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M Van Geel

Showing results (61-70 of 171) with videos related to

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The British Journal of Dermatology|September 15, 2017
Novel CLDN1 mutation in ichthyosis-hypotrichosis-sclerosing cholangitis syndrome without signs of liver diseaseI F Nagtzaam, V P M Peeters, M Vreeburg, et al.
European Journal of Surgical Oncology : the Journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology|June 13, 2021
Dealing with indeterminate pulmonary nodules in colorectal cancer patients; a systematic reviewJoris J van den Broek, Tess van Gestel, Sabrine Q Kol, et al.
Journal of Clinical Medicine|September 14, 2024
Added Value of Histological Evaluation of Muscle Biopsies in Porcine Vascularized Composite AllograftsKaj Brouwers, Shannen R W M van Geel, Dominique van Midden, et al.
Resuscitation|August 25, 2009
Deadly vasospasmD P H Eijking, C L A Reichert, A M Wagenvoort, et al.
Human Mutation|September 18, 2009
Novel missense mutations in the FOXC2 gene alter transcriptional activityM A M van Steensel, R J Damstra, M V Heitink, et al.
Human Mutation|January 1, 1995
Two intronic mutations in the adrenoleukodystrophy geneS Kemp, M J Ligtenberg, B M van Geel, et al.
Clinical and Experimental Dermatology|June 25, 2016
Clustered unilateral trichoepitheliomas indicate Type 1 segmental manifestation of multiple familial trichoepitheliomaL J M T Parren, K Munte, V Winnepenninckx, et al.
The British Journal of Dermatology|April 16, 2008
Chanarin-Dorfman syndrome caused by a novel splice site mutation in ABHD5S Badeloe, M van Geel, I Nagtzaam, et al.
Clinical Neurology and Neurosurgery|June 1, 1993
Delay in diagnosis of X-linked adrenoleukodystrophyB M van Geel, J Assies, E B Haverkort, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
ALDP expression in fibroblasts of patients with X-linked adrenoleukodystrophyS Kemp, P A Mooyer, P A Bolhuis, et al.
Pageof 18

Showing results (61-70 of 171) with videos related to

Sort By:
Pageof 18
The British Journal of Dermatology|September 15, 2017
Novel CLDN1 mutation in ichthyosis-hypotrichosis-sclerosing cholangitis syndrome without signs of liver diseaseI F Nagtzaam, V P M Peeters, M Vreeburg, et al.
European Journal of Surgical Oncology : the Journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology|June 13, 2021
Dealing with indeterminate pulmonary nodules in colorectal cancer patients; a systematic reviewJoris J van den Broek, Tess van Gestel, Sabrine Q Kol, et al.
Journal of Clinical Medicine|September 14, 2024
Added Value of Histological Evaluation of Muscle Biopsies in Porcine Vascularized Composite AllograftsKaj Brouwers, Shannen R W M van Geel, Dominique van Midden, et al.
Resuscitation|August 25, 2009
Deadly vasospasmD P H Eijking, C L A Reichert, A M Wagenvoort, et al.
Human Mutation|September 18, 2009
Novel missense mutations in the FOXC2 gene alter transcriptional activityM A M van Steensel, R J Damstra, M V Heitink, et al.
Human Mutation|January 1, 1995
Two intronic mutations in the adrenoleukodystrophy geneS Kemp, M J Ligtenberg, B M van Geel, et al.
Clinical and Experimental Dermatology|June 25, 2016
Clustered unilateral trichoepitheliomas indicate Type 1 segmental manifestation of multiple familial trichoepitheliomaL J M T Parren, K Munte, V Winnepenninckx, et al.
The British Journal of Dermatology|April 16, 2008
Chanarin-Dorfman syndrome caused by a novel splice site mutation in ABHD5S Badeloe, M van Geel, I Nagtzaam, et al.
Clinical Neurology and Neurosurgery|June 1, 1993
Delay in diagnosis of X-linked adrenoleukodystrophyB M van Geel, J Assies, E B Haverkort, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
ALDP expression in fibroblasts of patients with X-linked adrenoleukodystrophyS Kemp, P A Mooyer, P A Bolhuis, et al.
Pageof 18