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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.Journal of Endocrinological Investigation|August 12, 1999
Growth hormone and body composition in athletesH FrischPadiatrie Und Padologie|January 1, 1976
[Differential diagnosis of chronic myeloic leucemia in infancy (author's transl)]C Binder, E Pichler, T Radaskiewicz, et al.Padiatrie Und Padologie|January 1, 1976
[Reduction of expected height in excessively tall boys (author's transl)]H FrischZeitschrift Fur Geburtshilfe Und Neonatologie|December 29, 2000
[Maternal phenylketonuria: dietary treatment of a 2 generation illness]D Möslinger, S Scheibenreiter, E Spoula, et al.Acta Paediatrica Scandinavica|January 1, 1988
Familial pseudohypoaldosteronismC Popow, A Pollak, K Herkner, 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.Padiatrie Und Padologie|January 1, 1985
[Percutaneously implanted silastic catheters in the neonate]O Luz, H FrischPageof 25