M. Wilschanski

发表

Recommendations for the classification of diseases as CFTR-related disorders.

B. Kerem, J. Zieleński, P. Pignatti, 2011, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Pediatric chronic pancreatitis is associated with genetic risk factors and substantial disease burden.

B. Barth, S. Freedman, M. Bellin, 2015, The Journal of pediatrics.

Early‐Onset Acute Recurrent and Chronic Pancreatitis Is Associated with PRSS1 or CTRC Gene Mutations

B. Barth, S. Freedman, B. Zimmerman, 2017, The Journal of pediatrics.

Exocrine Pancreatic Function Testing in Patients With Cystic Fibrosis and Pancreatic Sufficiency: A Correlation Study

E. Picard, H. Mussaffi, H. Blau, 2009, Journal of pediatric gastroenterology and nutrition.

Functional gastro‐intestinal disorder algorithms focus on early recognition, parental reassurance and nutritional strategies

F. Gottrand, H. Szajewska, A. Staiano, 2016, Acta paediatrica.

A pilot study of the effect of gentamicin on nasal potential difference measurements in cystic fibrosis patients carrying stop mutations.

A. Avital, B. Kerem, H. Blau, 2000, American journal of respiratory and critical care medicine.

Nonsense-mediated mRNA decay affects nonsense transcript levels and governs response of cystic fibrosis patients to gentamicin.

B. Kerem, M. Nissim-Rafinia, E. Kerem, 2007, The Journal of clinical investigation.

PTC124 treatment over 3 months improves pharmacodynamic and clinical parameters in patients with nonsense-mutation-mediated CF

H. Blau, E. Kerem, M. Wilschanski, 2008 .

An international randomized multicenter comparison of nasal potential difference techniques.

J. Clancy, F. Accurso, F. Vermeulen, 2010, Chest.

European Society for Pae Hepatology and Nutrition Guidelines for the Evaluation and Treatment of Gastrointestinal and Nutritional Complications in Children With Neurological Impairment

R. Orel, M. Wilschanski, N. F. Mis, 2017 .

European Society for Paediatric Gastroenterology, Hepatology and Nutrition Guidelines for the Evaluation and Treatment of Gastrointestinal and Nutritional Complications in Children With Neurological Impairment.

F. Gottrand, R. Orel, M. Wilschanski, 2017, Journal of pediatric gastroenterology and nutrition.

Risk Factors Associated With Pediatric Acute Recurrent and Chronic Pancreatitis: Lessons From INSPPIRE.

B. Barth, S. Freedman, M. Bellin, 2016, JAMA pediatrics.

CFTR: A New Horizon in the Pathomechanism and Treatment of Pancreatitis.

S. Muallem, G. Lukács, P. Hegyi, 2016, Reviews of physiology, biochemistry and pharmacology.

Ivacaftor in People with Cystic Fibrosis and a 3849+10kb C→T or D1152H Residual Function Mutation

E. Kerem, J. Davies, J. R. Doyle, 2020, Annals of the American Thoracic Society.

Causal Evaluation of Acute Recurrent and Chronic Pancreatitis in Children: Consensus From the INSPPIRE Group

B. Barth, S. Freedman, M. Lowe, 2017, Journal of pediatric gastroenterology and nutrition.

Ataluren for the treatment of nonsense-mutation cystic fibrosis: a randomised, double-blind, placebo-controlled phase 3 trial.

S. Peltz, S. McColley, E. Kerem, 2014, The Lancet. Respiratory medicine.

Cystic Fibrosis–related Liver Disease: Research Challenges and Future Perspectives

M. Trauner, P. Witters, S. Ling, 2017, Journal of pediatric gastroenterology and nutrition.

Guidelines for the diagnosis and management of distal intestinal obstruction syndrome in cystic fibrosis patients.

R. Houwen, M. Wilschanski, A. Munck, 2011, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Direct Costs of Acute Recurrent and Chronic Pancreatitis in Children in the INSPPIRE Registry

B. Barth, S. Freedman, M. Bellin, 2016, Journal of pediatric gastroenterology and nutrition.

The EFFect of dietary fat content on the recurrence of pancreaTitis (EFFORT): Protocol of a multicenter randomized controlled trial.

P. Hegyi, M. Papp, G. Capurso, 2021, Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.].

Differences in the pattern of structural abnormalities on CT scan in patients with cystic fibrosis and pancreatic sufficiency or insufficiency.

E. Kerem, M. Wilschanski, N. Simanovsky, 2013, Chest.

Clinical and Genetic Risk Factors for Cystic Fibrosis-related Liver Disease

C. Springer, B. Kerem, H. Blau, 1999, Pediatrics.

In vivo measurements of ion transport in long-living CF mice.

L. Tsui, R. Rozmahel, C. Bear, 1996, Biochemical and biophysical research communications.

Helicobacter pylori Genotypes in Israeli Children: The Significance of Geography

M. Wilschanski, D. Branski, B. Rudensky, 2002, Journal of pediatric gastroenterology and nutrition.

Impact of Obesity on Pediatric Acute Recurrent and Chronic Pancreatitis

B. Barth, S. Freedman, M. Bellin, 2018, Pancreas.

Hereditary Pancreatitis and Chronic Pancreatitis

M. Wilschanski, A. Uc, 2016 .

Definitions of Pediatric Pancreatitis and Survey of Present Clinical Practices

B. Barth, S. Freedman, M. Lowe, 2012, Journal of pediatric gastroenterology and nutrition.

Diabetes Mellitus in Children with Acute Recurrent and Chronic Pancreatitis: Data From the INternational Study Group of Pediatric Pancreatitis: In Search for a CuRE Cohort.

B. Barth, S. Freedman, M. Bellin, 2019, Journal of pediatric gastroenterology and nutrition.

WNK4 regulates airway Na+ transport: study of familial hyperkalaemia and hypertension.

M. Shaharabany, E. Kerem, H. Mayan, 2005, European journal of clinical investigation.

WNK4 regulates Na+ transport in airways

M. Shaharabany, E. Kerem, H. Mayan, 2005 .

Chronic Pancreatitis: Pediatric and Adult Cohorts Show Similarities in Disease Progress Despite Different Risk Factors.

Michelle A. Anderson, Vikesh K. Singh, B. Barth, 2019, Journal of pediatric gastroenterology and nutrition.

Treatment of cystic fibrosis in low-income countries.

E. Kerem, M. Wilschanski, D. Shoseyov, 2016, The Lancet. Respiratory medicine.

Cancer risk among lung transplant recipients with cystic fibrosis.

G. Copeland, C. Lynch, E. Engels, 2017, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Erratum: Modulation of disease severity in cystic fibrosis transmembrane conductance regulator deficient mice by a secondary genetic factor (Nature Genetics (1996) 12 (280-287))

L. Tsui, J. Nadeau, R. Rozmahel, 1996 .

Diagnosis of Cystic Fibrosis in Screened Populations

D. Sanders, M. Rosenfeld, H. Blau, 2017, The Journal of pediatrics.

Comparison of Nasal Potential Difference and Intestinal Current Measurements as Surrogate Markers for CFTR Function

S. Freedman, E. Kerem, S. Sheth, 2016, Journal of pediatric gastroenterology and nutrition.

CFTR biomarkers: time for promotion to surrogate end-point

M. Amaral, N. Derichs, M. Proesmans, 2012, European Respiratory Journal.

New clinical diagnostic procedures for cystic fibrosis in Europe.

N. Derichs, F. Vermeulen, I. Fajac, 2011, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Nasal potential difference measurements in patients with atypical cystic fibrosis.

B. Kerem, H. Blau, M. Kramer, 2001, The European respiratory journal.

Phenotypic characterisation of patients with intermediate sweat chloride values: towards validation of the European diagnostic algorithm for cystic fibrosis

P. Lebecque, N. Derichs, K. De Boeck, 2009, Thorax.

A Novel Familial Mutation in the PCSK1 Gene That Alters the Oxyanion Hole Residue of Proprotein Convertase 1/3 and Impairs Its Enzymatic Activity

I. Lindberg, O. Pappo, Martín G. Martín, 2014, PloS one.

Cystic Fibrosis

M. Wilschanski, Z. Davidovics, 2021, Textbook of Pediatric Gastroenterology, Hepatology and Nutrition.

Maintenance of nutritional status in patients with cystic fibrosis: new and emerging therapies

M. Wilschanski, D. Kalnins, 2012, Drug design, development and therapy.

Efficacy and safety of ataluren in patients with nonsense-mutation cystic fibrosis not receiving chronic inhaled aminoglycosides: The international, randomized, double-blind, placebo-controlled Ataluren Confirmatory Trial in Cystic Fibrosis (ACT CF).

E. Kerem, M. Konstan, I. Sermet-Gaudelus, 2017, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Reproducibility of nasal potential difference measurements in cystic fibrosis.

E. Picard, H. Blau, E. Kerem, 2007, Chest.

The effect of probiotic administration on metabolomics and glucose metabolism in CF patients

L. Laghi, M. Wilschanski, L. Bentur, 2022, Pediatric pulmonology.

Vitamins A and E and Pulmonary Exacerbations in Patients With Cystic Fibrosis

E. Kerem, M. Wilschanski, J. Rivlin, 2007, Journal of pediatric gastroenterology and nutrition.

M. Bellin, M. Lowe, Maisam Abu-El-Haija, 2022, Journal of pediatric gastroenterology and nutrition.

Increasing Vitamin D Serum Levels Is Associated With Reduced Pulmonary Exacerbations in Patients With Cystic Fibrosis

E. Kerem, M. Wilschanski, D. Shoseyov, 2019, Journal of pediatric gastroenterology and nutrition.

A randomized placebo-controlled trial of ataluren for the treatment of nonsense mutation cystic fibrosis

S. Peltz, S. McColley, F. Accurso, 2014 .

Nonsense-mediated mRNA decay affects nonsense transcript levels and governs response of cystic fibrosis patients

B. Kerem, M. Nissim-Rafinia, E. Kerem, 2007 .

Relative Expression and Localization of the Insulin-Like Growth Factor System Components in the Fetal, Child and Adult Intestine

M. Wilschanski, I. Ariel, S. Freier, 2005, Journal of pediatric gastroenterology and nutrition.

Combination of Helicobacter pylori Strain and Tumor Necrosis Factor-α Polymorphism of the Host Increases the Risk of Peptic Ulcer Disease in Children

M. Wilschanski, Y. Schlesinger, D. Halle, 2007, Journal of pediatric gastroenterology and nutrition.

ECFS standards of care on CFTR-related disorders: Diagnostic criteria of CFTR dysfunction.

F. Vermeulen, I. Sermet-Gaudelus, P. Melotti, 2022, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Role of Indigenous Lactobacilli in Gastrin-Mediated Acid Production in the Mouse Stomach

L. Messerini, P. Bechi, I. Novak, 2015 .

Hepatopulmonary Syndrome in Patients With Cystic Fibrosis and Liver Disease.

E. Kerem, M. Wilschanski, D. Shoseyov, 2016, Chest.

Nutritional Status Improved in Cystic Fibrosis Patients with the G551D Mutation After Treatment with Ivacaftor

S. Schwarzenberg, M. Wilschanski, A. Munck, 2015, Digestive Diseases and Sciences.

An international consensus report on a new algorithm for the management of infant diarrhoea

F. Gottrand, H. Szajewska, A. Staiano, 2016, Acta paediatrica.

Management Guidelines of Eosinophilic Esophagitis in Childhood

M. Mearin, F. Gottrand, A. Staiano, 2014, Journal of pediatric gastroenterology and nutrition.

Supplementary enteral nutrition maintains remission in paediatric Crohn's disease.

M. Corey, A. Griffiths, P. Pencharz, 1996, Gut.

Obesogenic habits among children and their families in response to initiation of gluten-free diet

M. Wilschanski, E. Shteyer, M. Moskovitz, 2018, European Journal of Pediatrics.

Nasal potential difference in non‐classic cystic fibrosis—long term follow up

E. Picard, H. Blau, E. Kerem, 2008, Pediatric pulmonology.

Shwachman syndrome: exocrine pancreatic dysfunction and variable phenotypic expression.

M. Wilschanski, P. Durie, D. Mack, 1996, Gastroenterology.

The impact of a national population carrier screening program on cystic fibrosis birth rate and age at diagnosis: Implications for newborn screening.

E. Picard, H. Mussaffi, D. Prais, 2016, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Ataluren for the treatment of cystic fibrosis

M. Wilschanski, D. Shoseyov, M. Cohen-Cymberknoh, 2016, Expert review of respiratory medicine.

Probiotics in cystic fibrosis patients: A double blind crossover placebo controlled study: Pilot study from the ESPGHAN Working Group on Pancreas/CF.

S. Verhulst, M. Wilschanski, B. Pot, 2018, Clinical nutrition ESPEN.

Prevention of malnutrition in cystic fibrosis.

M. Wilschanski, M. Slae, 2019, Current opinion in pulmonary medicine.

3.19 Nutrition in cystic fibrosis.

M. Wilschanski, 2015, World review of nutrition and dietetics.

International Survey on Severe Acute Respiratory Syndrome Coronavirus 2 and Acute Pancreatitis Co-occurrence in Children

M. Wilschanski, M. Slae, Z. Sellers, 2021, Pancreas.

Insights into the variability of nasal potential difference, a biomarker of CFTR activity.

J. Jais, J. Davies, I. Sermet-Gaudelus, 2019, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Pediatric endoscopy training across Europe: a survey of the ESPGHAN National Societies Network 2016–2019

R. Orel, M. Thomson, C. Ribes-Koninckx, 2022, Endoscopy international open.

Evidence of Intestinal Inflammation in Patients With Cystic Fibrosis

H. Mussaffi, E. Kerem, M. Wilschanski, 2010, Journal of pediatric gastroenterology and nutrition.

A multiple reader scoring system for Nasal Potential Difference parameters.

F. Vermeulen, I. Sermet-Gaudelus, S. Rowe, 2017, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Nasal potential difference measurements to assess CFTR ion channel activity.

J. Clancy, S. Rowe, M. Wilschanski, 2011, Methods in molecular biology.

Modulation of disease severity in cystic fibrosis transmembrane conductance regulator deficient mice by a secondary genetic factor

L. Tsui, J. Nadeau, C. Bear, 1996, Nature Genetics.

Genetic and Electrophysiological Characteristics of Recurrent Acute Pancreatitis

Z. Halpern, E. Kerem, P. Ruszniewski, 2015, Journal of pediatric gastroenterology and nutrition.

Oral probiotics prevent necrotizing enterocolitis in very low birth weight neonates.

M. Caplan, M. Wilschanski, C. Hammerman, 2005, The Journal of pediatrics.

Idiopathic Pancreatitis Preceding the Diagnosis of Inflammatory Bowel Disease Is More Frequent in Pediatric Patients

B. Weiss, I. Dotan, M. Wilschanski, 2011, Journal of pediatric gastroenterology and nutrition.

EPC/HPSG evidence-based guidelines for the management of pediatric pancreatitis.

P. Hegyi, R. Sutton, L. Czakó, 2018, Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.].

Incomplete rescue of cystic fibrosis transmembrane conductance regulator deficient mice by the human CFTR cDNA.

L. Tsui, R. Rozmahel, C. Bear, 1997, Human molecular genetics.

Oral Health Status and Salivary Properties in Relation to Gluten-free Diet in Children With Celiac Disease

D. Steinberg, M. Wilschanski, E. Shteyer, 2013, Journal of pediatric gastroenterology and nutrition.

Basic protocol for transepithelial nasal potential difference measurements.

Michael R Knowles, Jean Lebacq, Patrick Lebecque, 2004, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Cystic fibrosis transmembrane conductance regulator and obstructive azoospermia

L. Tsui, J. Zieleński, K. Jarvi, 1995, The Lancet.

Gentamicin-induced correction of CFTR function in patients with cystic fibrosis and CFTR stop mutations.

B. Kerem, H. Blau, Z. Bebők, 2003, The New England journal of medicine.

Correlation of sweat chloride concentration with classes of the cystic fibrosis transmembrane conductance regulator gene mutations.

M. Corey, J. Zieleński, H. Levison, 1995, The Journal of pediatrics.

Cystic fibrosis, pregnancy, and recurrent, acute pancreatitis.

E. Picard, A. Samueloff, E. Kerem, 2003, Journal of pediatric gastroenterology and nutrition.

Autoimmune Pancreatitis in Children: Characteristic Features, Diagnosis, and Management

B. Barth, S. Freedman, B. Zimmerman, 2017, The American Journal of Gastroenterology.

Endoscopic Retrograde Cholangiopancreatography in Neonatal Cholestasis

D. Gozal, M. Wilschanski, D. Wengrower, 2012, Journal of pediatric gastroenterology and nutrition.

ESPEN-ESPGHAN-ECFS guidelines on nutrition care for infants, children, and adults with cystic fibrosis.

B. Strandvik, D. Turck, S. Schneider, 2016, Clinical nutrition.

Prolonged TPN during pregnancy in a cystic fibrosis patient with chronic pancreatitis.

M. Wilschanski, Y. Sciaky-Tamir, H. Elyashar-Earon, 2009, European journal of obstetrics, gynecology, and reproductive biology.

Findings on routine abdominal ultrasonography in cystic fibrosis patients.

E. Picard, E. Kerem, M. Wilschanski, 1999, Journal of pediatric gastroenterology and nutrition.

The Use of Fecal Calprotectin Testing in Paediatric Disorders: A Position Paper of the European Society for Paediatric Gastroenterology and Nutrition Gastroenterology Committee

F. Gottrand, E. Miele, M. Benninga, 2021, Journal of pediatric gastroenterology and nutrition.

Colon Cancer Associated Transcript-1 (CCAT1) Expression in Adenocarcinoma of the Stomach

Alexander Stojadinovic, Itzhak Avital, A. Stojadinovic, 2015, Journal of Cancer.

Nutritional supplementation with polymeric diet enriched with transforming growth factor-beta 2 for children with Crohn's disease.

R. Shapira, B. Weiss, M. Wilschanski, 2008, The Israel Medical Association journal : IMAJ.

Primary sclerosing cholangitis in 32 children: Clinical, laboratory, and radiographic features, with survival analysis

M. Corey, A. Griffiths, L. Blendis, 1995, Hepatology.

Class 1 CF Mutations

M. Wilschanski, 2012, Front. Pharmacol..

Chronic ataluren (PTC124) treatment of nonsense mutation cystic fibrosis

H. Blau, E. Kerem, T. Ajayi, 2011, European Respiratory Journal.

The Use of Jejunal Tube Feeding in Children: A Position Paper by the Gastroenterology and Nutrition Committees of the European Society for Paediatric Gastroenterology, Hepatology and Nutrition 2019.

F. Gottrand, C. Ribes-Koninckx, M. Wilschanski, 2019, Journal of pediatric gastroenterology and nutrition.

Cystic fibrosis: terminology and diagnostic algorithms

K De Boeck, C Castellani, C. Castellani, 2005, Thorax.

The cystic fibrosis of exocrine pancreas.

I. Novak, M. Wilschanski, 2013, Cold Spring Harbor perspectives in medicine.

Patterns of GI disease in adulthood associated with mutations in the CFTR gene

M. Wilschanski, P. Durie, 2007, Gut.

Defining DIOS and Constipation in Cystic Fibrosis With a Multicentre Study on the Incidence, Characteristics, and Treatment of DIOS

R. Houwen, I. Sermet, M. Wilschanski, 2010, Journal of pediatric gastroenterology and nutrition.

Nutritional Considerations in Pediatric Pancreatitis: A Position Paper from the NASPGHAN Pancreas Committee and ESPGHAN Cystic Fibrosis/Pancreas Working Group

M. Wilschanski, V. Morinville, S. Werlin, 2018, Journal of pediatric gastroenterology and nutrition.

Nutritional Considerations in Pediatric Pancreatitis : A Position Paper from the NASPGHAN Pancreas Committee and ESPGHAN Cystic Fibrosis / Pancreas Working Group

M. Wilschanski, V. Morinville, S. Werlin, 2019 .

Hijab Pin Ingestions

M. Wilschanski, Z. Davidovics, Y. Berkun, 2020, Pediatrics.

Real life practice of sweat testing in Europe.

N. Derichs, K. De Boeck, M. Wilschanski, 2017, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

ESPGHAN- Guidelines for the Evaluation and Treatment of Gastrointestinal and Nutritional Complications in Children with Neurological Impairment.

F. Gottrand, R. Orel, M. Wilschanski, 2017, Journal of pediatric gastroenterology and nutrition.

Preconditioning allows engraftment of mouse and human embryonic lung cells, enabling lung repair in mice

I. Biton, D. Hagin, E. Shezen, 2015, Nature Medicine.

Nutritional and metabolic management for cystic fibrosis in a post-cystic fibrosis transmembrane conductance modulator era

M. Wilschanski, D. Peckham, 2022, Current opinion in pulmonary medicine.

Cystic fibrosis and the gut

M. Wilschanski, M. Slae, 2020, Frontline Gastroenterology.

International prospective study of distal intestinal obstruction syndrome in cystic fibrosis: Associated factors and outcome.

R. Houwen, M. Wilschanski, A. Munck, 2016, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Design and Implementation of INSPPIRE

Steven D. Freedman, Monika Ahuja, Sarah Jane Schwarzenberg, 2014, Journal of pediatric gastroenterology and nutrition.

ESPGHAN Position Paper on Management of Percutaneous Endoscopic Gastrostomy in Children and Adolescents

F. Gottrand, R. Orel, S. Husby, 2015, Journal of pediatric gastroenterology and nutrition.

DEFINITIONS OF PEDIATRIC PANCREATITIS AND SURVEY OF CURRENT CLINICAL PRACTICES: REPORT FROM INSPPIRE (INTERNATIONAL STUDY GROUP OF PEDIATRIC PANCREATITIS: IN SEARCH FOR A CURE)

B. Barth, S. Freedman, M. Lowe, 2022 .

Cystic Fibrosis Transmembrane Conductance Regulator Ion Channel Function Testing in Recurrent Acute Pancreatitis

H. Blau, E. Kerem, R. Mountford, 2008, Journal of clinical gastroenterology.

The changing face of the exocrine pancreas in cystic fibrosis: the correlation between pancreatic status, pancreatitis and cystic fibrosis genotype

B. Kerem, H. Blau, M. Wilschanski, 2008, European journal of gastroenterology & hepatology.

Drugs in Focus: Proton Pump Inhibitors

F. Gottrand, M. Benninga, R. Orel, 2021, Journal of pediatric gastroenterology and nutrition.

ESPGHAN and NASPGHAN Report on the Assessment of Exocrine Pancreatic Function and Pancreatitis in Children.

M. Thomson, M. Lowe, M. Wilschanski, 2015, Journal of pediatric gastroenterology and nutrition.

Analysis of INSPPIRE-2 Cohort: Risk Factors and Disease Burden in Children With Acute Recurrent or Chronic Pancreatitis

M. Lowe, S. Schwarzenberg, M. Wilschanski, 2022, Journal of pediatric gastroenterology and nutrition.

INternational Study Group of Pediatric Pancreatitis: In Search for a CuRE Cohort Study: Design and Rationale for INSPPIRE 2 From the Consortium for the Study of Chronic Pancreatitis, Diabetes, and Pancreatic Cancer.

B. Barth, M. Bellin, M. Lowe, 2018, Pancreas.

Therapeutic Endoscopic Retrograde Cholangiopancreatography in Pediatric Patients With Acute Recurrent and Chronic Pancreatitis: Data From the INSPPIRE (INternational Study group of Pediatric Pancreatitis: In search for a cuRE) Study.

B. Barth, S. Freedman, M. Bellin, 2017, Pancreas.

Clinical and Practice Variations in Pediatric Acute Recurrent or Chronic Pancreatitis: Report From The Insppire Study.

B. Barth, B. Zimmerman, M. Bellin, 2020, Journal of pediatric gastroenterology and nutrition.

Recommendations for Diagnosis and Management of Autoimmune Pancreatitis in Childhood: Consensus From INSPPIRE

B. Barth, B. Zimmerman, M. Lowe, 2018, Journal of pediatric gastroenterology and nutrition.

Risk Factors for Rapid Progression From Acute Recurrent to Chronic Pancreatitis in Children: Report From INSPPIRE.

B. Barth, S. Freedman, M. Bellin, 2019, Journal of pediatric gastroenterology and nutrition.

Pancreas Divisum in Pediatric Acute Recurrent and Chronic Pancreatitis

B. Barth, S. Freedman, M. Bellin, 2019, Journal of clinical gastroenterology.

B. Barth, S. Freedman, M. Bellin, 2017, Pancreas.

Management of Gastrointestinal and Nutritional Problems in Children with Neurological Impairment: A Survey of Practice.

F. Gottrand, R. Orel, M. Van Winckel, 2020, Journal of pediatric gastroenterology and nutrition.

Role of Polyethylene Glycol in the Treatment of Functional Constipation in Children

F. Gottrand, I. Koppen, M. Benninga, 2017, Journal of pediatric gastroenterology and nutrition.

Treatment Regimens for Helicobacter pylori Infection in Children: Is In Vitro Susceptibility Testing Helpful?

M. Wilschanski, B. Rudensky, Y. Schlesinger, 2005, Journal of pediatric gastroenterology and nutrition.

Supplementary enterai nutrition maintains remission in paediatric Crohn's disease

M. Corey, A. Griffiths, P. Pencharz, 1996 .

Toxic effects of atenolol consumed during breast feeding.

G. Koren, A. Eidelman, M. Wilschanski, 1989, The Journal of pediatrics.

Hepatobiliary Involvement in Cystic Fibrosis

M. Wilschanski, M. Slae, A. Bertolini, 2020 .

Effects of new and emerging therapies on gastrointestinal outcomes in cystic fibrosis

R. Houwen, M. Wilschanski, M. Slae, 2017, Current opinion in pulmonary medicine.

Effectiveness of PTC124 treatment of cystic fibrosis caused by nonsense mutations: a prospective phase II trial

Eitan Kerem, B. Kerem, H. Blau, 2008, The Lancet.

Neonatal sclerosing cholangitis associated with autoimmune phenomena.

M. Wilschanski, D. Branski, C. Brautbar, 2000, Journal of pediatric gastroenterology and nutrition.

Pathology of pancreatic and intestinal disorders in cystic fibrosis

M. Wilschanski, P. Durie, 1998, Journal of the Royal Society of Medicine.

Severe Clostridium difficile-associated colitis in young patients with cystic fibrosis.

E. Kerem, M. Wilschanski, A. Lerner, 1998, The Journal of pediatrics.

Training in Paediatric Clinical Nutrition Across Europe: A Survey of the National Societies Network (2016–2019) of the European Society for Paediatric Gastroenterology, Hepatology and Nutrition

G. Veres, B. Koletzko, R. Orel, 2022, Journal of pediatric gastroenterology and nutrition.

The Q359K/T360K mutation causes cystic fibrosis in Georgian Jews.

H. Mussaffi, D. Prais, M. Mei-Zahav, 2018, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Genetic modifiers of liver disease in cystic fibrosis.

M. Corey, J. Zieleński, M. Drumm, 2009, JAMA.

Cystic fibrosis and the role of gastrointestinal outcome measures in the new era of therapeutic CFTR modulation.

M. Wilschanski, H. Verkade, J. Taminiau, 2015, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

3.22 Nutrition in Cystic Fibrosis.

M. Wilschanski, M. Slae, 2022, World review of nutrition and dietetics.

Mutations in the cystic fibrosis transmembrane regulator gene and in vivo transepithelial potentials.

M. Corey, L. Tsui, J. Zieleński, 2006, American journal of respiratory and critical care medicine.

Factors Associated With Frequent Opioid Use in Children With Acute Recurrent and Chronic Pancreatitis.

B. Barth, S. Freedman, M. Bellin, 2019, Journal of pediatric gastroenterology and nutrition.

Infantile-onset inflammatory bowel disease has variable long-term outcomes

B. Weiss, M. Wilschanski, R. Shaoul, 2023, Frontiers in Pediatrics.

Initial Development and Validation of a Transition Readiness Scale for Adolescents with Inflammatory Bowel Disease

M. Wilschanski, R. Shamir, D. Turner, 2019, Gastroenterology research and practice.

Decreased postnatal docosahexaenoic and arachidonic acid blood levels in premature infants are associated with neonatal morbidities.

J. Ware, S. Freedman, Camilia R. Martin, 2011, The Journal of pediatrics.

651 – International Study Group of Pediatric Pancreatitis: in Search for a Cure(INSPPIRE 2) Cohort Study: Design and Rationale from the Consortium for the Study of Chronic Pancreatitis, Diabetes, and Pancreatic Cancer (CPDPC)

B. Barth, M. Bellin, M. Lowe, 2019, Gastroenterology.

Haemophilus Influenzae Neonatal Sepsis—What is Appropriate Initial Therapy?

A. Eidelman, M. Wilschanski, M. Schimmel, 1988, Acta paediatrica Scandinavica.

Shwachman-Diamond syndrome presenting as hepatosplenomegaly.

B. Shuckett, M. Wilschanski, P. Durie, 1994, Journal of pediatric gastroenterology and nutrition.

Ambulatory quantitative waking and sleeping cough assessment in patients with cystic fibrosis.

Temitayo Ajayi, Eitan Kerem, S. Peltz, 2011, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Quantitative cough assessment in cystic fibrosis (CF)

S. Peltz, E. Kerem, M. Wilschanski, 2008 .

Highlights of the ESPEN-ESPGHAN-ECFS Guidelines on Nutrition Care for Infants and Children With Cystic Fibrosis

B. Strandvik, S. Schneider, M. Stern, 2016, Journal of pediatric gastroenterology and nutrition.

Changes of CFTR functional measurements and clinical improvements in cystic fibrosis patients with non p.Gly551Asp gating mutations treated with ivacaftor.

I. Sermet-Gaudelus, M. Wilschanski, T. Nguyen-Khoa, 2017, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Nasal potential difference measurements in diagnosis of cystic fibrosis: an international survey.

B. Tümmler, N. Derichs, M. Ballmann, 2014, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Evaluation of the intestinal current measurement method as a diagnostic test for cystic fibrosis

E. Picard, E. Kerem, M. Wilschanski, 2013, Pediatric Pulmonology.

Patterns of gastrointestinal disease associated with mutations of CFTR

M. Wilschanski, 2008, Current gastroenterology reports.

Recurrent abdominal pain in children: is constipation an issue?

M. Wilschanski, D. Branski, 2004, The Israel Medical Association journal : IMAJ.

Celiac Disease and Celiac Antibodies in DM1 Patients: When Are Screening and Biopsy Recommended?

M. Wilschanski, O. Toker, M. Slae, 2018, Digestive Diseases and Sciences.

Liprotamase Long-term Safety and Support of Nutritional Status in Pancreatic-insufficient Cystic Fibrosis

M. Wilschanski, M. Campion, D. Borowitz, 2012, Journal of pediatric gastroenterology and nutrition.

Novel therapeutic modalities in pediatric inflammatory bowel disease.

M. Wilschanski, E. Shteyer, 2008, The Israel Medical Association journal : IMAJ.

Standardized Measurement of Nasal Membrane Transepithelial Potential Difference (NPD).

I. Sermet-Gaudelus, S. Rowe, P. Melotti, 2018, Journal of visualized experiments : JoVE.

Nasal potential difference in suspected cystic fibrosis patients with 5T polymorphism.

N. Derichs, P. Melotti, K. De Boeck, 2020, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Primary sclerosing cholangitis is associated with abnormalities in CFTR.

C. Férec, M. Audrézet, M. Wilschanski, 2018, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Nasal potential difference in non classic cystic fibrosis – long term follow up

E. Picard, H. Blau, E. Kerem, 2008 .

Reaching the diagnosis of cystic fibrosis--the limits of the spectrum.

H. Mussaffi, H. Blau, M. Wilschanski, 2000, The Israel Medical Association journal : IMAJ.

New drugs for cystic fibrosis

E. Kerem, M. Wilschanski, 2011, Expert opinion on investigational drugs.

Small molecules to treat cystic fibrosis.

M. Wilschanski, 2010, Proceedings of the American Thoracic Society.

algorithmsfibrosis: terminology and diagnostic

C. Castellani, J. Dodge, M. Wilschanski, 2008 .

Assessment of the efficacy of in vivo CFTR protein replacement therapy in CF mice.

Y. Wang, C. Ackerley, L. Huan, 1998, Human gene therapy.

Pain medication Steroids Pancreatic enzymes Diabetes medication Family history of pancreatic cancer Family history of pancreatitis Constant pain Episodic pain Chronic pancreatitis

B. Barth, S. Freedman, M. Bellin, 2016 .

41* PTC124 activity in CF patients carrying stop mutations: results of a phase 2 study

H. Blau, E. Kerem, M. Wilschanski, 2007 .

Clinical and functional efficacy of elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis carrying the N1303K mutation.

B. Kerem, E. Kerem, F. Ratjen, 2023, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

ESPGHAN Position Statement on the Management of Percutaneous Endoscopic Gastrostomy (PEG) in Children and Adolescents.

F. Gottrand, R. Orel, S. Husby, 2014 .

Increased Risk of Celiac Disease in Patients with Uveitis.

M. Wilschanski, Z. Davidovics, R. Amer, 2023, Ocular immunology and inflammation.

Novel therapeutic approaches for cystic fibrosis.

M. Wilschanski, 2013, Discovery medicine.

CFTR Protein Function Modulation Therapy Is Finally Targeting Cystic Fibrosis-related Gastrointestinal Disease.

M. Wilschanski, F. Bodewes, 2017, Journal of pediatric gastroenterology and nutrition.

Diversity of reproductive tract abnormalities in men with cystic fibrosis.

M. Corey, K. Jarvi, E. Tullis, 1996, JAMA.

New drugs for cystic fibrosis

E. Kerem, M. Wilschanski, 2011, Expert opinion on investigational drugs.

Cystic fibrosis and the role of gastrointestinal outcome measures in the new era of therapeutic CFTR modulation.

M. Wilschanski, H. Verkade, J. Taminiau, 2015, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Decreased postnatal docosahexaenoic and arachidonic acid blood levels in premature infants are associated with neonatal morbidities.

J. Ware, S. Freedman, Camilia R. Martin, 2011, The Journal of pediatrics.

Oral probiotics prevent necrotizing enterocolitis in very low birth weight neonates.

M. Caplan, M. Wilschanski, C. Hammerman, 2005, The Journal of pediatrics.

Obesogenic habits among children and their families in response to initiation of gluten-free diet

M. Wilschanski, E. Shteyer, M. Moskovitz, 2018, European Journal of Pediatrics.

ESPGHAN- Guidelines for the Evaluation and Treatment of Gastrointestinal and Nutritional Complications in Children with Neurological Impairment.

F. Gottrand, R. Orel, M. Wilschanski, 2017, Journal of pediatric gastroenterology and nutrition.

Recommendations for the classification of diseases as CFTR-related disorders.

B. Kerem, J. Zieleński, P. Pignatti, 2011, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

New clinical diagnostic procedures for cystic fibrosis in Europe.

N. Derichs, F. Vermeulen, P. Melotti, 2011, Journal of Cystic Fibrosis.

Influence of perfusate temperature on nasal potential difference

F. Vermeulen, P. Melotti, K. De Boeck, 2012, European Respiratory Journal.

Phenotypic characterisation of patients with intermediate sweat chloride values: towards validation of the European diagnostic algorithm for cystic fibrosis

P. Lebecque, N. Derichs, I. Sermet, 2009, Thorax.

Standards for the care of people with cystic fibrosis (CF); recognising and addressing CF health issues.

M. Wilschanski, J. Bouchara, S. van Koningsbruggen-Rietschel, 2024, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

ESPEN-ESPGHAN-ECFS guideline on nutrition care for cystic fibrosis.

C. Ribes-Koninckx, M. Wilschanski, S. Van Biervliet, 2023, Clinical nutrition.

ESPEN Guideline ESPEN-ESPGHAN-ECFS guideline on nutrition care for cystic ﬁ brosis

C. Ribes-Koninckx, M. Wilschanski, E. Hatziagorou, 2022 .

Evolution of nutritional management in children with cystic fibrosis - a narrative review.

M. Wilschanski, Chris Smith, Jacqueline Lowdon, 2024, Journal of human nutrition and dietetics : the official journal of the British Dietetic Association.