Adalbert Raimann

Vienna, Austria

Last Updated: 09/26/2026

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Found 50 publications

Clinical Course of Hyperostosis Due to SP7 (Osterix) Gain-of Function Mutation.

Clinical Course of Hyperostosis Due to SP7 (Osterix) Gain-of Function Mutation.

Journal: Klinische Padiatrie

Published: March 19, 2026

The use of denosumab in rare bone diseases in adults: a systematic review from the ECTS Rare Bone Disease Action Group.

The use of denosumab in rare bone diseases in adults: a systematic review from the ECTS Rare Bone Disease Action Group.

Journal: The Journal of clinical endocrinology and metabolism

Published: December 13, 2025

The use of denosumab in rare bone diseases in adults: a systematic review from the ECTS Rare Bone Disease Action Group.

The use of denosumab in rare bone diseases in adults: a systematic review from the ECTS Rare Bone Disease Action Group.

Journal: The Journal of clinical endocrinology and metabolism

Published: December 13, 2025

EndoCompass Project: Research Roadmap for Calcium and Bone Endocrinology.

EndoCompass Project: Research Roadmap for Calcium and Bone Endocrinology.

Journal: Hormone research in paediatrics

Published: October 14, 2025

Lower Limb Deformity in Different Types of Rickets.

Lower Limb Deformity in Different Types of Rickets.

Journal: Journal of clinical medicine

Published: September 29, 2025

Bone Health in Young Individuals with Primary Ciliary Dyskinesia: Insights from a Comparison with Cystic Fibrosis and Healthy Controls.

Bone Health in Young Individuals with Primary Ciliary Dyskinesia: Insights from a Comparison with Cystic Fibrosis and Healthy Controls.

Journal: Hormone research in paediatrics

Published: July 05, 2025

Prevalence of enthesopathies in X-linked hypophosphatemia: an explorative ultrasound study.

Prevalence of enthesopathies in X-linked hypophosphatemia: an explorative ultrasound study.

Journal: JBMR plus

Published: April 15, 2025

Transition Care for Young Persons with Rare Bone Mineral Conditions: A Consensus Recommendation from the ECTS Rare Bone Disease Action Group.

Transition Care for Young Persons with Rare Bone Mineral Conditions: A Consensus Recommendation from the ECTS Rare Bone Disease Action Group.

Journal: Calcified tissue international

Published: February 21, 2025

EndoCompass project: research roadmap for calcium and bone endocrinology.

EndoCompass project: research roadmap for calcium and bone endocrinology.

Journal: European journal of endocrinology

Published: February 16, 2025

XLH Matters: an evolving programme to discuss new advances and share clinical experiences to improve patient outcomes.

XLH Matters: an evolving programme to discuss new advances and share clinical experiences to improve patient outcomes.

Journal: Orphanet journal of rare diseases

Published: February 03, 2025

Inadequate pediatric reference ranges impede the diagnosis of X-linked hypophosphatemia and hypophosphatasia in Austria.

Inadequate pediatric reference ranges impede the diagnosis of X-linked hypophosphatemia and hypophosphatasia in Austria.

Journal: Wiener klinische Wochenschrift

Published: December 21, 2024

Developing a standard dataset in the European registries for rare endocrine and bone conditions-a Melorheostosis dataset.

Developing a standard dataset in the European registries for rare endocrine and bone conditions-a Melorheostosis dataset.

Journal: Orphanet journal of rare diseases

Published: December 04, 2024

Showing 1-12 of 50

Last Updated: 09/26/2026