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21 February 2020

issue

3

1 reference

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21 February 2020

page(s)

252-257

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HEREDITARY FAMILIAL CONGENITAL HAEMORRHAGIC NEPHRITIS.

21 February 2020

cites work

1 reference

Identification of mutations in the COL4A5 collagen gene in Alport syndrome

21 January 2018

1 reference

Identification of mutations in the alpha 3(IV) and alpha 4(IV) collagen genes in autosomal recessive Alport syndrome

21 January 2018

1 reference

Autosomal dominant Alport syndrome caused by a COL4A3 splice site mutation

21 January 2018

1 reference

COL4A3/COL4A4 mutations: from familial hematuria to autosomal-dominant or recessive Alport syndrome

21 January 2018

1 reference

Autosomal dominant Alport syndrome: molecular analysis of the COL4A4 gene and clinical outcome.

21 January 2018

1 reference

Autosomal-dominant Alport syndrome: natural history of a disease due to COL4A3 or COL4A4 gene

21 January 2018

1 reference

Advances in Alport syndrome diagnosis using next-generation sequencing

21 January 2018

1 reference

Incidence of renal failure and nephroprotection by RAAS inhibition in heterozygous carriers of X-chromosomal and autosomal recessive Alport mutations

21 January 2018

1 reference

Genetics of classic Alport's syndrome

21 January 2018

1 reference

The value of clinical criteria in identifying patients with X-linked Alport syndrome

21 January 2018

1 reference

Early angiotensin-converting enzyme inhibition in Alport syndrome delays renal failure and improves life expectancy

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1111/CGE.12258

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24033287%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

1 reference