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Wiener Medizinische Wochenschrift (1946)
|
January 27, 2021
Bone and growth: basic principles behind rare disorders
Adalbert Raimann, Diana-Alexandra Ertl, Gabriele Haeusler
The Spine Journal : Official Journal of the North American Spine Society
|
June 25, 2017
A journey through growth plates: tracking differences in morphology and regulation between the spine and the long bones in a pig model
Adalbert Raimann, Alireza Javanmardi, Monika Egerbacher, et al.
Klinische Padiatrie
|
March 19, 2026
Clinical Course of Hyperostosis Due to SP7 (Osterix) Gain-of Function Mutation
Uwe Wintergerst, Rainer Biedermann, Bernd Wegener, et al.
Current Osteoporosis Reports
|
October 28, 2023
Bone Material Properties in Bone Diseases Affecting Children
Adalbert Raimann, Barbara M Misof, Peter Fratzl, et al.
Wiener Klinische Wochenschrift
|
May 19, 2025
Inadequate pediatric reference ranges impede the diagnosis of X-linked hypophosphatemia and hypophosphatasia in Austria
Jojo Steininger, Magdalena Jablonska, Susanne Sagmeister, et al.
Bone
|
June 23, 2012
A novel homozygous mutation in the parathyroid hormone gene (PTH) in a girl with isolated hypoparathyroidism
Diana-Alexandra Ertl, Susanne Stary, Berthold Streubel, et al.
Hormone Research in Paediatrics
|
July 31, 2024
Accelerated Linear Growth during Erdafitinib Treatment: An FGFR-Related, but Growth Factor and Sex Steroid-Independent Mechanism?
Adalbert Raimann, Natalia Stepien, Amedeo A Azizi, et al.
Orthopadie (Heidelberg, Germany)
|
July 1, 2022
[Osteogenesis imperfecta : A multidisciplinary challenge]
Gabriel T Mindler, Rudolf Ganger, Alexandra Stauffer, et al.
Journal of Clinical Medicine
|
May 14, 2022
Disorders of the Calcium Sensing Signaling Pathway: From Familial Hypocalciuric Hypercalcemia (FHH) to Life Threatening Conditions in Infancy
Jakob Höppner, Kathrin Sinningen, Adalbert Raimann, et al.
Gait & Posture
|
July 21, 2020
Disease-specific gait deviations in pediatric patients with X-linked hypophosphatemia
Gabriel T Mindler, Andreas Kranzl, Alexandra Stauffer, et al.
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of 5
Search research articles
Search
Showing results (1-10 of 50) with videos related to
Sort By:
Page
of 5
Wiener Medizinische Wochenschrift (1946)
|
January 27, 2021
Bone and growth: basic principles behind rare disorders
Adalbert Raimann, Diana-Alexandra Ertl, Gabriele Haeusler
The Spine Journal : Official Journal of the North American Spine Society
|
June 25, 2017
A journey through growth plates: tracking differences in morphology and regulation between the spine and the long bones in a pig model
Adalbert Raimann, Alireza Javanmardi, Monika Egerbacher, et al.
Klinische Padiatrie
|
March 19, 2026
Clinical Course of Hyperostosis Due to SP7 (Osterix) Gain-of Function Mutation
Uwe Wintergerst, Rainer Biedermann, Bernd Wegener, et al.
Current Osteoporosis Reports
|
October 28, 2023
Bone Material Properties in Bone Diseases Affecting Children
Adalbert Raimann, Barbara M Misof, Peter Fratzl, et al.
Wiener Klinische Wochenschrift
|
May 19, 2025
Inadequate pediatric reference ranges impede the diagnosis of X-linked hypophosphatemia and hypophosphatasia in Austria
Jojo Steininger, Magdalena Jablonska, Susanne Sagmeister, et al.
Bone
|
June 23, 2012
A novel homozygous mutation in the parathyroid hormone gene (PTH) in a girl with isolated hypoparathyroidism
Diana-Alexandra Ertl, Susanne Stary, Berthold Streubel, et al.
Hormone Research in Paediatrics
|
July 31, 2024
Accelerated Linear Growth during Erdafitinib Treatment: An FGFR-Related, but Growth Factor and Sex Steroid-Independent Mechanism?
Adalbert Raimann, Natalia Stepien, Amedeo A Azizi, et al.
Orthopadie (Heidelberg, Germany)
|
July 1, 2022
[Osteogenesis imperfecta : A multidisciplinary challenge]
Gabriel T Mindler, Rudolf Ganger, Alexandra Stauffer, et al.
Journal of Clinical Medicine
|
May 14, 2022
Disorders of the Calcium Sensing Signaling Pathway: From Familial Hypocalciuric Hypercalcemia (FHH) to Life Threatening Conditions in Infancy
Jakob Höppner, Kathrin Sinningen, Adalbert Raimann, et al.
Gait & Posture
|
July 21, 2020
Disease-specific gait deviations in pediatric patients with X-linked hypophosphatemia
Gabriel T Mindler, Andreas Kranzl, Alexandra Stauffer, et al.
Page
of 5