248 results on '"Kamenicky, Peter"'
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2. X-linked hypophosphataemia
3. Aberrant hormone receptors regulate a wide spectrum of endocrine tumors
4. Safety of growth hormone replacement in survivors of cancer and intracranial and pituitary tumours: a consensus statement.
5. Acromegalic Cardiomyopathy: An Entity on its own? The Effects of GH and IGF-I Excess and Treatment on Cardiovascular Risk Factors
6. Position statement on the diagnosis and management of acromegaly: The French National Diagnosis and Treatment Protocol (NDTP)
7. Efficacy of Burosumab in Adults with X-linked Hypophosphatemia (XLH): A Post Hoc Subgroup Analysis of a Randomized Double-Blind Placebo-Controlled Phase 3 Study
8. Improved Oral Health in Adults with X-Linked Hypophosphatemia Treated with Burosumab
9. Results of systematic KDM1A genotyping in a large series of Primary Bilateral Macronodular Adrenal Hyperplasia (PBMAH) patients and analysis of the genotype/phenotype correlation
10. Increased urinary excretion of calcium and nephrolithiasis: Real-life data from the epi-hypo cohort of hypoparathyroidism patients
11. Consensus statement by the French Society of Endocrinology (SFE) and French Society of Pediatric Endocrinology & Diabetology (SFEDP) on diagnosis of Cushing's syndrome
12. Loss of KDM1A in GIP-dependent primary bilateral macronodular adrenal hyperplasia with Cushing's syndrome: a multicentre, retrospective, cohort study
13. Anatomy of the medial wall of the cavernous sinus: A systematic review of the literature
14. Hypertension in Acromegaly
15. X-linked hypophosphatemia and burosumab: Practical clinical points from the French experience
16. Cardiovascular complications of acromegaly
17. Management of X-linked hypophosphatemia in adults
18. Differentiating pathologic parathyroid glands from thyroid nodules on neck ultrasound: the PARATH-US cross-sectional study
19. Mechanism of ectopic hormone receptors in adrenal tumors and hyperplasia
20. Adult Height Improved Over Decades in Patients with X-Linked Hypophosphatemia: a cohort study
21. OR17-05 Lysine Demethylase KDM1A And Ectopic Expression Of GIP-Receptor In Somatotropinomas Of Patients With Paradoxical Response To Oral Glucose
22. SAT278 Thyroid Hormones Regulate 11bhsd Enzymes: A Novel Function In Glucocorticoid Hormone Metabolism
23. SAT237 AZP-3601, A Novel PTH 1 Receptor Agonist, Induces Rapid Reduction And Normalization Of Urinary Calcium In Chronic Hypoparathyroid Patients
24. THU059 Increased Intracellular And Extracellular Myocardial Masses On Cardiac Magnetic Resonance Imaging In Patents With Acromegaly
25. FRI163 Central Role Of Mirnas During Kidney Development And Establishment Of The Mineralocorticoid Signaling Pathway Establishment Of The Mineralocorticoid Signaling Pathway
26. OR23-04 Treatment Of Chronic Hypoparathyroidism With Eneboparatide (AZP-3601), A Novel PTH 1 Receptor Agonist: Results From A Phase 2 Trial
27. OR11-03 A Novel Mutation In The Ligand-binding Domain Of The NR3C1 Gene Associated With Fluctuating Resistance To Glucocorticoids
28. Continued Beneficial Effects of Burosumab in Adults with X-Linked Hypophosphatemia: Results from a 24-Week Treatment Continuation Period After a 24-Week Double-Blind Placebo-Controlled Period
29. Clinical practice recommendations for the diagnosis and management of X-linked hypophosphataemia
30. Germline loss-of-function PAM variants are enriched in subjects with pituitary hypersecretion
31. Eneboparatide, a novel PTH 1 receptor agonist, induces rapid reduction and normalization of urinary calcium in chronic hypoparathyroid patients
32. Lysine demethylase KDM1A and ectopic expression of GIP-receptor in somatotropinomas of patients with paradoxical response to oral glucose
33. Treatment of chronic hypoparathyroidism by Eneboparatide, a novel PTH receptor-1 agonist: Results from a phase 2a study
34. Description of 38 novel ARMC5 variants and review of the literature: the updated mutational landscape of ARMC5 in Bilateral Macronodular Adrenocortical Disease
35. Increased intracellular and extracellular myocardial mass on cardiac magnetic resonance imaging in patients with acromegaly
36. Similarities and differences between thyroid and parathyroid nodules on ultrasound: the PARATH-US study
37. Pivotal Role of miRNAs during Establishment of the Mineralocorticoid Signaling Pathway and Kidney Development
38. Impact of Cushing's syndrome on the gonadotrope axis and testicular functions in men.
39. Challenging pre-surgical localization of hyperfunctioning parathyroid glands in primary hyperparathyroidism: the added value of 18F-Fluorocholine PET/CT
40. Benefit of burosumab in adults with X-linked hypophosphataemia (XLH) is maintained with long-term treatment
41. Germline loss-of-function PAM variants are enriched in subjects with pituitary hypersecretion
42. Primary hyperparathyroidism in pregnancy
43. Values of osteoprotegerin in aortic valve tissue in patients with significant aortic stenosis depend on the existence of concomitant coronary artery disease
44. Germline loss-of-functionPAMvariants are enriched in subjects with pituitary hypersecretion
45. Combining metabolomics and machine learning models as a tool to distinguish non-classic 21-hydroxylase deficiency from polycystic ovary syndrome without adrenocorticotropic hormone testing
46. Genotype-phenotype Description of Vitamin D–dependent Rickets 1A: CYP27B1 p.(Ala129Thr) Variant Induces a Milder Disease
47. OR12-3 Identification of Predictive Criteria for the Primary Bilateral Macronodular Adrenal Hyperplasia Gene ARMC5: A European Series of 352 Unselected Patients.
48. RF13 | PMON146 Molecular determinants of cavernous sinus invasion by pituitary adenomas: functional in vitro studies and in vivo investigations in a rat model of invasive pituitary tumorigenesis obtained by stereotactic pituitary GC cells injection
49. OR04-4 Loss of KDM1A in Bilateral Macronodular Adrenal Hyperplasia With GIP-Dependent Cushing's Syndrome and in Acromegaly With Paradoxical GH Response to Oral Glucose
50. Identification of predictive criteria for pathogenic variants of primary bilateral macronodular adrenal hyperplasia (PBMAH) gene ARMC5 in 352 unselected patients
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