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B Cabalska

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Medycyna Wieku Rozwojowego|November 28, 2000
[Non-ketonic hyperglycinemia]B Cabalska
Medycyna Wieku Rozwojowego|March 29, 2001
[Standards for diagnosis and treatment of phenylketonuria]E Sendecka, B Cabalska
Acta Anthropogenetica|January 1, 1985
Hyperphenylalaninemia in Polish children's populationB Cabalska, N Duczynska, I Nowaczewska, et al.
Journal of Medical Genetics|January 16, 1998
Molecular basis of mild hyperphenylalaninaemia in PolandC Zekanowski, M Nowacka, B Cabalska, et al.
Journal of Medical Screening|October 27, 2001
Should newborn mutation scanning for hyperphenylalaninaemia and galactosaemia be implemented? A Polish experienceC Zekanowski, M Nowacka, B Radomyska, et al.
Problemy Medycyny Wieku Rozwojowego|January 1, 1990
[Evaluation of amino acids in plasma and amniotic fluid of women from genetic risk groups]N Duczyńska, B Cabalska, I Nowaczewska, et al.
Problemy Medycyny Wieku Rozwojowego|January 1, 1979
[Neurological status and psychomotor development of children with phenylketonuria treated early]J Czochańska, A Wilmowska-Pietruszyńska, K Zorska, et al.
Problemy Medycyny Wieku Rozwojowego|January 1, 1979
[Clinical and biochemical diagnosis of galactosemia among our cases]K Bozkowa, E Zbieg-Sendecka, Z Grodzka, et al.
European Journal of Pediatrics|July 1, 1996
Longitudinal study on early diagnosis and treatment of phenylketonuria in PolandM B Cabalska, I Nowaczewska, E Sendecka, et al.
Ginekologia Polska|May 4, 1999
[Maternal PKU syndrome as an obstetric problem: literature review and own clinical experience]E Rogowiecka, E Sendecka, B Chazan, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Medycyna Wieku Rozwojowego|November 28, 2000
[Non-ketonic hyperglycinemia]B Cabalska
Medycyna Wieku Rozwojowego|March 29, 2001
[Standards for diagnosis and treatment of phenylketonuria]E Sendecka, B Cabalska
Acta Anthropogenetica|January 1, 1985
Hyperphenylalaninemia in Polish children's populationB Cabalska, N Duczynska, I Nowaczewska, et al.
Journal of Medical Genetics|January 16, 1998
Molecular basis of mild hyperphenylalaninaemia in PolandC Zekanowski, M Nowacka, B Cabalska, et al.
Journal of Medical Screening|October 27, 2001
Should newborn mutation scanning for hyperphenylalaninaemia and galactosaemia be implemented? A Polish experienceC Zekanowski, M Nowacka, B Radomyska, et al.
Problemy Medycyny Wieku Rozwojowego|January 1, 1990
[Evaluation of amino acids in plasma and amniotic fluid of women from genetic risk groups]N Duczyńska, B Cabalska, I Nowaczewska, et al.
Problemy Medycyny Wieku Rozwojowego|January 1, 1979
[Neurological status and psychomotor development of children with phenylketonuria treated early]J Czochańska, A Wilmowska-Pietruszyńska, K Zorska, et al.
Problemy Medycyny Wieku Rozwojowego|January 1, 1979
[Clinical and biochemical diagnosis of galactosemia among our cases]K Bozkowa, E Zbieg-Sendecka, Z Grodzka, et al.
European Journal of Pediatrics|July 1, 1996
Longitudinal study on early diagnosis and treatment of phenylketonuria in PolandM B Cabalska, I Nowaczewska, E Sendecka, et al.
Ginekologia Polska|May 4, 1999
[Maternal PKU syndrome as an obstetric problem: literature review and own clinical experience]E Rogowiecka, E Sendecka, B Chazan, et al.
Pageof 2