1,618 results on '"Marini, Francesca"'
Search Results
2. Association of vitamin D and bisphenol A levels with cardiovascular risk in an elderly Italian population: results from the InCHIANTI study
3. The challenge of hypophosphatasia diagnosis in adults: results from the HPP International Working Group Literature Surveillance
4. Hypophosphatasia diagnosis: current state of the art and proposed diagnostic criteria for children and adults
5. Congenital Hyperparathyroidism
6. Proposed diagnostic criteria for the diagnosis of hypophosphatasia in children and adolescents: results from the HPP International Working Group
7. Correction: Hypophosphatasia diagnosis: current state of the art and proposed diagnostic criteria for children and adults
8. Parathyroid carcinoma: molecular therapeutic targets
9. Molecular genetics of parathyroid tumors
10. Building Low-Resource NER Models Using Non-Speaker Annotation
11. Paget’s Disease of Bone
12. Role of Wnt signaling and sclerostin in bone and as therapeutic targets in skeletal disorders
13. Genetic Causes of Primary Hyperparathyroidism
14. Influence of Neck Pain, Cervical Extensor Muscle Fatigue, and Manual Therapy on Wrist Proprioception
15. The ground beetle Pseudoophonus rufipes gut microbiome is influenced by the farm management system
16. Hyperparathyroidism in Complex Genetic Disorders
17. Skeletal abnormalities, pediatric-onset severe osteoporosis, and multiple fragility fractures in a patient with a novel CTNNB1 de novo variant
18. Role of Nutrition in the Management of Patients with Multiple Endocrine Neoplasia Type 1
19. Genetics of congenital hypoparathyroidism and pseudohypoparathyroidism: results of a multigenic screening in an Italian cohort of affected patients
20. Increased bone fragility over time in women with chronic hypoparathyroidism: Real-world data from the HypoparaNet Italian Cohort
21. Comparison of the performance of an eriophyid mite, Aceria salsolae, on nontarget plants in the laboratory and in the field
22. List of contributors
23. Genetic Causes of Primary Hyperparathyroidism
24. Synthesis of organochalcogens: use of nonconventional solvents/reaction media
25. Parathyroid carcinoma and atypical parathyroid tumor: analysis of an Italian database.
26. Iodine/Oxone® oxidative system for the synthesis of selenylindoles bearing a benzenesulfonamide moiety as carbonic anhydrase I, II, IX, and XII inhibitors.
27. Selenosulfones, A Meetup of Chalcogens: A Journey into their Recent Chemistry.
28. Cyclopropanation of Aryl and Styryl Acetonitriles With Selenium‐Based Dielectrophiles.
29. Genetic disorders and insulinoma/glucagonoma
30. The Orlando Fringe: An Overview
31. Quantitative Muscle Fatigue Assessment in Neuromuscular Disorders: A Pilot Study on Duchenne Pediatric Subjects
32. Quality of life in Italian patients with Multiple endocrine neoplasia type 1 (MEN 1): results of an extensive survey
33. Electrostatic attraction-repulsion model with Cinchona alkaloid-based zwitterionic chiral stationary phases exemplified for zwitterionic analytes
34. Mapping Breeding Birds in a Karstic Sinkhole with a Comparison between Different Sampling Methods.
35. 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
36. Hypophosphatasia diagnosis: current state of the art and proposed diagnostic criteria for children and adults
37. Proposed diagnostic criteria for the diagnosis of hypophosphatasia in children and adolescents: results from the HPP International Working Group
38. Hereditary Syndromes and Abdominal Neuroendocrine Tumors
39. Genetics of Osteoporosis
40. Come monitorare i carrier di mutazioni del gene MEN1
41. A domino approach to pyrazino- indoles and pyrroles using vinyl selenones
42. Proprioceptive identification of joint position versus kinaesthetic movement reproduction
43. Calcifediol: Mechanisms of Action
44. Pancreatic Neuroendocrine Tumors in MEN1 Patients: Difference in Post-Operative Complications and Tumor Progression between Major and Minimal Pancreatic Surgeries
45. OR23-02 Genotype-Phenotype Correlation In Calcium Sensing Receptor (Casr) Gene Gain-Of-Function Mutations: A Case Series And Report Of 2 Novel Mutations
46. Case Report: Calcium sensing receptor gene gain of function mutations: a case series and report of 2 novel mutations
47. Vinylation of N-Heteroarenes through Addition/Elimination Reactions of Vinyl Selenones
48. Robotic wrist training after stroke: Adaptive modulation of assistance in pediatric rehabilitation
49. Study of vitamin D status and vitamin D receptor polymorphisms in a cohort of Italian patients with juvenile idiopathic arthritis
50. Bone tissue and mineral metabolism in hereditary endocrine tumors: clinical manifestations and genetic bases
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