Lista de obras - Wojciech Cichy - Dominio Público Uruguay

A method of rapid and cost-effective screening for small mutations in patients with Peutz-Jeghers Syndrome

A simplified method for detection of the mutations predominantly causing cystic fibrosis and phenylketonuria in Polish families

scientific article published on 01 July 1993

Acid steatocrit determination is not helpful in cystic fibrosis patients without or with mild steatorrhea.

artículo científico publicado en 2010

Activity of arylsulfatase and beta-glucuronidase in small intestine mucosa in children with malabsorption syndromes

artículo científico publicado el 1 de septiembre de 1979

Activity of glucosamine synthetase in the small intestine mucosa in children with malabsorption syndromes

artículo científico publicado el 1 de septiembre de 1979

Activity of jejunal peptidases in malabsorption syndrome in children (author's transl)

artículo científico publicado el 1 de enero de 1979

Activity of lipolytic enzymes of the duodenal juice in children with pancreopathy

artículo científico publicado en 1976

An Evaluation of the Ability of the Probiotic Strain Lactobacillus rhamnosus GG to Eliminate the Gastrointestinal Carrier State of Vancomycin-resistant Enterococci in Colonized Children ⬇️

artículo científico publicado el 1 de noviembre de 2011

Analysis of exocrine pancreatic function in cystic fibrosis: one mild CFTR mutation does not exclude pancreatic insufficiency

scientific article published on 01 September 2001

Association of c.802C>T polymorphism of NOD2/CARD15 gene with the chronic gastritis and predisposition to cancer in H. pylori infected patients

artículo científico publicado en 2010

Atherosclerotic Risk Factors in Children with Celiac Disease

scientific article published on 27 March 2020

Changes in elementary indices of electrolyte metabolism during secretion of gastric acid in diabetic children

artículo científico publicado el 23 de mayo de 1973

Chronic diarrhea due to VIPoma in two children

scientific article published on 01 January 1984

Chronic diarrhea in 3 children with ganglioneuroma

artículo científico publicado el 6 de febrero de 1984

Crohn's Disease Susceptibility and Onset Are Strongly Related to Three Gene Haplotypes

artículo científico publicado en 2021

Current views on the etiopathogenesis, clinical manifestation, diagnostics, treatment and correlation with other nosological entities of SIBO.

artículo científico

Cystic fibrosis is a risk factor for celiac disease.

artículo científico publicado en 2010

Determination of faecal inflammatory marker concentration as a noninvasive method of evaluation of pathological activity in children with inflammatory bowel diseases

artículo científico publicado en 2015

Disease specific knowledge about cystic fibrosis, patient education and counselling in Poland

artículo científico publicado en 2014

Evaluation of serum pancreatic polypeptide estimations following hormonal stimulation for the diagnosis of exocrine pancreatic insufficiency

artículo científico publicado en 1984

Exocrine and endocrine pancreatic functions in children with the short bowel syndrome

artículo científico publicado en 1987

Fecal pyruvate kinase: a potential new marker for intestinal inflammation in children with inflammatory bowel disease

artículo científico publicado en 2007

First Polish Cowden syndrome patient with confirmed PTEN gene mutation

artículo científico publicado en 2010

Gastric HCl excretion in hypothyroidism and hyperthyroidism

artículo científico publicado el 1 de marzo de 1976

Gastric acid secretion in diabetic children

artículo científico publicado el 30 de mayo de 1973

Gastric secretion and some indices of electrolyte metabolism in Turner's syndrome

artículo científico publicado el 26 de mayo de 1976

Gastric secretion of acid in healthy children

artículo científico publicado el 1 de mayo de 1975

Hamartomatous polyposis syndromes

scientific article published on 01 June 2013

High Resolution Melting analysis as a rapid and efficient method of screening for small mutations in the STK11 gene in patients with Peutz-Jeghers syndrome.

artículo científico publicado en 2013

How a motivation programme can affect complex treatment compliance in a rare disease? Results of a questionnaire-based, self-reported study to evaluate “Life Club CF”, a programme intended for patients with cystic fibrosis.

artículo científico publicado en 2010

How to inspire and involve future medical doctors in CF care?

artículo científico publicado en 2007

Insulin and growth hormone levels following alimentary stimulation in children with dystrophy and malabsorption syndrome

artículo científico publicado el 1 de septiembre de 1979

Intestinal dipeptidase and disaccharidase activity in malabsorption syndrome in children

artículo científico publicado el 1 de septiembre de 1977

Juvenile polyposis syndrome.

artículo científico publicado en 2014

Liver disease in cystic fibrosis

artículo científico publicado en 2014

Marie-Sainton syndrome (cleidocranial dysostosis) associated with osseous changes in the hand

artículo científico publicado el 1 de marzo de 1975

Medical control of sport activities in children and adolescents and its organizational forms

artículo científico publicado en 1972

Microsatellite Haplotypes of Polish Cystic Fibrosis Alleles: ΔF508 Chromosomes Demonstrate a North-South Haplotype Frequency Gradient

scientific article published on 01 November 1996

Molecular genetics of PKU in Poland and potential impact of mutations on BH4 responsiveness

artículo científico publicado en 2013

Mutations spectrum in hereditary disorders predisposing to occurrence of intestine polyposis in Poland

artículo científico publicado en 2012

Organ-sparing surgery of the bilateral testicular large cell calcifying sertoli cell tumor in patient with atypical Peutz-Jeghers syndrome

artículo científico publicado en 2011

Parenteral nutrition in patients with inborn errors of metabolism - a therapeutic problem

Pattern of hydroxyproline indices during the developmental period (between the ages of 6 months and 18 years)

artículo científico publicado el 5 de enero de 1976

Postprandial release of some enterohormones in children with chronic persistent hepatitis and posthepatitic cirrhosis

artículo científico publicado en 1987

Psychosomatic development of children with malabsorption syndrome

artículo científico publicado el 1 de octubre de 1975

Qualitative and Quantitative Characteristics of Selected Bacterial Groups in Children with Inflammatory Bowel Diseases

artículo científico publicado en 2016

Qualitative and Quantitative Characteristics of Selected Bacterial Groups in Children with Inflammatory Bowel Diseases

Quality of life in noncompliant adults with phenylketonuria after resumption of the diet

artículo científico publicado en 2008

Recovery of phenol from aqueous streams in hollow fiber modules

artículo científico publicado en 2002

Release of pancreatic polypeptide after administration of cholecystokinin in children with mucoviscidosis

artículo científico publicado en 1985

Serum Concentrations of Insulin, Ghrelin, Adiponectin, Leptin, Leptin Receptor and Lipocalin-2 in Children with Celiac Disease Who Do and Do Not Adhere to a Gluten-Free Diet

artículo científico publicado en 2016

Serum PP-release after hormonal (CCK) and mixed test-meal (MTM) stimulation by children with exocrine pancreatic insufficiency (EPI).

artículo científico publicado en 1986

Serum pancreatic polypeptide and glucagon immunoreactivity in fasting healthy and diabetic children

artículo científico publicado en 1989

Skin reactions to penicillin

artículo científico

Smoking problem in developmental age

artículo científico publicado en 2006

Somatostatin in the treatment of gastrointestinal diseases in children

scientific article published on 01 January 1988

The usefulness of trypsin determination in the serum in the diagnosis of pancreatic diseases in children

scientific article published on 01 July 1987

Value of load tests in the assessment of digestion and absorption in children

artículo científico publicado el 1 de diciembre de 1972

Watery diarrhea in a child with ganglioneuroma and increased serum level of vasoactive intestinal hormone

artículo científico publicado el 1 de septiembre de 1979

[Alkaptonuria in a 3-month-old girl]

scientific article published on 01 December 1973

[Comparative effects of somatostatin and ranitidine on gastric function in children with hyperchlorhydria]

artículo científico publicado en 1986

[Congenital fructose intolerance diagnosed in a 13-year-old boy]

artículo científico publicado en 1994

[Cystic fibrosis: now and in the future]

scientific article published on 01 January 1995

[Diagnosis of hemorrhage of Meckel's diverticulum using technetium scintigraphy]

scientific article published on 01 May 1989

[Effect of a diet rich in fiber on enterohormones in the blood serum of obese children]

artículo científico publicado en 1988

[Evaluation of treatment efficacy in gastritis and duodenitis in children with Helicobacter pylori infection]

scientific article published on 01 January 1995

[Food stimulated release of IRI and HGH in children with malabsorption (author's transl)]

artículo científico publicado en 1980

[Hydroxyproline indicators in the evaluation of nutritional status of children with various metabolic diseases]

scientific article published on 01 February 1974

[Trisomy group D chromosomes (47,XX, D+) syndrome]

artículo científico publicado en 1977

[Vitamin K deficiency in patients with CF despite supplementation]

artículo científico publicado en 2010

Lista de obras de Wojciech Cichy

A method of rapid and cost-effective screening for small mutations in patients with Peutz-Jeghers Syndrome

A simplified method for detection of the mutations predominantly causing cystic fibrosis and phenylketonuria in Polish families

Acid steatocrit determination is not helpful in cystic fibrosis patients without or with mild steatorrhea.

Activity of arylsulfatase and beta-glucuronidase in small intestine mucosa in children with malabsorption syndromes

Activity of glucosamine synthetase in the small intestine mucosa in children with malabsorption syndromes

Activity of jejunal peptidases in malabsorption syndrome in children (author's transl)

Activity of lipolytic enzymes of the duodenal juice in children with pancreopathy

An Evaluation of the Ability of the Probiotic Strain Lactobacillus rhamnosus GG to Eliminate the Gastrointestinal Carrier State of Vancomycin-resistant Enterococci in Colonized Children ⬇️

Analysis of exocrine pancreatic function in cystic fibrosis: one mild CFTR mutation does not exclude pancreatic insufficiency

Association of c.802C>T polymorphism of NOD2/CARD15 gene with the chronic gastritis and predisposition to cancer in H. pylori infected patients

Atherosclerotic Risk Factors in Children with Celiac Disease

Changes in elementary indices of electrolyte metabolism during secretion of gastric acid in diabetic children

Chronic diarrhea due to VIPoma in two children

Chronic diarrhea in 3 children with ganglioneuroma

Crohn's Disease Susceptibility and Onset Are Strongly Related to Three Gene Haplotypes

Current views on the etiopathogenesis, clinical manifestation, diagnostics, treatment and correlation with other nosological entities of SIBO.

Cystic fibrosis is a risk factor for celiac disease.

Determination of faecal inflammatory marker concentration as a noninvasive method of evaluation of pathological activity in children with inflammatory bowel diseases

Disease specific knowledge about cystic fibrosis, patient education and counselling in Poland

Evaluation of serum pancreatic polypeptide estimations following hormonal stimulation for the diagnosis of exocrine pancreatic insufficiency

Exocrine and endocrine pancreatic functions in children with the short bowel syndrome

Fecal pyruvate kinase: a potential new marker for intestinal inflammation in children with inflammatory bowel disease

First Polish Cowden syndrome patient with confirmed PTEN gene mutation

Gastric HCl excretion in hypothyroidism and hyperthyroidism

Gastric acid secretion in diabetic children

Gastric secretion and some indices of electrolyte metabolism in Turner's syndrome

Gastric secretion of acid in healthy children

Hamartomatous polyposis syndromes

High Resolution Melting analysis as a rapid and efficient method of screening for small mutations in the STK11 gene in patients with Peutz-Jeghers syndrome.

How a motivation programme can affect complex treatment compliance in a rare disease? Results of a questionnaire-based, self-reported study to evaluate “Life Club CF”, a programme intended for patients with cystic fibrosis.

How to inspire and involve future medical doctors in CF care?

Insulin and growth hormone levels following alimentary stimulation in children with dystrophy and malabsorption syndrome

Intestinal dipeptidase and disaccharidase activity in malabsorption syndrome in children

Juvenile polyposis syndrome.

Liver disease in cystic fibrosis

Marie-Sainton syndrome (cleidocranial dysostosis) associated with osseous changes in the hand

Medical control of sport activities in children and adolescents and its organizational forms

Microsatellite Haplotypes of Polish Cystic Fibrosis Alleles: ΔF508 Chromosomes Demonstrate a North-South Haplotype Frequency Gradient

Molecular genetics of PKU in Poland and potential impact of mutations on BH4 responsiveness

Mutations spectrum in hereditary disorders predisposing to occurrence of intestine polyposis in Poland

Organ-sparing surgery of the bilateral testicular large cell calcifying sertoli cell tumor in patient with atypical Peutz-Jeghers syndrome

Parenteral nutrition in patients with inborn errors of metabolism - a therapeutic problem

Pattern of hydroxyproline indices during the developmental period (between the ages of 6 months and 18 years)

Postprandial release of some enterohormones in children with chronic persistent hepatitis and posthepatitic cirrhosis

Psychosomatic development of children with malabsorption syndrome

Qualitative and Quantitative Characteristics of Selected Bacterial Groups in Children with Inflammatory Bowel Diseases

Qualitative and Quantitative Characteristics of Selected Bacterial Groups in Children with Inflammatory Bowel Diseases

Quality of life in noncompliant adults with phenylketonuria after resumption of the diet

Recovery of phenol from aqueous streams in hollow fiber modules

Release of pancreatic polypeptide after administration of cholecystokinin in children with mucoviscidosis

Serum Concentrations of Insulin, Ghrelin, Adiponectin, Leptin, Leptin Receptor and Lipocalin-2 in Children with Celiac Disease Who Do and Do Not Adhere to a Gluten-Free Diet

Serum PP-release after hormonal (CCK) and mixed test-meal (MTM) stimulation by children with exocrine pancreatic insufficiency (EPI).

Serum pancreatic polypeptide and glucagon immunoreactivity in fasting healthy and diabetic children

Skin reactions to penicillin

Smoking problem in developmental age

Somatostatin in the treatment of gastrointestinal diseases in children

The usefulness of trypsin determination in the serum in the diagnosis of pancreatic diseases in children

Value of load tests in the assessment of digestion and absorption in children

Watery diarrhea in a child with ganglioneuroma and increased serum level of vasoactive intestinal hormone

[Alkaptonuria in a 3-month-old girl]

[Comparative effects of somatostatin and ranitidine on gastric function in children with hyperchlorhydria]

[Congenital fructose intolerance diagnosed in a 13-year-old boy]

[Cystic fibrosis: now and in the future]

[Diagnosis of hemorrhage of Meckel's diverticulum using technetium scintigraphy]

[Effect of a diet rich in fiber on enterohormones in the blood serum of obese children]

[Evaluation of treatment efficacy in gastritis and duodenitis in children with Helicobacter pylori infection]

[Food stimulated release of IRI and HGH in children with malabsorption (author's transl)]

[Hydroxyproline indicators in the evaluation of nutritional status of children with various metabolic diseases]

[Trisomy group D chromosomes (47,XX, D+) syndrome]

[Vitamin K deficiency in patients with CF despite supplementation]