P. Witters
发表
P. Carmeliet,
L. Treps,
M. Declercq,
2021,
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
P. Carmeliet,
A. Ramalho,
D. Cassiman,
2020,
European Respiratory Journal.
V. Traver,
M. Boon,
C. Ribes-Koninckx,
2018,
PloS one.
E. Martins,
A. Harroche,
P. Witters,
2020,
Journal of Inherited Metabolic Disease.
H. Andersson,
C. V. van Karnebeek,
D. Cassiman,
2021,
Orphanet Journal of Rare Diseases.
H. Freeze,
F. Tort,
Christina Lam,
2020,
Journal of inherited metabolic disease.
F. Scaglia,
K. Õunap,
M. He,
2020,
Genetics in Medicine.
P. Rutgeerts,
S. Vermeire,
G. Assche,
2013
.
M. Trauner,
P. Witters,
S. Ling,
2017,
Journal of pediatric gastroenterology and nutrition.
D. Mekahli,
E. Levtchenko,
P. Witters,
2018,
Pediatric Nephrology.
M. Baumgartner,
H. Andersson,
P. Witters,
2016,
Molecular genetics and metabolism.
Noncirrhotic presinusoidal portal hypertension is common in cystic fibrosis–associated liver disease
B. Strandvik,
T. Roskams,
F. Nevens,
2011,
Hepatology.
Zhen Wang,
G. Engelmann,
D. Cassiman,
2020,
Liver international : official journal of the International Association for the Study of the Liver.
H. Freeze,
G. Matthijs,
A. Ribes,
2021,
American Journal of Human Genetics.
F. Cools,
P. Witters,
2006,
Acta cardiologica.
G. Francis,
R. Hegele,
M. Reijman,
2022,
The Lancet.
F. Nevens,
D. Cassiman,
P. Witters,
2010,
Journal of Thrombosis and Haemostasis.
P. Witters,
K. Driesen,
2022,
Metabolites.
M. Patterson,
H. Plotkin,
Christina Lam,
2021,
Molecular genetics and metabolism.
Rachel B. Keller,
D. Nickerson,
M. Bamshad,
2021,
HGG advances.
J. Mainz,
M. Boon,
C. Ribes-Koninckx,
2020,
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
H. Freeze,
M. Patterson,
Christina Lam,
2019,
Journal of inherited metabolic disease.
P. Witters,
K. De Boeck,
S. Demeyer,
2016,
European Journal of Pediatrics.
E. Levtchenko,
D. Cassiman,
P. Witters,
2020,
Journal of pediatric gastroenterology and nutrition.
P. Witters,
E. Morava,
J. Jaeken,
2018,
European Journal of Human Genetics.
D. Cassiman,
C. Thiel,
P. Vermeersch,
2019,
American journal of human genetics.
F. Nevens,
S. Sarin,
D. Valla,
2020,
Hepatology.
M. Boon,
C. Ribes-Koninckx,
P. Witters,
2017,
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
D. Cassiman,
P. Vermeersch,
P. Witters,
2019,
Metabolites.
T. Roskams,
D. Mekahli,
D. Cassiman,
2018,
Orphanet Journal of Rare Diseases.
D. Cassiman,
P. Vermeersch,
P. Witters,
2022,
Molecular metabolism.
G. Matthijs,
R. Wevers,
C. Thiel,
2016,
Journal of Inherited Metabolic Disease.
K. Jansen,
P. Vermeersch,
P. Witters,
2018,
Journal of Inherited Metabolic Disease.
I. Casteels,
E. Denayer,
P. Witters,
2021,
Ophthalmic genetics.
P. Carmeliet,
L. Treps,
M. Declercq,
2019,
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
F. Nevens,
C. Verslype,
D. Cassiman,
2008,
Alimentary pharmacology & therapeutics.
Marc Gewillig,
Geert Maleux,
Johan Fevery,
2008,
Journal of gastroenterology and hepatology.
P. Witters,
2016,
Journal of Inherited Metabolic Disease.
J. Vockley,
S. Wortmann,
T. Derks,
2020,
Genetics in Medicine.
D. Cassiman,
P. Witters,
J. Jaeken,
2017,
Journal of Inherited Metabolic Disease.
P. Witters,
E. Morava,
T. Kozicz,
2019,
Genetics in Medicine.
H. Waterham,
L. de Meirleir,
P. Witters,
2016,
American journal of medical genetics. Part A.
P. Witters,
E. Sokal,
X. Stephenne,
2022,
Acta gastro-enterologica Belgica.
D. Cassiman,
P. Witters,
G. Maleux,
2018,
Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver.
L. Weber,
D. Mekahli,
M. Liebau,
2018,
Front. Pediatr..
R. Horvath,
M. Tesařová,
Ann Saada,
2017,
Genetics in Medicine.
L. Hoefsloot,
J. Saris,
A. de Klein,
2020,
Molecular therapy. Methods & clinical development.
D. Cassiman,
P. Witters,
E. Morava,
2021,
Genes.
J. Ceuppens,
H. Mages,
R. Kroczek,
2004,
The Journal of Immunology.
F. Nevens,
C. Verslype,
W. Laleman,
2009,
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
D. Cassiman,
P. Witters,
E. Morava,
2017,
Nutrients.
G. Enns,
P. Witters,
E. Morava,
2019,
JIMD reports.
Nicole M. Armstrong,
G. Diaz,
R. Giugliani,
2022,
Orphanet Journal of Rare Diseases.
Z. Saifudeen,
E. Levtchenko,
D. Cassiman,
2017,
Molecular genetics and metabolism.
T. Roskams,
D. Cassiman,
L. Dupont,
2017,
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
D. Cassiman,
P. Witters,
M. Laurent,
2020,
Journal of clinical densitometry : the official journal of the International Society for Clinical Densitometry.
G. Matthijs,
D. Cassiman,
T. Gadomski,
2017,
The Journal of clinical endocrinology and metabolism.
L. Forbat,
D. Cassiman,
P. Witters,
2019,
JIMD reports.
G. Matthijs,
D. Cassiman,
P. Witters,
2018,
Genetics in Medicine.
F. Nevens,
C. Verslype,
W. Laleman,
2010,
European journal of gastroenterology & hepatology.
P. Witters,
I. Hoffman,
Ilse Van Horebeek,
2017,
Journal of paediatrics and child health.
G. Matthijs,
D. Cassiman,
P. Witters,
2018,
Genetics in Medicine.
L. Lagae,
C. Wouters,
B. Ceulemans,
2007,
Epilepsia.
P. Witters,
E. Morava,
2016
.
E. Perlstein,
Christina Lam,
D. Cassiman,
2021,
Annals of neurology.
P. Witters,
E. Morava,
T. Kozicz,
2019,
Genetics in Medicine.
M. Davenport,
P. Witters,
A. Dhawan,
2017,
Journal of pediatric gastroenterology and nutrition.
K. Devriendt,
D. Cassiman,
M. Declercq,
2020,
Journal of hepatology.
G. Opdenakker,
P. Proost,
P. Witters,
2018,
The FEBS journal.
H. Freeze,
M. Patterson,
Christina Lam,
2021,
Orphanet Journal of Rare Diseases.
Christina Lam,
M. Schultz,
D. Cassiman,
2023,
Cell reports. Medicine.
H. Freeze,
Christina Lam,
G. Enns,
2023,
Journal of inherited metabolic disease.
P. Witters,
E. Morava,
S. Radenkovic,
2018,
Molecular genetics and metabolism.
D. Cassiman,
L. Dupont,
P. Witters,
2013,
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
A. Novelli,
P. Witters,
B. Ghesquière,
2022,
Genetics in medicine : official journal of the American College of Medical Genetics.
P. Witters,
2017,
Journal of Inherited Metabolic Disease.
Noncirrhotic presinusoidal portal hypertension is common in cystic fibrosis–associated liver disease
B. Strandvik,
T. Roskams,
F. Nevens,
2011,
Hepatology.
P. Witters,
2016,
Journal of Inherited Metabolic Disease.
Z. Saifudeen,
E. Levtchenko,
D. Cassiman,
2017,
Molecular genetics and metabolism.
F. Nevens,
C. Verslype,
D. Cassiman,
2008,
Alimentary pharmacology & therapeutics.
J. Ceuppens,
H. Mages,
R. Kroczek,
2004,
The Journal of Immunology.
M. Boon,
C. Ribes-Koninckx,
P. Witters,
2016
.