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H Reimann

Showing results (21-30 of 36) with videos related to

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Microvascular Research|September 1, 1975
Capillary red blood cell velocity measurements in human nailfold by videodensitometric methodP Butti, M Intaglietta, H Reimann, et al.
Bibliotheca Anatomica|January 1, 1975
Capillary red blood cell velocity measurements in human nailfold by videodensitometric methodP Butti, M Intaglietta, H Reimann, et al.
Zeitschrift Fur Medizinische Laboratoriumsdiagnostik|January 1, 1990
[Recording protein metabolism and cell proliferation with the stable isotope 15N]C Wagenknecht, H Barleben, L Junker, et al.
Folia Haematologica (Leipzig, Germany : 1928)|January 1, 1989
[Influencing the fibrinolytic activity by antithrombotics in patients with atherosclerosis]C Norden, H Reimann, G Grunow, et al.
VASA. Supplementum|January 1, 1991
[Prognosis of peripheral arterial occlusive disease following angioplasty]J Lieske, C Norden, U Krünes, et al.
Klinische Wochenschrift|May 17, 1990
[15N tracer technical studies of protein metabolism in arteriosclerosis patients]H Barleben, C Wagenknecht, K Jung, et al.
Genomics|September 2, 1998
The human dead ringer/bright homolog, DRIL1: cDNA cloning, gene structure, and mapping to D19S886, a marker on 19p13.3 that is strictly linked to the Peutz-Jeghers syndromeR D Kortschak, H Reimann, M Zimmer, et al.
American Journal of Human Genetics|July 27, 2001
Molecular characterization and gene content of breakpoint boundaries in patients with neurofibromatosis type 1 with 17q11.2 microdeletionsD E Jenne, S Tinschert, H Reimann, et al.
Genomics|June 14, 2000
A common set of at least 11 functional genes is lost in the majority of NF1 patients with gross deletionsD E Jenne, S Tinschert, E Stegmann, et al.
Nature Genetics|January 13, 1998
Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinaseD E Jenne, H Reimann, J Nezu, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
Microvascular Research|September 1, 1975
Capillary red blood cell velocity measurements in human nailfold by videodensitometric methodP Butti, M Intaglietta, H Reimann, et al.
Bibliotheca Anatomica|January 1, 1975
Capillary red blood cell velocity measurements in human nailfold by videodensitometric methodP Butti, M Intaglietta, H Reimann, et al.
Zeitschrift Fur Medizinische Laboratoriumsdiagnostik|January 1, 1990
[Recording protein metabolism and cell proliferation with the stable isotope 15N]C Wagenknecht, H Barleben, L Junker, et al.
Folia Haematologica (Leipzig, Germany : 1928)|January 1, 1989
[Influencing the fibrinolytic activity by antithrombotics in patients with atherosclerosis]C Norden, H Reimann, G Grunow, et al.
VASA. Supplementum|January 1, 1991
[Prognosis of peripheral arterial occlusive disease following angioplasty]J Lieske, C Norden, U Krünes, et al.
Klinische Wochenschrift|May 17, 1990
[15N tracer technical studies of protein metabolism in arteriosclerosis patients]H Barleben, C Wagenknecht, K Jung, et al.
Genomics|September 2, 1998
The human dead ringer/bright homolog, DRIL1: cDNA cloning, gene structure, and mapping to D19S886, a marker on 19p13.3 that is strictly linked to the Peutz-Jeghers syndromeR D Kortschak, H Reimann, M Zimmer, et al.
American Journal of Human Genetics|July 27, 2001
Molecular characterization and gene content of breakpoint boundaries in patients with neurofibromatosis type 1 with 17q11.2 microdeletionsD E Jenne, S Tinschert, H Reimann, et al.
Genomics|June 14, 2000
A common set of at least 11 functional genes is lost in the majority of NF1 patients with gross deletionsD E Jenne, S Tinschert, E Stegmann, et al.
Nature Genetics|January 13, 1998
Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinaseD E Jenne, H Reimann, J Nezu, et al.
Pageof 4