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Methods and Findings in Experimental and Clinical Pharmacology
|
January 1, 1985
Erythrocyte cationic transport systems in normal male and female volunteers
P Lijnen, J R M'Buyamba-Kabangu, W Lissens, et al.
Pediatric Research
|
December 5, 2000
Analysis of exonic mutations leading to exon skipping in patients with pyruvate dehydrogenase E1 alpha deficiency
A K Cardozo, L De Meirleir, I Liebaers, et al.
Reproductive Biomedicine Online
|
December 4, 2010
Mutation analysis of three genes in patients with maturation arrest of spermatogenesis and couples with recurrent miscarriages
K Stouffs, D Vandermaelen, H Tournaye, et al.
Human Genetics
|
September 1, 1990
The deletion F508 is the major gene mutation in a representative Belgian cystic fibrosis population
M Bonduelle, W Lissens, A Malfroot, et al.
Human Molecular Genetics
|
September 1, 1992
A serine to proline substitution (S1255P) in the second nucleotide binding fold of the cystic fibrosis gene
W Lissens, M Bonduelle, A Malfroot, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Pyruvate dehydrogenase deficiency due to a mutation of the E1 alpha subunit
L J de Meirleir, W Lissens, E Vamos, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1991
The prevalence of the deletion F508 in a Belgian cystic fibrosis population
W Lissens, M Bonduelle, A Malfroot, et al.
Acta Clinica Belgica
|
January 1, 1975
Effects of long-term anticonvulsant therapy on calcium metabolism in adult epileptics: influence of age and sex
J Dequeker, G De Backer, D Van Dessel, et al.
Journal of Cardiovascular Pharmacology
|
August 1, 1989
Long-term double-blind comparison of doxazosin and atenolol in patients with mild to moderate hypertension
P Lijnen, R Fagard, J Staessen, et al.
Pediatric Neurology
|
October 1, 1995
Bilateral striatal necrosis with a novel point mutation in the mitochondrial ATPase 6 gene
L De Meirleir, S Seneca, W Lissens, et al.
Page
of 20
Search research articles
Search
Showing results (21-30 of 195) with videos related to
Sort By:
Page
of 20
Methods and Findings in Experimental and Clinical Pharmacology
|
January 1, 1985
Erythrocyte cationic transport systems in normal male and female volunteers
P Lijnen, J R M'Buyamba-Kabangu, W Lissens, et al.
Pediatric Research
|
December 5, 2000
Analysis of exonic mutations leading to exon skipping in patients with pyruvate dehydrogenase E1 alpha deficiency
A K Cardozo, L De Meirleir, I Liebaers, et al.
Reproductive Biomedicine Online
|
December 4, 2010
Mutation analysis of three genes in patients with maturation arrest of spermatogenesis and couples with recurrent miscarriages
K Stouffs, D Vandermaelen, H Tournaye, et al.
Human Genetics
|
September 1, 1990
The deletion F508 is the major gene mutation in a representative Belgian cystic fibrosis population
M Bonduelle, W Lissens, A Malfroot, et al.
Human Molecular Genetics
|
September 1, 1992
A serine to proline substitution (S1255P) in the second nucleotide binding fold of the cystic fibrosis gene
W Lissens, M Bonduelle, A Malfroot, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Pyruvate dehydrogenase deficiency due to a mutation of the E1 alpha subunit
L J de Meirleir, W Lissens, E Vamos, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1991
The prevalence of the deletion F508 in a Belgian cystic fibrosis population
W Lissens, M Bonduelle, A Malfroot, et al.
Acta Clinica Belgica
|
January 1, 1975
Effects of long-term anticonvulsant therapy on calcium metabolism in adult epileptics: influence of age and sex
J Dequeker, G De Backer, D Van Dessel, et al.
Journal of Cardiovascular Pharmacology
|
August 1, 1989
Long-term double-blind comparison of doxazosin and atenolol in patients with mild to moderate hypertension
P Lijnen, R Fagard, J Staessen, et al.
Pediatric Neurology
|
October 1, 1995
Bilateral striatal necrosis with a novel point mutation in the mitochondrial ATPase 6 gene
L De Meirleir, S Seneca, W Lissens, et al.
Page
of 20