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I F de Coo

Showing results (1-10 of 18) with videos related to

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Journal of the Neurological Sciences|February 1, 1996
Leber's hereditary optic neuropathy with the 11 778 mtDNA mutation and white matter disease resembling multiple sclerosis: clinical, MRI and MRS findingsP H Jansen, M S van der Knaap, I F de Coo
Tijdschrift Voor Kindergeneeskunde|December 1, 1991
[Subdural empyema. The importance of rapid diagnosis]A T Hageman, F J Gabreëls, I F De Coo, et al.
Cephalalgia : an International Journal of Headache|September 24, 2015
Evaluation of the new ICHD-III beta cluster headache criteriaI F de Coo, L A Wilbrink, J Haan, et al.
Journal of the Neurological Sciences|July 1, 1997
A PCR test for progressive external ophthalmoplegia and Kearns-Sayre syndrome on DNA from blood samplesI F De Coo, T Gussinklo, P J Arts, et al.
Clinical Neurology and Neurosurgery|January 1, 1982
Recessively inherited 'pure' spastic paraplegia: case studyI F de Coo, F J Gabreëls, W O Renier, et al.
Nederlands Tijdschrift Voor Geneeskunde|March 20, 2001
[Williams syndrome: new insights into genetic etiology, pathogenesis and clinical aspects]J M van Hagen, L C Govaerts, I F de Coo, et al.
Nederlands Tijdschrift Voor Geneeskunde|September 26, 1992
[Chorea and primary antiphospholipid syndrome]H A van Heereveld, F H van den Hoogen, G de Vaan, et al.
Annals of Neurology|January 23, 1999
A 4-base pair deletion in the mitochondrial cytochrome b gene associated with parkinsonism/MELAS overlap syndromeI F De Coo, W O Renier, W Ruitenbeek, et al.
Neurology|November 9, 2000
Mutations in noncoding regions of the proteolipid protein gene in Pelizaeus-Merzbacher diseaseG M Hobson, A P Davis, N C Stowell, et al.
Journal of the Neurological Sciences|July 1, 1997
Clinical heterogeneity in respiratory chain complex III deficiency in childhoodJ Mourmans, U Wendel, H A Bentlage, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Journal of the Neurological Sciences|February 1, 1996
Leber's hereditary optic neuropathy with the 11 778 mtDNA mutation and white matter disease resembling multiple sclerosis: clinical, MRI and MRS findingsP H Jansen, M S van der Knaap, I F de Coo
Tijdschrift Voor Kindergeneeskunde|December 1, 1991
[Subdural empyema. The importance of rapid diagnosis]A T Hageman, F J Gabreëls, I F De Coo, et al.
Cephalalgia : an International Journal of Headache|September 24, 2015
Evaluation of the new ICHD-III beta cluster headache criteriaI F de Coo, L A Wilbrink, J Haan, et al.
Journal of the Neurological Sciences|July 1, 1997
A PCR test for progressive external ophthalmoplegia and Kearns-Sayre syndrome on DNA from blood samplesI F De Coo, T Gussinklo, P J Arts, et al.
Clinical Neurology and Neurosurgery|January 1, 1982
Recessively inherited 'pure' spastic paraplegia: case studyI F de Coo, F J Gabreëls, W O Renier, et al.
Nederlands Tijdschrift Voor Geneeskunde|March 20, 2001
[Williams syndrome: new insights into genetic etiology, pathogenesis and clinical aspects]J M van Hagen, L C Govaerts, I F de Coo, et al.
Nederlands Tijdschrift Voor Geneeskunde|September 26, 1992
[Chorea and primary antiphospholipid syndrome]H A van Heereveld, F H van den Hoogen, G de Vaan, et al.
Annals of Neurology|January 23, 1999
A 4-base pair deletion in the mitochondrial cytochrome b gene associated with parkinsonism/MELAS overlap syndromeI F De Coo, W O Renier, W Ruitenbeek, et al.
Neurology|November 9, 2000
Mutations in noncoding regions of the proteolipid protein gene in Pelizaeus-Merzbacher diseaseG M Hobson, A P Davis, N C Stowell, et al.
Journal of the Neurological Sciences|July 1, 1997
Clinical heterogeneity in respiratory chain complex III deficiency in childhoodJ Mourmans, U Wendel, H A Bentlage, et al.
Pageof 2