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TAVR in Patients with Pure Aortic Regurgitation: Ready to Use?

Current cardiology reports, 2020-07, Vol.22 (9), p.98-98, Article 98

2020

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Experimental study on relation between scour and complex 3D flow field

Scientia Iranica. Transaction A, Civil engineering, 2017-12, Vol.24 (6), p.2696-2711

2017

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DHA-Rich Fish Oil Increases the Omega-3 Index in Healthy Adults and Slows Resting Heart Rate without Altering Cardiac Autonomic Reflex Modulation

Journal of the American College of Nutrition, 2022-10, Vol.ahead-of-print (ahead-of-print), p.1-9

2022

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Protective spur dike for scour mitigation of existing spur dikes

Journal of hydraulic research, 2011-12, Vol.49 (6), p.809-813

2011

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Alcohol Consumption Between the Ages of 16 and 23 in Britain: a longitudinal study

British Journal of Addiction, 1987-02, Vol.82 (2), p.175-180

1987

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Evaluation of Metastatic Meningioma With 2-Deoxy-2-[18F]Fluoro-D-Glucose PET/CT

Clinical nuclear medicine, 2005-11, Vol.30 (11), p.717-720

2005

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A LONGITUDINAL STUDY OF MATERNAL DEPRESSION AND CHILD BEHAVIOUR PROBLEMS

Journal of child psychology and psychiatry, 1984-01, Vol.25 (1), p.91-109

1984

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Evidence for a low upper limit of heritability of mental test performance in a national sample of twins

Nature (London), 1976-09, Vol.263 (5575), p.314-316

1976

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Depression in mothers 6 years after the birth of a first child

Social Psychiatry, 1986-01, Vol.21 (2), p.76-82

1986

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Comparative study of social and family correlates of children's behaviour ratings

Child : care, health & development, 1985-07, Vol.11 (4), p.209-228

1985

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Evaluating the ≤10:1 wholegrain criterion in identifying nutrient quality and health implications of UK breads and breakfast cereals

Public health nutrition, 2018-04, Vol.21 (6), p.1186-1193

2018

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Evaluation of flow characteristics in labyrinth weirs using response surface methodology

Flow measurement and instrumentation, 2019-10, Vol.69, p.101617, Article 101617

2019

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Defining the impact of mutation accumulation on replicative lifespan in yeast using cancer-associated mutator phenotypes

Proceedings of the National Academy of Sciences - PNAS, 2019-02, Vol.116 (8), p.3062-3071

2019

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Mutation in TRMU Related to Transfer RNA Modification Modulates the Phenotypic Expression of the Deafness-Associated Mitochondrial 12S Ribosomal RNA Mutations

American journal of human genetics, 2006-08, Vol.79 (2), p.291-302

2006

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Age-related hearing loss and the ahl locus in mice

Hearing research, 2004-02, Vol.188 (1), p.21-28

2004

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Spontaneous Polyploids and Antimutators Compete During the Evolution of Saccharomyces cerevisiae Mutator Cells

Genetics (Austin), 2020-08, Vol.215 (4), p.959-974

2020

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Nuclear background determines biochemical phenotype in the deafness-associated mitochondrial 12S rRNA mutation

Human molecular genetics, 2001-03, Vol.10 (6), p.573-580

2001

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A biochemical basis for the inherited susceptibility to aminoglycoside ototoxicity

Human molecular genetics, 2000-07, Vol.9 (12), p.1787-1793

2000

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Cu/Zn superoxide dismutase and age-related hearing loss

Hearing research, 2005-11, Vol.209 (1), p.76-85

2005

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Mitochondrial Myopathy, Sideroblastic Anemia, and Lactic Acidosis: An Autosomal Recessive Syndrome in Persian Jews Caused by a Mutation in the PUS1 Gene

Journal of child neurology, 2005-05, Vol.20 (5), p.449-452

2005

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Association of TNF-α G308A gene polymorphism in essential hypertensive patients without type 2 diabetes mellitus

Genetics and molecular research, 2015-12, Vol.14 (4), p.18974-18979

2015

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Inflammatory bowel disease susceptibility loci defined by genome scan meta-analysis of 1952 affected relative pairs

Human molecular genetics, 2004-04, Vol.13 (7), p.763-770

2004

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Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNA(Ser(UCN)) gene

Neurology, 1999-06, Vol.52 (9), p.1905

1999

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A Novel NOD2/CARD15 Haplotype Conferring Risk for Crohn Disease in Ashkenazi Jews

American journal of human genetics, 2003-03, Vol.72 (3), p.509-518

2003

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Human mitochondrial transcription factor B1 as a modifier gene for hearing loss associated with the mitochondrial A1555G mutation

Molecular genetics and metabolism, 2004-05, Vol.82 (1), p.27-32

2004

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TAVR in Patients with Pure Aortic Regurgitation: Ready to Use?

Experimental study on relation between scour and complex 3D flow field

DHA-Rich Fish Oil Increases the Omega-3 Index in Healthy Adults and Slows Resting Heart Rate without Altering Cardiac Autonomic Reflex Modulation

Protective spur dike for scour mitigation of existing spur dikes

Alcohol Consumption Between the Ages of 16 and 23 in Britain: a longitudinal study

Evaluation of Metastatic Meningioma With 2-Deoxy-2-[18F]Fluoro-D-Glucose PET/CT

A LONGITUDINAL STUDY OF MATERNAL DEPRESSION AND CHILD BEHAVIOUR PROBLEMS

Evidence for a low upper limit of heritability of mental test performance in a national sample of twins

Depression in mothers 6 years after the birth of a first child

Comparative study of social and family correlates of children's behaviour ratings

Evaluating the ≤10:1 wholegrain criterion in identifying nutrient quality and health implications of UK breads and breakfast cereals

Evaluation of flow characteristics in labyrinth weirs using response surface methodology

Defining the impact of mutation accumulation on replicative lifespan in yeast using cancer-associated mutator phenotypes

Mutation in TRMU Related to Transfer RNA Modification Modulates the Phenotypic Expression of the Deafness-Associated Mitochondrial 12S Ribosomal RNA Mutations

Age-related hearing loss and the ahl locus in mice

Spontaneous Polyploids and Antimutators Compete During the Evolution of Saccharomyces cerevisiae Mutator Cells

Nuclear background determines biochemical phenotype in the deafness-associated mitochondrial 12S rRNA mutation

A biochemical basis for the inherited susceptibility to aminoglycoside ototoxicity

Cu/Zn superoxide dismutase and age-related hearing loss

Mitochondrial Myopathy, Sideroblastic Anemia, and Lactic Acidosis: An Autosomal Recessive Syndrome in Persian Jews Caused by a Mutation in the PUS1 Gene

Association of TNF-α G308A gene polymorphism in essential hypertensive patients without type 2 diabetes mellitus

Inflammatory bowel disease susceptibility loci defined by genome scan meta-analysis of 1952 affected relative pairs

Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNA(Ser(UCN)) gene

A Novel NOD2/CARD15 Haplotype Conferring Risk for Crohn Disease in Ashkenazi Jews

Human mitochondrial transcription factor B1 as a modifier gene for hearing loss associated with the mitochondrial A1555G mutation

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