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Dirk Schnabel

Showing results (1-10 of 76) with videos related to

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Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz|June 12, 2020
[Biopsychosocial care concept for children with X‑chromosomal hypophosphatemia (XLH) : Example of the multiprofessional approach of social pediatric centers]Dirk Schnabel
BMC Pediatrics|May 15, 2024
Longitudinal analysis of vitamin D levels considering sunshine duration and suggestion for a standardised approach for vitamin D supplementation in children and adolescents with obesityKatja Wechsung, Dirk Schnabel, Susanna Wiegand
Deutsches Arzteblatt International|December 5, 2023
The Treatment of Growth Disorders in Childhood and AdolescenceJoachim Woelfle, Dirk Schnabel, Gerhard Binder
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz|July 2, 2020
[Comprehensive care for complex diseases]Rüdiger von Kries, Florian Heinen, Dirk Schnabel
The Journal of Clinical Endocrinology and Metabolism|February 13, 2014
A homozygous CaSR mutation causing a FHH phenotype completely masked by vitamin D deficiency presenting as ricketsDorothea Szczawinska, Dirk Schnabel, Saskia Letz, et al.
Metabolism: Clinical and Experimental|April 1, 2019
Diagnosis, treatment-monitoring and follow-up of children and adolescents with X-linked hypophosphatemia (XLH)Anya Rothenbuhler, Dirk Schnabel, Wolfgang Högler, et al.
Expert Review of Medical Devices|July 18, 2015
A web-based survey assessing the impact of storage flexibility on the daily life of patients and caregivers administering growth hormoneAnne-Marie Kappelgaard, Catherine P Metzinger, Dirk Schnabel
Deutsches Arzteblatt International|December 1, 2009
Treatment of dwarfism with recombinant human insulin-like growth factor-1Michael B Ranke, Joachim Wölfle, Dirk Schnabel, et al.
European Journal of Endocrinology|December 10, 2015
GENETICS IN ENDOCRINOLOGY: Gain and loss of function mutations of the calcium-sensing receptor and associated proteins: current treatment conceptsBernhard Mayr, Dirk Schnabel, Helmuth-Günther Dörr, et al.
Pediatric Nephrology (Berlin, Germany)|December 15, 2021
Rickets guidance: part I-diagnostic workupDieter Haffner, Maren Leifheit-Nestler, Andrea Grund, et al.
Pageof 8

Showing results (1-10 of 76) with videos related to

Sort By:
Pageof 8
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz|June 12, 2020
[Biopsychosocial care concept for children with X‑chromosomal hypophosphatemia (XLH) : Example of the multiprofessional approach of social pediatric centers]Dirk Schnabel
BMC Pediatrics|May 15, 2024
Longitudinal analysis of vitamin D levels considering sunshine duration and suggestion for a standardised approach for vitamin D supplementation in children and adolescents with obesityKatja Wechsung, Dirk Schnabel, Susanna Wiegand
Deutsches Arzteblatt International|December 5, 2023
The Treatment of Growth Disorders in Childhood and AdolescenceJoachim Woelfle, Dirk Schnabel, Gerhard Binder
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz|July 2, 2020
[Comprehensive care for complex diseases]Rüdiger von Kries, Florian Heinen, Dirk Schnabel
The Journal of Clinical Endocrinology and Metabolism|February 13, 2014
A homozygous CaSR mutation causing a FHH phenotype completely masked by vitamin D deficiency presenting as ricketsDorothea Szczawinska, Dirk Schnabel, Saskia Letz, et al.
Metabolism: Clinical and Experimental|April 1, 2019
Diagnosis, treatment-monitoring and follow-up of children and adolescents with X-linked hypophosphatemia (XLH)Anya Rothenbuhler, Dirk Schnabel, Wolfgang Högler, et al.
Expert Review of Medical Devices|July 18, 2015
A web-based survey assessing the impact of storage flexibility on the daily life of patients and caregivers administering growth hormoneAnne-Marie Kappelgaard, Catherine P Metzinger, Dirk Schnabel
Deutsches Arzteblatt International|December 1, 2009
Treatment of dwarfism with recombinant human insulin-like growth factor-1Michael B Ranke, Joachim Wölfle, Dirk Schnabel, et al.
European Journal of Endocrinology|December 10, 2015
GENETICS IN ENDOCRINOLOGY: Gain and loss of function mutations of the calcium-sensing receptor and associated proteins: current treatment conceptsBernhard Mayr, Dirk Schnabel, Helmuth-Günther Dörr, et al.
Pediatric Nephrology (Berlin, Germany)|December 15, 2021
Rickets guidance: part I-diagnostic workupDieter Haffner, Maren Leifheit-Nestler, Andrea Grund, et al.
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