(Q50516054)

14 March 2018

title

Natural history of Alström syndrome in early childhood: onset with dilated cardiomyopathy (English)

1 reference

14 March 2018

1 reference

Michaud JL

1

1 reference

14 March 2018

Héon E

2

1 reference

14 March 2018

Guilbert F

3

1 reference

14 March 2018

Weill J

4

1 reference

14 March 2018

Puech B

5

1 reference

14 March 2018

Benson L

6

1 reference

14 March 2018

Smallhorn JF

7

1 reference

14 March 2018

Shuman CT

8

1 reference

14 March 2018

Buncic JR

9

1 reference

14 March 2018

Levin AV

10

1 reference

14 March 2018

Weksberg R

11

1 reference

14 March 2018

Brevière GM

12

1 reference

14 March 2018

language of work or name

English

0 references

publication date

1 February 1996

1 reference

14 March 2018

The Journal of Pediatrics

published in

1 reference

14 March 2018

volume

128

1 reference

14 March 2018

issue

2

1 reference

14 March 2018

page(s)

225-229

1 reference

14 March 2018

Familial syndrome of primary testicular insufficiency with normal virilization, blindness, deafness and metabolic abnormalities

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970394-3

The syndrome of Laurence-Moon-Bardet-Biedl and allied diseases in Switzerland. Clinical, genetic and epidemiological studies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970394-3

The Alström syndrome: ophthalmic histopathology and retinal ultrastructure

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970394-3

Late onset dilated cardiomyopathy in a unique familial syndrome of hypogonadism and metabolic abnormalities

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970394-3

Alstrom's syndrome: further evidence of autosomal recessive inheritance and endocrinological dysfunction

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970394-3

Hepatic dysfunction in Alström disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970394-3

Longitudinal study of the early electroretinographic changes in Alström's syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970394-3

Dystrophin expression in the human retina is required for normal function as defined by electroretinography

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970394-3

Adiposity indices in children

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970394-3

Classification and diagnosis of diabetes mellitus and other categories of glucose intolerance. National Diabetes Data Group

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970394-3

The clinical course of primary myocardial disease in infants and children

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970394-3

Findings on endomyocardial biopsy in infants and children with dilated cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970394-3

Natural history and prognostic risk factors in endocardial fibroelastosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970394-3

Clinical profile of congestive cardiomyopathy in children

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970394-3

Outcome of infants and children with dilated cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970394-3

The Frequency of Familial Dilated Cardiomyopathy in a Series of Patients with Idiopathic Dilated Cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970394-3

A new familial syndrome characterized by pigmentary retinopathy, hypogonadism, mental retardation, nerve deafness and glucose intolerance

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970394-3

Familial insulin resistant diabetes associated with acanthosis nigricans, polycystic ovaries, hypogonadism, pigmentary retinopathy, labyrinthine deafness, and mental retardation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970394-3

The cardinal manifestations of Bardet-Biedl syndrome, a form of Laurence-Moon-Biedl syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970394-3

HEART DISEASE IN THE LAURENCE-MOON-BIEDL-BARDET SYNDROME: A REVIEW AND A REPORT OF 3 BROTHERS.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970394-3

Cardiac abnormalities in the Bardet-Biedl syndrome: echocardiographic studies of 22 patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970394-3

Natural course of visual functions in the Bardet-Biedl syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970394-3

Bardet-Biedl syndrome and related disorders

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970394-3

Standard for clinical electroretinography. International Standardization Committee

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970394-3

inferred from DOI database lookup

7 January 2021

based on heuristic

Patterns of rod and cone dysfunction in Bardet-Biedl syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970394-3

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0022-3476(96)70394-3

1 reference

14 March 2018

release_skrzohqpkvhm5ngeqqiod23i2y

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/skrzohqpkvhm5ngeqqiod23i2y

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

14 March 2018