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Prevalence of monogenic diabetes amongst Polish children after a nationwide genetic screening campaign

Diabetologia, 2012-10, Vol.55 (10), p.2631-2635

2012

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Mutations at the BLK locus linked to maturity onset diabetes of the young and β-cell dysfunction

Proceedings of the National Academy of Sciences - PNAS, 2009-08, Vol.106 (34), p.14460-14465

2009

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Delayed recognition of Wolfram syndrome frequently misdiagnosed as type 1 diabetes with early chronic complications

Experimental and clinical endocrinology & diabetes, 2014-01, Vol.122 (1), p.35

2014

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Wolfram syndrome in the Polish population: novel mutations and genotype-phenotype correlation

Clinical endocrinology (Oxford), 2011-11, Vol.75 (5), p.636-641

2011

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Psychiatric Comorbidities in Pediatric Monogenic Diabetes due to GCK Mutation: Impact on Diabetes-Related Quality of Life

Journal of the Academy of Consultation-Liaison Psychiatry, 2022-11, Vol.63 (6), p.548-556

2022

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Glycemic variability in patients with Wolfram syndrome is lower than in type 1 diabetes

Acta diabetologica, 2015-12, Vol.52 (6), p.1057-1062

2015

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Switching to sulphonylureas in children with iDEND syndrome caused by KCNJ11 mutations results in improved cerebellar perfusion

Diabetes care, 2013-08, Vol.36 (8), p.2311-2316

2013

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Non-dipping and arterial hypertension depend on clinical factors rather than on genetic variability of ACE and RGS2 genes in patients with type 1 diabetes

Acta diabetologica, 2014-08, Vol.51 (4), p.633-640

2014

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HbA1c-based diabetes diagnosis among patients with glucokinase mutation (GCK-MODY) is affected by a genetic variant of glucose-6-phosphatase (G6PC2)

Diabetic medicine, 2012-11, Vol.29 (11), p.1465-1469

2012

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Mutations in the SLC30A8 gene are not a major cause of MODY or other forms of early-onset, autosomal dominant type 2 diabetes

Diabetologia, 2007-10, Vol.50 (10), p.2224-2226

2007

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Thyroid Autoimmunity in Girls with Turner Syndrome

Advances in experimental medicine and biology, 2017, Vol.1022, p.71-76

Pokorski, Mieczyslaw

2017

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Disturbed release of gastrointestinal peptides in anorexia nervosa and in obesity

Diabetes, obesity & metabolism, 2000-04, Vol.2 (2), p.99-103

2000

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Association of asthma and total IgE levels with human leucocyte antigen-DR in patients with grass allergy

The European respiratory journal, 2002-07, Vol.20 (1), p.79-85

2002

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85-kDa cytosolic phospholipase A2 group IValpha gene promoter polymorphisms in patients with severe asthma: a gene expression and case-control study

Clinical and experimental immunology, 2007-10, Vol.150 (1), p.124-131

2007

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C-reactive protein and alpha2-macroglobulin plasma activity in medium-severe and severe psoriasis

Journal of the European Academy of Dermatology and Venereology, 2004-03, Vol.18 (2), p.180-183

2004

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The Role of VIP and Somatostatin in the Control of GH and Prolactin Release in Anorexia Nervosa and in Obesity

Annals of the New York Academy of Sciences, 2000-12, Vol.921 (1), p.443-455

2000

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The protective role of the HLA-DR locus in patients with various clinical types of alopecia areata

Archivum Immunologiae et Therapiae Experimentalis, 2002, Vol.50 (5), p.333-336

2002

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Study on activity of interleukin-6, C-reactive protein and alpha-2 macroglobulin in psoriatic patients during the acute clinical stage and remission

Annales Universitatis Mariae Curie-Skłodowska. Sectio D, Medicina, 2000, Vol.55, p.29

2000

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The behavior of T and B lymphocyte subpopulations in infectious and atopic bronchial asthma

Archivum Immunologiae et Therapiae Experimentalis, 1982, Vol.30 (1-2), p.63-66

1982

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Prevalence of monogenic diabetes amongst Polish children after a nationwide genetic screening campaign

Mutations at the BLK locus linked to maturity onset diabetes of the young and β-cell dysfunction

Delayed recognition of Wolfram syndrome frequently misdiagnosed as type 1 diabetes with early chronic complications

Wolfram syndrome in the Polish population: novel mutations and genotype-phenotype correlation

Psychiatric Comorbidities in Pediatric Monogenic Diabetes due to GCK Mutation: Impact on Diabetes-Related Quality of Life

Glycemic variability in patients with Wolfram syndrome is lower than in type 1 diabetes

Switching to sulphonylureas in children with iDEND syndrome caused by KCNJ11 mutations results in improved cerebellar perfusion

Non-dipping and arterial hypertension depend on clinical factors rather than on genetic variability of ACE and RGS2 genes in patients with type 1 diabetes

HbA1c-based diabetes diagnosis among patients with glucokinase mutation (GCK-MODY) is affected by a genetic variant of glucose-6-phosphatase (G6PC2)

Mutations in the SLC30A8 gene are not a major cause of MODY or other forms of early-onset, autosomal dominant type 2 diabetes

Thyroid Autoimmunity in Girls with Turner Syndrome

Disturbed release of gastrointestinal peptides in anorexia nervosa and in obesity

Association of asthma and total IgE levels with human leucocyte antigen-DR in patients with grass allergy

85-kDa cytosolic phospholipase A2 group IValpha gene promoter polymorphisms in patients with severe asthma: a gene expression and case-control study

C-reactive protein and alpha2-macroglobulin plasma activity in medium-severe and severe psoriasis

The Role of VIP and Somatostatin in the Control of GH and Prolactin Release in Anorexia Nervosa and in Obesity

The protective role of the HLA-DR locus in patients with various clinical types of alopecia areata

Study on activity of interleukin-6, C-reactive protein and alpha-2 macroglobulin in psoriatic patients during the acute clinical stage and remission

The behavior of T and B lymphocyte subpopulations in infectious and atopic bronchial asthma

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