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Results of search for 'au:"Kolníková, M"'
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Authors
Behulova, D
Bzduch, V
Böhmer, D
Chandoga, J
Kantarská, D
Klcova, V
Kolnikova, M
Kolníková, M
Konkoľová, J
Kršiaková, J
Petrovič, R
Repiský, M
Sykora, P
Zelinková, H
Šutovský, S
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Topics
Base Sequence
Brain Diseases, Metabolic
DNA Mutational Analysis
Epilepsy
Female
Glucose Transporter Type 1
Heterozygote
Humans
Infant
Male
Mutation, Missense
Peroxisomal Multifunctional Protein-2
Peroxisomes
Slovakia
deficiency
diagnosis
enzymology
etiology
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English
Your search returned 3 results.
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1.
Glucose transporter type 1 (GLUT-1) deficiency.
[electronic resource]
by
Bzduch, V
Sykora, P
Behulova, D
Kolnikova, M
Klcova, V
Producer:
20090211
In:
Bratislavske lekarske listy
vol. 109
Availability:
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2.
Glucose transporter type 1 (GLUT-1) deficiency.
[electronic resource]
by
Bzduch, V
Sykora, P
Behulova, D
Kolnikova, M
Klcova, V
Producer:
20080829
In:
Bratislavske lekarske listy
vol. 109
Availability:
No items available.
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3.
Peroxisomal D-bifunctional protein deficiency: First case reports from Slovakia.
[electronic resource]
by
Konkoľová, J
Petrovič, R
Chandoga, J
Repiský, M
Zelinková, H
Kršiaková, J
Kolníková, M
Kantarská, D
Šutovský, S
Böhmer, D
Producer:
20150819
In:
Gene
vol. 568
Online resources:
Available from publisher's website
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