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Nederlands Tijdschrift Voor Geneeskunde
|
October 10, 2013
[Increased CK activity in serum without symptoms: further investigations often unnecessary]
Nicol C Voermans, Marianne de Visser, John H J Wokke, et al.
Neurology
|
December 10, 2009
Dural ectasia in Marfan syndrome
Nicol C Voermans, Isabel Sánchez, L Concepción, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
March 31, 2015
The neuromuscular differential diagnosis of joint hypermobility
S Donkervoort, C G Bonnemann, B Loeys, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
July 7, 2005
[Epileptic seizures during childbirth in a patient with idiopathic generalised epilepsy]
N C Voermans, M J Zwarts, W O Renier, et al.
Vox Sanguinis
|
June 24, 2004
The (patho)physiology of megakaryocytopoiesis: from thrombopoietin in diagnostics and therapy to ex vivo generated cellular products
M R Tijssen, C E van der Schoot, C Voermans, et al.
Neuromuscular Disorders : NMD
|
November 24, 2024
My second life with mechanical ventilation: A golden anniversary
E Verhees, N A M Cobben, R van den Biggelaar, et al.
Muscle & Nerve
|
February 26, 2013
Exertional hyperckemia might be the first manifestation of a genetic disorder
Nicol C Voermans, Heinz Jungbluth, Esther Brusse, et al.
Acta Neuropathologica
|
February 7, 2024
"RYR1 and the cerebellum": scientific commentary on "Defective Cerebellar Ryanodine Receptor Type 1 and Endoplasmic Reticulum Calcium 'Leak' in Tremor Pathophysiology"
Heinz Jungbluth, Dennis T Famili, Rick C Helmich, et al.
Neuromuscular Disorders : NMD
|
November 18, 2005
The effect of dantrolene sodium in Very Long Chain Acyl-CoA Dehydrogenase Deficiency
N C Voermans, P J Poels, L A Kluijtmans, et al.
Journal of Neuromuscular Diseases
|
August 15, 2018
Mastication and Oral Motor Function in McArdle Disease: Patient Reported Complaints
C V Kouwenberg, N C Voermans, R Quinlivan, et al.
Page
of 35
Search research articles
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Showing results (31-40 of 344) with videos related to
Sort By:
Page
of 35
Nederlands Tijdschrift Voor Geneeskunde
|
October 10, 2013
[Increased CK activity in serum without symptoms: further investigations often unnecessary]
Nicol C Voermans, Marianne de Visser, John H J Wokke, et al.
Neurology
|
December 10, 2009
Dural ectasia in Marfan syndrome
Nicol C Voermans, Isabel Sánchez, L Concepción, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
March 31, 2015
The neuromuscular differential diagnosis of joint hypermobility
S Donkervoort, C G Bonnemann, B Loeys, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
July 7, 2005
[Epileptic seizures during childbirth in a patient with idiopathic generalised epilepsy]
N C Voermans, M J Zwarts, W O Renier, et al.
Vox Sanguinis
|
June 24, 2004
The (patho)physiology of megakaryocytopoiesis: from thrombopoietin in diagnostics and therapy to ex vivo generated cellular products
M R Tijssen, C E van der Schoot, C Voermans, et al.
Neuromuscular Disorders : NMD
|
November 24, 2024
My second life with mechanical ventilation: A golden anniversary
E Verhees, N A M Cobben, R van den Biggelaar, et al.
Muscle & Nerve
|
February 26, 2013
Exertional hyperckemia might be the first manifestation of a genetic disorder
Nicol C Voermans, Heinz Jungbluth, Esther Brusse, et al.
Acta Neuropathologica
|
February 7, 2024
"RYR1 and the cerebellum": scientific commentary on "Defective Cerebellar Ryanodine Receptor Type 1 and Endoplasmic Reticulum Calcium 'Leak' in Tremor Pathophysiology"
Heinz Jungbluth, Dennis T Famili, Rick C Helmich, et al.
Neuromuscular Disorders : NMD
|
November 18, 2005
The effect of dantrolene sodium in Very Long Chain Acyl-CoA Dehydrogenase Deficiency
N C Voermans, P J Poels, L A Kluijtmans, et al.
Journal of Neuromuscular Diseases
|
August 15, 2018
Mastication and Oral Motor Function in McArdle Disease: Patient Reported Complaints
C V Kouwenberg, N C Voermans, R Quinlivan, et al.
Page
of 35