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van Engelen

Showing results (71-80 of 831) with videos related to

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HGG Advances|January 12, 2024
PABPN1 loss-of-function causes APA-shift in oculopharyngeal muscular dystrophyMilad Shademan, Hailiang Mei, Baziel van Engelen, et al.
Nederlands Tijdschrift Voor Geneeskunde|February 11, 2000
[Endovascular stent implantation as a treatment for iliac artery disease]E Tetteroo, A D van Engelen, Y van der Graaf, et al.
Headache|June 1, 1991
Bilateral episodic mydriasis as a migraine equivalent in childhood: a case reportB G van Engelen, W O Renier, F J Gabreëls, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|November 6, 2003
Auditory processing in patients with Charcot-Marie-Tooth disease type 1AKarin Neijenhuis, Andy Beynon, Ad Snik, et al.
Human Mutation|April 4, 2003
Oculopharyngeal muscular dystrophy (OPMD) due to a small duplication in the PABPN1 geneBarbara M van der Sluijs, Baziel G M van Engelen, Lies H Hoefsloot
Human Molecular Genetics|April 22, 2010
Molecular therapy in myotonic dystrophy: focus on RNA gain-of-functionSusan A M Mulders, Baziel G M van Engelen, Bé Wieringa, et al.
Acta Neurologica Scandinavica|November 1, 1993
Diagnosing multiple sclerosis in childhoodH B van Lieshout, B G van Engelen, E A Sanders, et al.
Toxicology and Applied Pharmacology|June 1, 1997
Effect of coexposure to methyl ethyl ketone (MEK) on n-hexane toxicokinetics in human volunteersJ G van Engelen, W Rebel-de Haan, J J Opdam, et al.
Neuromuscular Disorders : NMD|July 26, 2024
Improving Heckmatt muscle ultrasound grading scale through Rasch analysisJuerd Wijntjes, Christiaan Saris, Jonne Doorduin, et al.
Epilepsy Research|January 1, 1994
Serologic HLA typing in cryptogenic Lennox-Gastaut syndromeB G van Engelen, L P de Waal, C M Weemaes, et al.
Pageof 84

Showing results (71-80 of 831) with videos related to

Sort By:
Pageof 84
HGG Advances|January 12, 2024
PABPN1 loss-of-function causes APA-shift in oculopharyngeal muscular dystrophyMilad Shademan, Hailiang Mei, Baziel van Engelen, et al.
Nederlands Tijdschrift Voor Geneeskunde|February 11, 2000
[Endovascular stent implantation as a treatment for iliac artery disease]E Tetteroo, A D van Engelen, Y van der Graaf, et al.
Headache|June 1, 1991
Bilateral episodic mydriasis as a migraine equivalent in childhood: a case reportB G van Engelen, W O Renier, F J Gabreëls, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|November 6, 2003
Auditory processing in patients with Charcot-Marie-Tooth disease type 1AKarin Neijenhuis, Andy Beynon, Ad Snik, et al.
Human Mutation|April 4, 2003
Oculopharyngeal muscular dystrophy (OPMD) due to a small duplication in the PABPN1 geneBarbara M van der Sluijs, Baziel G M van Engelen, Lies H Hoefsloot
Human Molecular Genetics|April 22, 2010
Molecular therapy in myotonic dystrophy: focus on RNA gain-of-functionSusan A M Mulders, Baziel G M van Engelen, Bé Wieringa, et al.
Acta Neurologica Scandinavica|November 1, 1993
Diagnosing multiple sclerosis in childhoodH B van Lieshout, B G van Engelen, E A Sanders, et al.
Toxicology and Applied Pharmacology|June 1, 1997
Effect of coexposure to methyl ethyl ketone (MEK) on n-hexane toxicokinetics in human volunteersJ G van Engelen, W Rebel-de Haan, J J Opdam, et al.
Neuromuscular Disorders : NMD|July 26, 2024
Improving Heckmatt muscle ultrasound grading scale through Rasch analysisJuerd Wijntjes, Christiaan Saris, Jonne Doorduin, et al.
Epilepsy Research|January 1, 1994
Serologic HLA typing in cryptogenic Lennox-Gastaut syndromeB G van Engelen, L P de Waal, C M Weemaes, et al.
Pageof 84