41 results on '"Lips, Cornelis J. M."'
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2. ETHICS: Genetic testing for MEN1—whose responsibility?
3. Exclusion of the phosphatidylinositol-specific phospholipase C β3 (PLC β3) gene as candidate for the multiple endocrine neoplasia type 1 (MEN 1) gene
4. Mutation analysis of the RET proto-oncogene in Dutch families with MEN 2A, MEN 2B and FMTC: two novel mutations and one de novo mutation for MEN 2A
5. Pancreatic islet amyloid formation in patients with noninsulin-dependent diabetes mellitus: Impliation for therapeutic strategy
6. RET as a Diagnostic and Therapeutic Target in Sporadic and Hereditary Endocrine Tumors
7. Clinical Case Seminar: Repeated [131I]Metaiodobenzylguanidine Therapy in Two Patients with Malignant Pheochromocytoma
8. Pheochromocytoma in Von Hippel-Lindau Disease
9. Atypical MEN Type 2B Associated with Two Germline RET Mutations on the Same Allele Not Involving Codon 918
10. The Relationship Between Specific RET Proto-oncogene Mutations and Disease Phenotype in Multiple Endocrine Neoplasia Type 2: International RET Mutation Consortium Analysis
11. Radioiodine treatment of hyperthyroidism: fixed or calculated doses; intelligent design or science?
12. Clinical review 155
13. Genetic testing for MEN1—whose responsibility?
14. The Multiple Endocrine Neoplasia Type 1 (MEN1) Tumor Suppressor Regulates Peroxisome Proliferator-Activated Receptor γ-Dependent Adipocyte Differentiation
15. Tissue Selectivity in Multiple Endocrine Neoplasia Type 1-Associated Tumorigenesis
16. The success rate of I-131 ablation in differentiated thyroid cancer: comparison of uptake-related and fixed-dose strategies
17. A patient with bilateral pheochromocytoma as part of a Von Hippel-Lindau (VHL) syndrome type 2C
18. Acromegaly in a multiple endocrine neoplasia type 1 (MEN1) family with low penetrance of the disease
19. Repeated [131I]Metaiodobenzylguanidine Therapy in Two Patients with Malignant Pheochromocytoma
20. Prognostic significance of successful ablation with radioiodine of differentiated thyroid cancer patients
21. Inhibition of Amyloid Fibril Formation of Human Amylin by N-Alkylated Amino Acid and -Hydroxy Acid Residue Containing Peptides
22. Medullary thyroid carcinoma: role of genetic testing and calcitonin measurement
23. Molecular physiology of the islet amyloid polypeptide (IAPP)/amylin gene in man, rat, and transgenic mice
24. IAPP/amylin transgenic mice as an in vivo modelsystem for type-2 diabetes mellitus?
25. Multiple endocrine neoplasia type 2.
26. Multiple endocrine neoplasia type 1.
27. Inhibition of Amyloid Fibril Formation of Human Amylin by N-Alkylated Amino Acid and α-Hydroxy Acid Residue Containing Peptides.
28. Identification of the Multiple Endocrine Neoplasia Type 1 (MEN1) Gene.
29. Introduction.
30. <em>RET</em> Mutation Screening in Familial Cutaneous Lichen Amyloidosis and in Skin Amyloidosis Associated With Multiple Endocrine Neoplasia.
31. Regulation of vitamin D receptor function in MEN1-related parathyroid adenomas.
32. The multiple endocrine neoplasia type 1 (MEN1) tumor suppressor regulates peroxisome proliferator-activated receptor gamma-dependent adipocyte differentiation.
33. Serine protease inhibitor 8 is a novel immunohistochemical marker for neuroendocrine tumors of the pancreas.
34. P18 is a tumor suppressor gene involved in human medullary thyroid carcinoma and pheochromocytoma development.
35. Synergistic effect of oncogenic RET and loss of p18 on medullary thyroid carcinoma development.
36. Liver metastases of neuroendocrine tumours; early reduction of tumour load to improve life expectancy.
37. Menin links estrogen receptor activation to histone H3K4 trimethylation.
38. Do patients with multiple endocrine neoplasia syndrome type 1 benefit from periodical screening?
39. The spectrum of carcinoid tumours and carcinoid syndromes.
40. Clinical review 155: Pheochromocytoma in Von Hippel-Lindau disease.
41. Inhibition of amyloid fibril formation of human amylin by N-alkylated amino acid and alpha-hydroxy acid residue containing peptides.
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