M. Langeveld
发表
Wyeth W. Wasserman,
Ron A. Wevers,
Clara D. M. van Karnebeek,
2018,
Journal of Inherited Metabolic Disease.
M. Nieuwdorp,
M. Langeveld,
J. Langendonk,
2021,
Molecular genetics and metabolism reports.
J. Romijn,
K. V. van Dijk,
M. Langeveld,
2012,
Metabolism: clinical and experimental.
M. Langeveld,
S. Houten,
K. V. Dijk,
2009
.
J. M. Aerts,
M. Langeveld,
C. Hollak,
2008,
Blood cells, molecules & diseases.
J. Kastelein,
M. Langeveld,
C. Hollak,
2009,
Atherosclerosis.
Gaucher disease type I : associated morbidities and long term efficacy of enzyme replacement therapy
J. Kastelein,
E. Groot,
M. Langeveld,
2008
.
Marjana R. Lima,
M. Dijkgraaf,
M. Langeveld,
2020,
Journal of Neurology, Neurosurgery, and Psychiatry.
M. Baumgartner,
R. Hagendijk,
B. Bembi,
2016,
Orphanet Journal of Rare Diseases.
M. Langeveld,
J. Wilson,
E. Friesema,
2017,
The British journal of dermatology.
A. V. van Kuilenburg,
M. Langeveld,
C. Hollak,
2021,
Molecular genetics and metabolism.
M. Langeveld,
C. Hollak,
Anton P. Bussink,
2005
.
M. Langeveld,
J. F. Aerts,
J. F. G. Aerts,
2009,
Progress in lipid research.
M. Langeveld,
C. Hollak,
P. Dubbelhuis,
2007,
Metabolism: clinical and experimental.
W. Wiersinga,
M. Langeveld,
C. Hollak,
2007,
Journal of Inherited Metabolic Disease.
M. Langeveld,
C. Hollak,
2018,
Reviews in Endocrine and Metabolic Disorders.
S. Ferdinandusse,
R. Wanders,
R. Houtkooper,
2020,
Clinical nutrition.
M. Langeveld,
2009
.
Type I Gaucher disease, a glycosphingolipid storage disorder, is associated with insulin resistance.
J. M. Aerts,
M. Langeveld,
C. Hollak,
2008,
The Journal of clinical endocrinology and metabolism.
M. Langeveld,
C. Hollak,
M. Boekholdt,
2021,
Heart.
C. Wanner,
A. V. van Kuilenburg,
M. Langeveld,
2017,
Molecular genetics and metabolism.
R. Schiffmann,
P. Elliott,
J. Moon,
2021,
Molecular genetics and metabolism.
L. Vissers,
A. Hoischen,
H. Prokisch,
2022,
Journal of inherited metabolic disease.
T. Takken,
K. Clarke,
S. Ferdinandusse,
2020,
Journal of inherited metabolic disease.
S. Ferdinandusse,
M. Langeveld,
G. Visser,
2022,
Journal of inherited metabolic disease.
M. Langeveld,
C. Hollak,
A. B. Kuilenburg,
2020,
Journal of inherited metabolic disease.
P. Murgatroyd,
M. Langeveld,
A. Vidal-Puig,
2017,
The American journal of clinical nutrition.
M. Langeveld,
C. Hollak,
M. Arends,
2018,
Drug discovery today.
M. Langeveld,
M. Cornel,
W. Dondorp,
2021,
Frontiers in Pediatrics.
M. Langeveld,
J. Jans,
M. D. De Vries,
2019,
Journal of inherited metabolic disease.
L. Bour,
M. Langeveld,
C. Hollak,
2011,
Blood cells, molecules & diseases.
M. Langeveld,
C. Hollak,
R. Lachmann,
2017,
The lancet. Diabetes & endocrinology.
M. Langeveld,
C. Hollak,
C. Beishuizen,
2022,
Orphanet Journal of Rare Diseases.
S. Praet,
M. Langeveld,
M. Michels,
2016,
JIMD reports.
M. Langeveld,
S. Schoenmakers,
J. Langendonk,
2020,
BMJ Case Reports.
M. Langeveld,
C. Hollak,
J. Weening,
2006,
Journal of Inherited Metabolic Disease.
M. Hoek,
M. Langeveld,
H. Bax,
2020
.
M. Langeveld,
W. Pijnappel,
A. T. van der Ploeg,
2020,
Bone.
M. Langeveld,
L. J. van der Giessen,
A. T. van der Ploeg,
2017,
Molecular genetics and metabolism.
M. Langeveld,
I. Mathijssen,
R. Verdijk,
2018,
Journal of Inherited Metabolic Disease.
M. Langeveld,
P. Moerland,
M. Sokolovic,
2009,
Hepatology.
M. Langeveld,
T. Wennekes,
H. Overkleeft,
2011,
Advances in experimental medicine and biology.
M. Langeveld,
2009
.
M. Langeveld,
C. Hollak,
J. Aerts,
2008,
Clinica chimica acta; international journal of clinical chemistry.
L. Hoefsloot,
M. Langeveld,
C. Hollak,
2018,
Journal of Inherited Metabolic Disease.
Marjana R. Lima,
M. Dijkgraaf,
G. Geurtsen,
2020,
Orphanet journal of rare diseases.
A. V. van Kuilenburg,
M. Langeveld,
C. Hollak,
2019,
Molecular genetics and metabolism.
P. Ciet,
M. Langeveld,
A. T. van der Ploeg,
2016,
Orphanet Journal of Rare Diseases.
P. Postema,
J. Kors,
M. Langeveld,
2023,
Diagnostics.
M. Langeveld,
T. Coşkun,
S. Huijbregts,
2021,
Molecular genetics and metabolism.
M. Langeveld,
J. Wilson,
J. Langendonk,
2017,
Parkinsonism & related disorders.
Development and clinical consequences of white matter lesions in Fabry disease: a systematic review.
M. Langeveld,
C. Hollak,
Mirjam Langeveld,
2018,
Molecular genetics and metabolism.
S. Ferdinandusse,
M. Langeveld,
C. Hollak,
2022,
JIMD reports.
Marjana R. Lima,
M. Dijkgraaf,
G. Geurtsen,
2020,
Journal of inherited metabolic disease.
S. Ferdinandusse,
R. Wanders,
A. Nederveen,
2020,
Journal of inherited metabolic disease.
S. Ferdinandusse,
H. Waterham,
R. Wanders,
2019,
Journal of inherited metabolic disease.
S. Ferdinandusse,
H. Waterham,
R. Wanders,
2019
.
M. Langeveld,
J. Bakker,
M. Arbous,
2017,
JIMD reports.
Marjana R. Lima,
M. Dijkgraaf,
G. Geurtsen,
2019,
Scientific Reports.
G. Geurtsen,
M. Langeveld,
C. Hollak,
2019,
JIMD reports.
Wytze J. Vlietstra,
C. Wanner,
A. V. van Kuilenburg,
2020,
International journal of molecular sciences.
V K Chatterjee,
P. Murgatroyd,
M. Langeveld,
2016,
Endocrine connections.
M. Langeveld,
R. Lachmann,
F. Mochel,
2019,
JIMD reports.
L. Lynd,
C. Stratakis,
M. Langeveld,
2019,
The lancet. Diabetes & endocrinology.
M. Langeveld,
2018,
Trends in cardiovascular medicine.
M. Langeveld,
C. Hollak,
R. Lachmann,
2020,
Orphanet Journal of Rare Diseases.
J. Szer,
M. Langeveld,
C. Hollak,
2018,
Blood cells, molecules & diseases.
M. Langeveld,
L. Henneman,
G. Visser,
2023,
Orphanet Journal of Rare Diseases.
C. V. van Karnebeek,
M. Langeveld,
M. Buijs,
2023,
Frontiers in neurology.
H. Waterham,
M. Langeveld,
A. Bosch,
2022,
Neonatology.
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.
S. Ferdinandusse,
R. Wanders,
M. Langeveld,
2020,
JIMD reports.
M. Langeveld,
P. Moerland,
M. Sokolovic,
2009,
Hepatology.
M. Langeveld,
J. Langendonk,
L. Vroegindeweij,
2017,
Parkinsonism & related disorders.
S. Boekholdt,
M. Langeveld,
C. Hollak,
2023,
Clinical journal of the American Society of Nephrology : CJASN.
M. Langeveld,
K. Biermann,
L. H. Oterdoom,
2015,
Journal of gastrointestinal and liver diseases : JGLD.