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A Wevers

Showing results (111-120 of 543) with videos related to

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Clinical Chemistry|May 1, 1995
Standardized method for high-resolution 1H-NMR of cerebrospinal fluidR A Wevers, U Engelke, U Wendel, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 6, 2008
Decreased bone density and treatment in patients with autosomal recessive cutis laxaC Noordam, S Funke, N V Knoers, et al.
Prenatal Diagnosis|October 1, 1992
Prenatal analyses in a pregnancy at risk for beta-mannosidosisW J Kleijer, G C Geilen, O P Van Diggelen, et al.
Neuroscience Letters|August 23, 1996
Expression of alpha subunit genes of nicotinic acetylcholine receptors in human lymphocytesC Hiemke, M Stolp, S Reuss, et al.
Journal of Inherited Metabolic Disease|March 28, 2002
Prolidase deficiency diagnosed by 1H NMR spectroscopy of urineS H Moolenaar, U F Engelke, N G Abeling, et al.
Biochimica Et Biophysica Acta|January 28, 2009
Vacuolar H+-ATPase meets glycosylation in patients with cutis laxaMailys Guillard, Aikaterini Dimopoulou, Björn Fischer, et al.
Brain Research. Molecular Brain Research|August 1, 1994
Cellular distribution of nicotinic acetylcholine receptor subunit mRNAs in the human cerebral cortex as revealed by non-isotopic in situ hybridizationA Wevers, A Jeske, C Lobron, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 9, 1999
A mutation in the human ortholog of the Saccharomyces cerevisiae ALG6 gene causes carbohydrate-deficient glycoprotein syndrome type-IcT Imbach, P Burda, P Kuhnert, et al.
Neuroscience Letters|June 2, 1995
Cellular expression of alpha 4 subunit mRNA of the nicotinic acetylcholine receptor in the developing rat telencephalonC H Ostermann, J Grunwald, A Wevers, et al.
Journal of Neurology|March 5, 2004
Spinal phenotype of cerebrotendinous xanthomatosis--a pitfall in the diagnosis of multiple sclerosisD Bartholdi, D Zumsteg, A Verrips, et al.
Pageof 55

Showing results (111-120 of 543) with videos related to

Sort By:
Pageof 55
Clinical Chemistry|May 1, 1995
Standardized method for high-resolution 1H-NMR of cerebrospinal fluidR A Wevers, U Engelke, U Wendel, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 6, 2008
Decreased bone density and treatment in patients with autosomal recessive cutis laxaC Noordam, S Funke, N V Knoers, et al.
Prenatal Diagnosis|October 1, 1992
Prenatal analyses in a pregnancy at risk for beta-mannosidosisW J Kleijer, G C Geilen, O P Van Diggelen, et al.
Neuroscience Letters|August 23, 1996
Expression of alpha subunit genes of nicotinic acetylcholine receptors in human lymphocytesC Hiemke, M Stolp, S Reuss, et al.
Journal of Inherited Metabolic Disease|March 28, 2002
Prolidase deficiency diagnosed by 1H NMR spectroscopy of urineS H Moolenaar, U F Engelke, N G Abeling, et al.
Biochimica Et Biophysica Acta|January 28, 2009
Vacuolar H+-ATPase meets glycosylation in patients with cutis laxaMailys Guillard, Aikaterini Dimopoulou, Björn Fischer, et al.
Brain Research. Molecular Brain Research|August 1, 1994
Cellular distribution of nicotinic acetylcholine receptor subunit mRNAs in the human cerebral cortex as revealed by non-isotopic in situ hybridizationA Wevers, A Jeske, C Lobron, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 9, 1999
A mutation in the human ortholog of the Saccharomyces cerevisiae ALG6 gene causes carbohydrate-deficient glycoprotein syndrome type-IcT Imbach, P Burda, P Kuhnert, et al.
Neuroscience Letters|June 2, 1995
Cellular expression of alpha 4 subunit mRNA of the nicotinic acetylcholine receptor in the developing rat telencephalonC H Ostermann, J Grunwald, A Wevers, et al.
Journal of Neurology|March 5, 2004
Spinal phenotype of cerebrotendinous xanthomatosis--a pitfall in the diagnosis of multiple sclerosisD Bartholdi, D Zumsteg, A Verrips, et al.
Pageof 55