Ascertainment strategies and genotype:phenotype correlations in hypertrophic cardiomyopathy.

Ascertainment strategies and genotype:phenotype correlations in hypertrophic cardiomyopathy.

Bibliografiske detaljer
Main Authors:	Blair, E, Redwood, C, Watkins, H
Format:	Journal article
Sprog:	English
Udgivet:	2003

Lignende værker

Mutations in cis can confound genotype-phenotype correlations in hypertrophic cardiomyopathy.
af: Blair, E, et al.
Udgivet: (2001)

Double mutations in CIS can confound genotype-phenotype correlations in hypertrophic cardiomyopathy
af: Blair, E, et al.
Udgivet: (2000)

Hypertrophic cardiomyopathy:a paradigm for myocardial energy depletion.
af: Ashrafian, H, et al.
Udgivet: (2003)

A Genotype-phenotype Taxonomy of Hypertrophic Cardiomyopathy
af: Lara Curran, BSc, et al.
Udgivet: (2024-01-01)

Functional analysis of hypertrophic cardiomyopathy missense mutations in the light meromyosin region of beta myosin heavy chain
af: Redwood, C, et al.
Udgivet: (2003)

Pediatric Hypertrophic Cardiomyopathy: Exploring the Genotype‐Phenotype Association
af: Minh B. Nguyen, et al.
Udgivet: (2022-03-01)

A novel mutation in phospholamban causes a mixed hypertrophic and dilated cardiomyopathy phenotype with autosomal dominant inheritance
af: Carballo, S, et al.
Udgivet: (2004)

Altered regulatory properties of human cardiac troponin I mutants that cause hypertrophic cardiomyopathy.
af: Elliott, K, et al.
Udgivet: (2000)

Linked genetic modifiers in hypertrophic cardiomyopathy
af: Ektisham, J, et al.
Udgivet: (2004)

Investigation of troponin I mutations causing familial hypertrophic cardiomyopathy
af: Abdulrazzak, H, et al.
Udgivet: (2001)

Effects of hypertrophic cardiomyopathy mutations in troponin I on contractility of skinned cardiac muscle fibres
af: Burton, D, et al.
Udgivet: (2002)

Early onset malignant hypertrophic cardiomyopathy caused by mutations in MYBPC3
af: Carballo, S, et al.
Udgivet: (2003)

Sudden death in hypertrophic cardiomyopathy.
af: Watkins, H
Udgivet: (2000)

Correlates of myocardial fibrosis in hypertrophic cardiomyopathy
af: Kramer, CM, et al.
Udgivet: (2018)

Altered inhibitory and troponin C-binding activities in cardiac troponin I mutants known to cause hypertrophic cardiomyopathy
af: Elliott, K, et al.
Udgivet: (2000)

Novel mutations in cardiac MYBPC3 and early onset malignant hypertrophic cardiomyopathy
af: Carballo, S, et al.
Udgivet: (2005)

Myocardial dysfunction in hypertrophic cardiomyopathy.
af: Ashrafian, H, et al.
Udgivet: (2001)

Delineating the role of adenosine monophosphate (AMP)-activated protein kinase (AMP) gamma 2 subunit in hypertrophic cardiomyopathy (HCM)
af: Grignani, R, et al.
Udgivet: (2005)

Mutations of the light meromyosin domain of the beta-myosin heavy chain rod in hypertrophic cardiomyopathy.
af: Blair, E, et al.
Udgivet: (2002)

Hypertrophic cardiomyopathy mutations in the gamma 2 subunit of AMP-activated kinase suggest a central role of energy compromise in disease pathogenesis
af: Blair, E, et al.
Udgivet: (2001)

Is DNA testing for hypertrophic cardiomyopathy cost-effective?
af: Wordsworth, S, et al.
Udgivet: (2006)

Comparison of the functional effects of mutations in troponin T which cause dilated and hypertrophic cardiomyopathies
af: Robinson, P, et al.
Udgivet: (2002)

Novel mutations in cardiac MYBPC3 causing early onset malignant hypertrophic cardiomyopathy
af: Carballo, S, et al.
Udgivet: (2005)

Metabolic perturbations in the pathogenesis of hypertrophic cardiomyopathy
af: Ashrafian, H, et al.
Udgivet: (2005)

Novel mutations in cardiac MYPBC3 cause early onset malignant hypertrophic cardiomyopathy (HCM)
af: Carballo, S, et al.
Udgivet: (2005)

Spectrum and genotype–phenotype relationship of ALPK3 variants in Chinese patients with hypertrophic cardiomyopathy
af: Jing Wang, et al.
Udgivet: (2024-06-01)

Late gadolinium enhancement cardiovascular magnetic resonance in genotyped hypertrophic cardiomyopathy with normal phenotype
af: Jassal Davinder S, et al.
Udgivet: (2008-12-01)

Dilated and hypertrophic cardiomyopathy mutations in troponin and alpha-tropomyosin have opposing effects on the calcium affinity of cardiac thin filaments.
af: Robinson, P, et al.
Udgivet: (2007)

The genetics of hypertrophic cardiomyopathy: Teare redux.
af: Watkins, H, et al.
Udgivet: (2008)

Hypertrophic cardiomyopathy in Noonan Syndrome closely mimics familial hypertrophic cardiomyopathy due to sarcomeric mutations.
af: Hudsmith, L, et al.
Udgivet: (2006)

Genetic determinants of clinical phenotype in hypertrophic cardiomyopathy
af: Lazar Velicki, et al.
Udgivet: (2020-12-01)

Hypertrophic Cardiomyopathy: From Phenotype and Pathogenesis to Treatment
af: Zeyi Cheng, et al.
Udgivet: (2021-10-01)

A troponin I mutant known to cause hypertrophic cardiomyopathy shows reduced inhibition of Ca2+ independent tension
af: Burton, D, et al.
Udgivet: (2000)

DNA testing for hypertrophic cardiomyopathy: a cost-effectiveness model.
af: Wordsworth, S, et al.
Udgivet: (2010)

DNA testing for hypertrophic cardiomyopathy: a cost-effectiveness model
af: Wordsworth, S, et al.
Udgivet: (2010)

Genetic clues to disease pathways in hypertrophic and dilated cardiomyopathies.
af: Watkins, H
Udgivet: (2003)

[Abnormal tropomyosin function in ATPase cycle in hypertrophic and dilated cardiomyopathies].
af: Borovikov, I, et al.
Udgivet: (2013)

Hypertrophic cardiomyopathy mutations in MYBPC3 dysregulate myosin
af: Toepfer, C, et al.
Udgivet: (2019)

Two mutations in human cardiac troponin I known to cause hypertrophic cardiomyopathy have different effects on cardiac muscle contraction
af: Burton, D, et al.
Udgivet: (2000)

A protocol to ascertain whether sepsis-induced cardiomyopathy constitutes a phenotype of Takotsubo syndrome
af: John E. Madias
Udgivet: (2023-10-01)