(Q30773121)

26 June 2017

title

Cardio-cutaneous syndrome (the "LEOPARD" syndrome). Review of the literature and a new family (English)

1 reference

26 June 2017

Cardio‐cutaneous syndrome (the “LEOPARD” syndrome). Review of the literature and a new family (English)

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1976.TB01574.X

12 November 2023

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1976.TB01574.X

12 November 2023

author name string

H. Seuanez

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1261064

6 September 2022

F. Mañe-Garzon

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1261064

6 September 2022

R. Kolski

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1261064

6 September 2022

language of work or name

1 reference

1 March 1976

1 reference

full work available at URL

26 June 2017

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1399-0004.1976.tb01574.x

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1976.TB01574.X

https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1399-0004.1976.tb01574.x

12 November 2023

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1976.TB01574.X

12 November 2023

1 reference

26 June 2017

volume

9

1 reference

26 June 2017

issue

3

1 reference

26 June 2017

page(s)

266-276

1 reference

A case of unilateral lentigines with mental deficiency.

26 June 2017

cites work

2

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1976.TB01574.X

AN UNUSUAL HUMAN MOSAIC FOR SKIN PIGMENTATION.

12 November 2023

5

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1976.TB01574.X

Congenital heart disease, deafness, andskeletal malformations: A new syndrome?

12 November 2023

6

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1976.TB01574.X

CONGENITAL CARDIAC ARRHYTHMIA.

12 November 2023

8

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1976.TB01574.X

Heritable Q-T Prolongation Without Deafness

12 November 2023

9

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1976.TB01574.X

Multiple Lentigenes Syndrome

12 November 2023

10

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1976.TB01574.X

The Leopard (multiple lentigines) syndrome revisited

12 November 2023

11

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1976.TB01574.X

Congenital deafness and cardiac arrhythmias

12 November 2023

13

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1976.TB01574.X

Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death

12 November 2023

14

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1976.TB01574.X

The surdo-cardiac syndrome: three new cases of congenital deafness with syncopal attacks and Q-T prolongation in the electrocardiogram

12 November 2023

15

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1976.TB01574.X

Hereditary prolongation of QT interval

12 November 2023

16

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1976.TB01574.X

Congenital heart disease, deaf-mutism and associated somatic malformations occurring in several members of one family

12 November 2023

17

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1976.TB01574.X

Cardiocutaneous Syndrome Continued

12 November 2023

18

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1976.TB01574.X

Generalized lentigines associated with multiple congenital defects (leopard syndrome)

12 November 2023

20

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1976.TB01574.X

Congenital deaf-mutism, prolonged QT interval, syncopal attacks and sudden death

12 November 2023

22

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1976.TB01574.X

Lentigo and Electrocardiographic Changes

12 November 2023

25

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1976.TB01574.X

'Little leopard' syndrome. Description of 3 cases and review of 24

12 November 2023

33

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1976.TB01574.X

A pedigree of generalized lentigo

12 November 2023

34

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1976.TB01574.X

Cardio-auditory syndromes. Cardiac and genetic study of 511 deaf-mute children

12 November 2023

37

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1976.TB01574.X

Lentiginosis profusa in daughter and mother: multiple granular cell "myoblastomas" in the former

12 November 2023

39

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1976.TB01574.X

An unidentified syndrome with abnormality of skin and hair

12 November 2023

41

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1976.TB01574.X

Generalized lentigo: Electrocardiographic abnormalities, conduction disorders and arrhythmias in three cases

12 November 2023

42

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1976.TB01574.X

12 November 2023

Cohorts and conclusions.

44

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1976.TB01574.X

Electrocardiographic abnormalities in a family with generalized lentigo

12 November 2023

45

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1976.TB01574.X

Pulmonary stenosis, cafe-au-lait spots, and dull intelligence

12 November 2023

47

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1976.TB01574.X

12 November 2023

Identifiers

0 references

1 reference