E Schober|M Götz|S Scheibenreiter - JoVE Visualize

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Monatsschrift Fur Kinderheilkunde|November 1, 1977

[Treacher-Collins-syndrome (author's transl)]E Schober, M Götz, S Scheibenreiter

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

Wiener Klinische Wochenschrift|January 6, 1978

[Ring chromosome 15 in a child (author's transl)]S Scheibenreiter, H Frisch

Klinische Padiatrie|November 1, 1977

[Ophthalmologic follow-up examination in galactosemia (author's transl)]G Zehetbauer, S Scheibenreiter

Wiener Klinische Wochenschrift|January 1, 1992

[Long-term results in children with classical galactosemia]S Scheibenreiter, E Knoll, K Widhalm

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

Wiener Klinische Wochenschrift|April 16, 1976

[Partial trisomy 9 with partial retention of the long arm (author's transl)]S Scheibenreiter, J Szilvássy, H Ender

Klinische Padiatrie|November 1, 1979

[Phenylalanine-fetopathia in twins of an undiagnosed phenylketonuric mother (author's transl)]W D Müller, M Haidvogl, S Scheibenreiter

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.

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Showing results (1-10 of 629) with videos related to

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Pageof 63

Monatsschrift Fur Kinderheilkunde|November 1, 1977

[Treacher-Collins-syndrome (author's transl)]E Schober, M Götz, S Scheibenreiter

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

Wiener Klinische Wochenschrift|January 6, 1978

[Ring chromosome 15 in a child (author's transl)]S Scheibenreiter, H Frisch

Klinische Padiatrie|November 1, 1977

[Ophthalmologic follow-up examination in galactosemia (author's transl)]G Zehetbauer, S Scheibenreiter

Wiener Klinische Wochenschrift|January 1, 1992

[Long-term results in children with classical galactosemia]S Scheibenreiter, E Knoll, K Widhalm

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

Wiener Klinische Wochenschrift|April 16, 1976

[Partial trisomy 9 with partial retention of the long arm (author's transl)]S Scheibenreiter, J Szilvássy, H Ender

Klinische Padiatrie|November 1, 1979

[Phenylalanine-fetopathia in twins of an undiagnosed phenylketonuric mother (author's transl)]W D Müller, M Haidvogl, S Scheibenreiter

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.

Pageof 63