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J Spranger

Showing results (181-190 of 247) with videos related to

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Journal of Medical Genetics|August 28, 1999
Recessively inherited multiple epiphyseal dysplasia with normal stature, club foot, and double layered patella caused by a DTDST mutationA Superti-Furga, L Neumann, T Riebel, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|December 1, 1991
Effects of cycle exercise on intestinal absorption in humansC V Gisolfi, K J Spranger, R W Summers, et al.
Journal of Medical Genetics|August 1, 1996
The deletion of six amino acids at the C-terminus of the alpha 1 (II) chain causes overmodification of type II and type XI collagen: further evidence for the association between small deletions in COL2A1 and Kniest dysplasiaA Winterpacht, A Superti-Furga, U Schwarze, et al.
Radiology|July 1, 1981
Diastrophic dysplasia: the death of a variantR Lachman, D Sillence, D Rimoin, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|March 28, 2003
Insulin decreases human adiponectin plasma levelsM Möhlig, U Wegewitz, M Osterhoff, et al.
Neuroscience|January 2, 2019
High-fat Diet and Physical Exercise Differentially Modulate Adult Neurogenesis in the Mouse HypothalamusC Klein, W Jonas, P Wiedmer, et al.
Journal of Endocrinological Investigation|December 13, 2003
Post-prandial decrease of human plasma ghrelin in the absence of insulinJ Spranger, M Ristow, B Otto, et al.
Physiological Genomics|October 4, 2000
A novel mutation in FGFR-3 disrupts a putative N-glycosylation site and results in hypochondroplasiaA Winterpacht, K Hilbert, C Stelzer, et al.
Diabetologia|April 8, 2010
Improved insulin sensitivity, preserved beta cell function and improved whole-body glucose metabolism after low-dose growth hormone replacement therapy in adults with severe growth hormone deficiency: a pilot studyA M Arafat, M Möhlig, M O Weickert, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|December 1, 1993
[Osteogenesis imperfecta in childhood and adolescence]R E Brenner, B Schiller, B F Pontz, et al.
Pageof 25

Showing results (181-190 of 247) with videos related to

Sort By:
Pageof 25
Journal of Medical Genetics|August 28, 1999
Recessively inherited multiple epiphyseal dysplasia with normal stature, club foot, and double layered patella caused by a DTDST mutationA Superti-Furga, L Neumann, T Riebel, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|December 1, 1991
Effects of cycle exercise on intestinal absorption in humansC V Gisolfi, K J Spranger, R W Summers, et al.
Journal of Medical Genetics|August 1, 1996
The deletion of six amino acids at the C-terminus of the alpha 1 (II) chain causes overmodification of type II and type XI collagen: further evidence for the association between small deletions in COL2A1 and Kniest dysplasiaA Winterpacht, A Superti-Furga, U Schwarze, et al.
Radiology|July 1, 1981
Diastrophic dysplasia: the death of a variantR Lachman, D Sillence, D Rimoin, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|March 28, 2003
Insulin decreases human adiponectin plasma levelsM Möhlig, U Wegewitz, M Osterhoff, et al.
Neuroscience|January 2, 2019
High-fat Diet and Physical Exercise Differentially Modulate Adult Neurogenesis in the Mouse HypothalamusC Klein, W Jonas, P Wiedmer, et al.
Journal of Endocrinological Investigation|December 13, 2003
Post-prandial decrease of human plasma ghrelin in the absence of insulinJ Spranger, M Ristow, B Otto, et al.
Physiological Genomics|October 4, 2000
A novel mutation in FGFR-3 disrupts a putative N-glycosylation site and results in hypochondroplasiaA Winterpacht, K Hilbert, C Stelzer, et al.
Diabetologia|April 8, 2010
Improved insulin sensitivity, preserved beta cell function and improved whole-body glucose metabolism after low-dose growth hormone replacement therapy in adults with severe growth hormone deficiency: a pilot studyA M Arafat, M Möhlig, M O Weickert, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|December 1, 1993
[Osteogenesis imperfecta in childhood and adolescence]R E Brenner, B Schiller, B F Pontz, et al.
Pageof 25