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H M Van Minderhout

Showing results (1-10 of 15) with videos related to

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Strabismus|February 15, 2011
Sixty strabismus cases operated with the Computerized Strabismus Model 1.0: When does it benefit, when not ?H J Simonsz, H M Van Minderhout, H Spekreijse
Strabismus|June 16, 2000
Perinatally ruptured dermoid cyst presenting as congenital oculomotor palsyH M Coevoet, H M van Minderhout, C M Mooy, et al.
Strabismus|March 23, 2001
The optimal stimulus to elicit suppression in small-angle convergent strabismusM V Joosse, H J Simonsz, H Spekreijse, et al.
Strabismus|December 17, 2009
Nightblindness-associated transient tonic downgaze (NATTD) in infant boys with chin-up head postureH J Simonsz, R J Florijn, H M van Minderhout, et al.
Strabismus|February 15, 2011
2 Quantitative visual field assessment of squinting eye under binocular conditions in ten patients with microstrabismus. Preliminary reportM V Joosse, H J Simonsz, H M Van Minderhout, et al.
Vision Research|November 28, 1997
Quantitative perimetry under binocular viewing conditions in microstrabismusM V Joosse, H J Simonsz, H M van Minderhout, et al.
Scientific Reports|March 30, 2024
Clinical and mutational characteristics of oculocutaneous albinism type 7C C Kruijt, G C de Wit, H M van Minderhout, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|July 24, 2012
Randomised comparison of three tools for improving compliance with occlusion therapy: an educational cartoon story, a reward calendar, and an information leaflet for parentsA M Tjiam, G Holtslag, H M Van Minderhout, et al.
The Journal of Molecular Diagnostics : JMD|July 12, 2015
A Novel Targeted Approach for Noninvasive Detection of Paternally Inherited Mutations in Maternal PlasmaJessica M E van den Oever, Ivonne J H M van Minderhout, Cornelis L Harteveld, et al.
Oncogene|April 6, 2004
Somatic loss of maternal chromosome 11 causes parent-of-origin-dependent inheritance in SDHD-linked paraganglioma and phaeochromocytoma familiesErik F Hensen, Ekaterina S Jordanova, Ivonne J H M van Minderhout, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Strabismus|February 15, 2011
Sixty strabismus cases operated with the Computerized Strabismus Model 1.0: When does it benefit, when not ?H J Simonsz, H M Van Minderhout, H Spekreijse
Strabismus|June 16, 2000
Perinatally ruptured dermoid cyst presenting as congenital oculomotor palsyH M Coevoet, H M van Minderhout, C M Mooy, et al.
Strabismus|March 23, 2001
The optimal stimulus to elicit suppression in small-angle convergent strabismusM V Joosse, H J Simonsz, H Spekreijse, et al.
Strabismus|December 17, 2009
Nightblindness-associated transient tonic downgaze (NATTD) in infant boys with chin-up head postureH J Simonsz, R J Florijn, H M van Minderhout, et al.
Strabismus|February 15, 2011
2 Quantitative visual field assessment of squinting eye under binocular conditions in ten patients with microstrabismus. Preliminary reportM V Joosse, H J Simonsz, H M Van Minderhout, et al.
Vision Research|November 28, 1997
Quantitative perimetry under binocular viewing conditions in microstrabismusM V Joosse, H J Simonsz, H M van Minderhout, et al.
Scientific Reports|March 30, 2024
Clinical and mutational characteristics of oculocutaneous albinism type 7C C Kruijt, G C de Wit, H M van Minderhout, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|July 24, 2012
Randomised comparison of three tools for improving compliance with occlusion therapy: an educational cartoon story, a reward calendar, and an information leaflet for parentsA M Tjiam, G Holtslag, H M Van Minderhout, et al.
The Journal of Molecular Diagnostics : JMD|July 12, 2015
A Novel Targeted Approach for Noninvasive Detection of Paternally Inherited Mutations in Maternal PlasmaJessica M E van den Oever, Ivonne J H M van Minderhout, Cornelis L Harteveld, et al.
Oncogene|April 6, 2004
Somatic loss of maternal chromosome 11 causes parent-of-origin-dependent inheritance in SDHD-linked paraganglioma and phaeochromocytoma familiesErik F Hensen, Ekaterina S Jordanova, Ivonne J H M van Minderhout, et al.
Pageof 2