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G H Boers

Showing results (21-30 of 88) with videos related to

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The New England Journal of Medicine|January 17, 1991
Neural-tube defects and derangement of homocysteine metabolismR P Steegers-Theunissen, G H Boers, F J Trijbels, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|July 25, 1991
Cerebral infarction after caesarean section due to heterozygosity for homocystinuria; a case reportA G Minkhorst, P W van Dongen, G H Boers, et al.
Annals of Vascular Surgery|May 5, 2000
Hyperhomocysteinemia as a cause of superior vena cava syndromeH C Buscher, W B Barendregt, G H Boers, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Alternative methionine degradation via the transamination pathway: an option for therapy for homocystinuria due to cystathionine synthase deficiencyH J Blom, G H Boers, A Tangerman, et al.
Acta Paediatrica (Oslo, Norway : 1992)|June 26, 1998
Optic neuropathy in McCune-Albright syndrome: an indication for aggressive treatmentG Bocca, J de Vries, J R Cruysberg, et al.
Metabolism: Clinical and Experimental|June 1, 1989
Cystathionine-synthase-deficient patients do not use the transamination pathway of methionine to reduce hypermethioninemia and homocystinemiaH J Blom, G H Boers, J M Trijbels, et al.
European Heart Journal|August 24, 1999
Homocysteine, vitamin status and risk of vascular disease; effects of gender and menopausal status. European COMAC GroupP Verhoef, R Meleady, L E Daly, et al.
European Radiology|January 1, 1997
Imaging of vascular pathology in hyperhomocysteinemic patients with digital subtraction angiography and magnetic resonance techniquesD G Franken, J O Barentsz, F M Heijstraten, et al.
Nederlands Tijdschrift Voor Geneeskunde|June 27, 1992
[Cardiovascular abnormalities in Marfan syndrome]J H Fast, G H Boers, S Meijers-Jacobs, et al.
Nederlands Tijdschrift Voor Geneeskunde|October 3, 2003
[Hemopyrrollactamuria (HPU); from spots to pseudo-disease]J W van der Meer, R van de Kerkhof, G K The, et al.
Pageof 9

Showing results (21-30 of 88) with videos related to

Sort By:
Pageof 9
The New England Journal of Medicine|January 17, 1991
Neural-tube defects and derangement of homocysteine metabolismR P Steegers-Theunissen, G H Boers, F J Trijbels, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|July 25, 1991
Cerebral infarction after caesarean section due to heterozygosity for homocystinuria; a case reportA G Minkhorst, P W van Dongen, G H Boers, et al.
Annals of Vascular Surgery|May 5, 2000
Hyperhomocysteinemia as a cause of superior vena cava syndromeH C Buscher, W B Barendregt, G H Boers, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Alternative methionine degradation via the transamination pathway: an option for therapy for homocystinuria due to cystathionine synthase deficiencyH J Blom, G H Boers, A Tangerman, et al.
Acta Paediatrica (Oslo, Norway : 1992)|June 26, 1998
Optic neuropathy in McCune-Albright syndrome: an indication for aggressive treatmentG Bocca, J de Vries, J R Cruysberg, et al.
Metabolism: Clinical and Experimental|June 1, 1989
Cystathionine-synthase-deficient patients do not use the transamination pathway of methionine to reduce hypermethioninemia and homocystinemiaH J Blom, G H Boers, J M Trijbels, et al.
European Heart Journal|August 24, 1999
Homocysteine, vitamin status and risk of vascular disease; effects of gender and menopausal status. European COMAC GroupP Verhoef, R Meleady, L E Daly, et al.
European Radiology|January 1, 1997
Imaging of vascular pathology in hyperhomocysteinemic patients with digital subtraction angiography and magnetic resonance techniquesD G Franken, J O Barentsz, F M Heijstraten, et al.
Nederlands Tijdschrift Voor Geneeskunde|June 27, 1992
[Cardiovascular abnormalities in Marfan syndrome]J H Fast, G H Boers, S Meijers-Jacobs, et al.
Nederlands Tijdschrift Voor Geneeskunde|October 3, 2003
[Hemopyrrollactamuria (HPU); from spots to pseudo-disease]J W van der Meer, R van de Kerkhof, G K The, et al.
Pageof 9