Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

S Scheibenreiter

Showing results (21-30 of 46) with videos related to

Pageof 5
Sort By:
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
Padiatrie Und Padologie|January 1, 1982
[Wolf-Hirschhorn-syndrome with high urinary level of heparan sulfate (author's transl)]G Lubec, S Scheibenreiter, J Szilvassy, et al.
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.
Zeitschrift Fur Geburtshilfe Und Perinatologie|February 1, 1974
[Prevention of prematurity and prenatal dystrophy. II. Preliminary results with a simple method of pre-calculating the risk of prematurity (author's transl)]H Coradello, A Pollak, S Scheibenreiter, et al.
Archiv Fur Genetik|January 1, 1975
[Inherited brachydactyly (Drinkwater I, Bell's Al type)]H Frisch, H Hayek, S Scheibenreiter, et al.
Padiatrie Und Padologie|January 1, 1976
[Differential diagnosis of chronic myeloic leucemia in infancy (author's transl)]C Binder, E Pichler, T Radaskiewicz, et al.
Zeitschrift 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.
Wiener Klinische Wochenschrift|January 1, 1972
[5 years of the Austrian program for the early detection of inborn errors of metabolism. Activity report]O Thalhammer, S Scheibenreiter, R Schön, et al.
Pageof 5

Showing results (21-30 of 46) with videos related to

Sort By:
Pageof 5
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
Padiatrie Und Padologie|January 1, 1982
[Wolf-Hirschhorn-syndrome with high urinary level of heparan sulfate (author's transl)]G Lubec, S Scheibenreiter, J Szilvassy, et al.
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.
Zeitschrift Fur Geburtshilfe Und Perinatologie|February 1, 1974
[Prevention of prematurity and prenatal dystrophy. II. Preliminary results with a simple method of pre-calculating the risk of prematurity (author's transl)]H Coradello, A Pollak, S Scheibenreiter, et al.
Archiv Fur Genetik|January 1, 1975
[Inherited brachydactyly (Drinkwater I, Bell's Al type)]H Frisch, H Hayek, S Scheibenreiter, et al.
Padiatrie Und Padologie|January 1, 1976
[Differential diagnosis of chronic myeloic leucemia in infancy (author's transl)]C Binder, E Pichler, T Radaskiewicz, et al.
Zeitschrift 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.
Wiener Klinische Wochenschrift|January 1, 1972
[5 years of the Austrian program for the early detection of inborn errors of metabolism. Activity report]O Thalhammer, S Scheibenreiter, R Schön, et al.
Pageof 5