35 results on '"Höppner, Jakob"'
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2. PLS3 Mutations in X-Linked Osteoporosis: Clinical and Genetic Features in Five New Families
3. Rare genetic disorders that impair parathyroid hormone synthesis, secretion, or bioactivity provide insights into the diagnostic utility of different parathyroid hormone assays
4. Transition for adolescents with a rare disease: results of a nationwide German project
5. Autosomal recessive hypophosphatemic rickets type 2 (ARHR2) due to ENPP1-deficiency
6. Prednisone prevents particle induced bone loss in the calvaria mouse model
7. Systemic sclerosis-associated myositis features minimal inflammation and characteristic capillary pathology
8. PLS3 Mutations in X-Linked Osteoporosis: Clinical and Genetic Features in Five New Families
9. Progressive pulmonary fibrosis in patients with connective tissue disease-associated interstitial lung disease: An explorative study.
10. Pulmonale Beteiligung bei idiopathischen inflammatorischen Myopathien.
11. Pulmonale Beteiligung bei idiopathischen inflammatorischen Myopathien
12. Lichen Planus After Denosumab
13. PLS3 mutations in X-linked osteoporosis : clinical and genetic features in five new families
14. Cardiorespiratory fitness in adolescents and young adults with Klinefelter syndrome – a pilot study
15. Comprehensive autoantibody profiles in systemic sclerosis: Clinical cluster analysis
16. Comprehensive Autoantibody Profiles in Systemic Sclerosis: Clinical Cluster Analysis
17. SIGLEC-1 in Systemic Sclerosis: A Useful Biomarker for Differential Diagnosis
18. Purinergic signaling in systemic sclerosis
19. Endothelin B Receptor Immunodynamics in Pulmonary Arterial Hypertension
20. Disorders of the Calcium Sensing Signaling Pathway: From Familial Hypocalciuric Hypercalcemia (FHH) to Life Threatening Conditions in Infancy
21. SIGLEC-1 in Systemic Sclerosis: A Useful Biomarker for Differential Diagnosis
22. Purinergic signalling in systemic sclerosis
23. Case Report: Severe Neonatal Course in Paternally Derived Familial Hypocalciuric Hypercalcemia
24. Prednisone prevents particle induced bone loss in the calvaria mouse model
25. Rhizomelia and impaired linear growth in a girl with juvenile paget disease
26. Clinical course in two children with Juvenile Paget's disease during long-term treatment with intravenous bisphosphonates
27. Severe courses of neonatal FHH in paternally inherited CaSR mutations: Implications for perinatal monitoring and treatment
28. Rhizomelia and Impaired Linear Growth in a Girl with Juvenile Paget Disease: The Natural History of the Condition
29. Recurring Fever
30. Diagnostik und Therapie der hypophosphatämischen Rachitis im Kindesalter
31. Eiken syndrome with parathyroid hormone resistance due to a novel parathyroid hormone receptor type 1 mutation: clinical features and functional analysis.
32. High parathyroid hormone rather than low vitamin D is associated with reduced event-free survival in childhood cancer.
33. [Pulmonary involvement in idiopathic inflammatory myopathies].
34. Purinergic signalling in systemic sclerosis.
35. Recurring Fever.
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