Lista de obras -

1H NMR-based metabolomics studies of urine reveal differences between type 1 diabetic patients with high and low HbAc1 values

artículo científico publicado en 2013

A high frequency of apoptosis was found in cultures of lymphocytes isolated from the venous blood of children born with a low birth weight

artículo científico publicado en 2004

A new case of cerebro-facio-thoracic dysplasia in a 3-year-old girl with short stature and hypothyroidism

artículo científico publicado el 1 de julio de 2012

Analysis of chosen polymorphisms in FoxP3 gene in children and adolescents with autoimmune thyroid diseases.

artículo científico publicado en 2014

Assessment of coeliac disease prevalence in patients with Down syndrome in Poland - a multi-centre study

artículo científico publicado en 2016

Congenital hyperinsulinism in Polish patients--how can we optimize clinical management?

artículo científico publicado en 2015

Congenital hypoaldosteronism associated with nails hypothrophy - case report and review of the literature

scientific article published on January 2008

Familial distal monosomy 3p26.3-pter with trisomy 4q32.2-qter, presenting with progressive ataxia, intellectual disability, and dysmorphic features

artículo científico publicado en 2012

Graves' disease in 2.5 years old girl - 6-years-long observation

artículo científico publicado en 2016

Hypomelanosis of Ito and precocious adrenarche in a girl

artículo científico publicado en 2006

Indices of insulin resistance and dyslipidemia are correlated with lymphocyte proneness to apoptosis in obese or overweight low birth weight children

artículo científico publicado en 2013

Influence of GnRH analog therapy on body mass in central precocious puberty

artículo científico publicado en 2009

L-thyroxine therapy and growth processes in children with Down syndrome.

artículo científico publicado en 2013

Lipid Complications after Hematopoietic Stem Cell Transplantation (HSCT) in Pediatric Patients

artículo científico publicado en 2020

Lipoprotein a (Lp(a)) in patients with Turner's syndrome

artículo científico publicado en 2010

Low birth weight infants (less than 2500g)--common problems for obstetricians and pediatricians

artículo científico publicado en 2003

Metabolic Disturbances in Children Treated for Solid Tumors

scientific article published on 15 December 2019

Metabolic syndrome in obese children

artículo científico publicado en 2005

Multihormonal hypopituitarism, hypothyroidism and hypoparathyroidism in a 17-years-old girl with Diamond-Blackfan anemia and secondary hemochromatosis

artículo científico publicado en 2013

Nutritional status at the moment of diagnosis in childhood cancer patients.

artículo científico publicado en 2017

Oesophageal atresia with tracheoesophageal fistula and anal atresia in a patient with a de novo microduplication in 17q12.

artículo científico publicado en 2013

PC12 Cell Line: Cell Types, Coating of Culture Vessels, Differentiation and Other Culture Conditions

scientific article published on 14 April 2020

Polymorphisms of lipoprotein lipase gene and their participation in metabolic processes

artículo científico publicado el 1 de enero de 2011

Roles of PPARs in the origin of metabolic disturbances in children with low birth weight (below 2500 g)

artículo científico publicado en 2009

The Influence of GnRH Analog Therapy on Growth in Central Precocious Puberty.

artículo científico publicado en 2016

The analysis of psychological and social problems, the physical development in young people with congenital adrenal hyperplasia - owner experience

artículo científico publicado el 1 de enero de 2010

Treatment of severe primary IGF-1 deficiency using rhIGF-1 preparation - first three years of Polish experience

artículo científico publicado en 2018

Uncommon constellation of multiglandular deficiency with 2 mutations in AIRE gene in an 18-year-old girl - 12 years of observation

artículo científico publicado en 2014

Urinary Deoxypyridinoline, Serum Osteocalcin and Bone Mineral Density in Girls with Turner's Syndrome ⬇️

artículo científico publicado el 1 de octubre de 2003

Vitamin D and metabolic, autoimmunologic and neoplasm diseases

artículo científico publicado en 2016

[Analysis of some risk factors for abnormal growth velocity in children treated with haematopoetic stem cell transplantation]

artículo científico publicado en 2006

[Carbohydrate and lipid metabolism disorders in obese children and adolescents]

scientific article published on 01 July 2004

[Effects of oncological therapy on bone disorders].

artículo científico publicado en 2017

[Evaluation of selected endocrine complications in patients treated with auto- and allo-haematopoietic stem cell transplantation]

artículo científico publicado en 2008

[Familial chromosome X structural aberrations - case report]

artículo científico publicado en 2010

[Impact of SIRT1 gene expression on the development and treatment of the metabolic syndrome in oncological patients].

artículo científico publicado en 2016

[Mosaic trisomy of chromosome 20 in a patient with congenital anomalies--10-years observation]

artículo científico publicado en 2009

[Multiplex minisequencing applied in detection of human functional CYP21 gene mutations]

artículo científico publicado en 2007

[Papillary thyroid carcinoma and meningioma in 17-year-old boy- a late effect of acute lymphoblastic leukemia treatment or a new disease? Case report and literature review]

artículo científico publicado en 2009

[Precocious puberty and von Recklinghausen's disease]

artículo científico publicado en 2006

[Psychosexual problem in young people with Down syndrome in parents' opinions - personal experience]

artículo científico publicado en 2008

[Suspicion of anorexia nervosa as a cause of delayed diagnosis of brain tumor. A case report].

artículo científico publicado en 2015

[The impact of VDR gene polymorphisms on obesity, metabolic changes, bone mass disorders and neoplastic processes]

artículo científico publicado en 2018

[The prevalence of thyro-peroxidase antibodies and thyroid function in Turner's syndrome]

scientific article published on 01 January 2006

Lista de obras de

1H NMR-based metabolomics studies of urine reveal differences between type 1 diabetic patients with high and low HbAc1 values

A high frequency of apoptosis was found in cultures of lymphocytes isolated from the venous blood of children born with a low birth weight

A new case of cerebro-facio-thoracic dysplasia in a 3-year-old girl with short stature and hypothyroidism

Analysis of chosen polymorphisms in FoxP3 gene in children and adolescents with autoimmune thyroid diseases.

Assessment of coeliac disease prevalence in patients with Down syndrome in Poland - a multi-centre study

Congenital hyperinsulinism in Polish patients--how can we optimize clinical management?

Congenital hypoaldosteronism associated with nails hypothrophy - case report and review of the literature

Familial distal monosomy 3p26.3-pter with trisomy 4q32.2-qter, presenting with progressive ataxia, intellectual disability, and dysmorphic features

Graves' disease in 2.5 years old girl - 6-years-long observation

Hypomelanosis of Ito and precocious adrenarche in a girl

Indices of insulin resistance and dyslipidemia are correlated with lymphocyte proneness to apoptosis in obese or overweight low birth weight children

Influence of GnRH analog therapy on body mass in central precocious puberty

L-thyroxine therapy and growth processes in children with Down syndrome.

Lipid Complications after Hematopoietic Stem Cell Transplantation (HSCT) in Pediatric Patients

Lipoprotein a (Lp(a)) in patients with Turner's syndrome

Low birth weight infants (less than 2500g)--common problems for obstetricians and pediatricians

Metabolic Disturbances in Children Treated for Solid Tumors

Metabolic syndrome in obese children

Multihormonal hypopituitarism, hypothyroidism and hypoparathyroidism in a 17-years-old girl with Diamond-Blackfan anemia and secondary hemochromatosis

Nutritional status at the moment of diagnosis in childhood cancer patients.

Oesophageal atresia with tracheoesophageal fistula and anal atresia in a patient with a de novo microduplication in 17q12.

PC12 Cell Line: Cell Types, Coating of Culture Vessels, Differentiation and Other Culture Conditions

Polymorphisms of lipoprotein lipase gene and their participation in metabolic processes

Roles of PPARs in the origin of metabolic disturbances in children with low birth weight (below 2500 g)

The Influence of GnRH Analog Therapy on Growth in Central Precocious Puberty.

The analysis of psychological and social problems, the physical development in young people with congenital adrenal hyperplasia - owner experience

Treatment of severe primary IGF-1 deficiency using rhIGF-1 preparation - first three years of Polish experience

Uncommon constellation of multiglandular deficiency with 2 mutations in AIRE gene in an 18-year-old girl - 12 years of observation

Urinary Deoxypyridinoline, Serum Osteocalcin and Bone Mineral Density in Girls with Turner's Syndrome ⬇️

Vitamin D and metabolic, autoimmunologic and neoplasm diseases

[Analysis of some risk factors for abnormal growth velocity in children treated with haematopoetic stem cell transplantation]

[Carbohydrate and lipid metabolism disorders in obese children and adolescents]

[Effects of oncological therapy on bone disorders].

[Evaluation of selected endocrine complications in patients treated with auto- and allo-haematopoietic stem cell transplantation]

[Familial chromosome X structural aberrations - case report]

[Impact of SIRT1 gene expression on the development and treatment of the metabolic syndrome in oncological patients].

[Mosaic trisomy of chromosome 20 in a patient with congenital anomalies--10-years observation]

[Multiplex minisequencing applied in detection of human functional CYP21 gene mutations]

[Papillary thyroid carcinoma and meningioma in 17-year-old boy- a late effect of acute lymphoblastic leukemia treatment or a new disease? Case report and literature review]

[Precocious puberty and von Recklinghausen's disease]

[Psychosexual problem in young people with Down syndrome in parents' opinions - personal experience]

[Suspicion of anorexia nervosa as a cause of delayed diagnosis of brain tumor. A case report].

[The impact of VDR gene polymorphisms on obesity, metabolic changes, bone mass disorders and neoplastic processes]

[The prevalence of thyro-peroxidase antibodies and thyroid function in Turner's syndrome]