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

H Kaloud

Showing results (1-10 of 31) with videos related to

Pageof 4
Sort By:
Padiatrie Und Padologie|January 1, 1972
[Make the diagnosis]H Kaloud
Wiener Medizinische Wochenschrift (1946)|November 28, 1970
[Somatic development and motor activity of blind children]H Kaloud
Zeitschrift Fur Kinderheilkunde|January 1, 1972
[Gene frequency of hereditary galactosemia with reference to the Duarte variant]H Kaloud, F C Sitzmann
Wiener Klinische Wochenschrift|October 18, 1970
[Galactose-1-phosphate-uridyltransferase in erythrocytes of children with hepatitis epidemica]H Kaloud, F C Sitzmann
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 1, 1976
Biokinetics of galactose in the homozygotes and heterozygotes of both forms of galactosemiaF C Sitzmann, H Kaloud
Medizinische Klinik|March 21, 1975
[Congenital disorders of galactose metabolism]F C Sitzmann, H Kaloud
Zeitschrift Fur Kinderheilkunde|February 11, 1974
[The galactokinase deficiency in two human populations: Styria (Austria) and Franconia (Bavaria). A comparative investigation on gen frequency (author's transl)]H Kaloud, F C Sitzmann
Padiatrie Und Padologie|January 1, 1971
[Activity of galaktose-1-phosphate-uridyltransferase in erythrozytes of galactosemia heterocygotes of different ages (author's transl)]H Kaloud, F C Sitzmann
Padiatrie Und Padologie|January 1, 1973
[EEG studies in totally and almost blind children]S Enge, H Kaloud, H Lechner
Electroencephalography and Clinical Neurophysiology|March 1, 1970
EEG investigations in children with lesions in the peripheral part of the visual systemH Lechner, S Enge, H Kaloud
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
Padiatrie Und Padologie|January 1, 1972
[Make the diagnosis]H Kaloud
Wiener Medizinische Wochenschrift (1946)|November 28, 1970
[Somatic development and motor activity of blind children]H Kaloud
Zeitschrift Fur Kinderheilkunde|January 1, 1972
[Gene frequency of hereditary galactosemia with reference to the Duarte variant]H Kaloud, F C Sitzmann
Wiener Klinische Wochenschrift|October 18, 1970
[Galactose-1-phosphate-uridyltransferase in erythrocytes of children with hepatitis epidemica]H Kaloud, F C Sitzmann
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 1, 1976
Biokinetics of galactose in the homozygotes and heterozygotes of both forms of galactosemiaF C Sitzmann, H Kaloud
Medizinische Klinik|March 21, 1975
[Congenital disorders of galactose metabolism]F C Sitzmann, H Kaloud
Zeitschrift Fur Kinderheilkunde|February 11, 1974
[The galactokinase deficiency in two human populations: Styria (Austria) and Franconia (Bavaria). A comparative investigation on gen frequency (author's transl)]H Kaloud, F C Sitzmann
Padiatrie Und Padologie|January 1, 1971
[Activity of galaktose-1-phosphate-uridyltransferase in erythrozytes of galactosemia heterocygotes of different ages (author's transl)]H Kaloud, F C Sitzmann
Padiatrie Und Padologie|January 1, 1973
[EEG studies in totally and almost blind children]S Enge, H Kaloud, H Lechner
Electroencephalography and Clinical Neurophysiology|March 1, 1970
EEG investigations in children with lesions in the peripheral part of the visual systemH Lechner, S Enge, H Kaloud
Pageof 4