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Dirk Schnabel

Showing results (41-50 of 76) with videos related to

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Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|November 8, 2023
LMS-based continuous pediatric reference values for soluble receptor activator of nuclear factor kappa B ligand (sRANKL) and osteoprotegerin (OPG) in the HARP cohortHelene Tietze, Veronika Pott, Nele Kanzelmeyer, et al.
Kidney International Reports|March 11, 2026
Kidney Injury Urine Biomarker Normal Ranges in ChildrenHannah Weber, Katharina Schermuly, Anna Tschirner, et al.
The Journal of Clinical Endocrinology and Metabolism|January 12, 2018
Mean High-Dose l-Thyroxine Treatment Is Efficient and Safe to Achieve a Normal IQ in Young Adult Patients With Congenital HypothyroidismPaulina E Aleksander, Michaela Brückner-Spieler, Anne-Marie Stoehr, et al.
Clinical Endocrinology|June 8, 2011
Activating mutations in the calcium-sensing receptor: genetic and clinical spectrum in 25 patients with autosomal dominant hypocalcaemia - a German surveyFriedhelm Raue, Josef Pichl, Helmuth-G Dörr, et al.
American Journal of Human Genetics|December 17, 2005
Hereditary hypophosphatemic rickets with hypercalciuria is caused by mutations in the sodium-phosphate cotransporter gene SLC34A3Bettina Lorenz-Depiereux, Anna Benet-Pages, Gertrud Eckstein, et al.
BMC Medical Genetics|April 11, 2012
Mutations in LRP5 cause primary osteoporosis without features of OI by reducing Wnt signaling activityJohanna Korvala, Harald Jüppner, Outi Mäkitie, et al.
The Journal of Clinical Endocrinology and Metabolism|October 18, 2023
LMS-Based Pediatric Reference Values for Parameters of Phosphate Homeostasis in the HARP CohortVeronika Pott, Helene Tietze, Nele Kanzelmeyer, et al.
The Journal of Clinical Investigation|June 1, 2021
Mild COVID-19 despite autoantibodies against type I IFNs in autoimmune polyendocrine syndrome type 1Christian Meisel, Bengisu Akbil, Tim Meyer, et al.
The Journal of Clinical Investigation|February 21, 2002
Choreoathetosis, hypothyroidism, and pulmonary alterations due to human NKX2-1 haploinsufficiencyHeiko Krude, Barbara Schütz, Heike Biebermann, et al.
European Journal of Endocrinology|September 27, 2016
Heterozygous inactivating CaSR mutations causing neonatal hyperparathyroidism: function, inheritance and phenotypeMarkus Glaudo, Saskia Letz, Marcus Quinkler, et al.
Pageof 8

Showing results (41-50 of 76) with videos related to

Sort By:
Pageof 8
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|November 8, 2023
LMS-based continuous pediatric reference values for soluble receptor activator of nuclear factor kappa B ligand (sRANKL) and osteoprotegerin (OPG) in the HARP cohortHelene Tietze, Veronika Pott, Nele Kanzelmeyer, et al.
Kidney International Reports|March 11, 2026
Kidney Injury Urine Biomarker Normal Ranges in ChildrenHannah Weber, Katharina Schermuly, Anna Tschirner, et al.
The Journal of Clinical Endocrinology and Metabolism|January 12, 2018
Mean High-Dose l-Thyroxine Treatment Is Efficient and Safe to Achieve a Normal IQ in Young Adult Patients With Congenital HypothyroidismPaulina E Aleksander, Michaela Brückner-Spieler, Anne-Marie Stoehr, et al.
Clinical Endocrinology|June 8, 2011
Activating mutations in the calcium-sensing receptor: genetic and clinical spectrum in 25 patients with autosomal dominant hypocalcaemia - a German surveyFriedhelm Raue, Josef Pichl, Helmuth-G Dörr, et al.
American Journal of Human Genetics|December 17, 2005
Hereditary hypophosphatemic rickets with hypercalciuria is caused by mutations in the sodium-phosphate cotransporter gene SLC34A3Bettina Lorenz-Depiereux, Anna Benet-Pages, Gertrud Eckstein, et al.
BMC Medical Genetics|April 11, 2012
Mutations in LRP5 cause primary osteoporosis without features of OI by reducing Wnt signaling activityJohanna Korvala, Harald Jüppner, Outi Mäkitie, et al.
The Journal of Clinical Endocrinology and Metabolism|October 18, 2023
LMS-Based Pediatric Reference Values for Parameters of Phosphate Homeostasis in the HARP CohortVeronika Pott, Helene Tietze, Nele Kanzelmeyer, et al.
The Journal of Clinical Investigation|June 1, 2021
Mild COVID-19 despite autoantibodies against type I IFNs in autoimmune polyendocrine syndrome type 1Christian Meisel, Bengisu Akbil, Tim Meyer, et al.
The Journal of Clinical Investigation|February 21, 2002
Choreoathetosis, hypothyroidism, and pulmonary alterations due to human NKX2-1 haploinsufficiencyHeiko Krude, Barbara Schütz, Heike Biebermann, et al.
European Journal of Endocrinology|September 27, 2016
Heterozygous inactivating CaSR mutations causing neonatal hyperparathyroidism: function, inheritance and phenotypeMarkus Glaudo, Saskia Letz, Marcus Quinkler, et al.
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