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Erratum to: Trimethylamine-N-oxide: A Novel Biomarker for the Identification of Inflammatory Bowel Disease.
- Published in:
- 2016
- By:
- Publication type:
- corrected article
Trimethylamine-N-oxide: A Novel Biomarker for the Identification of Inflammatory Bowel Disease.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Clinical and Mutation Spectra of Cockayne Syndrome in India.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Elderly patients with very high plasma lipoprotein(a) concentrations and few cardiovascular consequences: a case series.
- Published in:
- Journal of International Medical Research, 2024, v. 52, n. 8, p. 1, doi. 10.1177/03000605241271876
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- Publication type:
- Article
Cover Image, Volume 58, Number 7, July 2023.
- Published in:
- Pediatric Pulmonology, 2023, v. 58, n. 7, p. i, doi. 10.1002/ppul.26552
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- Publication type:
- Article
First reports of primary ciliary dyskinesia caused by a shared DNAH11 allele in Canadian Inuit.
- Published in:
- Pediatric Pulmonology, 2023, v. 58, n. 7, p. 1942, doi. 10.1002/ppul.26414
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- Publication type:
- Article
Integrated Analysis of the Pancreas and Islets Reveals Unexpected Findings in Human Male With Type 1 Diabetes.
- Published in:
- Journal of the Endocrine Society, 2021, v. 5, n. 12, p. 1, doi. 10.1210/jendso/bvab162
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- Publication type:
- Article
Multisystem Progeroid Syndrome With Lipodystrophy, Cardiomyopathy, and Nephropathy Due to an LMNA p.R349W Variant.
- Published in:
- Journal of the Endocrine Society, 2020, v. 4, n. 10, p. 1, doi. 10.1210/jendso/bvaa104
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- Publication type:
- Article
Differentiating Familial Chylomicronemia Syndrome From Multifactorial Severe Hypertriglyceridemia by Clinical Profiles.
- Published in:
- Journal of the Endocrine Society, 2019, v. 3, n. 12, p. 2397, doi. 10.1210/js.2019-00214
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- Publication type:
- Article
Whole-genome sequencing in French Canadians from Quebec.
- Published in:
- Human Genetics, 2016, v. 135, n. 11, p. 1213, doi. 10.1007/s00439-016-1702-6
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- Publication type:
- Article
Genomic basis of cystathioninuria (MIM 219500) revealed by multiple mutations in cystathionine gamma-lyase (CTH).
- Published in:
- Human Genetics, 2003, v. 112, n. 4, p. 404, doi. 10.1007/s00439-003-0906-8
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- Publication type:
- Article
Blood pressure among the Inuit (Eskimo) populations in the Arctic.
- Published in:
- Scandinavian Journal of Public Health, 2003, v. 31, n. 2, p. 92, doi. 10.1080/14034940210133924
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- Publication type:
- Article
Fatty liver in a non-obese patient.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
A novel MC4R mutation associated with childhood-onset obesity: A case report.
- Published in:
- Paediatrics & Child Health (1205-7088), 2014, v. 19, n. 10, p. 515, doi. 10.1093/pch/19.10.515
- By:
- Publication type:
- Article
Survival in Academy Award-winning actors and actresses.
- Published in:
- 2003
- By:
- Publication type:
- letter
Rapid development of massive tendon xanthomas following highly active antiretroviral therapy.
- Published in:
- 2002
- By:
- Publication type:
- letter
A Novel APOC2 Missense Mutation Causing Apolipoprotein C-II Deficiency With Severe Triglyceridemia and Pancreatitis.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Comment on Huh et al. Remnant Cholesterol Is an Independent Predictor of Type 2 Diabetes: A Nationwide Population-Based Cohort Study. Diabetes Care 2023;46:305–312.
- Published in:
- Diabetes Care, 2023, v. 46, n. 10, p. e204, doi. 10.2337/dc23-0992
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- Publication type:
- Article
Complex genetic architecture in severe hypobetalipoproteinemia.
- Published in:
- Lipids in Health & Disease, 2018, v. 17, p. 1, doi. 10.1186/s12944-018-0680-1
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- Publication type:
- Article
Ezetimibe prescriptions in older Canadian adults after an acute myocardial infarction: a population-based cohort study.
- Published in:
- Lipids in Health & Disease, 2018, v. 17, p. 1, doi. 10.1186/s12944-017-0649-5
- By:
- Publication type:
- Article
Secondary causes of chylomicronemia: defining the underside of the iceberg.
- Published in:
- 2018
- By:
- Publication type:
- editorial
Kinase mutations in human disease: interpreting genotype-phenotype relationships.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Plasma lipoproteins: genetic influences and clinical implications.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Progression to hepatitis and fibrosis secondary to lomitapide use-reply.
- Published in:
- 2014
- By:
- Publication type:
- Journal Article
Progression to Hepatitis and Fibrosis Secondary to Lomitapide Use: Selecting the Next Course of Action.
- Published in:
- JAMA Internal Medicine, 2014, v. 174, n. 9, p. 1522, doi. 10.1001/jamainternmed.2014.1538
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- Publication type:
- Article
Severe hypertriglyceridemia with pancreatitis: thirteen years' treatment with lomitapide.
- Published in:
- 2014
- By:
- Publication type:
- Journal Article
Severe Hypertriglyceridemia With Pancreatitis.
- Published in:
- JAMA Internal Medicine, 2014, v. 174, n. 3, p. 443, doi. 10.1001/jamainternmed.2013.13309
- By:
- Publication type:
- Article
Cost-Effectiveness of Icosapent Ethyl (IPE) for the Reduction of the Risk of Ischemic Cardiovascular Events in Canada.
- Published in:
- ClinicoEconomics & Outcomes Research, 2023, v. 15, p. 295, doi. 10.2147/CEOR.S377935
- By:
- Publication type:
- Article
Apolipoprotein E in hyperlipidemia.
- Published in:
- 1994
- By:
- Publication type:
- journal article
Bioinformatic detection of copy number variation in HNF4A causing maturity onset diabetes of the young.
- Published in:
- Clinical Genetics, 2019, v. 96, n. 4, p. 376, doi. 10.1111/cge.13599
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- Publication type:
- Article
Complex effects of laminopathy mutations on nuclear structure and function.
- Published in:
- Clinical Genetics, 2019, v. 95, n. 2, p. 199, doi. 10.1111/cge.13455
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- Publication type:
- Article
Genetic variation in paraoxonase-2 is associated with variation in plasma lipoproteins in Canadian Oji-Cree.
- Published in:
- Clinical Genetics, 1998, v. 54, n. 5, p. 394, doi. 10.1111/j.1399-0004.1998.tb03752.x
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- Publication type:
- Article
Exome Sequencing: New Insights into Lipoprotein Disorders.
- Published in:
- Current Cardiology Reports, 2014, v. 16, n. 7, p. 1, doi. 10.1007/s11886-014-0507-2
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- Publication type:
- Article
Lipoprotein(a) and coronary heart disease risk.
- Published in:
- Current Cardiology Reports, 1999, v. 1, n. 2, p. 105, doi. 10.1007/s11886-999-0067-z
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- Publication type:
- Article
Perivascular spaces, plasma GFAP, and speeded executive function in neurodegenerative diseases.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, n. 8, p. 5800, doi. 10.1002/alz.14081
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- Publication type:
- Article
Decreased Abdominal Girth and Increased Blood Pressure Associated With a Single Nucleotide Variant of Human Adenylyl Cyelase 6.
- Published in:
- FASEB Journal, 2007, v. 21, n. 6, p. A795, doi. 10.1096/fasebj.21.6.a795-d
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- Publication type:
- Article
Review of Evolocumab for the Reduction of LDL Cholesterol and Secondary Prevention of Atherosclerotic Cardiovascular Disease.
- Published in:
- Reviews in Cardiovascular Medicine, 2024, v. 25, n. 5, p. 1, doi. 10.31083/j.rcm2505190
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- Publication type:
- Article
Severe Hypertriglyceridemia due to a novel p.Q240H mutation in the Lipoprotein Lipase gene.
- Published in:
- Lipids in Health & Disease, 2015, v. 14, n. 1, p. 1, doi. 10.1186/s12944-015-0107-1
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- Publication type:
- Article
Heterozygous CAV1 frameshift mutations (MIM 601047) in patients with atypical partial lipodystrophy and hypertriglyceridemia.
- Published in:
- Lipids in Health & Disease, 2008, v. 7, p. 1, doi. 10.1186/1476-511X-7-3
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- Publication type:
- Article
Genetic determinants of statin intolerance.
- Published in:
- Lipids in Health & Disease, 2007, v. 6, p. 7, doi. 10.1186/1476-511X-6-7
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- Publication type:
- Article
Homozygous missense mutation (G56R) in glycosylphosphatidylinositol-anchored high-density lipoprotein-binding protein 1 (GPI-HBP1) in two siblings with fasting chylomicronemia (MIM 144650).
- Published in:
- Lipids in Health & Disease, 2007, v. 6, p. 23, doi. 10.1186/1476-511X-6-23
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- Publication type:
- Article
Treatment of dyslipidemia with lovastatin and ezetimibe in an adolescent with cholesterol ester storage disease.
- Published in:
- Lipids in Health & Disease, 2005, v. 4, p. 26, doi. 10.1186/1476-511X-4-26
- By:
- Publication type:
- Article
NPC1L1 haplotype is associated with inter-individual variation in plasma low-density lipoprotein response to ezetimibe.
- Published in:
- Lipids in Health & Disease, 2005, v. 4, p. 1, doi. 10.1186/1476-511X-4-16
- By:
- Publication type:
- Article
Expanding the phenotypic and molecular spectrum of NFS1‐related disorders that cause functional deficiencies in mitochondrial and cytosolic iron–sulfur cluster containing enzymes.
- Published in:
- Human Mutation, 2022, v. 43, n. 3, p. 305, doi. 10.1002/humu.24330
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- Publication type:
- Article
Stability of lipids on peritoneal dialysis in a patient with familial LCAT deficiency.
- Published in:
- 2007
- By:
- Publication type:
- Case Study
'Keep on keeping on': persistence with lipid-lowering treatment in familial hypercholesterolaemia.
- Published in:
- European Journal of Preventive Cardiology, 2023, v. 30, n. 4, p. 318, doi. 10.1093/eurjpc/zwac297
- By:
- Publication type:
- Article
Homozigot ailevi hiperkolesterolemi: klinisyenlerin tanıyı ve klinik yönetimi geliştirmelerine yönelik yeni anlayışlar ve rehberlik. Avrupa Ateroskleroz Derneği’nin Ailevi Hiperkolesterolemi Üzerine Uzlaşı Paneli yazılı görüşü
- Published in:
- Archives of the Turkish Society of Cardiology / Türk Kardiyoloji Derneği Arşivi, 2015, v. 43, p. 1
- By:
- Publication type:
- Article
Clinical utility gene card for: Familial hypobetalipoproteinaemia (APOB) - Update 2014.
- Published in:
- European Journal of Human Genetics, 2015, v. 23, n. 6, p. 1, doi. 10.1038/ejhg.2014.225
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- Publication type:
- Article
Clinical utility gene card for: Abetalipoproteinaemia - Update 2014.
- Published in:
- European Journal of Human Genetics, 2015, v. 23, n. 6, p. 1, doi. 10.1038/ejhg.2014.224
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- Publication type:
- Article
Clinical utility gene card for: Abetalipoproteinaemia.
- Published in:
- European Journal of Human Genetics, 2012, v. 20, n. 8, p. e1, doi. 10.1038/ejhg.2012.30
- By:
- Publication type:
- Article