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Klinische Padiatrie
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April 27, 2017
Bilateral Infiltrative Dacryoadenitis and Granulomatous Pneumonia in an 11-Year-Old Boy: A Case Report
Susanne C Diesner, Julius Lukas, Eva Stifter, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
January 12, 2016
1,25-Dihydroxyvitamin D Alone Improves Skeletal Growth, Microarchitecture, and Strength in a Murine Model of XLH, Despite Enhanced FGF23 Expression
Eva S Liu, Janaina S Martins, Adalbert Raimann, et al.
Pediatric Blood & Cancer
|
January 4, 2024
Feasibility and antitumour activity of the FGFR inhibitor erdafitnib in three paediatric CNS tumour patients
Natalia Stepien, Lisa Mayr, Maria T Schmook, et al.
Hormone Research in Paediatrics
|
November 26, 2023
Successful Use of Metyrapone Suppositories in an Infant with Neonatal Cushing and McCune Albright Syndrome: A Case Report
Diana-Alexandra Ertl, Gerda Ratzinger-Stoeger, Adalbert Raimann, et al.
Orphanet Journal of Rare Diseases
|
July 2, 2025
Developing a standard dataset in the European registries for rare endocrine and bone conditions-a Melorheostosis dataset
Natasha M Appelman-Dijkstra, Mariya Cherenko, Gavin P R Clunie, et al.
Frontiers in Endocrinology
|
February 17, 2023
Burosumab for X-linked hypophosphatemia in children and adolescents: Opinion based on early experience in seven European countries
M Zulf Mughal, Giampiero I Baroncelli, Carmen de Lucas-Collantes, et al.
JBMR Plus
|
August 13, 2025
Prevalence of enthesopathies in X-linked hypophosphatemia: an explorative ultrasound study
Lisa Bachfischer, Martina Behanova, Eva Rath, et al.
Nature Communications
|
February 5, 2022
A neomorphic variant in SP7 alters sequence specificity and causes a high-turnover bone disorder
Julian C Lui, Adalbert Raimann, Hironori Hojo, et al.
Bone
|
February 4, 2025
Mineralised bone properties in a child with recessive osteogenesis imperfecta type XIV and in a conditional Tmem38b knockout murine model (Runx2-Cre; Tmem38b<sup>fl/fl</sup>)
Chloe E Jones, Stéphane Blouin, Adalbert Raimann, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
December 6, 2021
An Expert Perspective on Phosphate Dysregulation With a Focus on Chronic Hypophosphatemia
Fahad Aljuraibah, Justine Bacchetta, Maria Luisa Brandi, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 50) with videos related to
Sort By:
Page
of 5
Klinische Padiatrie
|
April 27, 2017
Bilateral Infiltrative Dacryoadenitis and Granulomatous Pneumonia in an 11-Year-Old Boy: A Case Report
Susanne C Diesner, Julius Lukas, Eva Stifter, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
January 12, 2016
1,25-Dihydroxyvitamin D Alone Improves Skeletal Growth, Microarchitecture, and Strength in a Murine Model of XLH, Despite Enhanced FGF23 Expression
Eva S Liu, Janaina S Martins, Adalbert Raimann, et al.
Pediatric Blood & Cancer
|
January 4, 2024
Feasibility and antitumour activity of the FGFR inhibitor erdafitnib in three paediatric CNS tumour patients
Natalia Stepien, Lisa Mayr, Maria T Schmook, et al.
Hormone Research in Paediatrics
|
November 26, 2023
Successful Use of Metyrapone Suppositories in an Infant with Neonatal Cushing and McCune Albright Syndrome: A Case Report
Diana-Alexandra Ertl, Gerda Ratzinger-Stoeger, Adalbert Raimann, et al.
Orphanet Journal of Rare Diseases
|
July 2, 2025
Developing a standard dataset in the European registries for rare endocrine and bone conditions-a Melorheostosis dataset
Natasha M Appelman-Dijkstra, Mariya Cherenko, Gavin P R Clunie, et al.
Frontiers in Endocrinology
|
February 17, 2023
Burosumab for X-linked hypophosphatemia in children and adolescents: Opinion based on early experience in seven European countries
M Zulf Mughal, Giampiero I Baroncelli, Carmen de Lucas-Collantes, et al.
JBMR Plus
|
August 13, 2025
Prevalence of enthesopathies in X-linked hypophosphatemia: an explorative ultrasound study
Lisa Bachfischer, Martina Behanova, Eva Rath, et al.
Nature Communications
|
February 5, 2022
A neomorphic variant in SP7 alters sequence specificity and causes a high-turnover bone disorder
Julian C Lui, Adalbert Raimann, Hironori Hojo, et al.
Bone
|
February 4, 2025
Mineralised bone properties in a child with recessive osteogenesis imperfecta type XIV and in a conditional Tmem38b knockout murine model (Runx2-Cre; Tmem38b<sup>fl/fl</sup>)
Chloe E Jones, Stéphane Blouin, Adalbert Raimann, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
December 6, 2021
An Expert Perspective on Phosphate Dysregulation With a Focus on Chronic Hypophosphatemia
Fahad Aljuraibah, Justine Bacchetta, Maria Luisa Brandi, et al.
Page
of 5