G. Visser
发表
S. Ferdinandusse,
R. Wanders,
B. van der Zwaag,
2014,
The New England journal of medicine.
I. van der Made,
E. Creemers,
C. Argmann,
2020,
bioRxiv.
S. Wortmann,
M. Rubio-Gozalbo,
G. Visser,
2013,
Journal of Inherited Metabolic Disease.
R. Ophoff,
E. Strengman,
J. Luykx,
2014,
The American journal of clinical nutrition.
L. Kluijtmans,
A. Heijboer,
A. Boelen,
2020,
JIMD reports.
H. Waterham,
T. Derks,
M. D. De Vries,
2019,
Journal of inherited metabolic disease.
J. Dittman,
T. A. Ryan,
S. Thoms,
2017,
The Journal of clinical investigation.
S. Ferdinandusse,
R. Wanders,
R. Houtkooper,
2018,
Reviews in Endocrine and Metabolic Disorders.
R. Berger,
T. D. de Koning,
P. V. van Hasselt,
2008,
Annals of neurology.
R. Wanders,
S. Houten,
G. Visser,
2013
.
R. Berger,
T. D. de Koning,
P. V. van Hasselt,
2009
.
S. Waisbren,
M. Hochuli,
S. Wortmann,
2019,
Orphanet Journal of Rare Diseases.
S. Ferdinandusse,
R. Wanders,
R. Houtkooper,
2020,
Clinical nutrition.
H. Sauerwein,
M. Ackermans,
G. Visser,
2010,
Journal of Inherited Metabolic Disease.
H. Sauerwein,
M. Ackermans,
G. Visser,
2008
.
L. Dorland,
G. Visser,
H. Engbers,
2005,
Journal of Inherited Metabolic Disease.
M. Hendriks,
N. D. de Roos,
M. Bonthuis,
2010,
Journal of Inherited Metabolic Disease.
T. Derks,
T. D. de Koning,
G. Visser,
2016,
Neonatology.
T. D. de Koning,
G. Visser,
N. Verhoeven-Duif,
2012,
Analytica chimica acta.
T. Suormala,
E. R. Baumgartner,
D. Reijngoud,
2000,
European Journal of Pediatrics.
F. Vaz,
J. Jans,
P. V. van Hasselt,
2013,
Molecular genetics and metabolism.
T. Takken,
K. Clarke,
S. Ferdinandusse,
2020,
Journal of inherited metabolic disease.
S. Ferdinandusse,
M. Langeveld,
G. Visser,
2022,
Journal of inherited metabolic disease.
Sharyn A. Lincoln,
F. Zou,
L. Medne,
2017,
Journal of neurogenetics.
T. Kuijpers,
A. Tool,
D. Roos,
2003,
Blood.
J. Jans,
P. V. van Hasselt,
G. Visser,
2015,
PloS one.
F. Groenendaal,
W. Visser,
T. D. de Koning,
2012,
Pediatrics.
J. Leonard,
G. Visser,
K. Ullrich,
2007,
European Journal of Pediatrics.
J. Leonard,
G. Visser,
K. Ullrich,
2002,
European Journal of Pediatrics.
S. Ferdinandusse,
R. Wanders,
R. Coronel,
2020,
International journal of molecular sciences.
M. Hellerstein,
R. Neese,
F. Kuipers,
2002,
The Journal of pediatrics.
G. Visser,
G. Smit,
J. Rake,
2006
.
B. Prakken,
P. Coffer,
M. Buitenhuis,
2012,
Journal of Inherited Metabolic Disease.
H. Waterham,
R. Wanders,
J. Fock,
2012,
Journal of Medical Genetics.
T. Takken,
P. Helders,
L. Dorland,
2005,
Nutrition & metabolism.
S. Ferdinandusse,
R. Houtkooper,
R. Wanders,
2022,
Journal of Inherited Metabolic Disease.
R. Wanders,
F. Vaz,
G. Visser,
2015
.
A. Verhoeven,
G. Visser,
R. Zwieten,
1999,
Pediatric Research.
W. Schlack,
C. Hollak,
J. Hermanides,
2016,
JIMD Reports.
R. Wanders,
S. Houten,
G. Visser,
2014,
FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
S. Ferdinandusse,
R. Wanders,
R. Houtkooper,
2020,
Journal of lipid and atherosclerosis.
H. Scheffer,
C. Buys,
G. Visser,
2000,
European journal of pediatrics.
H. Scheffer,
C. Buys,
G. Visser,
1999
.
R. Hochstenbach,
L. T. van der Veken,
P. Terhal,
2014,
Cytogenetic and Genome Research.
S. Ferdinandusse,
H. Waterham,
P. Nikkels,
2017,
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.
J. Leonard,
G. Visser,
K. Ullrich,
2002,
European Journal of Pediatrics.
A. Balemans,
K. V. van Gassen,
P. V. van Hasselt,
2018,
JIMD reports.
Glycogen storage disease type Ia: Four novel mutations (175delGG, R170X, G266V and V338F) identified
H. Scheffer,
C. Buys,
G. Visser,
1999
.
G. Matthijs,
R. Wevers,
C. Thiel,
2016,
Journal of Inherited Metabolic Disease.
J. Jans,
K. V. van Gassen,
G. Visser,
2019,
JIMD reports.
Robert W. Taylor,
A. Ballabio,
E. Bertini,
2020,
Journal of inherited metabolic disease.
J. Jans,
P. V. van Hasselt,
G. Visser,
2015,
Analytica chimica acta.
E. van der Veer,
G. Visser,
G. Smit,
2003,
Journal of Inherited Metabolic Disease.
P. Bosco,
M. Durán,
F. Calì,
2019,
Nature Communications.
J. Jans,
P. V. van Hasselt,
G. Visser,
2016,
Journal of Inherited Metabolic Disease.
K. V. van Gassen,
P. V. van Hasselt,
G. Visser,
2015,
JIMD reports.
C. Vrinten,
G. Ceccarini,
A. Federico,
2020,
Orphanet Journal of Rare Diseases.
J. Leonard,
G. Visser,
U. Wendel,
2007,
European Journal of Pediatrics.
J. Leonard,
J. Fernandes,
G. Visser,
2000,
The Journal of pediatrics.
J. Leonard,
G. Visser,
U. Wendel,
2002,
European Journal of Pediatrics.
H. Waterham,
R. Wanders,
M. Durán,
2010,
Journal of Inherited Metabolic Disease.
P. Sauer,
P. Nikkels,
F. Kokke,
2002,
Journal of Inherited Metabolic Disease.
T. Wieland,
T. Strom,
J. Veltman,
2014,
Human Genetics.
H. Scheffer,
C. Buys,
G. Visser,
2000,
European Journal of Pediatrics.
J. Leonard,
K. Groenier,
G. Visser,
2007,
European Journal of Pediatrics.
J. Leonard,
K. Groenier,
G. Visser,
2002,
European Journal of Pediatrics.
A. Verhoeven,
G. Visser,
G. Smit,
1998,
Journal of Inherited Metabolic Disease.
R. Rodenburg,
V. Wolters,
J. V. van Montfrans,
2017,
Human Genetics.
Anke M Hövels,
Peter M van Hasselt,
Nanda M Verhoeven-Duif,
2016,
Genetics in Medicine.
L. Vissers,
T. Wieland,
T. Strom,
2014,
Human Genetics.
R. Pfundt,
N. de Leeuw,
B. D. de Vries,
2007,
Developmental medicine and child neurology.
H. Scheffer,
A. Smit,
G. Visser,
1998
.
S. Houten,
R. Nievelstein,
G. Visser,
2013,
Journal of Inherited Metabolic Disease.
W. Gahl,
T. Eggermann,
E. Babu,
2004,
Nature Genetics.
J. M. Aerts,
R. Wevers,
C. Hollak,
2012,
Molecular genetics and metabolism.
C. Toro,
C. Tifft,
C. Gellera,
2020,
Journal of clinical medicine.
Mitochondrial trifunctional protein deficiency in human cultured fibroblasts: effects of bezafibrate
S. Ferdinandusse,
R. Wanders,
B. Andresen,
2016,
Journal of Inherited Metabolic Disease.
J. Jans,
G. Visser,
N. Verhoeven-Duif,
2013,
Molecular genetics and metabolism.
G. Visser,
G. Smit,
J. Rake,
2003,
Journal of Inherited Metabolic Disease.
T. Takken,
N. V. van Riel,
J. Jeneson,
2016,
PloS one.
G. Visser,
S. Fuchs,
Susanne J. Boers,
2014,
Orphanet Journal of Rare Diseases.
S. Biskup,
G. Visser,
J. Breur,
2019,
JIMD reports.
S. Grünert,
J. Sass,
T. Derks,
2017,
Molecular genetics and metabolism.
G. Visser,
F. Wijburg,
F. V. van Spronsen,
2016,
European Journal of Pediatrics.
S. Ferdinandusse,
R. Wanders,
R. Houtkooper,
2021,
Frontiers in Pharmacology.
R. Rodenburg,
H. Venselaar,
S. Wortmann,
2014,
European Journal of Human Genetics.
S. Ferdinandusse,
H. Waterham,
R. Wanders,
2015,
Genetics in Medicine.
J. Kimpen,
G. Visser,
J. V. Woensel,
1995,
European Journal of Pediatrics.
R. Rodenburg,
S. Wortmann,
J. Smeitink,
2015,
Journal of Inherited Metabolic Disease.
S. Ferdinandusse,
R. Wanders,
A. Nederveen,
2020,
Journal of inherited metabolic disease.
Prediction of VLCAD deficiency phenotype by a metabolic fingerprint in newborn screening bloodspots.
S. Ferdinandusse,
R. Houtkooper,
M. Pras-Raves,
2020,
Biochimica et biophysica acta. Molecular basis of disease.
M. Heiner-Fokkema,
G. Visser,
M. G. M. de Sain-van der Velden,
2022,
JIMD reports.
N. Verhoeven,
T. D. de Koning,
P. V. van Hasselt,
2011,
Pediatrics.
H. Waterham,
R. Wanders,
M. Durán,
2013,
JIMD reports.
S. Ferdinandusse,
H. Waterham,
R. Wanders,
2019,
Journal of inherited metabolic disease.
S. Ferdinandusse,
N. Darín,
J. Ruiter,
2022,
Journal of inherited metabolic disease.
S. Ferdinandusse,
R. Wanders,
T. Derks,
2019,
Journal of inherited metabolic disease.
S. Ferdinandusse,
H. Waterham,
T. Derks,
2018,
Journal of inherited metabolic disease.
S. Ferdinandusse,
H. Waterham,
R. Wanders,
2019
.
S. Ferdinandusse,
H. Waterham,
T. Derks,
2018,
Journal of Inherited Metabolic Disease.
S. Ferdinandusse,
H. Waterham,
L. Kluijtmans,
2016,
JIMD reports.
H. Waterham,
R. Wanders,
T. Derks,
2012,
Orphanet Journal of Rare Diseases.
H. Waterham,
R. Wanders,
T. Derks,
2012
.
C. Bergmann,
R. Nievelstein,
F. Beemer,
2005,
American journal of medical genetics. Part A.
J. Jans,
K. V. van Gassen,
P. V. van Hasselt,
2016,
JIMD reports.
E. Turro,
J. Jaeken,
K. Freson,
2017,
Orphanet Journal of Rare Diseases.
M. D. De Vries,
P. V. van Hasselt,
G. Visser,
2011,
Molecular genetics and metabolism.
J. Leonard,
G. Visser,
K. Ullrich,
2007,
European Journal of Pediatrics.
M. Kroos,
J. Kimpen,
G. Visser,
2002,
Pediatrics.
M. D. de Barse,
R. Berger,
A. Verrips,
2008,
Journal of Inherited Metabolic Disease.
G. Sinnema,
T. D. de Koning,
P. V. van Hasselt,
2014,
The Journal of pediatrics.
A. van der Lelij,
G. Visser,
R. Wisse,
2012,
BMJ Case Reports.
G. Matthijs,
E. Legius,
J. Cassiman,
1996,
Genomics.
M. Langeveld,
L. Henneman,
G. Visser,
2023,
Orphanet Journal of Rare Diseases.
Newborn screening for primary carnitine deficiency: who will benefit? – a retrospective cohort study
S. Ferdinandusse,
M. Langeveld,
M. D. De Vries,
2023,
Journal of Medical Genetics.
J. Schweizer,
D. Reijngoud,
K. D. de Jong,
2000,
European Journal of Pediatrics.
H. Waterham,
L. Ijlst,
N. Abeling,
2017
.
S. Ferdinandusse,
R. Wanders,
M. Langeveld,
2020,
JIMD reports.
J. Dittman,
T. A. Ryan,
S. Thoms,
2017,
The Journal of clinical investigation.
N. Verhoeven,
T. D. de Koning,
P. V. van Hasselt,
2011,
Pediatrics.
P. Bosco,
M. Durán,
F. Calì,
2019,
Nature Communications.
S. Ferdinandusse,
H. Waterham,
T. Derks,
2018,
Journal of Inherited Metabolic Disease.
H. Scheffer,
C. Buys,
G. Visser,
2000,
Human mutation.
Sharyn A. Lincoln,
F. Zou,
L. Medne,
2017,
Journal of neurogenetics.