604 results on '"Saeger, Wolfgang"'
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2. Xanthogranulomatöse Adrenalitis: Seltene und schwierige Differentialdiagnose von Nebennierentumoren
3. Pituitary neuroendocrine tumors with PIT1/SF1 co-expression show distinct clinicopathological and molecular features
4. Metastases to the pituitary gland: insights from the German pituitary tumor registry
5. Inflammatory and Infectious Disorders in Endocrine Pathology
6. Cystic versus non-cystic silent corticotrophic adenomas: clinical and histological analysis of 62 cases after microscopic transsphenoidal surgery—a retrospective, single-center study
7. Exoscopic vs. microscopic transsphenoidal surgery for Cushing’s disease: a retrospective single-center study on 388 patients
8. Multiple tumorous lesions of the pituitary gland
9. Two Pituitary Neuroendocrine Tumors (PitNETs) with Very High Proliferation and TP53 Mutation — High-Grade PitNET or PitNEC?
10. The Diagnostic Impact of Epigenomics in Pituicyte-derived Tumors: Report of an Unusual Sellar Lesion with Extensive Hemorrhage and Necrotic Debris
11. Post-mortem histopathology of pituitary and adrenals of COVID-19 patients
12. ACTH-secreting pituitary carcinoma with TP53, NF1, ATRX and PTEN mutations Case report and review of the literature
13. Differences in somatostatin receptor subtype expression in patients with acromegaly: new directions for targeted therapy?
14. TP53 mutations in functional corticotroph tumors are linked to invasion and worse clinical outcome
15. Co-occurrence of Pituitary Neuroendocrine Tumors (PitNETs) and Tumors of the Neurohypophysis
16. Double adenomas of the pituitary reveal distinct lineage markers, copy number alterations, and epigenetic profiles
17. Xanthogranulomatous adrenalitis
18. Pituitary neuroendocrine tumors: a model for neuroendocrine tumor classification
19. WHO-Klassifikation der Hypophysentumoren des Jahres 2017
20. Co-expression of intermediate filaments glial fibrillary acidic protein and cytokeratin in pituitary adenoma
21. Pituitary neuroendocrine tumors (PitNETs): nomenclature evolution, not clinical revolution
22. Hypoxia and the hypoxia inducible factor 1α activate protein kinase A by repressing RII beta subunit transcription
23. Pathology of pituitary adenoma
24. Contributors
25. Pathology of nonadenomatous pituitary tumors and tumor-like lesions
26. Correction to: Two Pituitary Neuroendocrine Tumors (PitNETs) with Very High Proliferation and TP53 Mutation – High‑Grade PitNET or PitNEC?
27. Intratumoral morphological heterogeneity can be an indicator of genetic heterogeneity in colorectal cancer
28. Nebennierenrinde
29. Hypophyse
30. IgG4-Associated Adrenalitis—a Case Report
31. Spindle cell oncocytoma of the neurohypophysis with metastasis to the sphenoparietal sinus and immunohistochemical negativity for S100 and epithelial membrane antigen (EMA).
32. Unveiling the identities of null cell tumours: Epigenomics corroborate subtle histological cues in pituitary neuroendocrine tumour/adenoma classification
33. Sarcomatoid Adrenal Carcinoma: Case Report with Contribution to Pathogenesis
34. Immunoprofiling of glial tumours of the neurohypophysis suggests a common pituicytic origin of neoplastic cells
35. Teratoma of the Sellar Region: a Case Report
36. Somatotropinomas inadequately controlled with octreotide may over-respond to pasireotide: the importance of dose adjustment to achieve long-term biochemical control
37. Classical Histopathology and Immunohistochemistry
38. Functioning Adenomas
39. IgG4‐related hypophysitis is highly prevalent among cases of histologically confirmed hypophysitis
40. Functioning Adenomas
41. Pasireotide for malignant insulinoma
42. Exoscopic vs. microscopic transsphenoidal surgery for Cushing’s disease: A retrospective single-center study on 388 patients
43. Tumor-like Lesions of the Sellar Region
44. Cushing’s Syndrome Due to CRH and ACTH Co-secreting Pancreatic Tumor—Presentation of a New Case Focusing on Diagnostic Pitfalls
45. Additional file 1 of TP53 mutations in functional corticotroph tumors are linked to invasion and worse clinical outcome
46. Molecular Diagnosis of Pituitary Adenoma Predisposition Caused by Aryl Hydrocarbon Receptor-Interacting Protein Gene Mutations
47. Correction to: Two Pituitary Neuroendocrine Tumors (PitNETs) with Very High Proliferation and TP53 Mutation – High‑Grade PitNET or PitNEC?
48. Hypophyse
49. Nebennierenrinde
50. Epidermal growth factor receptor in adrenocortical tumors: analysis of gene sequence, protein expression and correlation with clinical outcome
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