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Depression and quality of sleep in patients with type 1 diabetes being under regular diabetes care

European psychiatry, 2023-03, Vol.66 (S1), p.S347-S348

2023

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Switching from Neutral Protamine Hagedorn Insulin to Insulin Glargine 300 U/mL Improves Glycaemic Control and Reduces Hypoglycaemia Risk: Results of a Multicentre, Prospective, Observational Study

Journal of diabetes research, 2020, Vol.2020 (2020), p.1-8

2020

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A single dose of dapagliflozin, an SGLT-2 inhibitor, induces higher glycosuria in GCK- and HNF1A-MODY than in type 2 diabetes mellitus

Endocrine, 2017-08, Vol.57 (2), p.272-279

2017

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Clinical Usefulness of a Bolus Calculator in Maintaining Normoglycaemia in Active Professional Patients with Type 1 Diabetes Treated with Continuous Subcutaneous Insulin Infusion

Journal of international medical research, 2008-09, Vol.36 (5), p.1112-1116

2008

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Switching from Neutral Protamine Hagedorn (NPH) Insulin to Insulin Glargine 300 U/mL in Older and Younger Patients with Type 2 Diabetes: A Post Hoc Analysis of a Multicenter, Prospective, Observational Study

Diabetes therapy, 2022-02, Vol.13 (2), p.301-310

2022

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Prevalence of Retinopathy in Adult Patients with GCK-MODY and HNF1A-MODY

Experimental and clinical endocrinology & diabetes, 2015-10, Vol.123 (9), p.524-528

2015

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The identification of a R201H mutation in KCNJ11, which encodes Kir6.2, and successful transfer to sustained-release sulphonylurea therapy in a subject with neonatal diabetes: evidence for heterogeneity of beta cell function among carriers of the R201H mutation

Diabetologia, 2005-05, Vol.48 (5), p.1029-1031

2005

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Vitamin D receptor gene polymorphisms and association with type 2 diabetes mellitus in a Polish population

Experimental and clinical endocrinology & diabetes, 2003-12, Vol.111 (8), p.505-509

2003

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Molecular background and clinical characteristics of HNF1A MODY in a Polish population

Diabetes & metabolism, 2008-11, Vol.34 (5), p.524-528

2008

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Further evidence for a susceptibility locus for type 2 diabetes on chromosome 20q13.1-q13.2

Diabetes (New York, N.Y.), 2000-12, Vol.49 (12), p.2212-2216

2000

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Clinical risk factors and the role of VDR gene polymorphisms in diabetic retinopathy in Polish type 2 diabetes patients

Acta diabetologica, 2006-12, Vol.43 (4), p.114-119

2006

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Diabetic retinopathy in permanent neonatal diabetes due to Kir6.2 gene mutations: the results of a minimum 2-year follow-up after the transfer from insulin to sulphonylurea

Diabetic medicine, 2009-06, Vol.26 (6), p.663-664

2009

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The Influence of Dietary Carbohydrate Content on Glycaemia in Patients with Glucokinase Maturity-Onset Diabetes of the Young

Journal of international medical research, 2011-12, Vol.39 (6), p.2296-2301

2011

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Lack of association between polymorphisms in the gene encoding protein tyrosine phosphatase 1B (PTPN1) and risk of Type 2 diabetes

Diabetic medicine, 2007-06, Vol.24 (6), p.650-655

2007

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Pancreatic exocrine insufficiency is not common in HNF-1α MODY

Diabetic medicine, 2008-05, Vol.25 (5), p.627-630

2008

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24-HOUR CENTRAL BLOOD PRESSURE PROFILE IN TYPE 1 DIABETICS

Journal of hypertension, 2018-06, Vol.36 (Supplement 1), p.e263-e264

2018

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Switching from Neutral Protamine Hagedorn Insulin to Insulin Glargine 300U/mL Improves Glycaemic Control and Reduces Hypoglycaemia Risk: Results of a Multicentre, Prospective, Observational Study

Journal of Diabetes Research, 2020-04

2020

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The Ala45Thr polymorphism of BETA2/NeuroD1 gene and susceptibility to type 2 diabetes mellitus in a Polish population

Acta diabetologica, 2003-06, Vol.40 (2), p.109-111

2003

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Association study of the Vitamin D: 1alpha-hydroxylase (CYP1alpha) gene and type 2 diabetes mellitus in a Polish population

Diabetes & metabolism, 2003-04, Vol.29 (2), p.119-124

2003

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Effectiveness and safety of long-term treatment with sulfonylureas in patients with neonatal diabetes due to KCNJ11 mutations: an international cohort study

The lancet. Diabetes & endocrinology, 2018-08, Vol.6 (8), p.637-646

2018

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The Ala45Thr polymorphism of BETA2/NeuroD1 gene and susceptibility to type 1 diabetes mellitus in caucasians

Experimental and clinical endocrinology & diabetes, 2003-08, Vol.111 (5), p.251-254

2003

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Routine sensor-augmented pump therapy in type 1 diabetes: the INTERPRET study

Diabetes technology & therapeutics, 2013-04, Vol.15 (4), p.273-280

2013

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Homozygous combination of calpain 10 gene haplotypes is associated with type 2 diabetes mellitus in a Polish population

European journal of endocrinology, 2002-05, Vol.146 (5), p.695-699

2002

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Type 2 diabetes mellitus: from genes to disease

Pharmacological reports, 2005-01, Vol.57 Suppl, p.20-32

2005

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Determinants of the development of diabetes (maturity-onset diabetes of the young-3) in carriers of HNF-1α mutations: Evidence for parent-of-origin effect

Diabetes care, 2002-12, Vol.25 (12), p.2292-2301

2002

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Depression and quality of sleep in patients with type 1 diabetes being under regular diabetes care

Switching from Neutral Protamine Hagedorn Insulin to Insulin Glargine 300 U/mL Improves Glycaemic Control and Reduces Hypoglycaemia Risk: Results of a Multicentre, Prospective, Observational Study

A single dose of dapagliflozin, an SGLT-2 inhibitor, induces higher glycosuria in GCK- and HNF1A-MODY than in type 2 diabetes mellitus

Clinical Usefulness of a Bolus Calculator in Maintaining Normoglycaemia in Active Professional Patients with Type 1 Diabetes Treated with Continuous Subcutaneous Insulin Infusion

Switching from Neutral Protamine Hagedorn (NPH) Insulin to Insulin Glargine 300 U/mL in Older and Younger Patients with Type 2 Diabetes: A Post Hoc Analysis of a Multicenter, Prospective, Observational Study

Prevalence of Retinopathy in Adult Patients with GCK-MODY and HNF1A-MODY

The identification of a R201H mutation in KCNJ11, which encodes Kir6.2, and successful transfer to sustained-release sulphonylurea therapy in a subject with neonatal diabetes: evidence for heterogeneity of beta cell function among carriers of the R201H mutation

Vitamin D receptor gene polymorphisms and association with type 2 diabetes mellitus in a Polish population

Molecular background and clinical characteristics of HNF1A MODY in a Polish population

Further evidence for a susceptibility locus for type 2 diabetes on chromosome 20q13.1-q13.2

Clinical risk factors and the role of VDR gene polymorphisms in diabetic retinopathy in Polish type 2 diabetes patients

Diabetic retinopathy in permanent neonatal diabetes due to Kir6.2 gene mutations: the results of a minimum 2-year follow-up after the transfer from insulin to sulphonylurea

The Influence of Dietary Carbohydrate Content on Glycaemia in Patients with Glucokinase Maturity-Onset Diabetes of the Young

Lack of association between polymorphisms in the gene encoding protein tyrosine phosphatase 1B (PTPN1) and risk of Type 2 diabetes

Pancreatic exocrine insufficiency is not common in HNF-1α MODY

24-HOUR CENTRAL BLOOD PRESSURE PROFILE IN TYPE 1 DIABETICS

Switching from Neutral Protamine Hagedorn Insulin to Insulin Glargine 300U/mL Improves Glycaemic Control and Reduces Hypoglycaemia Risk: Results of a Multicentre, Prospective, Observational Study

The Ala45Thr polymorphism of BETA2/NeuroD1 gene and susceptibility to type 2 diabetes mellitus in a Polish population

Association study of the Vitamin D: 1alpha-hydroxylase (CYP1alpha) gene and type 2 diabetes mellitus in a Polish population

Effectiveness and safety of long-term treatment with sulfonylureas in patients with neonatal diabetes due to KCNJ11 mutations: an international cohort study

The Ala45Thr polymorphism of BETA2/NeuroD1 gene and susceptibility to type 1 diabetes mellitus in caucasians

Routine sensor-augmented pump therapy in type 1 diabetes: the INTERPRET study

Homozygous combination of calpain 10 gene haplotypes is associated with type 2 diabetes mellitus in a Polish population

Type 2 diabetes mellitus: from genes to disease

Determinants of the development of diabetes (maturity-onset diabetes of the young-3) in carriers of HNF-1α mutations: Evidence for parent-of-origin effect

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