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C Bachmann

Showing results (161-170 of 233) with videos related to

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Helvetica Paediatrica Acta|January 1, 1979
Congenital defect in intracellular cobalamin metabolism resulting in homocystinuria and methylmalonic aciduria. II. Biochemical investigationsE R Baumgartner, H Wick, J C Linnell, et al.
Biochemical and Biophysical Research Communications|March 15, 1989
In vivo 31P NMR spectroscopy of energy rich phosphates in the brain of the hyperammonemic ratR Friolet, J P Colombo, F Lazeyras, et al.
European Journal of Clinical Pharmacology|January 1, 1985
Effects of the dopaminergic agonist cianergoline on blood pressure, the renin-angiotensin-aldosterone axis and the sympathetic nervous system in patients with essential hypertensionG Bise, C Foletti, C Beretta-Piccoli, et al.
Surgical Endoscopy|June 11, 2021
Technology development of hyperthermic pressurized intraperitoneal aerosol chemotherapy (hPIPAC)C Bachmann, I Sautkin, G Nadiradze, et al.
Metabolism: Clinical and Experimental|March 1, 1980
Increased serum low-density lipoprotein cholesterol in men treated short-term with the diuretic chlorthalidoneZ Glück, P Weidmann, R Mordasini, et al.
The Journal of Biological Chemistry|February 7, 2001
Amyloid and non-amyloid forms of 5q31-linked corneal dystrophy resulting from kerato-epithelin mutations at Arg-124 are associated with abnormal turnover of the proteinE Korvatska, H Henry, Y Mashima, et al.
Clinical Science and Molecular Medicine. Supplement|December 1, 1978
Increased ratio between serum beta- and alpha-lipoproteins during diuretic therapy: an adverse effect?Z Glück, G Baumgartner, P Weidmann, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
Different organic acid patterns in urine and in cerebrospinal fluid in a patient with biotinidase deficiencyM Di Rocco, A Superti-Furga, P Durand, et al.
Pediatric Research|September 1, 1989
Biotinidase deficiency: a cause of subacute necrotizing encephalomyelopathy (Leigh syndrome). Report of a case with lethal outcomeE R Baumgartner, T M Suormala, H Wick, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Partial N-acetylglutamate synthetase deficiency: a new case with uncontrollable movement disordersA B Burlina, C Bachmann, B Wermuth, et al.
Pageof 24

Showing results (161-170 of 233) with videos related to

Sort By:
Pageof 24
Helvetica Paediatrica Acta|January 1, 1979
Congenital defect in intracellular cobalamin metabolism resulting in homocystinuria and methylmalonic aciduria. II. Biochemical investigationsE R Baumgartner, H Wick, J C Linnell, et al.
Biochemical and Biophysical Research Communications|March 15, 1989
In vivo 31P NMR spectroscopy of energy rich phosphates in the brain of the hyperammonemic ratR Friolet, J P Colombo, F Lazeyras, et al.
European Journal of Clinical Pharmacology|January 1, 1985
Effects of the dopaminergic agonist cianergoline on blood pressure, the renin-angiotensin-aldosterone axis and the sympathetic nervous system in patients with essential hypertensionG Bise, C Foletti, C Beretta-Piccoli, et al.
Surgical Endoscopy|June 11, 2021
Technology development of hyperthermic pressurized intraperitoneal aerosol chemotherapy (hPIPAC)C Bachmann, I Sautkin, G Nadiradze, et al.
Metabolism: Clinical and Experimental|March 1, 1980
Increased serum low-density lipoprotein cholesterol in men treated short-term with the diuretic chlorthalidoneZ Glück, P Weidmann, R Mordasini, et al.
The Journal of Biological Chemistry|February 7, 2001
Amyloid and non-amyloid forms of 5q31-linked corneal dystrophy resulting from kerato-epithelin mutations at Arg-124 are associated with abnormal turnover of the proteinE Korvatska, H Henry, Y Mashima, et al.
Clinical Science and Molecular Medicine. Supplement|December 1, 1978
Increased ratio between serum beta- and alpha-lipoproteins during diuretic therapy: an adverse effect?Z Glück, G Baumgartner, P Weidmann, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
Different organic acid patterns in urine and in cerebrospinal fluid in a patient with biotinidase deficiencyM Di Rocco, A Superti-Furga, P Durand, et al.
Pediatric Research|September 1, 1989
Biotinidase deficiency: a cause of subacute necrotizing encephalomyelopathy (Leigh syndrome). Report of a case with lethal outcomeE R Baumgartner, T M Suormala, H Wick, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Partial N-acetylglutamate synthetase deficiency: a new case with uncontrollable movement disordersA B Burlina, C Bachmann, B Wermuth, et al.
Pageof 24