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Journal of Inherited Metabolic Disease
|
January 1, 1984
Diagnosis and treatment of argininaemia. Characteristics of arginase in human erythrocytes and tissues
W Endres, R Schaller, Y S Shin
Metabolism: Clinical and Experimental
|
April 1, 1994
Effect of high-protein meal plus aspartame ingestion on plasma phenylalanine concentrations in obligate heterozygotes for phenylketonuria
H C Curtius, W Endres, N Blau
Journal of Inherited Metabolic Disease
|
January 1, 1991
Purification of alpha and beta subunits of phosphorylase-b-kinase in human liver and cardiac muscle by affinity chromatography and immunodetection
T Podskarbi, W Endres, Y S Shin
Acta Paediatrica Japonica : Overseas Edition
|
August 1, 1988
Clinical course of hereditary fructose intolerance in 56 patients
W Endres, T Sierck, Y S Shin
Neuroscience Letters
|
December 3, 1986
Excitatory amino acids and intracellular pH in motoneurons of the isolated frog spinal cord
W Endres, K Ballanyi, G Serve, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
|
November 24, 2022
Incidence and follow-up of persistent lung perfusion abnormalities as a result of suspected air trapping or microthrombosis in non-hospitalised COVID-19 patients during the early half of the pandemic - experience in a tertiary institution in South Afr
O Evbuomwan, W Endres, T Tebieia, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
March 25, 2011
A high-throughput sequencing-based methodology to identify all uncapped and cleaved RNA molecules in eukaryotic genomes
Matthew W Endres, Rebecca T Cook, Brian D Gregory
Virchows Archiv. A, Pathological Anatomy and Histology
|
January 1, 1981
[Morphology and diagnosis of Zellweger syndrome. A contribution to combined cytochemical-finestructural identification of peroxisomes in autopsy material and frozen liver tissue with case report]
J Müller-Höcker, K Bise, W Endres, et al.
Clinical Chemistry
|
October 1, 1984
A simple assay for amylo-1,6-glucosidase to detect heterozygotes for glycogenosis type III in erythrocytes
Y S Shin, R Ungar, M Rieth, et al.
Health Physics
|
June 1, 1970
Thermoluminescence personnel dosimetry at Hanford. II. Energy dependence and application of TLD materials in operational health physics
G W Endres, R L Kathren, L F Kocher
Page
of 12
Search research articles
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Showing results (31-40 of 112) with videos related to
Sort By:
Page
of 12
Journal of Inherited Metabolic Disease
|
January 1, 1984
Diagnosis and treatment of argininaemia. Characteristics of arginase in human erythrocytes and tissues
W Endres, R Schaller, Y S Shin
Metabolism: Clinical and Experimental
|
April 1, 1994
Effect of high-protein meal plus aspartame ingestion on plasma phenylalanine concentrations in obligate heterozygotes for phenylketonuria
H C Curtius, W Endres, N Blau
Journal of Inherited Metabolic Disease
|
January 1, 1991
Purification of alpha and beta subunits of phosphorylase-b-kinase in human liver and cardiac muscle by affinity chromatography and immunodetection
T Podskarbi, W Endres, Y S Shin
Acta Paediatrica Japonica : Overseas Edition
|
August 1, 1988
Clinical course of hereditary fructose intolerance in 56 patients
W Endres, T Sierck, Y S Shin
Neuroscience Letters
|
December 3, 1986
Excitatory amino acids and intracellular pH in motoneurons of the isolated frog spinal cord
W Endres, K Ballanyi, G Serve, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
|
November 24, 2022
Incidence and follow-up of persistent lung perfusion abnormalities as a result of suspected air trapping or microthrombosis in non-hospitalised COVID-19 patients during the early half of the pandemic - experience in a tertiary institution in South Afr
O Evbuomwan, W Endres, T Tebieia, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
March 25, 2011
A high-throughput sequencing-based methodology to identify all uncapped and cleaved RNA molecules in eukaryotic genomes
Matthew W Endres, Rebecca T Cook, Brian D Gregory
Virchows Archiv. A, Pathological Anatomy and Histology
|
January 1, 1981
[Morphology and diagnosis of Zellweger syndrome. A contribution to combined cytochemical-finestructural identification of peroxisomes in autopsy material and frozen liver tissue with case report]
J Müller-Höcker, K Bise, W Endres, et al.
Clinical Chemistry
|
October 1, 1984
A simple assay for amylo-1,6-glucosidase to detect heterozygotes for glycogenosis type III in erythrocytes
Y S Shin, R Ungar, M Rieth, et al.
Health Physics
|
June 1, 1970
Thermoluminescence personnel dosimetry at Hanford. II. Energy dependence and application of TLD materials in operational health physics
G W Endres, R L Kathren, L F Kocher
Page
of 12