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Klinische Padiatrie|November 1, 1980
[Hypergalactosemia in newborns as uncovered by the Austrian screening program in 12 years (author's transl)]O Thalhammer, S Scheibenreiter, E Knoll, et al.Human Genetics|January 1, 1982
Intracellular phenylalanine and tyrosine concentration in homozygotes and heterozygotes for phenylketonuria (PKU) and hyperphenylalaninemia compared with normalsO Thalhammer, G Lubec, H Königshofer, et al.Klinische Padiatrie|November 1, 1980
[12 years Austrian newborn screening for inborn errors of metabolism. Results with special reference to phenylketonuria, hyperphenylalaninemia and histidinemia (author's transl)]O Thalhammer, S Scheibenreiter, E Knoll, et al.Journal of Perinatal Medicine|January 1, 1976
Prospective and retrospective examination of an easily applicable score to predict the probability of premature birth defined by weightO Thalhammer, H Coradello, A Pollak, et al.Pediatrics|June 1, 1992
Long-term follow-up of 12 patients with the late-onset variant of argininosuccinic acid lyase deficiency: no impairment of intellectual and psychomotor development during therapyK Widhalm, S Koch, S Scheibenreiter, et al.Wiener Klinische Wochenschrift|October 7, 1988
[21 years "Austrian Program for Early Detection of Congenital Metabolic Abnormalities." Did the screening programs also contribute scientific knowledge?]O ThalhammerKlinische Padiatrie|September 1, 1981
[Screening for congenital hypothyroidism in Austria (author's transl)]O ThalhammerWiener Klinische Wochenschrift|October 31, 1975
[Toxoplasmosis investigation of pregnant women and newborn infants (author's transl)]O ThalhammerWiener Klinische Wochenschrift|January 6, 1978
[Ring chromosome 15 in a child (author's transl)]S Scheibenreiter, H FrischKlinische Padiatrie|November 1, 1977
[Ophthalmologic follow-up examination in galactosemia (author's transl)]G Zehetbauer, S ScheibenreiterPageof 5