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Familial chylomicronemia syndrome: an under‐recognized cause of severe hypertriglyceridaemia

Journal of internal medicine, 2020-04, Vol.287 (4), p.340-348

2020

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Ambroxol as a novel disease-modifying treatment for Parkinson's disease dementia: protocol for a single-centre, randomized, double-blind, placebo-controlled trial

BMC neurology, 2019-02, Vol.19 (1), p.20-20, Article 20

2019

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Conservative management in hypertriglyceridemia‐associated pancreatitis

Journal of internal medicine, 2019-12, Vol.286 (6), p.644-650

2019

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Gas production and transport during bench-scale electrical resistance heating of water and trichloroethene

Journal of contaminant hydrology, 2014-09, Vol.165, p.24-36

2014

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Nuclear lamin A/C R482Q mutation in Canadian kindreds with Dunnigan-type familial partial lipodystrophy

Human molecular genetics, 2000, Vol.9 (1), p.109-112

2000

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Mutations in LPL, APOC2, APOA5, GPIHBP1 and LMF1 in patients with severe hypertriglyceridaemia

Journal of internal medicine, 2012-08, Vol.272 (2), p.185-196

2012

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Evaluation of apolipoprotein A5 variants: A cohort of patients with severe hypertriglyceridemia from Turkiye

Journal of clinical lipidology, 2024-05, Vol.18 (3), p.e423-e429

2024

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The lipid-lowering effects of lomitapide are unaffected by adjunctive apheresis in patients with homozygous familial hypercholesterolaemia – A post-hoc analysis of a Phase 3, single-arm, open-label trial

Atherosclerosis, 2015-06, Vol.240 (2), p.408-414

2015

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Differences in risk factors, atherosclerosis, and cardiovascular disease between ethnic groups in Canada: the Study of Health Assessment and Risk in Ethnic groups (SHARE)

The Lancet (British edition), 2000-07, Vol.356 (9226), p.279-284

2000

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Vascular calcifications in homozygote familial hypercholesterolemia

Arteriosclerosis, thrombosis, and vascular biology, 2008-04, Vol.28 (4), p.777

2008

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Novel lamin A/C gene (LMNA) mutations in atypical progeroid syndromes

Journal of medical genetics, 2004-04, Vol.41 (4), p.304-308

2004

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Hutchinson-Gilford progeria syndrome

Clinical genetics, 2004-11, Vol.66 (5), p.375-381

2004

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Thermal Treatment of Trichloroethene by Electrical Resistance Heating: Visualization of Gas Production in Coarse Layers

Water (Basel), 2023-05, Vol.15 (11), p.1976

2023

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Using Mendelian randomization to determine causative factors in cardiovascular disease

Journal of internal medicine, 2013-01, Vol.273 (1), p.44-47

2013

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Respiratory syncytial virus therapy and prophylaxis: have we finally turned the corner?

The European respiratory journal, 2011-08, Vol.38 (2), p.246-247

Hegele, R G

2011

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Lessons from human mutations in PPARγ

International Journal of Obesity, 2005-03, Vol.29 (S1), p.S31-S35

Hegele, R A

2005

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LMNA mutation position predicts organ system involvement in laminopathies

Clinical genetics, 2005-07, Vol.68 (1), p.31-34

Hegele, RA

2005

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Depression, marijuana use and early-onset marijuana use conferred unique effects on neural connectivity and cognition

Acta psychiatrica Scandinavica, 2016-11, Vol.134 (5), p.399-409

2016

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Characterization of the I4399M variant of apolipoprotein(a): implications for altered prothrombotic properties of lipoprotein(a)

Journal of thrombosis and haemostasis, 2017-09, Vol.15 (9), p.1834-1844

2017

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Biallelic mutations at PPARG cause a congenital, generalized lipodystrophy similar to the Berardinelli–Seip syndrome

European journal of medical genetics, 2014-09, Vol.57 (9), p.524-526

2014

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The failure of torcetrapib: what have we learned?

British journal of pharmacology, 2008-08, Vol.154 (7), p.1379-1381

2008

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Monogenic Dyslipidemias: Window on Determinants of Plasma Lipoprotein Metabolism

American journal of human genetics, 2001-12, Vol.69 (6), p.1161-1177

Hegele, Robert A.

2001

Volltextzugriff (PDF)

The Canadian Healthy Infant Longitudinal Development Birth Cohort Study: Biological Samples and Biobanking

Paediatric and perinatal epidemiology, 2015-01, Vol.29 (1), p.84-92

2015

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Inflammation of small airways in asthma

Journal of allergy and clinical immunology, 1997-07, Vol.100 (1), p.44-51

1997

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Compound heterozygosity for two non-synonymous polymorphisms in NPC1L1 in a non-responder to ezetimibe

Clinical genetics, 2005-02, Vol.67 (2), p.175-177

2005

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Familial chylomicronemia syndrome: an under‐recognized cause of severe hypertriglyceridaemia

Ambroxol as a novel disease-modifying treatment for Parkinson's disease dementia: protocol for a single-centre, randomized, double-blind, placebo-controlled trial

Conservative management in hypertriglyceridemia‐associated pancreatitis

Gas production and transport during bench-scale electrical resistance heating of water and trichloroethene

Nuclear lamin A/C R482Q mutation in Canadian kindreds with Dunnigan-type familial partial lipodystrophy

Mutations in LPL, APOC2, APOA5, GPIHBP1 and LMF1 in patients with severe hypertriglyceridaemia

Evaluation of apolipoprotein A5 variants: A cohort of patients with severe hypertriglyceridemia from Turkiye

The lipid-lowering effects of lomitapide are unaffected by adjunctive apheresis in patients with homozygous familial hypercholesterolaemia – A post-hoc analysis of a Phase 3, single-arm, open-label trial

Differences in risk factors, atherosclerosis, and cardiovascular disease between ethnic groups in Canada: the Study of Health Assessment and Risk in Ethnic groups (SHARE)

Vascular calcifications in homozygote familial hypercholesterolemia

Novel lamin A/C gene (LMNA) mutations in atypical progeroid syndromes

Hutchinson-Gilford progeria syndrome

Thermal Treatment of Trichloroethene by Electrical Resistance Heating: Visualization of Gas Production in Coarse Layers

Using Mendelian randomization to determine causative factors in cardiovascular disease

Respiratory syncytial virus therapy and prophylaxis: have we finally turned the corner?

Lessons from human mutations in PPARγ

LMNA mutation position predicts organ system involvement in laminopathies

Depression, marijuana use and early-onset marijuana use conferred unique effects on neural connectivity and cognition

Characterization of the I4399M variant of apolipoprotein(a): implications for altered prothrombotic properties of lipoprotein(a)

Biallelic mutations at PPARG cause a congenital, generalized lipodystrophy similar to the Berardinelli–Seip syndrome

The failure of torcetrapib: what have we learned?

Monogenic Dyslipidemias: Window on Determinants of Plasma Lipoprotein Metabolism

The Canadian Healthy Infant Longitudinal Development Birth Cohort Study: Biological Samples and Biobanking

Inflammation of small airways in asthma

Compound heterozygosity for two non-synonymous polymorphisms in NPC1L1 in a non-responder to ezetimibe

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