A. Bosch
发表
I. Eijgelshoven,
S. Demirdas,
T. A. Smith,
2013,
Molecular genetics and metabolism.
L. Kluijtmans,
A. Heijboer,
A. Boelen,
2020,
JIMD reports.
H. Waterham,
T. Derks,
M. D. De Vries,
2019,
Journal of inherited metabolic disease.
C. Hollak,
Rani H. Singh,
P. Bisschop,
2015,
Orphanet Journal of Rare Diseases.
Outcome of infants diagnosed with 3-methyl-crotonyl-CoA-carboxylase deficiency by newborn screening.
G. Enns,
B. Graham,
B. Lanpher,
2012,
Molecular genetics and metabolism.
J. Burgerhof,
C. Hollak,
N. Blau,
2013,
Orphanet Journal of Rare Diseases.
Hubertus C M T Prinsen,
M. Huigen,
L. Kluijtmans,
2020,
JIMD reports.
M. Grootenhuis,
F. Wijburg,
A. Bosch,
2004,
Pediatrics.
A. Bosch,
A. E. ten Hoedt,
J. Gentile,
2009
.
M. Baumgartner,
R. Hagendijk,
B. Bembi,
2016,
Orphanet Journal of Rare Diseases.
M. Gautschi,
E. Treacy,
R. Saldova,
2021,
JIMD reports.
M. Caan,
S. Roosendaal,
C. Hollak,
2020,
Molecular genetics and metabolism.
Merel E. Hermans,
G. Geurtsen,
K. Oostrom,
2019,
Orphanet Journal of Rare Diseases.
J. H. van der Lee,
S. Waisbren,
K. Õunap,
2016,
Journal of Inherited Metabolic Disease.
S. Waisbren,
F. Eyskens,
E. Treacy,
2017,
JIMD reports.
Merel E. Hermans,
G. Geurtsen,
C. Hollak,
2020,
Orphanet Journal of Rare Diseases.
N. Blau,
S. Huijbregts,
A. Macdonald,
2017,
Orphanet Journal of Rare Diseases.
M. Contarino,
B. Post,
M. Tijssen,
2014,
Orphanet Journal of Rare Diseases.
S. Waisbren,
N. Leslie,
J. Fridovich-Keil,
2012,
Journal of Inherited Metabolic Disease.
S. Ferdinandusse,
C. Hollak,
M. D. De Vries,
2019,
Journal of inherited metabolic disease.
S. Waisbren,
M. Hochuli,
S. Wortmann,
2019,
Orphanet Journal of Rare Diseases.
A. Bosch,
Galactosaemia − Should,
IT BE Screened,
2019
.
S. Ferdinandusse,
R. Wanders,
M. van Weeghel,
2018,
Orphanet Journal of Rare Diseases.
I. Knerr,
P. Doran,
E. Treacy,
2018,
Orphanet Journal of Rare Diseases.
R. Wanders,
F. Wijburg,
A. Bosch,
2004,
Archives of Disease in Childhood.
A. Bosch,
2004
.
T. Derks,
A. Boelen,
M. D. De Vries,
2017,
Molecular Genetics and Metabolism.
C. Welt,
J. Geraedts,
G. de Wert,
2013,
Orphanet Journal of Rare Diseases.
A. Bosch,
2010,
Journal of Inherited Metabolic Disease.
H. Maurice‐Stam,
M. Grootenhuis,
F. Wijburg,
2009,
Journal of Inherited Metabolic Disease.
H. Sauerwein,
M. Ackermans,
F. Wijburg,
2005,
Molecular genetics and metabolism.
R. Wanders,
F. Wijburg,
A. Bosch,
2003,
Journal of Inherited Metabolic Disease.
J. Moreno-Navarrete,
J. Fernández-Real,
A. Pontecorvi,
2012,
Annals of Nutrition and Metabolism.
C. Hollak,
S. Demirdas,
A. Bosch,
2013,
Orphanet Journal of Rare Diseases.
C. Hollak,
M. Heiner-Fokkema,
M. Vries,
2011,
Molecular genetics and metabolism.
D. Rizopoulos,
J. Jans,
M. D. De Vries,
2020,
Clinical nutrition.
H. Waterham,
L. Ijlst,
R. Wanders,
2012,
Orphanet Journal of Rare Diseases.
"MY PKU": increasing self-management in patients with phenylketonuria. A randomized controlled trial
C. Hollak,
F. Wijburg,
A. Bosch,
2011,
Orphanet journal of rare diseases.
M. Benninga,
B. Koot,
A. Bosch,
2018,
Atherosclerosis.
T. Koning,
A. Bosch,
E. Rubio-Gozalbo,
2005,
Journal of Inherited Metabolic Disease.
C. Hollak,
F. Eyskens,
D. Cassiman,
2022,
Journal of inherited metabolic disease.
M. Langeveld,
J. Jans,
M. D. De Vries,
2019,
Journal of inherited metabolic disease.
Robert de Jonge,
A. Heijboer,
A. Boelen,
2018,
Molecular genetics and metabolism.
I. Rivera,
P. Verloo,
D. Timson,
2020,
Genetics in Medicine.
C. Hollak,
L. D. de Sonneville,
S. Huijbregts,
2018,
Molecular genetics and metabolism.
C. Hollak,
L. D. de Sonneville,
S. Huijbregts,
2017,
Behavior Genetics.
A. Bosch,
F. V. van Spronsen,
M. Giżewska,
2012,
Annals of Nutrition and Metabolism.
S. Ferdinandusse,
R. Houtkooper,
R. Wanders,
2022,
Journal of Inherited Metabolic Disease.
A. Bosch,
B. Jaeger,
2016,
Journal of Inherited Metabolic Disease.
H. Heymans,
M. Grootenhuis,
F. Wijburg,
2009,
Acta paediatrica.
N. Blau,
S. Huijbregts,
A. Burlina,
2017,
The lancet. Diabetes & endocrinology.
J. H. van der Lee,
C. Hollak,
P. Bisschop,
2017,
Annals of Nutrition and Metabolism.
N. Longo,
N. Blau,
C. Harding,
1964,
Neurology.
B. Dorgelo,
T. Koning,
A. Bosch,
2009,
Journal of Inherited Metabolic Disease.
J. H. van der Lee,
C. Hollak,
M. Wagenmakers,
2020,
Journal of inherited metabolic disease.
R. Rodenburg,
E. Kamsteeg,
J. Cobben,
2018,
Molecular genetics and metabolism reports.
S. Huijbregts,
V. Leuzzi,
A. Bosch,
2011,
Molecular genetics and metabolism.
A. Bosch,
C. Acquaviva,
C. Vianey-Saban,
2022,
Physician's Guide to the Diagnosis, Treatment, and Follow-Up of Inherited Metabolic Diseases.
M. Durán,
B. Poll-The,
C. Majoie,
2014,
Molecular genetics and metabolism.
R. Lachmann,
T. Derks,
M. Tijssen,
2019,
Journal of inherited metabolic disease.
A. Bosch,
2006,
Journal of Inherited Metabolic Disease.
C. Hollak,
A. Bosch,
Stephanie C M Nijmeijer,
2019,
Journal of inherited metabolic disease.
C. Vrinten,
G. Ceccarini,
A. Federico,
2020,
Orphanet Journal of Rare Diseases.
E. Bettiol,
A. Regnault,
A. Burlina,
2015,
Orphanet Journal of Rare Diseases.
H. Waterham,
R. Wanders,
M. Durán,
2010,
Journal of Inherited Metabolic Disease.
N. Blau,
S. Huijbregts,
A. Burlina,
2017
.
C. Hollak,
L. D. de Sonneville,
S. Huijbregts,
2016,
Journal of Inherited Metabolic Disease.
L. Sonneville,
C. Hollak,
S. Huijbregts,
2016
.
C. Hollak,
L. D. de Sonneville,
Leo M. J. Sonneville,
2010,
Journal of Inherited Metabolic Disease.
H. Houlden,
A. Bosch,
B. O'Callaghan,
2019,
Journal of inherited metabolic disease.
M. Eijkemans,
F. Broekmans,
B. Fauser,
2007,
Reproductive Sciences.
H. Waterham,
L. Ijlst,
R. Wanders,
2005,
Human mutation.
J. Fridovich-Keil,
B. Mendelsohn,
I. Knerr,
2022,
Journal of inherited metabolic disease.
A. Bosch,
2018,
Developmental period medicine.
M. Grootenhuis,
F. Wijburg,
A. Bosch,
2007,
Journal of Inherited Metabolic Disease.
M. Durán,
A. Boelen,
F. Wijburg,
2007,
Journal of Inherited Metabolic Disease.
M. Langeveld,
T. Coşkun,
S. Huijbregts,
2021,
Molecular genetics and metabolism.
A. Verrips,
A. Bosch,
F. Vaz,
2015,
European Journal of Pediatrics.
J. H. van der Lee,
S. Waisbren,
M. Gautschi,
2017,
JIMD reports.
A. Heijboer,
M. Finken,
M. Ackermans,
2021,
The Journal of clinical endocrinology and metabolism.
P. Struijs,
A. Bosch,
R. Hemke,
2020,
BMC Rheumatology.
M. Baumgartner,
S. Grünert,
M. Landolt,
2019,
Orphanet Journal of Rare Diseases.
Nenad Blau,
Roberto Cerone,
N. Blau,
2013,
Pediatrics.
S. Ferdinandusse,
H. Waterham,
R. Wanders,
2019,
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.
H. Waterham,
R. Wanders,
T. Derks,
2012,
Orphanet Journal of Rare Diseases.
H. Waterham,
R. Wanders,
T. Derks,
2012
.
R. Fingerhut,
A. Boelen,
A. Bosch,
2016,
JIMD reports.
Merel E. Hermans,
S. Ferdinandusse,
A. V. van Kuilenburg,
2022,
Journal of inherited metabolic disease.
J. H. van der Lee,
S. Ferdinandusse,
S. Roosendaal,
2020,
Brain communications.
S. Ferdinandusse,
C. Hollak,
M. D. De Vries,
2020,
Molecular genetics and metabolism.
S. Waisbren,
H. Maurice‐Stam,
M. Grootenhuis,
2011
.
H. Maurice‐Stam,
M. Grootenhuis,
F. Wijburg,
2011,
Journal of Inherited Metabolic Disease.
M. Durán,
A. V. van Kuilenburg,
A. Bosch,
2008,
Nucleosides, nucleotides & nucleic acids.
M. Durán,
A. V. van Kuilenburg,
L. Zoetekouw,
2007,
Molecular genetics and metabolism.
E. Bettiol,
A. Regnault,
A. Burlina,
2015,
Orphanet Journal of Rare Diseases.
T. van Amelsvoort,
A. Bassett,
L. Bour,
2017,
Psychological Medicine.
C. Hollak,
L. D. de Sonneville,
S. Huijbregts,
2015,
Molecular genetics and metabolism.
Merel E. Hermans,
G. Geurtsen,
C. Hollak,
2023,
Orphanet Journal of Rare Diseases.
C. Hollak,
L. D. de Sonneville,
S. Huijbregts,
2013,
Molecular genetics and metabolism.
C. Hollak,
L. D. de Sonneville,
S. Huijbregts,
2017,
Neuropsychology.
A. Burlina,
G. Berry,
E. Treacy,
2017,
Journal of Inherited Metabolic Disease.
H. Waterham,
M. Langeveld,
A. Bosch,
2022,
Neonatology.
L. Sonneville,
C. Hollak,
S. Huijbregts,
2017
.
H. Maurice‐Stam,
M. Grootenhuis,
M. D. De Vries,
2013,
Molecular genetics and metabolism.
C. Hollak,
P. Bisschop,
S. Demirdas,
2018,
Annals of Nutrition and Metabolism.
A. Bosch,
Bosch,
2010,
Journal of inherited metabolic disease.
A. Bosch,
J. Gentile,
A. E. Hoedt,
2010,
Molecular genetics and metabolism.
T. van Gelder,
A. Bosch,
Noa Rosenberg,
2023,
Journal of inherited metabolic disease.
A. Heijboer,
M. Heijnen,
A. Boelen,
2020,
European journal of endocrinology.
M. Hoogendoorn,
A. Heijboer,
A. Boelen,
2023,
Clinical biochemistry.
A. Heijboer,
A. Boelen,
N. Zwaveling-Soonawala,
2021,
European Thyroid Journal.
N. Blau,
M. Couce,
S. Keil,
2013,
Pediatrics.
M. D. De Vries,
A. Bosch,
F. V. van Spronsen,
2016,
Orphanet Journal of Rare Diseases.
Merel E. Hermans,
G. Geurtsen,
C. Hollak,
2020,
Orphanet Journal of Rare Diseases.
A. Meester‐Delver,
C. Hollak,
T. Derks,
2018,
Disability and rehabilitation.
A. Nederveen,
C. Hollak,
S. Huijbregts,
2017,
Psychological Medicine.
S. Ferdinandusse,
H. Waterham,
T. Derks,
2018,
Journal of Inherited Metabolic Disease.
N. Longo,
N. Blau,
C. Harding,
2021,
Nature Reviews Disease Primers.
G. Boers,
M. Janssen,
A. Bosch,
2009,
European Journal of Pediatrics.
H. Maurice‐Stam,
M. Grootenhuis,
F. Wijburg,
2009,
Journal of Inherited Metabolic Disease.