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Andreas R Huber

Showing results (51-60 of 68) with videos related to

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Clinica Chimica Acta; International Journal of Clinical Chemistry|August 19, 2008
Stability of hematological analytes depends on the hematology analyser used: a stability study with Bayer Advia 120, Beckman Coulter LH 750 and Sysmex XE 2100Fatime Imeri, Roberto Herklotz, Lorenz Risch, et al.
Blood Cells, Molecules & Diseases|March 16, 2013
Detection of germline rearrangements in patients with α- and β-thalassemia using high resolution array CGHAriane Blattner, Saskia Brunner-Agten, Katja Ludin, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 29, 2006
Effective control of persistent hyperparathyroidism with cinacalcet in renal allograft recipientsAndreas L Serra, Reto Savoca, Andreas R Huber, et al.
American Journal of Medical Genetics. Part A|April 2, 2010
Interstitial deletion 1q42 in a patient with agenesis of corpus callosum: Phenotype-genotype comparison to the 1q41q42 microdeletion suggests a contiguous 1q4 syndromeIsabel Filges, Benno Röthlisberger, Nemya Boesch, et al.
European Journal of Applied Physiology|January 29, 2016
Increased endothelial microparticles and oxidative stress at extreme altitudeJacqueline Pichler Hefti, Alexander Leichtle, Monika Stutz, et al.
Swiss Medical Weekly|October 2, 2009
Body mass index, blood pressure, and serum cholesterol in young Swiss men: an analysis on 56784 army conscriptsChristoph H Saely, Lorenz Risch, Franz Frey, et al.
The British Journal of Ophthalmology|October 20, 2010
Cerebrospinal fluid dynamics between the basal cisterns and the subarachnoid space of the optic nerve in patients with papilloedemaHanspeter Esriel Killer, Gregor Peter Jaggi, Neil R Miller, et al.
American Journal of Medical Genetics. Part A|January 24, 2009
Familial 14.5 Mb interstitial deletion 13q21.1-13q21.33: clinical and array-CGH study of a benign phenotype in a three-generation familyIsabel Filges, Benno Röthlisberger, Christoph Noppen, et al.
Journal of Medical Genetics|November 2, 2010
Reduced expression by SETBP1 haploinsufficiency causes developmental and expressive language delay indicating a phenotype distinct from Schinzel-Giedion syndromeIsabel Filges, Keiko Shimojima, Nobuhiko Okamoto, et al.
Digestion|July 1, 2006
Glucagon-like peptide-1 is involved in sodium and water homeostasis in humansJean-Pierre Gutzwiller, Petr Hruz, Andreas R Huber, et al.
Pageof 7

Showing results (51-60 of 68) with videos related to

Sort By:
Pageof 7
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 19, 2008
Stability of hematological analytes depends on the hematology analyser used: a stability study with Bayer Advia 120, Beckman Coulter LH 750 and Sysmex XE 2100Fatime Imeri, Roberto Herklotz, Lorenz Risch, et al.
Blood Cells, Molecules & Diseases|March 16, 2013
Detection of germline rearrangements in patients with α- and β-thalassemia using high resolution array CGHAriane Blattner, Saskia Brunner-Agten, Katja Ludin, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 29, 2006
Effective control of persistent hyperparathyroidism with cinacalcet in renal allograft recipientsAndreas L Serra, Reto Savoca, Andreas R Huber, et al.
American Journal of Medical Genetics. Part A|April 2, 2010
Interstitial deletion 1q42 in a patient with agenesis of corpus callosum: Phenotype-genotype comparison to the 1q41q42 microdeletion suggests a contiguous 1q4 syndromeIsabel Filges, Benno Röthlisberger, Nemya Boesch, et al.
European Journal of Applied Physiology|January 29, 2016
Increased endothelial microparticles and oxidative stress at extreme altitudeJacqueline Pichler Hefti, Alexander Leichtle, Monika Stutz, et al.
Swiss Medical Weekly|October 2, 2009
Body mass index, blood pressure, and serum cholesterol in young Swiss men: an analysis on 56784 army conscriptsChristoph H Saely, Lorenz Risch, Franz Frey, et al.
The British Journal of Ophthalmology|October 20, 2010
Cerebrospinal fluid dynamics between the basal cisterns and the subarachnoid space of the optic nerve in patients with papilloedemaHanspeter Esriel Killer, Gregor Peter Jaggi, Neil R Miller, et al.
American Journal of Medical Genetics. Part A|January 24, 2009
Familial 14.5 Mb interstitial deletion 13q21.1-13q21.33: clinical and array-CGH study of a benign phenotype in a three-generation familyIsabel Filges, Benno Röthlisberger, Christoph Noppen, et al.
Journal of Medical Genetics|November 2, 2010
Reduced expression by SETBP1 haploinsufficiency causes developmental and expressive language delay indicating a phenotype distinct from Schinzel-Giedion syndromeIsabel Filges, Keiko Shimojima, Nobuhiko Okamoto, et al.
Digestion|July 1, 2006
Glucagon-like peptide-1 is involved in sodium and water homeostasis in humansJean-Pierre Gutzwiller, Petr Hruz, Andreas R Huber, et al.
Pageof 7