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Current Opinion in Chemical Biology|May 18, 2023
A phenazine-inspired framework for identifying biological functions of microbial redox-active metabolitesKorbinian O Thalhammer, Dianne K Newman
Human Genetics|October 14, 1977
Intellectual level (IQ) in heterozygotes for phenylketonuria (PKU). Is the PKU gene also acting by means other than phenylalanine-blood level elevation?O Thalhammer, L Havelec, E Knoll, et al.
Wiener Klinische Wochenschrift|October 28, 1977
[The IQ of heterozygotes for phenylketonuria (PKU). indication of a blood phenylalanine-independent action of the PKU mutant (author's transl)]O Thalhammer, L Havelec, E Knoll, et al.
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.
Klinische Padiatrie|November 1, 1980
[Intracellular concentration of phenylalanine, tyrosine and alpha-amino butyric acid in 13 homozygotes and 19 heterozygotes for phenylketonuria (PKU) compared with 26 normals (author's transl)]O Thalhammer, A Pollak, G Lubec, 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. Supplementum|January 1, 1977
[Screening for hypothyroidism in the newborn with a total T 4-RIA method (author's transl)]H Fritzsche, M Weissel, R Höfer, 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.
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