M. Krawczyński

发表

Serum Lipase After Secretin Stimulation Detects Mild Pancreatic Involvement in Cystic Fibrosis

K. Herzig, J. Walkowiak, A. Galli-Tsinopoulou, 2004, Journal of pediatric gastroenterology and nutrition.

Fecal elastase-1 is superior to fecal chymotrypsin in the assessment of pancreatic involvement in cystic fibrosis.

K. Herzig, J. Przysławski, J. Walkowiak, 2002, Pediatrics.

The predominance of ω‐6 polyunsaturated fatty acids in cystic fibrosis despite low arachidonic acid levels

I. Bolesławska, J. Przysławski, J. Walkowiak, 2003, Acta paediatrica.

Faecal elastase‐1 test is superior to faecal lipase test in the assessment of exocrine pancreatic function in cystic fibrosis

K. Herzig, J. Przysławski, M. Grzymisławski, 2004, Acta paediatrica.

Vegetarian Diet Alters the Assessment of Exocrine Pancreatic Function With the Use of Fecal Tests

L. Wądołowska, K. Herzig, J. Książyk, 2004, Journal of pediatric gastroenterology and nutrition.

Giardiasis aggravates malabsorption in cystic fibrosis

K. Herzig, J. Walkowiak, M. Krawczyński, 2004, Scandinavian journal of gastroenterology.

Comparative study of clinical characteristics of amniotic rupture sequence with and without body wall defect: further evidence for separation.

Aleksander Jamsheer, A. Latos-Bieleńska, J. Limon, 2009, Birth defects research. Part A, Clinical and molecular teratology.

Current status and prospects for cannabinoids ("medical marihuana") used in children therapy. Review of opinions and standpoints

B. Steinborn, M. Krawczyński, R. Wachowiak, 2016 .

Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene.

R. Hennekam, A. Latos-Bieleńska, H. Ropers, 2010, American journal of human genetics.

Genetic evaluation of patients with Alström syndrome in the Polish population

M. Borowiec, M. Krawczyński, R. Płoski, 2016, Clinical genetics.

Parental age as a risk factor for isolated congenital malformations in a Polish population.

Elzbieta Gajewska, A. Latos-Bieleńska, J. Limon, 2009, Paediatric and Perinatal Epidemiology.

Cranioectodermal Dysplasia, Sensenbrenner Syndrome, Is a Ciliopathy Caused by Mutations in the IFT122 Gene

R. Hennekam, A. Latos-Bieleńska, H. Ropers, 2022 .

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

M. Witt, J. Walkowiak, D. Sands, 2001, European journal of clinical investigation.

Both fecal elastase-1 and fecal chymotrypsin concentrations are decreased i vegetarians

K. Herzig, J. Przysławski, J. Walkowiak, 2001 .