Found: 29
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Association Between Eight Adiponectin Polymorphisms, Obesity, and Metabolic Syndrome Parameters in Tunisian Volunteers.
- Published in:
- Metabolic Syndrome & Related Disorders, 2011, v. 9, n. 6, p. 419, doi. 10.1089/met.2011.0035
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- Publication type:
- Article
Apolipoprotein B and Non-High-Density Lipoprotein Cholesterol Are Better Risk Markers for Coronary Artery Disease than Low-Density Lipoprotein Cholesterol in Hypertriglyceridemic Metabolic Syndrome Patients.
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- Metabolic Syndrome & Related Disorders, 2010, v. 8, n. 6, p. 515, doi. 10.1089/met.2010.0006
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- Publication type:
- Article
Elevated Liver Enzymes in Metabolic Syndrome Are Associated with Coronary Stenosis in a Tunisian Population.
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- Metabolic Syndrome & Related Disorders, 2010, v. 8, n. 3, p. 249, doi. 10.1089/met.2009.0077
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- Article
Designing a Simple Electrochemical Genosensor for the Detection of Urinary PCA3, a Prostate Cancer Biomarker.
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- Micromachines, 2024, v. 15, n. 5, p. 602, doi. 10.3390/mi15050602
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- Article
A novel mutation in the AGXT gene causing primary hyperoxaluria type I: genotype-phenotype correlation.
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- Journal of Genetics, 2016, v. 95, n. 3, p. 659, doi. 10.1007/s12041-016-0676-4
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- Article
Association of four apolipoprotein B polymorphisms with lipid profile and stenosis in Tunisian coronary patients.
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- Journal of Genetics, 2012, v. 91, n. 1, p. 75, doi. 10.1007/s12041-012-0127-9
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- Publication type:
- Article
5′ ins/del and 3′ VNTR polymorphisms in the apolipoprotein B gene in relation to lipids and coronary artery disease.
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- Clinical Chemistry & Laboratory Medicine, 2008, v. 46, n. 3, p. 329, doi. 10.1515/CCLM.2008.067
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- Article
Unusual clinical outcome of primary Hyperoxaluria type 1 in Tunisian patients carrying 33_34InsC mutation.
- Published in:
- 2017
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- Publication type:
- journal article
Impairment of Spermatogenesis in Rats by Mercuric Chloride: Involvement of Low 17β-Estradiol Level in Induction of Acute Oxidative Stress.
- Published in:
- Biological Trace Element Research, 2011, v. 142, n. 3, p. 598, doi. 10.1007/s12011-010-8774-2
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- Publication type:
- Article
Association Between Haptoglobin 2 -2 Genotype and Coronary Artery Disease and Its Severity in a Tunisian Population.
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- Biochemical Genetics, 2014, v. 52, n. 5/6, p. 269, doi. 10.1007/s10528-014-9646-9
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- Article
Association of PON1 and PON2 Polymorphisms with PON1 Activity and Significant Coronary Stenosis in a Tunisian Population.
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- Biochemical Genetics, 2013, v. 51, n. 1/2, p. 76, doi. 10.1007/s10528-012-9544-y
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- Publication type:
- Article
Response to the Letter to the Editor Regarding "Polymorphisms in Pediatric Idiopathic Nephrotic Syndrome".
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- 2018
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- Publication type:
- Letter to the Editor
Leptin and Leptin receptor polymorphisms, plasma Leptin levels and obesity in Tunisian volunteers.
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- International Journal of Experimental Pathology, 2018, v. 99, n. 3, p. 121, doi. 10.1111/iep.12271
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- Article
Six lipoprotein lipase gene polymorphisms, lipid profile and coronary stenosis in a Tunisian population.
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- Molecular Biology Reports, 2012, v. 39, n. 11, p. 9893, doi. 10.1007/s11033-012-1856-9
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- Publication type:
- Article
Timing matters: diurnal variation of maximal fat oxidation and substrate oxidation rates in metabolic syndrome—a randomized crossover study.
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- European Journal of Applied Physiology, 2024, v. 124, n. 10, p. 3135, doi. 10.1007/s00421-024-05518-y
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- Publication type:
- Article
Hyperhomocysteinemia in Tunisian bipolar I patients.
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- Psychiatry & Clinical Neurosciences, 2011, v. 65, n. 7, p. 664, doi. 10.1111/j.1440-1819.2011.02284.x
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- Publication type:
- Article
Mutational Analysis of Agxt in Tunisian Population with Primary Hyperoxaluria Type 1.
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- Annals of Human Genetics, 2017, v. 81, n. 1, p. 1, doi. 10.1111/ahg.12178
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- Publication type:
- Article
Resistin polymorphims, plasma resistin levels and obesity in Tunisian volunteers.
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- 2018
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- Publication type:
- journal article
Association of ADIPOQ, leptin, LEPR, and resistin polymorphisms with obesity parameters in Hammam Sousse Sahloul Heart Study.
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- 2017
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- Publication type:
- journal article
HOGA1 Gene Mutations of Primary Hyperoxaluria Type 3 in Tunisian Patients.
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- 2017
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- Publication type:
- journal article
Influence of genetic and non-genetic factors on acenocoumarol maintenance dose requirement in a Tunisian population.
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- European Journal of Clinical Pharmacology, 2018, v. 74, n. 6, p. 711, doi. 10.1007/s00228-018-2423-7
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- Publication type:
- Article
Novel mutations in steroid-resistant nephrotic syndrome diagnosed in Tunisian children.
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- Pediatric Nephrology, 2011, v. 26, n. 2, p. 241, doi. 10.1007/s00467-010-1694-8
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- Publication type:
- Article
Paraoxonase 1 polymorphisms (L55M and Q192R) as a genetic marker of diabetic nephropathy in youths with type 1 diabetes.
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- Polish Journal of Endocrinology / Endokrynologia Polska, 2017, v. 68, n. 1, p. 35, doi. 10.5603/EP.a2016.0027
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- Article
Effect of cigarette smoking on paraoxonase 1 activity according to PON1 L55M and PON1 Q192R gene polymorphisms.
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- Environmental Health & Preventive Medicine, 2012, v. 17, n. 4, p. 316, doi. 10.1007/s12199-011-0256-4
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- Publication type:
- Article
Effect of Pre-Meal Metformin With or Without an Acute Exercise Bout on Postprandial Lipemic and Glycemic Responses in Metabolic Syndrome Patients: A Randomized, Open Label, Crossover Study.
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- Journal of Cardiovascular Pharmacology & Therapeutics, 2023, v. 28, p. 1, doi. 10.1177/10742484231156318
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- Publication type:
- Article
Variability in response to vitamin D supplementation according to vitamin D metabolism related gene polymorphisms in healthy adults.
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- European Journal of Clinical Nutrition, 2023, v. 77, n. 2, p. 189, doi. 10.1038/s41430-022-01218-y
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- Publication type:
- Article
Biological Activities Evaluation of Enantiopure Isoxazolidine Derivatives: In Vitro, In Vivo and In Silico Studies.
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- Applied Biochemistry & Biotechnology, 2019, v. 187, n. 3, p. 1113, doi. 10.1007/s12010-018-2868-2
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- Article
The C677T MTHFR genotypes influence the efficacy of B9 and B12 vitamins supplementation to lowering plasma total homocysteine in hemodialysis.
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- Journal of Nephrology (JNonline), 2016, v. 29, n. 5, p. 691, doi. 10.1007/s40620-015-0235-8
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- Publication type:
- Article
Selected AGXT gene mutations analysis provides a genetic diagnosis in 28% of Tunisian patients with primary hyperoxaluria.
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- BMC Nephrology, 2011, v. 12, n. 1, p. 25, doi. 10.1186/1471-2369-12-25
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- Publication type:
- Article