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Hereditäre hypophosphatämische Rachitis: Neue Aspekte zur Pathogenese, Diagnostik und Therapie
Translated title of the contribution
:
Hereditary hypophosphatemic rickets: New aspects of pathogenesis, diagnosis, and treatment
Ralf Oheim
*
,
Olaf Hiort
*
Corresponding author for this work
Clinic of Pediatric and Adolescent Medicine
University Hospital Hamburg-Eppendorf
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Dive into the research topics of 'Hereditary hypophosphatemic rickets: New aspects of pathogenesis, diagnosis, and treatment'. Together they form a unique fingerprint.
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Medicine and Dentistry
Fibroblast
100%
Rickets
40%
Osteomalacia
40%
Clinical Feature
20%
Osteoarthritis
20%
Autosomal Dominant Inheritance
20%
Short Stature
20%
Adolescence
20%
Metabolite
20%
Proteinase
20%
Autosomal Recessive Inheritance
20%
Keyphrases
Hypophosphatemic Rickets
100%
Rare Forms
28%
Extraskeletal
14%
Arthrosis
14%
Most Common Form
14%
Daily Dose
14%
Lower Extremity
14%
Misalignment
14%
Deformity
14%
Vitamin D Metabolites
14%
Diagnostic Significance
14%
INIS
rickets
100%