I. Jankowska

发表

Exocrine Pancreatic Function in Children with Progressive Familial Intrahepatic Cholestasis Type 2

Richard J. Thompson, K. Herzig, J. Walkowiak, 2006, Journal of pediatric gastroenterology and nutrition.

Recurrence of non‐alcoholic steatohepatitis after liver transplantation in a 13‐yr‐old boy

P. Socha, I. Jankowska, J. Pawłowska, 2007, Pediatric Transplantation.

Good and bad prognosis of alpha-1-antitrypsin deficiency in children: when to list for liver transplantation.

P. Socha, I. Jankowska, J. Pawłowska, 2007, Transplantation proceedings.

Long‐term monitoring of Epstein–Barr virus DNA load and humoral parameter abnormalities in pediatric liver transplant recipients before development of malignancy

A. Sawicka, K. Dzierżanowska-Fangrat, H. Gregorek, 2010, Pediatric transplantation.

Targeted Next-Generation Sequencing in Diagnostic Approach to Monogenic Cholestatic Liver Disorders—Single-Center Experience

R. Płoski, P. Socha, E. Ciara, 2020, Frontiers in Pediatrics.

Influence of Partial External Biliary Diversion on the Lipid Profile in Children With Progressive Familial Intrahepatic Cholestasis

P. Socha, A. Wierzbicka, I. Jankowska, 2016, Journal of pediatric gastroenterology and nutrition.

Autosomal Recessive Polycystic Kidney Disease—The Clinical Aspects and Diagnostic Challenges

Dorota Wicher, Łukasz Obrycki, I. Jankowska, 2020, Journal of Pediatric Genetics.

Hepatocellular carcinoma in ten children under five years of age with bile salt export pump deficiency

Richard J. Thompson, L. Pawlikowska, B. Portmann, 2006, Hepatology.

Lipid metabolism and oxidative stress in children after liver transplantation treated with sirolimus

P. Socha, A. Wierzbicka, I. Jankowska, 2012, Pediatric transplantation.

Obesity, lipid profiles and oxidative stress in children after liver transplantation.

P. Socha, A. Wierzbicka, I. Jankowska, 2017, Acta biochimica Polonica.

Graves' disease, Celiac disease and liver function abnormalities in a patient--clinical manifestation and diagnostic difficulties.

M. Woźniak, I. Jankowska, B. Kamińska, 2014, Acta biochimica Polonica.

Genotype correlates with the natural history of severe bile salt export pump deficiency.

Richard J. Thompson, B. Kamath, H. Arnell, 2020, Journal of hepatology.

Common variant p.D19H of the hepatobiliary sterol transporter ABCG8 increases the risk of gallstones in children

F. Lammert, M. Krawczyk, Z. Kułaga, 2022, Liver international : official journal of the International Association for the Study of the Liver.

Liver Transplantation in Polish Children With α1-Antitrypsin Deficiency: A Single-Center Experience.

P. Socha, I. Jankowska, J. Pawłowska, 2016, Transplantation proceedings.

Epstein–Barr virus gene expression and latent membrane protein 1 gene polymorphism in pediatric liver transplant recipients

K. Dzierżanowska-Fangrat, B. Kasztelewicz, I. Jankowska, 2011, Journal of medical virology.

The impact of cytokine gene polymorphisms on Epstein-Barr virus infection outcome in pediatric liver transplant recipients.

K. Dzierżanowska-Fangrat, B. Kasztelewicz, I. Jankowska, 2012, Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology.

Reversal of tacrolimus‐related hypertrophic cardiomyopathy after conversion to rapamycin in a pediatric liver transplant recipient

W. Kawalec, A. Turska-Kmieć, M. Markiewicz, 2007, Pediatric transplantation.

Percutaneous Treatment of Biliary Strictures After Pediatric Liver Transplantation

D. Kamińska, J. Pertkiewicz, I. Jankowska, 2018, Annals of transplantation.

Endoscopic treatment in biliary strictures after pediatric liver transplantation

J. Pertkiewicz, I. Jankowska, J. Pawłowska, 2018, Pediatric transplantation.

Epstein–Barr virus DNA load in peripheral blood mononuclear cells and whole blood from pediatric transplant recipients

M. Pronicki, R. Grenda, K. Dzierżanowska-Fangrat, 2011, Transplant infectious disease : an official journal of the Transplantation Society.

Fine-resolution mapping by haplotype evaluation: the examples of PFIC1 and BRIC

N. Freimer, R. Sinke, D. Barton, 1999, Human Genetics.

Apolipoprotein E Polymorphism in Alagille Syndrome and Progressive Familial Intrahepatic Cholestasis

P. Socha, I. Jankowska, J. Pawłowska, 2000, Digestive Diseases and Sciences.

Exocrine pancreatic function in children with Alagille syndrome

A. Wierzbicka, J. Walkowiak, Anna Miśkiewicz-Chotnicka, 2016, Scientific reports.

Small intestinal bacterial overgrowth in patients with progressive familial intrahepatic cholestasis.

J. Moczko, J. Walkowiak, A. Lisowska, 2014, Acta biochimica Polonica.

Cholestatic Syndromes in Childhood and Catch-Up Growth

P. Socha, I. Jankowska, J. Pawłowska, 2012 .

Normal levels of serum pancreatic enzymes in patients with progressive familial intrahepatic cholestasis type 2.

A. Wierzbicka, J. Walkowiak, M. Biczysko, 2010, Acta biochimica Polonica.

Treatment of progressive familial intrahepatic cholestasis: Liver transplantation or partial external biliary diversion

Y. Révillon, T. Drewniak, M. Markiewicz, 1999, Pediatric transplantation.

Normal pancreatic secretion in children with progressive familial intrahepatic cholestasis type 1

K. Herzig, J. Walkowiak, L. Bull, 2006, Scandinavian journal of gastroenterology.

On histOpathOlOgical features

S. Szymańska, I. Jankowska, Patryk Lipiński, 2019 .

Lipid, carbohydrate metabolism, and antioxidant status in children after liver transplantation.

P. Socha, A. Wierzbicka, I. Jankowska, 2007, Transplantation Proceedings.

Drug-resistant epilepsia and fulminant valproate liver toxicity. Alpers-Huttenlocher syndrome in two children confirmed post mortem by identification of p.W748S mutation in POLG gene

G. Węgrzyn, M. Pronicki, K. Kotulska, 2011, Medical science monitor : international medical journal of experimental and clinical research.

Autoimmune hepatitis in transplanted liver.

M. Woźniak, I. Jankowska, J. Pawłowska, 2004, Transplantation proceedings.

Successful sirolimus rescue in tacrolimus‐induced thrombotic microangiopathy after living‐related liver transplantation

D. Kamińska, M. Markiewicz, J. Ryżko, 2012, Pediatric transplantation.

Deficiency of the expression of CD45RA isoform of CD45 common leukocyte antigen in CD4+ T lymphocytes in children with infantile cholestasis.

P. Socha, C. Barth, J. Michalkiewicz, 2001, Immunology Letters.

Long-Term Systematic Monitoring of Four Polish Transaldolase Deficient Patients.

P. Socha, A. Tylki-Szymańska, E. Ciara, 2018, JIMD reports.

Prevalence of Cryptosporidium, Blastocystis, and other opportunistic infections in patients with primary and acquired immunodeficiency

M. Bednarska, A. Bajer, I. Jankowska, 2018, Parasitology Research.

The first case of Enterocytozoon bieneusi infection in Poland.

T. Graczyk, M. Bednarska, A. Bajer, 2013, Annals of agricultural and environmental medicine : AAEM.

Prevalence of Cryptosporidium, Blastocystis, and other opportunistic infections in patients with primary and acquired immunodeficiency

B. Wolska-Kuśnierz, M. Bednarska, A. Bajer, 2018, Parasitology Research.

Prevention of de novo hepatitis B virus infection by vaccination and high hepatitis B surface antibodies level in children receiving hepatitis B virus core antibody-positive living related donor liver: case reports.

M. Pronicki, I. Jankowska, J. Pawłowska, 2007, Transplantation proceedings.

Combined Liver-Kidney Transplantation in Children: Single-Center Experiences and Long-Term Results.

R. Grenda, G. Kowalewski, I. Jankowska, 2018, Transplantation proceedings.

Differences in presentation and progression between severe FIC1 and BSEP deficiencies.

Richard J. Thompson, N. Freimer, L. Pawlikowska, 2010, Journal of hepatology.

Liver transplantation in three family members after Amanita phalloides mushroom poisoning.

J. Pawlak, M. Krawczyk, I. Jankowska, 2002, Transplantation Proceedings.

Cholestasis Due to USP53 Deficiency

Richard J. Thompson, M. Deheragoda, B. Wagner, 2020, Journal of pediatric gastroenterology and nutrition.

Outcomes of surgical management of familial intrahepatic cholestasis 1 and bile salt export protein deficiencies

Richard J. Thompson, L. Pawlikowska, P. Rosenthal, 2018, Hepatology communications.

Acute liver failure in children—Is living donor liver transplantation justified?

G. Kowalewski, W. Patkowski, I. Jankowska, 2018, PloS one.

Neonatal cholestasis due to citrin deficiency: diagnostic pitfalls.

R. Płoski, P. Socha, A. Tylki-Szymańska, 2020, Acta biochimica Polonica.

Short-term effects of parenteral nutrition of cholestatic infants with lipid emulsions based on medium-chain and long-chain triacylglycerols.

B. Koletzko, P. Socha, H. Demmelmair, 2007, Nutrition.

The rs12532734 Polymorphism Near the Solute Carrier 26A3 Gene Locus Is Associated With Gallstone Disease in Children

F. Lammert, M. Krawczyk, Z. Kułaga, 2022, Journal of pediatric gastroenterology and nutrition.

Hemodynamic failure as an indication to urgent liver transplantation in infants with giant hepatic hemangiomas or vascular malformations – Report of four cases

B. Dembowska-Baginska, G. Brzezinska-Rajszys, I. Jankowska, 2009, Pediatric transplantation.

Congenital hepatic fibrosis in a 9-year-old female patient – a case report

I. Jankowska, J. Pawłowska, J. Cielecka-Kuszyk, 2017, Clinical and experimental hepatology.

Genotype-phenotype relationships of truncating mutations, p.E297G and p.D482G in bile salt export pump deficiency

Richard J. Thompson, M. H. Jørgensen, F. Suchy, 2022, JHEP Reports.

Cortisol deficiency as a rare cause of neonatal cholestasis.

Karolina Kot, M. Szalecki, I. Jankowska, 2018, Developmental period medicine.

Long-chain PUFA supplementation improves PUFA profile in infants with cholestasis

B. Koletzko, P. Socha, H. Demmelmair, 2006, Lipids.

Risk factors and outcomes associated with recurrent autoimmune hepatitis following liver transplantation.

Maciej K. Janik, M. Manns, V. Ronca, 2022, Journal of hepatology.

Surgical treatment of progressive familial intrahepatic cholestasis: comparison of partial external biliary diversion and ileal bypass.

T. Drewniak, M. Markiewicz, I. Jankowska, 2003, European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie.

Severe bile salt export pump deficiency: 82 different ABCB11 mutations in 109 families.

Richard J. Thompson, Bruno Stieger, Giorgina Mieli-Vergani, 2008, Gastroenterology.

Bile salt export pump (BSEP) deficiency is a significant risk factor for both paediatric and adult hepatobiliary malignancy

Richard J. Thompson, L. Pawlikowska, B. Portmann, 2005 .

A Report of 2 Infant Siblings with Progressive Intrahepatic Familial Cholestasis Type 1 and a Novel Homozygous Mutation in the ATP8B1 Gene Treated with Partial External Biliary Diversion and Liver Transplant

P. Socha, I. Jankowska, J. Pawłowska, 2021, The American journal of case reports.

Characterization of mutations in ATP8B1 associated with hereditary cholestasis

Richard J. Thompson, N. Freimer, L. Pawlikowska, 2004, Hepatology.

Progressive familial intrahepatic cholestasis and inborn errors of bile acid synthesis.

P. Socha, I. Jankowska, 2012, Clinics and research in hepatology and gastroenterology.

Impact of Genotype, Serum Bile Acids, and Surgical Biliary Diversion on Native Liver Survival in FIC1 Deficiency

Richard J. Thompson, P. Rosenthal, F. Suchy, 2021, Hepatology.

Ileal Exclusion in Children With Progressive Familial Intrahepatic Cholestasis

J. Ryżko, I. Jankowska, J. Pawłowska, 2014, Journal of pediatric gastroenterology and nutrition.

Progressive familial intrahepatic cholestasis type 3: report of four clinical cases, novel ABCB4 variants, and long-term follow-up.

R. Płoski, E. Ciara, D. Jurkiewicz, 2021, Annals of hepatology.

Progressive familial intrahepatic cholestasis — farnesoid X receptor deficiency due to NR1H4 mutation: A case report

Richard J. Thompson, L. Bull, I. Jankowska, 2021, World journal of clinical cases.

PS-195-Predicting long-term outcome after surgical biliary diversion in Bsep-deficiency patients: Results from the NAPPED consortium

Richard J. Thompson, D. Wessel, B. Kamath, 2019, Journal of Hepatology.

The Natural Course of Bsep Deficiency : Results from the Global Napped-Consortium

Richard J. Thompson, D. Wessel, H. Arnell, 2018 .

Long-term follow-up in children with progressive familial intrahepatic cholestasis type 2 after partial external biliary diversion with focus on histopathological features.

S. Szymańska, I. Jankowska, J. Cielecka-Kuszyk, 2019, Polish journal of pathology : official journal of the Polish Society of Pathologists.

Treatment of pruritus with Prometheus dialysis and absorption system in a patient with benign recurrent intrahepatic cholestasis

M. Jirsa, M. Krawczyk, M. Hartleb, 2014, Hepatology research : the official journal of the Japan Society of Hepatology.

The Course of Ulcerative Colitis After Pediatric Liver Transplantation for Sclerosing Cholangitis.

M. Dądalski, J. Kierkuś, M. Woźniak, 2020, Transplantation proceedings.

Case Report: Adenosine kinase deficiency diagnosed 10 years after liver transplantation: Novel phenotypic insights

R. Płoski, M. Pronicki, E. Ciara, 2022, Frontiers in Pediatrics.

Maralixibat for the treatment of PFIC: Long‐term, IBAT inhibition in an open‐label, Phase 2 study

Richard J. Thompson, Robert H. Squires, A. Dorenbaum, 2022, Hepatology communications.

Successful pregnancy after ileal exclusion in progressive familial intrahepatic cholestasis type 2.

I. Jankowska, J. Pawłowska, P. Czubkowski, 2015, Annals of hepatology.

Sterol 27-Hydroxylase Deficiency as a Cause of Neonatal Cholestasis: Report of 2 Cases and Review of the Literature

R. Płoski, P. Socha, E. Ciara, 2021, Frontiers in Pediatrics.

Outcome of four high-risk pregnancies in female liver transplant recipients on tacrolimus immunosuppression.

K. Zieniewicz, M. Krawczyk, L. Pączek, 2006, Transplantation proceedings.

Absence of teratogenicity of sirolimus used during early pregnancy in a liver transplant recipient.

L. Pączek, M. Markiewicz, I. Jankowska, 2004, Transplantation proceedings.

Progress in Molecular Diagnosis and Treatment of Genetic Based Pediatric Malignancies

I. Jankowska, J. Cielecka-Kuszyk, P. Czubkowski, 2006 .

Transient Elastography for Detection of Liver Fibrosis in Children With Autosomal Recessive Polycystic Kidney Disease

K. Chrzanowska, Dorota Wicher, P. Socha, 2019, Front. Pediatr..

Elevated serum transaminases in the course of rotavirus infection

I. Jankowska, A. Liberek, Patryk Lipiński, 2018 .

Cardiovascular Risk Assessment in Children with Chronic Cholestatic Liver Diseases.

M. Litwin, P. Socha, A. Wierzbicka-Rucińska, 2020, Journal of pediatric gastroenterology and nutrition.

Amoxicillin/clavulanic acid-induced cholestatic liver injury after pediatric liver transplantation.

D. Kamińska, M. Markiewicz, I. Jankowska, 2012, Annals of transplantation.

Beta-carotene and vitamin A serum concentration in children with progressive familial intrahepatic cholestasis with complete relief cholestasis after ursodeoxycholic acid or surgical treatment

P. Socha, Irena Jankowska, Joanna Pawłowska, 2003 .

M. Pronicki, I. Jankowska, J. Pawłowska, 2003 .

[Application of polymerase chain reaction (PCR) for the detection of DNA-HCMV in cerebrospinal fluid of neonates and infants with cytomegalovirus infection].

M. Idzik, D. Dzierżanowska, E. Augustynowicz, 1997, Neurologia i neurochirurgia polska.

Polar relaxation mode in PbZrO3 crystals

J. Dec, K. Roleder, I. Jankowska, 1993 .

[Evaluation of selected parameters in calcium and phosphate metabolism in acute liver failure following poisoning with Amanita phalloides].

J. Ryżko, I. Jankowska, J. Socha, 1990, Polski tygodnik lekarski.

Frequency dependent electrostrictive effect in the antiferroelectric PbZrO3 crystals

J. Dec, K. Roleder, I. Jankowska, 1993 .

Acute-on-chronic hepatitis. A case report of autoimmune hepatitis/primary sclerosing cholangitis/ulcerative colitis overlap syndrome in a 15-year-old patient

M. Dądalski, M. Woźniak, I. Jankowska, 2017, Clinical and experimental hepatology.

Liver transplantation for fulminant Wilson's disease in children.

P. Socha, I. Jankowska, P. Kaliciński, 2008, Annals of transplantation.

Antibody-mediated rejection in pediatric liver transplant recipients.

I. Jankowska, P. Kaliciński, B. Piątosa, 2014, Annals of transplantation.

Newborn presentation of Niemann-Pick disease type C - Difficulties and limitations of diagnostic methods.

M. Pronicki, A. Tylki-Szymańska, A. Ługowska, 2017, Pediatrics and neonatology.

Hepato- and splenomegaly in selected metabolic diseases – diagnostics and differentiation

A. Tylki-Szymańska, D. Rokicki, E. Szymańska, 2018 .

Effect of Lactobacillus casei DN-114001 application on the activity of fecal enzymes in children after liver transplantation.

B. Cukrowska, E. Klewicka, I. Jankowska, 2007, Transplantation proceedings.

The natural course of FIC1 deficiency and BSEP deficiency: Initial results from the NAPPED-consortium (Natural course and Prognosis of PFIC and Effect of biliary Diversion)

Richard J. Thompson, D. Wessel, H. Arnell, 2018 .

Scintiscanning in diagnostics of hepatopulmonary syndrome in children.

A. Kaminska, P. Socha, I. Jankowska, 2001, Medical Science Monitor.

Coronavirus Disease 2019-Liver Injury-Literature Review and Guidelines Based on the Recommendations of Hepatological Societies

D. Lebensztejn, I. Jankowska, J. Pawłowska, 2021, Pediatric gastroenterology, hepatology & nutrition.

Beneficial effect of liver transplantation on bone mineral density in small infants with cholestasis.

P. Socha, R. Lorenc, J. Ryżko, 2004, Transplantation proceedings.

Liver transplantation for severe hepatic graft-versus-host disease in two children after hematopoietic stem cell transplantation.

E. Bernatowska, I. Jankowska, J. Pawłowska, 2010, Transplantation proceedings.

Novel c.191C>G (p.Pro64Arg) MPV17 mutation identified in two pairs of unrelated Polish siblings with mitochondrial hepatoencephalopathy

R. Płoski, M. Pronicki, M. Wieckowski, 2014, Clinical genetics.

Clinical aspects of nutrition in children with chronic cholestasis – on the basis of a selected case

P. Socha, I. Jankowska, J. Pawłowska, 2008 .

Pediatric Liver Disease Patients and Secondary Glycosylation Abnormalities

P. Socha, A. Tylki-Szymańska, I. Jankowska, 2021, Frontiers in Pediatrics.

NBAS deficiency due to biallelic c.2809C > G variant presenting with recurrent acute liver failure with severe hyperammonemia, acquired microcephaly and progressive brain atrophy

P. Socha, A. Tylki-Szymańska, D. Rokicki, 2021, Metabolic brain disease.

Acute liver failure due to DGUOK deficiency-is liver transplantation justified?

R. Płoski, P. Socha, E. Ciara, 2020, Clinics and research in hepatology and gastroenterology.

Natural history of liver disease in a large international cohort of children with Alagille syndrome: Results from the GALA study

Richard J. Thompson, N. Spinner, J. Feinstein, 2022, Hepatology.

Treatment of cholestatic pruritus in children

I. Jankowska, J. Pawłowska, Praca Poglądowa, 2015 .

Hepatobiliary scanning in the diagnosis of biliary atresia.

A. Kaminska, P. Socha, I. Jankowska, 2001, Medical Science Monitor.

Reduction of naive CD4/CD45RA+ T cells in children with biliary atresia before and after liver transplantation.

P. Socha, J. Michalkiewicz, I. Jankowska, 2003, Transplantation proceedings.

β-Carotene Deficiency in Cholestatic Liver Disease of Childhood Is Caused by β-Carotene Malabsorption

P. Socha, A. Dhawan, A. Wierzbicka, 2010, Journal of pediatric gastroenterology and nutrition.

Immunological factors and liver fibrosis in pediatric liver transplant recipients.

I. Jankowska, P. Kaliciński, B. Piątosa, 2015, Annals of transplantation.

Are children with gallstone disease more overweight? Results of a matched case-control analysis.

Z. Kułaga, I. Jankowska, S. Więcek, 2023, Clinics and research in hepatology and gastroenterology.

Novel c.191C>G (p.Pro64Arg) MPV17 mutation identified in two pairs of unrelated Polish siblings with mitochondrial hepatoencephalopathy

M. Pronicki, M. Wieckowski, E. Ciara, 2014, Clinical genetics.

[Amanita phalloides poisoning as an indication for liver transplantation in three family members].

J. Pawlak, M. Krawczyk, I. Jankowska, 2006, Wiadomosci lekarskie.

Occurrence of Portal Hypertension and Its Clinical Course in Patients With Molecularly Confirmed Autosomal Recessive Polycystic Kidney Disease (ARPKD)

K. Chrzanowska, M. Rydzanicz, M. Liebau, 2020, Frontiers in Pediatrics.