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V Bzduch

Showing results (1-10 of 11) with videos related to

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Bratislavske Lekarske Listy|August 19, 2007
Cardiorenal syndrome and later-onset Fabry disease: is there a connection?V Bzduch
Journal of Inherited Metabolic Disease|March 10, 2007
Sacral dimple as a skin manifestation of the Smith-Lemli-Opitz syndromeV Bzduch, D Behulova, L Kozak
Bratislavske Lekarske Listy|January 27, 2009
Glucose transporter type 1 (GLUT-1) deficiencyV Bzduch, P Sykora, D Behulova, et al.
Bratislavske Lekarske Listy|July 18, 2008
Glucose transporter type 1 (GLUT-1) deficiencyV Bzduch, P Sykora, D Behulova, et al.
Bratislavske Lekarske Listy|November 8, 2003
Trisomy 18 mimicking Smith-Lemli-Opitz syndrome in the immediate neonatal periodV Bzduch, D Behulova, L Pevalova, et al.
Bratislavske Lekarske Listy|April 1, 2004
Serum free carnitine in medium chain acyl-CoA dehydrogenase deficiencyV Bzduch, D Behulova, A Salingova, et al.
Bratislavske Lekarske Listy|January 7, 2005
A case of Rett syndrome from Ukraine--clinical diagnosis confirmed by mutation analysis of the MECP2 geneV Bzduch, D Zahorakova, E Grechanina, et al.
Bratislavske Lekarske Listy|January 5, 2002
Metabolic cause of Reye-like syndromeV Bzduch, D Behulova, W Lehnert, et al.
Bratislavske Lekarske Listy|January 28, 2017
GAI - distinct genotype and phenotype characteristics in reported Slovak patientsJ Lisyova, R Petrovic, K Jurickova, et al.
Bratislavske Lekarske Listy|February 23, 2021
Congenital disorders of glycosylation - an umbrella term for rapidly expanding group of rare genetic metabolic disorders - importance of physical investigationD E Lekka, J Brucknerova, A Salingova, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Bratislavske Lekarske Listy|August 19, 2007
Cardiorenal syndrome and later-onset Fabry disease: is there a connection?V Bzduch
Journal of Inherited Metabolic Disease|March 10, 2007
Sacral dimple as a skin manifestation of the Smith-Lemli-Opitz syndromeV Bzduch, D Behulova, L Kozak
Bratislavske Lekarske Listy|January 27, 2009
Glucose transporter type 1 (GLUT-1) deficiencyV Bzduch, P Sykora, D Behulova, et al.
Bratislavske Lekarske Listy|July 18, 2008
Glucose transporter type 1 (GLUT-1) deficiencyV Bzduch, P Sykora, D Behulova, et al.
Bratislavske Lekarske Listy|November 8, 2003
Trisomy 18 mimicking Smith-Lemli-Opitz syndrome in the immediate neonatal periodV Bzduch, D Behulova, L Pevalova, et al.
Bratislavske Lekarske Listy|April 1, 2004
Serum free carnitine in medium chain acyl-CoA dehydrogenase deficiencyV Bzduch, D Behulova, A Salingova, et al.
Bratislavske Lekarske Listy|January 7, 2005
A case of Rett syndrome from Ukraine--clinical diagnosis confirmed by mutation analysis of the MECP2 geneV Bzduch, D Zahorakova, E Grechanina, et al.
Bratislavske Lekarske Listy|January 5, 2002
Metabolic cause of Reye-like syndromeV Bzduch, D Behulova, W Lehnert, et al.
Bratislavske Lekarske Listy|January 28, 2017
GAI - distinct genotype and phenotype characteristics in reported Slovak patientsJ Lisyova, R Petrovic, K Jurickova, et al.
Bratislavske Lekarske Listy|February 23, 2021
Congenital disorders of glycosylation - an umbrella term for rapidly expanding group of rare genetic metabolic disorders - importance of physical investigationD E Lekka, J Brucknerova, A Salingova, et al.
Pageof 2