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April 3, 2025
Phenotypic characterization of ENPP1 deficiency: generalized arterial calcification of infancy and autosomal recessive hypophosphatemic rickets type 2
Carlos R Ferreira, Mary E Hackbarth, Yvonne Nitschke, et al.
Pediatric Nephrology (Berlin, Germany)
|
October 24, 2017
Effects of growth hormone treatment on adult height in severely short children with X-linked hypophosphatemic rickets
Nadine Meyerhoff, Dieter Haffner, Hagen Staude, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
August 6, 2021
Ectopic Calcification and Hypophosphatemic Rickets: Natural History of ENPP1 and ABCC6 Deficiencies
Carlos R Ferreira, Kristina Kintzinger, Mary E Hackbarth, et al.
Molecular and Cellular Pediatrics
|
May 8, 2019
Vitamin D supplementation after the second year of life: joint position of the Committee on Nutrition, German Society for Pediatric and Adolescent Medicine (DGKJ e.V.), and the German Society for Pediatric Endocrinology and Diabetology (DGKED e.V.)
Thomas Reinehr, Dirk Schnabel, Martin Wabitsch, et al.
Circulation. Cardiovascular Genetics
|
December 18, 2009
Hypophosphatemia, hyperphosphaturia, and bisphosphonate treatment are associated with survival beyond infancy in generalized arterial calcification of infancy
Frank Rutsch, Petra Böyer, Yvonne Nitschke, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 13, 2018
A New Multisystem Disorder Caused by the Gαs Mutation p.F376V
Heike Biebermann, Gunnar Kleinau, Dirk Schnabel, et al.
Journal of Medical Genetics
|
October 24, 2006
Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations
Martin Zenker, Katarina Lehmann, Anna Leana Schulz, et al.
Nature Reviews. Nephrology
|
May 10, 2019
Clinical practice recommendations for the diagnosis and management of X-linked hypophosphataemia
Dieter Haffner, Francesco Emma, Deborah M Eastwood, et al.
Pediatric Nephrology (Berlin, Germany)
|
June 24, 2024
Health-related quality of life of children with X-linked hypophosphatemia in Germany
Martin Klein, Michael Obermaier, Helena Mutze, et al.
Therapeutic Advances in Chronic Disease
|
September 9, 2022
Post-authorisation safety study of burosumab use in paediatric, adolescent and adult patients with X-linked hypophosphataemia: rationale and description
Maria Luisa Brandi, Gema Ariceta, Signe Sparre Beck-Nielsen, et al.
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Search research articles
Search
Showing results (51-60 of 76) with videos related to
Sort By:
Page
of 8
JBMR Plus
|
April 3, 2025
Phenotypic characterization of ENPP1 deficiency: generalized arterial calcification of infancy and autosomal recessive hypophosphatemic rickets type 2
Carlos R Ferreira, Mary E Hackbarth, Yvonne Nitschke, et al.
Pediatric Nephrology (Berlin, Germany)
|
October 24, 2017
Effects of growth hormone treatment on adult height in severely short children with X-linked hypophosphatemic rickets
Nadine Meyerhoff, Dieter Haffner, Hagen Staude, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
August 6, 2021
Ectopic Calcification and Hypophosphatemic Rickets: Natural History of ENPP1 and ABCC6 Deficiencies
Carlos R Ferreira, Kristina Kintzinger, Mary E Hackbarth, et al.
Molecular and Cellular Pediatrics
|
May 8, 2019
Vitamin D supplementation after the second year of life: joint position of the Committee on Nutrition, German Society for Pediatric and Adolescent Medicine (DGKJ e.V.), and the German Society for Pediatric Endocrinology and Diabetology (DGKED e.V.)
Thomas Reinehr, Dirk Schnabel, Martin Wabitsch, et al.
Circulation. Cardiovascular Genetics
|
December 18, 2009
Hypophosphatemia, hyperphosphaturia, and bisphosphonate treatment are associated with survival beyond infancy in generalized arterial calcification of infancy
Frank Rutsch, Petra Böyer, Yvonne Nitschke, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 13, 2018
A New Multisystem Disorder Caused by the Gαs Mutation p.F376V
Heike Biebermann, Gunnar Kleinau, Dirk Schnabel, et al.
Journal of Medical Genetics
|
October 24, 2006
Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations
Martin Zenker, Katarina Lehmann, Anna Leana Schulz, et al.
Nature Reviews. Nephrology
|
May 10, 2019
Clinical practice recommendations for the diagnosis and management of X-linked hypophosphataemia
Dieter Haffner, Francesco Emma, Deborah M Eastwood, et al.
Pediatric Nephrology (Berlin, Germany)
|
June 24, 2024
Health-related quality of life of children with X-linked hypophosphatemia in Germany
Martin Klein, Michael Obermaier, Helena Mutze, et al.
Therapeutic Advances in Chronic Disease
|
September 9, 2022
Post-authorisation safety study of burosumab use in paediatric, adolescent and adult patients with X-linked hypophosphataemia: rationale and description
Maria Luisa Brandi, Gema Ariceta, Signe Sparre Beck-Nielsen, et al.
Page
of 8