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Helvetica Paediatrica Acta
|
January 1, 1979
Congenital defect in intracellular cobalamin metabolism resulting in homocystinuria and methylmalonic aciduria. II. Biochemical investigations
E 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 rat
R 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 hypertension
G 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 chlorthalidone
Z 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 protein
E 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 deficiency
M 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 outcome
E 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 disorders
A B Burlina, C Bachmann, B Wermuth, et al.
Page
of 24
Search research articles
Search
Showing results (161-170 of 233) with videos related to
Sort By:
Page
of 24
Helvetica Paediatrica Acta
|
January 1, 1979
Congenital defect in intracellular cobalamin metabolism resulting in homocystinuria and methylmalonic aciduria. II. Biochemical investigations
E 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 rat
R 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 hypertension
G 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 chlorthalidone
Z 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 protein
E 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 deficiency
M 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 outcome
E 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 disorders
A B Burlina, C Bachmann, B Wermuth, et al.
Page
of 24