65 results on '"Grossman, Ashley"'
Search Results
2. The diagnostic value of prolactin adjustment in bilateral inferior petrosal sinus sampling for differentiating Cushing’s disease from the ectopic ACTH syndrome: a systematic review and meta-analysis
3. Author Correction: International consensus statement on the diagnosis and management of phaeochromocytoma and paraganglioma in children and adolescents
4. Management of phaeochromocytoma and paraganglioma in patients with germline SDHB pathogenic variants: an international expert Consensus statement
5. The Driver Role of Pathologists in Endocrine Oncology: What Clinicians Seek in Pathology Reports
6. The Spectrum of Familial Pituitary Neuroendocrine Tumors
7. Paediatric Cushing’s disease: Epidemiology, pathogenesis, clinical management and outcome
8. “The past is a different country, they do things differently there”: using the SEER data-base to assess prognosis in neuroendocrine tumours
9. Pituitary neuroendocrine tumors: a model for neuroendocrine tumor classification
10. International consensus on initial screening and follow-up of asymptomatic SDHx mutation carriers
11. Investigation of the Hypothalamo-pituitary-adrenal (HPA) axis: a contemporary synthesis
12. Distinctive features of pancreatic neuroendocrine neoplasms exhibiting an increment in proliferative activity during the course of the disease
13. Molecular Pathology of Well-Differentiated Gastro-entero-pancreatic Neuroendocrine Tumors
14. The Pangenomic Classification of Pituitary Neuroendocrine Tumors: Quality Histopathology is Required for Accurate Translational Research
15. The role of the tumour microenvironment in the angiogenesis of pituitary tumours
16. GH deficiency in cancer survivors in the transition age: diagnosis and therapy
17. Pituitary neuroendocrine tumors (PitNETs): nomenclature evolution, not clinical revolution
18. Thyroid disease in the time of COVID-19
19. Difference in survival between right- versus left-sided colorectal neuroendocrine neoplasms
20. Tumor microenvironment defines the invasive phenotype of AIP-mutation-positive pituitary tumors
21. A prospective longitudinal study of Pasireotide in Nelson’s syndrome
22. A prolapsing pituitary adenoma
23. Chemokines modulate the tumour microenvironment in pituitary neuroendocrine tumours
24. Chemotherapy in NETs: When and how
25. Routine genetic screening with a multi-gene panel in patients with pheochromocytomas
26. Anti-PD-L1 atezolizumab-Induced Autoimmune Diabetes: a Case Report and Review of the Literature
27. Characterisation of myocardial structure and function in adult-onset growth hormone deficiency using cardiac magnetic resonance
28. Long-term outcomes of children treated for Cushing’s disease: a single center experience
29. Glucocorticoid-induced osteoporosis: pathophysiological role of GH/IGF-I and PTH/VITAMIN D axes, treatment options and guidelines
30. Do patients with incidentally discovered bilateral adrenal nodules represent an early form of ARMC5-mediated bilateral macronodular hyperplasia?
31. Chordoid glioma of the third ventricle: a patient presenting with SIADH and a review of this rare tumor
32. Therapeutic Strategies for the Treatment of Severe Cushing’s Syndrome
33. Treating prolactinomas with dopamine agonists: always worth the gamble?
34. Clinical and biochemical manifestations of Cushing’s
35. The Wnt Signalling Cascade and the Adherens Junction Complex in Craniopharyngioma Tumorigenesis
36. Predicting an adrenal crisis: can we do it?
37. A novel succinate dehydrogenase type B mutation in an Iranian family. Its genetic and clinical evaluation
38. The AIP (aryl hydrocarbon receptor-interacting protein) gene and its relation to the pathogenesis of pituitary adenomas
39. A thymic carcinoid tumour causing Zollinger-Ellison and Cushing’s syndromes due to ectopic ACTH and gastrin secretion
40. Mini-review: pheochromocytomas causing the ectopic ACTH syndrome
41. Oncogene-induced senescence in pituitary adenomas and carcinomas
42. Signaling Pathways in Pheochromocytomas and Paragangliomas: Prospects for Future Therapies
43. BRAF V600E mutations are characteristic for papillary craniopharyngioma and may coexist with CTNNB1-mutated adamantinomatous craniopharyngioma
44. Pheochromocytomas and paragangliomas: assessment of malignant potential
45. Everolimus in the treatment of renal cell carcinoma and neuroendocrine tumors
46. Recurrent pituitary ependymoma: a complex clinical problem
47. The ectopic ACTH syndrome
48. Pituitary gland and β-catenin signaling: from ontogeny to oncogenesis
49. The molecular biology of pituitary tumors: a personal perspective
50. Imaging in covert ectopic ACTH secretion: a CT pictorial review
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