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S Scheibenreiter

Showing results (11-20 of 46) with videos related to

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Klinische Monatsblatter Fur Augenheilkunde|May 1, 1973
[Morphology of galactosemia cataract]S Scheibenreiter, G Zehetbauer
Wiener Klinische Wochenschrift|January 1, 1992
[Long-term results in children with classical galactosemia]S Scheibenreiter, E Knoll, K Widhalm
Monatsschrift Fur Kinderheilkunde|November 1, 1973
[Bird headed dwarfism (Seckel's syndrome) in a girl (author's transl)]E Pichler, S Scheibenreiter, K Zhuber
Wiener Klinische Wochenschrift|January 2, 1970
[Austrian programm for the early detection of inborn errors of metabolism]O Thalhammer, S Scheibenreiter, E Biedl
Padiatrie Und Padologie|January 1, 1976
[Investigation of the frequency of heterozygotes for galactose-1-phosphate-uridyl-transferase-deficiency(galactosemia) in the Vienna area. Comparison with the frequency of homozygotes found by newborn screening (author's transl)]S Scheibenreiter, V Scheiber, A Kiefer
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|September 1, 1987
[Gonadotropin secretion in children with galactosemia]E Schober, S Scheibenreiter, H Frisch
Clinical Genetics|May 1, 1995
18p monosomy with GH-deficiency and empty sella: good response to GH-treatmentE Schober, S Scheibenreiter, H Frisch
Zeitschrift Fur Kinderheilkunde|January 1, 1971
Histidinemia: detection by routine newborn screening and biochemical observations on three unrelated casesO Thalhammer, S Scheibenreiter, M Pantlitschko
Monatsschrift Fur Kinderheilkunde|July 1, 1971
[Occurrence of histidinemia: results of mass screening in 48,000 newborn infants]O Thalhammer, S Scheibenreiter, M Pantlitschko
Monatsschrift Fur Kinderheilkunde|November 1, 1977
[Treacher-Collins-syndrome (author's transl)]E Schober, M Götz, S Scheibenreiter
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Showing results (11-20 of 46) with videos related to

Sort By:
Pageof 5
Klinische Monatsblatter Fur Augenheilkunde|May 1, 1973
[Morphology of galactosemia cataract]S Scheibenreiter, G Zehetbauer
Wiener Klinische Wochenschrift|January 1, 1992
[Long-term results in children with classical galactosemia]S Scheibenreiter, E Knoll, K Widhalm
Monatsschrift Fur Kinderheilkunde|November 1, 1973
[Bird headed dwarfism (Seckel's syndrome) in a girl (author's transl)]E Pichler, S Scheibenreiter, K Zhuber
Wiener Klinische Wochenschrift|January 2, 1970
[Austrian programm for the early detection of inborn errors of metabolism]O Thalhammer, S Scheibenreiter, E Biedl
Padiatrie Und Padologie|January 1, 1976
[Investigation of the frequency of heterozygotes for galactose-1-phosphate-uridyl-transferase-deficiency(galactosemia) in the Vienna area. Comparison with the frequency of homozygotes found by newborn screening (author's transl)]S Scheibenreiter, V Scheiber, A Kiefer
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|September 1, 1987
[Gonadotropin secretion in children with galactosemia]E Schober, S Scheibenreiter, H Frisch
Clinical Genetics|May 1, 1995
18p monosomy with GH-deficiency and empty sella: good response to GH-treatmentE Schober, S Scheibenreiter, H Frisch
Zeitschrift Fur Kinderheilkunde|January 1, 1971
Histidinemia: detection by routine newborn screening and biochemical observations on three unrelated casesO Thalhammer, S Scheibenreiter, M Pantlitschko
Monatsschrift Fur Kinderheilkunde|July 1, 1971
[Occurrence of histidinemia: results of mass screening in 48,000 newborn infants]O Thalhammer, S Scheibenreiter, M Pantlitschko
Monatsschrift Fur Kinderheilkunde|November 1, 1977
[Treacher-Collins-syndrome (author's transl)]E Schober, M Götz, S Scheibenreiter
Pageof 5