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L Verstraeten

Showing results (11-20 of 28) with videos related to

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Annales De Biologie Clinique|January 1, 1991
[Storage of granulocytes]L Verstraeten, M Marchand-Arvier, F Schooneman, et al.
Annales De Biologie Clinique|January 1, 1991
[Chemotaxis of polynuclear neutrophils during a four-day storage in a liquid medium]L Verstraeten, M Marchand-Arvier, F Schooneman, et al.
Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|October 1, 1989
Biochemical diagnosis of an hereditary aminolaevulinate dehydratase deficiency in a 63-year-old manA Hassoun, L Verstraeten, R Mercelis, et al.
Frontiers in Pharmacology|October 12, 2020
Lipid Membranes as Key Targets for the Pharmacological Actions of GinsenosidesSandrine L Verstraeten, Joseph H Lorent, Marie-Paule Mingeot-Leclercq
Acta Clinica Belgica|January 1, 1991
[Association of idiopathic hemochromatosis and tardive cutaneous porphyria]M Buysschaert, L Verstraeten, V Novik, et al.
Journal of the Neurological Sciences|January 1, 1990
Porphyric neuropathy and hereditary delta-aminolevulinic acid dehydratase deficiency in an adultR Mercelis, A Hassoun, L Verstraeten, et al.
Clinical Chemistry|December 1, 1992
Interference of Tienam in colorimetric determination of 5-aminolevulinic acid and porphobilinogen in serum and urineL Verstraeten, M C Ledoux, B Moos, et al.
Frontiers in Immunology|February 22, 2019
NKG2D and Its Ligand MULT1 Contribute to Disease Progression in a Mouse Model of Multiple SclerosisLaurine Legroux, Ana Carmena Moratalla, Cyril Laurent, et al.
European Journal of Clinical Investigation|April 1, 1991
Hereditary hepatic porphyria due to homozygous delta-aminolevulinic acid dehydratase deficiency: studies in lymphocytes and erythrocytesS Sassa, H Fujita, M Doss, et al.
Histochemistry and Cell Biology|October 31, 2001
Growth stimulatory angiotensin II type-1 receptor is upregulated in breast hyperplasia and in situ carcinoma but not in invasive carcinomaB De Paepe, V L Verstraeten, C R De Potter, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
Annales De Biologie Clinique|January 1, 1991
[Storage of granulocytes]L Verstraeten, M Marchand-Arvier, F Schooneman, et al.
Annales De Biologie Clinique|January 1, 1991
[Chemotaxis of polynuclear neutrophils during a four-day storage in a liquid medium]L Verstraeten, M Marchand-Arvier, F Schooneman, et al.
Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|October 1, 1989
Biochemical diagnosis of an hereditary aminolaevulinate dehydratase deficiency in a 63-year-old manA Hassoun, L Verstraeten, R Mercelis, et al.
Frontiers in Pharmacology|October 12, 2020
Lipid Membranes as Key Targets for the Pharmacological Actions of GinsenosidesSandrine L Verstraeten, Joseph H Lorent, Marie-Paule Mingeot-Leclercq
Acta Clinica Belgica|January 1, 1991
[Association of idiopathic hemochromatosis and tardive cutaneous porphyria]M Buysschaert, L Verstraeten, V Novik, et al.
Journal of the Neurological Sciences|January 1, 1990
Porphyric neuropathy and hereditary delta-aminolevulinic acid dehydratase deficiency in an adultR Mercelis, A Hassoun, L Verstraeten, et al.
Clinical Chemistry|December 1, 1992
Interference of Tienam in colorimetric determination of 5-aminolevulinic acid and porphobilinogen in serum and urineL Verstraeten, M C Ledoux, B Moos, et al.
Frontiers in Immunology|February 22, 2019
NKG2D and Its Ligand MULT1 Contribute to Disease Progression in a Mouse Model of Multiple SclerosisLaurine Legroux, Ana Carmena Moratalla, Cyril Laurent, et al.
European Journal of Clinical Investigation|April 1, 1991
Hereditary hepatic porphyria due to homozygous delta-aminolevulinic acid dehydratase deficiency: studies in lymphocytes and erythrocytesS Sassa, H Fujita, M Doss, et al.
Histochemistry and Cell Biology|October 31, 2001
Growth stimulatory angiotensin II type-1 receptor is upregulated in breast hyperplasia and in situ carcinoma but not in invasive carcinomaB De Paepe, V L Verstraeten, C R De Potter, et al.
Pageof 3