(Q63440935)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19449150%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

title

Genetic and clinical profile of Indian patients of idiopathic restrictive cardiomyopathy with and without hypertrophy (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19449150%20AND%20SRC:MED&resulttype=core&format=json

restrictive cardiomyopathy

28 January 2020

main subject

1 reference

1

1 reference

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28 January 2020

Kewal K Talwar

8

1 reference

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28 January 2020

Madhu Khullar

9

1 reference

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28 January 2020

author name string

Shamim Ahmad

2

1 reference

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28 January 2020

Tarunveer Singh Ahluwalia

3

1 reference

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28 January 2020

Monica Ahuja

4

1 reference

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28 January 2020

Ajay Bahl

5

1 reference

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28 January 2020

Uma Nahar Saikia

6

1 reference

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28 January 2020

Balvinder Singh

7

1 reference

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28 January 2020

publication date

17 May 2009

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19449150%20AND%20SRC:MED&resulttype=core&format=json

Molecular and Cellular Biochemistry

28 January 2020

published in

1 reference

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28 January 2020

volume

331

1 reference

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28 January 2020

issue

1-2

1 reference

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28 January 2020

page(s)

187-192

1 reference

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https://scigraph.springernature.com/pub.10.1007/s11010-009-0157-7

28 January 2020

exact match

0 references

cites work

Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1

1 reference

12 December 2020

Restrictive Cardiomyopathy

1 reference

12 December 2020

Genetics of hypertrophic cardiomyopathy: one, two, or more diseases?

1 reference

12 December 2020

Frequency and clinical expression of cardiac troponin I mutations in 748 consecutive families with hypertrophic cardiomyopathy.

1 reference

12 December 2020

Simulations of the myosin II motor reveal a nucleotide-state sensing element that controls the recovery stroke

1 reference

12 December 2020

Idiopathic restrictive cardiomyopathy is part of the clinical expression of cardiac troponin I mutations

1 reference

12 December 2020

Hypertrophic cardiomyopathy: histopathological features of sudden death in cardiac troponin T disease

1 reference

12 December 2020

Novel mutations in sarcomeric protein genes in dilated cardiomyopathy.

1 reference

12 December 2020

Prevalence, Clinical Significance, and Genetic Basis of Hypertrophic Cardiomyopathy With Restrictive Phenotype

1 reference

12 December 2020

A point mutation (R192H) in the C-terminus of human cardiac troponin I causes diastolic dysfunction in transgenic mice

1 reference

12 December 2020

Magnitude of left ventricular hypertrophy and risk of sudden death in hypertrophic cardiomyopathy

1 reference

12 December 2020

A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation

1 reference

12 December 2020