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F Baas

Showing results (81-90 of 245) with videos related to

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Human Mutation|January 1, 1995
Déjérine-Sottas neuropathy is associated with a de novo PMP22 mutationL J Valentijn, R A Ouvrier, N H van den Bosch, et al.
Nederlands Tijdschrift Voor Geneeskunde|November 24, 2004
[From gene to disease: amyotrophic lateral sclerosis]P W J van Vught, J H Veldink, F Baas, et al.
Oncogene|October 7, 1997
Allelotype of pediatric rhabdomyosarcomaM Visser, C Sijmons, J Bras, et al.
Acta Neuropathologica|June 24, 2005
The unfolded protein response is activated in Alzheimer's diseaseJ J M Hoozemans, R Veerhuis, E S Van Haastert, et al.
Journal of Psychopharmacology (Oxford, England)|May 2, 2009
Striatal D₂ receptor binding in 22q11 deletion syndrome: an [¹²³I]IBZM SPECT studyE Boot, J Booij, J R Zinkstok, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 16, 2010
The first case of protease-sensitive prionopathy (PSPr) in The Netherlands: a patient with an unusual GSS-like clinical phenotypeC Jansen, M W Head, W A van Gool, et al.
The Canadian Journal of Cardiology|May 13, 2021
Early Lethal Noncompaction Cardiomyopathy in Siblings With Compound Heterozygous RYR2 VariantJantiene C Duvekot, Annette F Baas, Catharina M L Volker-Touw, et al.
Neurology|March 1, 1996
Genetic localization of Bethlem myopathyG J Jobsis, P A Bolhuis, J M Boers, et al.
Chronic Respiratory Disease|February 14, 2015
Attitudes toward opioids for refractory dyspnea in COPD among Dutch chest physiciansDaisy J A Janssen, S M de Hosson, Eline bij de Vaate, et al.
European Journal of Clinical Investigation|March 27, 2026
MYH11 variants in thoracic aortic aneurysm pathophysiology: From bench to bedsideAria Atash, Barend M E Mees, Maarten J Cramer, et al.
Pageof 25

Showing results (81-90 of 245) with videos related to

Sort By:
Pageof 25
Human Mutation|January 1, 1995
Déjérine-Sottas neuropathy is associated with a de novo PMP22 mutationL J Valentijn, R A Ouvrier, N H van den Bosch, et al.
Nederlands Tijdschrift Voor Geneeskunde|November 24, 2004
[From gene to disease: amyotrophic lateral sclerosis]P W J van Vught, J H Veldink, F Baas, et al.
Oncogene|October 7, 1997
Allelotype of pediatric rhabdomyosarcomaM Visser, C Sijmons, J Bras, et al.
Acta Neuropathologica|June 24, 2005
The unfolded protein response is activated in Alzheimer's diseaseJ J M Hoozemans, R Veerhuis, E S Van Haastert, et al.
Journal of Psychopharmacology (Oxford, England)|May 2, 2009
Striatal D₂ receptor binding in 22q11 deletion syndrome: an [¹²³I]IBZM SPECT studyE Boot, J Booij, J R Zinkstok, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 16, 2010
The first case of protease-sensitive prionopathy (PSPr) in The Netherlands: a patient with an unusual GSS-like clinical phenotypeC Jansen, M W Head, W A van Gool, et al.
The Canadian Journal of Cardiology|May 13, 2021
Early Lethal Noncompaction Cardiomyopathy in Siblings With Compound Heterozygous RYR2 VariantJantiene C Duvekot, Annette F Baas, Catharina M L Volker-Touw, et al.
Neurology|March 1, 1996
Genetic localization of Bethlem myopathyG J Jobsis, P A Bolhuis, J M Boers, et al.
Chronic Respiratory Disease|February 14, 2015
Attitudes toward opioids for refractory dyspnea in COPD among Dutch chest physiciansDaisy J A Janssen, S M de Hosson, Eline bij de Vaate, et al.
European Journal of Clinical Investigation|March 27, 2026
MYH11 variants in thoracic aortic aneurysm pathophysiology: From bench to bedsideAria Atash, Barend M E Mees, Maarten J Cramer, et al.
Pageof 25