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U Tietze

Showing results (11-20 of 33) with videos related to

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Progress in Pediatric Surgery|January 1, 1983
The significance of diagnostic laparotomy in girls with disorders of sexual developmentW A Welte, H U Tietze, G Schwanitz
Acta Endocrinologica|June 1, 1970
Autoradiographic studies on nuclear DNA and RNA synthesis in the adenohypophysis of castrated ratsF Städtler, G Dhom, E Stöcker, et al.
Klinische Padiatrie|November 1, 1983
[Gonadal dysgenesis--possible variation of clinical, hormonal, cytogenetic and histologic findings]G Schwanitz, H U Tietze, K Zerres, et al.
Klinische Padiatrie|September 1, 1983
[Extreme tissue mosaicism in trisomy 8 syndrome. Trisomy 8 in fibroblasts and normal karyotype in lymphocytes]M Meisel-Stosiek, R A Pfeiffer, H U Tietze
Biomedizinische Technik. Biomedical Engineering|November 1, 1979
[A long term ECG-analysing system for quantitative evaluation of cardiac rhythm disturbances (author's transl)]U Tietze, E R von Leitner, D Andresen, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|January 1, 1983
[Spondylocostal dysostosis. Report of 5 cases including siblings and an atypical case]R A Pfeiffer, H G Hansen, B Böwing, et al.
Zeitschrift Fur Kardiologie|January 1, 1981
[Computer compatible long-term ECG analysing system for quantitative detection of low grade and complex dysrhythmias--Methods and evaluation of the analysing accuracy (author's transl)]E R von Leitner, U Tietze, D Andresen, et al.
Verhandlungen Der Deutschen Gesellschaft Fur Innere Medizin|January 1, 1978
[Incidence of myocardial infarct recurrences determined by means of serial measurements of creatine kinase and the isoenzyme CK-MB]V Kötter, E Prokein, T Linderer, et al.
Schweizerische Medizinische Wochenschrift|March 21, 1970
[Cortisol regulation in childhood hypoglycemia with adrenal medulla dysfunction]H U Tietze, R Zurbrugg, K Zuppinger, et al.
Journal of Medical Genetics|April 1, 1993
Simultaneous de novo interstitial deletion of 16q21 and intercalary duplication of 19q in a retarded infant with minor dysmorphic featuresU Trautmann, R A Pfeiffer, U Seufert-Satomi, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
Progress in Pediatric Surgery|January 1, 1983
The significance of diagnostic laparotomy in girls with disorders of sexual developmentW A Welte, H U Tietze, G Schwanitz
Acta Endocrinologica|June 1, 1970
Autoradiographic studies on nuclear DNA and RNA synthesis in the adenohypophysis of castrated ratsF Städtler, G Dhom, E Stöcker, et al.
Klinische Padiatrie|November 1, 1983
[Gonadal dysgenesis--possible variation of clinical, hormonal, cytogenetic and histologic findings]G Schwanitz, H U Tietze, K Zerres, et al.
Klinische Padiatrie|September 1, 1983
[Extreme tissue mosaicism in trisomy 8 syndrome. Trisomy 8 in fibroblasts and normal karyotype in lymphocytes]M Meisel-Stosiek, R A Pfeiffer, H U Tietze
Biomedizinische Technik. Biomedical Engineering|November 1, 1979
[A long term ECG-analysing system for quantitative evaluation of cardiac rhythm disturbances (author's transl)]U Tietze, E R von Leitner, D Andresen, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|January 1, 1983
[Spondylocostal dysostosis. Report of 5 cases including siblings and an atypical case]R A Pfeiffer, H G Hansen, B Böwing, et al.
Zeitschrift Fur Kardiologie|January 1, 1981
[Computer compatible long-term ECG analysing system for quantitative detection of low grade and complex dysrhythmias--Methods and evaluation of the analysing accuracy (author's transl)]E R von Leitner, U Tietze, D Andresen, et al.
Verhandlungen Der Deutschen Gesellschaft Fur Innere Medizin|January 1, 1978
[Incidence of myocardial infarct recurrences determined by means of serial measurements of creatine kinase and the isoenzyme CK-MB]V Kötter, E Prokein, T Linderer, et al.
Schweizerische Medizinische Wochenschrift|March 21, 1970
[Cortisol regulation in childhood hypoglycemia with adrenal medulla dysfunction]H U Tietze, R Zurbrugg, K Zuppinger, et al.
Journal of Medical Genetics|April 1, 1993
Simultaneous de novo interstitial deletion of 16q21 and intercalary duplication of 19q in a retarded infant with minor dysmorphic featuresU Trautmann, R A Pfeiffer, U Seufert-Satomi, et al.
Pageof 4