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Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|January 1, 1981
[Age dependency of normal and modified nucleobases in urine in correlation to growth velocity (author's transl)]G Schöch, H Lorenz, G Heller-Schöch, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 30, 1986
Metabolic conversion of L-[U-14C]phenylalanine to respiratory 14CO2 in healthy subjects, phenylketonuria heterozygotes and classic phenylketonuricsW D Lehmann, R Fischer, H C Heinrich, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 27, 1984
Detection of heterozygous carriers for phenylketonuria by a L-[2H5]phenylalanine stable isotope loading testW D Lehmann, N Theobald, H C Heinrich, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|January 1, 1985
[Neonatal screening for mucoviscidosis using the BM-test-meconium]R Grüttner, P Clemens, P Koepp, et al.
Child Development|August 1, 1984
The development of sex role stereotypes in the third year: relationships to gender labeling, gender identity, sex-typed toy preference, and family characteristicsM Weinraub, L P Clemens, A Sockloff, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|May 1, 1983
[Excretion of normal and modified RNA catabolites and creatinine in the urine as a function of nutrition in children]G Schöch, G Heller-Schöch, J Müller, et al.
Biochemical Society Transactions|July 20, 2007
Protein transduction: identification, characterization and optimizationJ Tilstra, K K Rehman, T Hennon, et al.
Padiatrie Und Padologie|January 1, 1982
[Excretion of methylated nucleosides in the initial therapy phase in a case of anorexia nervosa]P Clemens, G Schöch, G Ziemer, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|March 1, 1991
Technetium-99m-MRP20, a potential brain perfusion agent: in vivo biodistribution and SPECT studies in non-primate animalsG F Morgan, M Deblaton, P Clemens, et al.
Taiwan Yi Xue Hui Za Zhi. Journal of the Formosan Medical Association|January 1, 1989
Screening of congenital hypothyroidism, phenylketonuria, galactosemia, homocystinuria, and maple syrup urine disease in moderate to severe mentally retarded Chinese childrenK J Hsiao, C H Chen, T T Liu, et al.
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