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I Barić

Showing results (1-10 of 18) with videos related to

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Lijecnicki Vjesnik|October 1, 1987
[In vitro study of characteristics associated with the pathogenicity of strains of Yersinia enterocolitica]I Barić, I Stojiljković, S Kalenić
Croatian Medical Journal|July 27, 2001
Inborn errors of metabolism at the turn of the millenniumI Barić, K Fumić, G F Hoffmann
Lijecnicki Vjesnik|July 1, 1994
[Homocystinuria: case reports with a note on hyperhomocysteinemia as a risk factor for the early onset of vascular disease]I Barić, N Barisić, N Blau, et al.
Biochemical and Biophysical Research Communications|January 24, 2008
S-Adenosylhomocysteine hydrolase (AdoHcyase) deficiency: enzymatic capabilities of human AdoHcyase are highly effected by changes to codon 89 and its surrounding residuesR Beluzić, M Cuk, T Pavkov, et al.
Acta Paediatrica (Oslo, Norway : 1992)|July 13, 2002
Screening for fragile X syndrome: results from a school for mentally retarded childrenS Hećimović, I Petek Tarnik, I Barić, et al.
Acta Medica Croatica : Casopis Hravatske Akademije Medicinskih Znanosti|January 1, 1993
T-cell subsets in asthmatic childrenI Barić, Z Reiner-Banovac, E Verona, et al.
Clinical Genetics|October 23, 1997
Expand Long PCR for fragile X mutation detectionS Hećimović, I Barisić, A Müller, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Geographical distribution of the P281L mutation at the phenylalanine hydroxylase locus: possible origin in southeastern EuropeI Barić, D Mardesić, V Sarnavøka, et al.
Journal of Inherited Metabolic Disease|April 5, 2001
A new case of succinyl-CoA:acetoacetate transferase deficiency: favourable course despite very low residual activityI Barić, V Sarnavka, K Fumić, et al.
Journal of Inherited Metabolic Disease|September 15, 2006
Fumaric aciduria: mild phenotype in a 8-year-old girl with novel mutationsM Maradin, K Fumić, H Hansikova, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Lijecnicki Vjesnik|October 1, 1987
[In vitro study of characteristics associated with the pathogenicity of strains of Yersinia enterocolitica]I Barić, I Stojiljković, S Kalenić
Croatian Medical Journal|July 27, 2001
Inborn errors of metabolism at the turn of the millenniumI Barić, K Fumić, G F Hoffmann
Lijecnicki Vjesnik|July 1, 1994
[Homocystinuria: case reports with a note on hyperhomocysteinemia as a risk factor for the early onset of vascular disease]I Barić, N Barisić, N Blau, et al.
Biochemical and Biophysical Research Communications|January 24, 2008
S-Adenosylhomocysteine hydrolase (AdoHcyase) deficiency: enzymatic capabilities of human AdoHcyase are highly effected by changes to codon 89 and its surrounding residuesR Beluzić, M Cuk, T Pavkov, et al.
Acta Paediatrica (Oslo, Norway : 1992)|July 13, 2002
Screening for fragile X syndrome: results from a school for mentally retarded childrenS Hećimović, I Petek Tarnik, I Barić, et al.
Acta Medica Croatica : Casopis Hravatske Akademije Medicinskih Znanosti|January 1, 1993
T-cell subsets in asthmatic childrenI Barić, Z Reiner-Banovac, E Verona, et al.
Clinical Genetics|October 23, 1997
Expand Long PCR for fragile X mutation detectionS Hećimović, I Barisić, A Müller, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Geographical distribution of the P281L mutation at the phenylalanine hydroxylase locus: possible origin in southeastern EuropeI Barić, D Mardesić, V Sarnavøka, et al.
Journal of Inherited Metabolic Disease|April 5, 2001
A new case of succinyl-CoA:acetoacetate transferase deficiency: favourable course despite very low residual activityI Barić, V Sarnavka, K Fumić, et al.
Journal of Inherited Metabolic Disease|September 15, 2006
Fumaric aciduria: mild phenotype in a 8-year-old girl with novel mutationsM Maradin, K Fumić, H Hansikova, et al.
Pageof 2