1,590 results on '"Marini, Francesca"'
Search Results
2. The challenge of hypophosphatasia diagnosis in adults: results from the HPP International Working Group Literature Surveillance
3. Hypophosphatasia diagnosis: current state of the art and proposed diagnostic criteria for children and adults
4. Proposed diagnostic criteria for the diagnosis of hypophosphatasia in children and adolescents: results from the HPP International Working Group
5. Congenital Hyperparathyroidism
6. Correction: Hypophosphatasia diagnosis: current state of the art and proposed diagnostic criteria for children and adults
7. Parathyroid carcinoma: molecular therapeutic targets
8. Paget’s Disease of Bone
9. Molecular genetics of parathyroid tumors
10. Role of Wnt signaling and sclerostin in bone and as therapeutic targets in skeletal disorders
11. Building Low-Resource NER Models Using Non-Speaker Annotation
12. Genetic Causes of Primary Hyperparathyroidism
13. Skeletal abnormalities, pediatric-onset severe osteoporosis, and multiple fragility fractures in a patient with a novel CTNNB1 de novo variant
14. Role of Nutrition in the Management of Patients with Multiple Endocrine Neoplasia Type 1
15. Genetics of congenital hypoparathyroidism and pseudohypoparathyroidism: results of a multigenic screening in an Italian cohort of affected patients
16. Increased bone fragility over time in women with chronic hypoparathyroidism: Real-world data from the HypoparaNet Italian Cohort
17. Selenosulfones, A Meetup of Chalcogens: A Journey into their Recent Chemistry.
18. Cyclopropanation of Aryl and Styryl Acetonitriles With Selenium‐Based Dielectrophiles.
19. The ground beetle Pseudoophonus rufipes gut microbiome is influenced by the farm management system
20. Hyperparathyroidism in Complex Genetic Disorders
21. Influence of Neck Pain, Cervical Extensor Muscle Fatigue, and Manual Therapy on Wrist Proprioception
22. Iodine/Oxone® oxidative system for the synthesis of selenylindoles bearing a benzenesulfonamide moiety as carbonic anhydrase I, II, IX, and XII inhibitors.
23. List of contributors
24. Genetic Causes of Primary Hyperparathyroidism
25. Synthesis of organochalcogens: use of nonconventional solvents/reaction media
26. Genetic disorders and insulinoma/glucagonoma
27. The Orlando Fringe: An Overview
28. Mapping Breeding Birds in a Karstic Sinkhole with a Comparison between Different Sampling Methods.
29. Quantitative Muscle Fatigue Assessment in Neuromuscular Disorders: A Pilot Study on Duchenne Pediatric Subjects
30. A Novel Heterozygous Mutation c.1627G>T (p.Gly543Cys) in the SLC34A1 Gene in a Male Patient with Recurrent Nephrolithiasis and Early Onset Osteopenia: A Case Report
31. Hypophosphatasia diagnosis: current state of the art and proposed diagnostic criteria for children and adults
32. Proposed diagnostic criteria for the diagnosis of hypophosphatasia in children and adolescents: results from the HPP International Working Group
33. Calcifediol: Mechanisms of Action
34. Pancreatic Neuroendocrine Tumors in MEN1 Patients: Difference in Post-Operative Complications and Tumor Progression between Major and Minimal Pancreatic Surgeries
35. OR23-02 Genotype-Phenotype Correlation In Calcium Sensing Receptor (Casr) Gene Gain-Of-Function Mutations: A Case Series And Report Of 2 Novel Mutations
36. Quality of life in Italian patients with Multiple endocrine neoplasia type 1 (MEN 1): results of an extensive survey
37. Hereditary Syndromes and Abdominal Neuroendocrine Tumors
38. Genetics of Osteoporosis
39. A domino approach to pyrazino- indoles and pyrroles using vinyl selenones
40. Proprioceptive identification of joint position versus kinaesthetic movement reproduction
41. Reactivity of oxidants towards phenyl and benzyl substituted 5-selanylpentanoic acids: radiolytic and theoretical insights.
42. Case Report: Calcium sensing receptor gene gain of function mutations: a case series and report of 2 novel mutations
43. Vinylation of N-Heteroarenes through Addition/Elimination Reactions of Vinyl Selenones
44. List of Contributors
45. Multiple endocrine neoplasia type 1
46. Come monitorare i carrier di mutazioni del gene MEN1
47. Correction to: Multiple endocrine neoplasia type 1: analysis of germline MEN1 mutations in the Italian multicenter MEN1 patient database
48. Multiple endocrine neoplasia type 1: analysis of germline MEN1 mutations in the Italian multicenter MEN1 patient database
49. Study of vitamin D status and vitamin D receptor polymorphisms in a cohort of Italian patients with juvenile idiopathic arthritis
50. In vitro study of rapid non-genomic effects of 25(OH)D3 in preosteoblastic cells
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