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L Corbeel

Showing results (51-60 of 67) with videos related to

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Acta Paediatrica Belgica|July 1, 1976
On amino acid and ammonia metabolism in childhood hypothyroidismJ Jaeken, L Corbeel, E Eggermont, et al.
Lancet (London, England)|March 24, 1979
Treatment of purulent meningitis in infantsL Corbeel, K de Boeck, N Logghe, et al.
Pediatric Pulmonology|August 1, 1992
Aplasia of respiratory tract ciliaK DeBoeck, M Jorissen, K Wouters, et al.
Lancet (London, England)|August 2, 1980
Intraventricular gentamicin in meningitisL Corbeel, K de Boeck, N Logghe, et al.
Acta Paediatrica Belgica|October 1, 1980
Intraventricular and or intralumbar treatment of purulent meningitis in infantsR Eeckels, L Corbeel, C De Boeck, et al.
Acta Paediatrica Belgica|January 1, 1981
Growth hormone deficiency: clinical appearance and results of treatmentM Vanderschueren-Lodeweyckx, L Dooms, G Vanacker, et al.
The Journal of Clinical Investigation|March 1, 1985
Cytochrome b deficiency in an autosomal form of chronic granulomatous disease. A third form of chronic granulomatous disease recognized by monocyte hybridizationR S Weening, L Corbeel, M de Boer, et al.
American Journal of Human Genetics|November 1, 1992
Cytochrome b558-negative, autosomal recessive chronic granulomatous disease: two new mutations in the cytochrome b558 light chain of the NADPH oxidase (p22-phox)M de Boer, A de Klein, J P Hossle, et al.
Human Molecular Genetics|January 1, 1995
Mutations in the phosphorylase kinase gene PHKA2 are responsible for X-linked liver glycogen storage diseaseJ Hendrickx, P Coucke, E Dams, et al.
Neuropediatrics|August 1, 1984
Gamma-aminobutyric acid-transaminase deficiency: a newly recognized inborn error of neurotransmitter metabolismJ Jaeken, P Casaer, P de Cock, et al.
Pageof 7

Showing results (51-60 of 67) with videos related to

Sort By:
Pageof 7
Acta Paediatrica Belgica|July 1, 1976
On amino acid and ammonia metabolism in childhood hypothyroidismJ Jaeken, L Corbeel, E Eggermont, et al.
Lancet (London, England)|March 24, 1979
Treatment of purulent meningitis in infantsL Corbeel, K de Boeck, N Logghe, et al.
Pediatric Pulmonology|August 1, 1992
Aplasia of respiratory tract ciliaK DeBoeck, M Jorissen, K Wouters, et al.
Lancet (London, England)|August 2, 1980
Intraventricular gentamicin in meningitisL Corbeel, K de Boeck, N Logghe, et al.
Acta Paediatrica Belgica|October 1, 1980
Intraventricular and or intralumbar treatment of purulent meningitis in infantsR Eeckels, L Corbeel, C De Boeck, et al.
Acta Paediatrica Belgica|January 1, 1981
Growth hormone deficiency: clinical appearance and results of treatmentM Vanderschueren-Lodeweyckx, L Dooms, G Vanacker, et al.
The Journal of Clinical Investigation|March 1, 1985
Cytochrome b deficiency in an autosomal form of chronic granulomatous disease. A third form of chronic granulomatous disease recognized by monocyte hybridizationR S Weening, L Corbeel, M de Boer, et al.
American Journal of Human Genetics|November 1, 1992
Cytochrome b558-negative, autosomal recessive chronic granulomatous disease: two new mutations in the cytochrome b558 light chain of the NADPH oxidase (p22-phox)M de Boer, A de Klein, J P Hossle, et al.
Human Molecular Genetics|January 1, 1995
Mutations in the phosphorylase kinase gene PHKA2 are responsible for X-linked liver glycogen storage diseaseJ Hendrickx, P Coucke, E Dams, et al.
Neuropediatrics|August 1, 1984
Gamma-aminobutyric acid-transaminase deficiency: a newly recognized inborn error of neurotransmitter metabolismJ Jaeken, P Casaer, P de Cock, et al.
Pageof 7