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A decision algorithm to identify patients with high probability of monogenic diabetes due to HNF1A mutations

Endocrine, 2019-04, Vol.64 (1), p.75-81

2019

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GTP cyclohydrolase I gene polymorphisms are associated with endothelial dysfunction and oxidative stress in patients with type 2 diabetes mellitus

PloS one, 2014-11, Vol.9 (11), p.e108587-e108587

2014

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Genetics of type 2 diabetes mellitus

Diabetes research and clinical practice, 2005-06, Vol.68, p.S10-S21

Malecki, Maciej T.

2005

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Circulating ghrelin level is higher in HNF1A–MODY and GCK–MODY than in polygenic forms of diabetes mellitus

Endocrine, 2015-12, Vol.50 (3), p.643-649

2015

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Monogenic Models: What Have the Single Gene Disorders Taught Us?

Current diabetes reports, 2012-12, Vol.12 (6), p.659-666

2012

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Permanent neonatal diabetes mellitus - the importance of diabetes differential diagnosis in neonates and infants

European journal of clinical investigation, 2011-03, Vol.41 (3), p.323-333

2011

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Quality of life assessment in patients with HNF1A-MODY and GCK-MODY

Endocrine, 2019-05, Vol.64 (2), p.246-253

2019

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The utility of MODY Probability Calculator in probands of families with early-onset autosomal dominant diabetes from Poland

Minerva medica, 2019-12, Vol.110 (6), p.499

2019

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Intima-media thickness and endothelial dysfunction in GCK and HNF1A-MODY patients

European journal of endocrinology, 2015-03, Vol.172 (3), p.277-283

2015

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Negative pressure wound therapy in the treatment of diabetic foot ulcers may be mediated through differential gene expression

Acta diabetologica, 2019-01, Vol.56 (1), p.115-120

2019

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Mutations in NEUROD1 are associated with the development of type 2 diabetes mellitus

Nature genetics, 1999-11, Vol.23 (3), p.323-328

1999

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A family with the Arg103Pro mutation in the NEUROD1 gene detected by next-generation sequencing – Clinical characteristics of mutation carriers

European journal of medical genetics, 2016-02, Vol.59 (2), p.75-79

2016

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Genetic testing for monogenic diabetes using targeted next-generation sequencing in patients with maturity-onset diabetes of the young

Polskie archiwum medycyny wewne̦trznej, 2015-01, Vol.125 (11), p.845-851

2015

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Variants of the adiponectin gene and type 2 diabetes in a Polish population

Acta diabetologica, 2009-12, Vol.46 (4), p.317-322

2009

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HDL cholesterol as a diagnostic tool for clinical differentiation of GCK-MODY from HNF1A-MODY and type 1 diabetes in children and young adults

Clinical endocrinology (Oxford), 2011-09, Vol.75 (3), p.321-327

2011

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Monogenic diabetes: implications for therapy of rare types of disease

Diabetes, obesity & metabolism, 2008-08, Vol.10 (8), p.607-616

2008

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New Polymorphism of ENPP1 (PC-1) Is Associated With Increased Risk of Type 2 Diabetes Among Obese Individuals

Diabetes (New York, N.Y.), 2006-09, Vol.55 (9), p.2626-2630

2006

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The clinical application of non-genetic biomarkers for differential diagnosis of monogenic diabetes

Diabetes research and clinical practice, 2009-12, Vol.86, p.S15-S21

2009

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An analysis of the sequence of the BAD gene among patients with maturity-onset diabetes of the young (MODY)

Journal of Pediatric Endocrinology and Metabolism, 2017-01, Vol.30 (1), p.97

2017

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Can geneticists help clinicians to understand and treat non-autoimmune diabetes?

Diabetes research and clinical practice, 2008-12, Vol.82, p.S83-S93

2008

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Variants influencing age at diagnosis of HNF1A-MODY

Molecular medicine (Cambridge, Mass.), 2022-09, Vol.28 (1), p.113-113, Article 113

2022

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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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Nicotinamide adenine dinucleotide phosphate (NADPH) oxidase p22phox subunit polymorphisms, systemic oxidative stress, endothelial dysfunction, and atherosclerosis in type 2 diabetes mellitus

Polskie archiwum medycyny wewne̦trznej, 2021-05, Vol.131 (5), p.447-454

2021

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

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

2002

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A decision algorithm to identify patients with high probability of monogenic diabetes due to HNF1A mutations

GTP cyclohydrolase I gene polymorphisms are associated with endothelial dysfunction and oxidative stress in patients with type 2 diabetes mellitus

Genetics of type 2 diabetes mellitus

Circulating ghrelin level is higher in HNF1A–MODY and GCK–MODY than in polygenic forms of diabetes mellitus

Monogenic Models: What Have the Single Gene Disorders Taught Us?

Permanent neonatal diabetes mellitus - the importance of diabetes differential diagnosis in neonates and infants

Quality of life assessment in patients with HNF1A-MODY and GCK-MODY

The utility of MODY Probability Calculator in probands of families with early-onset autosomal dominant diabetes from Poland

Intima-media thickness and endothelial dysfunction in GCK and HNF1A-MODY patients

Negative pressure wound therapy in the treatment of diabetic foot ulcers may be mediated through differential gene expression

Mutations in NEUROD1 are associated with the development of type 2 diabetes mellitus

A family with the Arg103Pro mutation in the NEUROD1 gene detected by next-generation sequencing – Clinical characteristics of mutation carriers

Genetic testing for monogenic diabetes using targeted next-generation sequencing in patients with maturity-onset diabetes of the young

Variants of the adiponectin gene and type 2 diabetes in a Polish population

HDL cholesterol as a diagnostic tool for clinical differentiation of GCK-MODY from HNF1A-MODY and type 1 diabetes in children and young adults

Monogenic diabetes: implications for therapy of rare types of disease

New Polymorphism of ENPP1 (PC-1) Is Associated With Increased Risk of Type 2 Diabetes Among Obese Individuals

The clinical application of non-genetic biomarkers for differential diagnosis of monogenic diabetes

An analysis of the sequence of the BAD gene among patients with maturity-onset diabetes of the young (MODY)

Can geneticists help clinicians to understand and treat non-autoimmune diabetes?

Variants influencing age at diagnosis of HNF1A-MODY

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

Nicotinamide adenine dinucleotide phosphate (NADPH) oxidase p22phox subunit polymorphisms, systemic oxidative stress, endothelial dysfunction, and atherosclerosis in type 2 diabetes mellitus

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

Association of the calpain-10 gene with type 2 diabetes in Europeans: Results of pooled and meta-analyses

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