The acute effects of a lunch containing capsaicin on energy and substrate utilisation, hormones, and satiety

gan Smeets, Astrid J., Westerterp-Plantenga, Margriet S.
Cyhoeddwyd 2009

Evolution of the basal ganglia: new perspectives through a comparative approach

gan SMEETS, WILHELMUS J. A. J., MARÍN, OSCAR, GONZÁLEZ, AGUSTÍN
Cyhoeddwyd 2000

Z-effect after intramedullary nailing systems for trochanteric femur fractures

gan Smeets, S.J.M., Kuijt, G., van Eerten, P.V.
Cyhoeddwyd yn Chin J Traumatol (2017)

Effect of blood transfusion on survival after hip fracture surgery

gan Smeets, S. J. M., Verbruggen, J. P. A. M., Poeze, M.
Cyhoeddwyd yn Eur J Orthop Surg Traumatol (2018)

Human ApoCI HpaI restriction site polymorphism revealed by the polymerase chain reaction

gan Nillesen, W.M., Smeets, H.J.M., Van Oost, B.A.
Cyhoeddwyd 1990

Chemokine and chemokine receptor expression in paired peripheral blood mononuclear cells and synovial tissue of patients with rheumatoid arthritis, osteoarthritis, and reactive art...

gan Haringman, J J, Smeets, T J M, Reinders‐Blankert, P, Tak, P P
Cyhoeddwyd 2006

The effectiveness of generic self‐management interventions for patients with chronic musculoskeletal pain on physical function, self‐efficacy, pain intensity and physical activity:...

gan Elbers, S., Wittink, H., Pool, J.J.M., Smeets, R.J.E.M.
Cyhoeddwyd yn Eur J Pain (2018)

Successful Endovascular Treatment of a Giant Intraparenchymal Renal Artery Pseudoaneurysm in a Young Female Patient

gan Huizing, Floortje, Blok, Joris J., Urlings, Thijs A.J., Smeets, Harm J.
Cyhoeddwyd yn EJVES Short Rep (2019)

Methods in molecular cardiology: microarray technology

gan van den Bosch, B., Doevendans, P.A., Lips, D., Smeets, H.J.M.
Cyhoeddwyd 2003

Biochemical abnormalities in a patient with thymidine phosphorylase deficiency with fatal outcome

gan Bakker, Jaap A., Schlesser, Patrick, Smeets, Hubert J. M., Francois, Baudouin, Bierau, Jörgen
Cyhoeddwyd 2010

Cerebellar developmental deficits underlie neurodegenerative disorder spinocerebellar ataxia type 23

gan Smeets, Cleo J.L.M., Ma, Kai Yu, Fisher, Simon E., Verbeek, Dineke S.
Cyhoeddwyd yn Brain Pathol (2020)

Metabolism and growth inhibition of four retinoids in head and neck squamous normal and malignant cells

gan Klaassen, I, Brakenhoff, R H, Smeets, S J, Snow, G B, Braakhuis, B J M
Cyhoeddwyd 2001

Transition Metal Ions in Zeolites: Coordination and activation of O(2)

gan Smeets, Pieter J., Woertink, Julia S., Sels, Bert F., Solomon, Edward I., Schoonheydt, Robert A.
Cyhoeddwyd 2010

Is the impact of hospital performance data greater in patients who have compared hospitals?

gan de Groot, Ingrid B, Otten, Wilma, Smeets, Harm J, Marang-van de Mheen, Perla J
Cyhoeddwyd 2011

Fear of Movement Is Related to Trunk Stiffness in Low Back Pain

gan Karayannis, Nicholas V., Smeets, Rob J. E. M., van den Hoorn, Wolbert, Hodges, Paul W.
Cyhoeddwyd 2013

Isolated case of mental retardation and ataxia due to a de novo mitochondrial T8993G mutation.

gan de Coo, I. F., Smeets, H. J., Gabreëls, F. J., Arts, N., van Oost, B. A.
Cyhoeddwyd 1996

Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease

gan Blok, M J, Spruijt, L, de Coo, I F M, Schoonderwoerd, K, Hendrickx, A, Smeets, H J
Cyhoeddwyd 2007

Intensity-based analysis of dual-color gene expression data as an alternative to ratio-based analysis to enhance reproducibility

gan Bossers, Koen, Ylstra, Bauke, Brakenhoff, Ruud H, Smeets, Serge J, Verhaagen, Joost, van de Wiel, Mark A
Cyhoeddwyd 2010

Cu-ZSM-5: A biomimetic inorganic model for methane oxidation

gan Vanelderen, Pieter, Hadt, Ryan G., Smeets, Pieter J., Solomon, Edward I., Schoonheydt, Robert A., Sels, Bert F.
Cyhoeddwyd 2011

Transcriptome analysis of complex I-deficient patients reveals distinct expression programs for subunits and assembly factors of the oxidative phosphorylation system

gan van der Lee, Robin, Szklarczyk, Radek, Smeitink, Jan, Smeets, Hubert J M, Huynen, Martijn A., Vogel, Rutger
Cyhoeddwyd yn BMC Genomics (2015)