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G W Padberg

Showing results (41-50 of 114) with videos related to

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European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|August 1, 1989
Clinical evaluation of pneumococcal meningitis in adults over a twelve-year periodG A Bruyn, H P Kremer, S de Marie, et al.
Nederlands Tijdschrift Voor Tandheelkunde|February 26, 2010
[Facioscapulohumeral muscular dystrophy]J Wilbers, R R Frants, B G M van Engelen, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 1991
Syncope or seizure? The diagnostic value of the EEG and hyperventilation test in transient loss of consciousnessW A Hoefnagels, G W Padberg, J Overweg, et al.
Nederlands Tijdschrift Voor Geneeskunde|March 29, 1997
[Malignant hyperthermia as a complication of anesthesia: predisposition is hereditary]M M Snoeck, M J Gielen, R C Sengers, et al.
Neurology|December 1, 1991
Hearing loss in facioscapulohumeral muscular dystrophyO F Brouwer, G W Padberg, C J Ruys, et al.
Cancer Research|February 1, 1997
Differential loss of heterozygosity in the region of the Cowden locus within 10q22-23 in follicular thyroid adenomas and carcinomasD J Marsh, Z Zheng, J Zedenius, et al.
Neurology|February 25, 2005
The neuropathology of hereditary congenital facial palsy vs Möbius syndromeH T F M Verzijl, B van der Zwaag, M Lammens, et al.
Journal of the Neurological Sciences|February 1, 1990
Facioscapulohumeral muscular dystrophy gene in Dutch families is not linked to markers for familial adenomatous polyposis on the long arm of chromosome 5C Wijmenga, R R Frants, O F Brouwer, et al.
Neurology|July 14, 2004
Ventilatory support in facioscapulohumeral muscular dystrophyM Wohlgemuth, E L van der Kooi, R G van Kesteren, et al.
Journal of Medical Genetics|January 1, 1996
Diagnostic, predictive, and prenatal testing for facioscapulohumeral muscular dystrophy: diagnostic approach for sporadic and familial casesE Bakker, M J Van der Wielen, E Voorhoeve, et al.
Pageof 12

Showing results (41-50 of 114) with videos related to

Sort By:
Pageof 12
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|August 1, 1989
Clinical evaluation of pneumococcal meningitis in adults over a twelve-year periodG A Bruyn, H P Kremer, S de Marie, et al.
Nederlands Tijdschrift Voor Tandheelkunde|February 26, 2010
[Facioscapulohumeral muscular dystrophy]J Wilbers, R R Frants, B G M van Engelen, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 1991
Syncope or seizure? The diagnostic value of the EEG and hyperventilation test in transient loss of consciousnessW A Hoefnagels, G W Padberg, J Overweg, et al.
Nederlands Tijdschrift Voor Geneeskunde|March 29, 1997
[Malignant hyperthermia as a complication of anesthesia: predisposition is hereditary]M M Snoeck, M J Gielen, R C Sengers, et al.
Neurology|December 1, 1991
Hearing loss in facioscapulohumeral muscular dystrophyO F Brouwer, G W Padberg, C J Ruys, et al.
Cancer Research|February 1, 1997
Differential loss of heterozygosity in the region of the Cowden locus within 10q22-23 in follicular thyroid adenomas and carcinomasD J Marsh, Z Zheng, J Zedenius, et al.
Neurology|February 25, 2005
The neuropathology of hereditary congenital facial palsy vs Möbius syndromeH T F M Verzijl, B van der Zwaag, M Lammens, et al.
Journal of the Neurological Sciences|February 1, 1990
Facioscapulohumeral muscular dystrophy gene in Dutch families is not linked to markers for familial adenomatous polyposis on the long arm of chromosome 5C Wijmenga, R R Frants, O F Brouwer, et al.
Neurology|July 14, 2004
Ventilatory support in facioscapulohumeral muscular dystrophyM Wohlgemuth, E L van der Kooi, R G van Kesteren, et al.
Journal of Medical Genetics|January 1, 1996
Diagnostic, predictive, and prenatal testing for facioscapulohumeral muscular dystrophy: diagnostic approach for sporadic and familial casesE Bakker, M J Van der Wielen, E Voorhoeve, et al.
Pageof 12