Primary amyloidosis Ppts latest 50 Published articles

Primary amyloidosis: Primary amyloidosis is a disorder in which abnormal proteins build up in tissues and organs. Clumps of the abnormal proteins are called amyloid deposits.

Primary amyloidosis can lead to conditions that include:
    Carpal tunnel syndrome
    Heart muscle damage (cardiomyopathy) leading to congestive heart failure
    Intestinal malabsorption
    Liver enlargement
    Kidney failure
    Nephrotic syndrome
    Neuropathy (nerves that do not work properly)
    Orthostatic hypotension (abnormal drop in blood pressure with standing)

Primary  AL Amyloidosis
by Matthew  Volk
http://www.med.unc.edu/medicine/web/12.1.08%20Volk.%20Amyloid,%20LCDD.ppt

Cardiac  Amyloidosis
by Ann Isaksen
https://medicine.med.unc.edu/education/internal-medicine-residency-program/files/ppt/11.10.09%20Isaksen%20cardiac%20amyloid.ppt

Primary  Amyloidosis  Case Presentation & Discussion
By Warren  Brenner
http://hematology.wustl.edu/conferences/presentations/Brenner20031017.ppt

Immune Disorders:  HLA and Disease Associations and Amyloidosis
by Nancy L. Jones, M.D.
http://cmspath.edu/rfc/lectures11-12/jones/hla/jones-hla_and_amyloidosis.ppt

Protein  Structure Determination, Protein Folding, Molecular Chaperones, Prions Alzyheimer’s
http://www.uh.edu/sibs/faculty/glegge/lecture_18.ppt

Computational  Method for Predicting Amyloidogenic Sequences
by Bill Welsh
http://dimacs.rutgers.edu/Workshops/Neurodegenerative/slides/welsh.ppt

Alphabet  Soup and Interstitial Lung Disease
by Leslie  Scheunemann
http://www.med.unc.edu/medicine/web/3.26.08%20ILD%20Scheunemann.ppt

Latest 50 Published articles:

1. A case of amyloidosis of the ureter caused by primary macroglobulinemia].
2. A case of primary colon amyloidosis presenting as hematochezia].
3. A case report of primary amyloidosis manifested by bilateral lower extremity edema and dyspnea
4. Anesthesia for a man with bullous amyloidosis as the first sign of advanced primary amyloidosis
5. Primary amyloidosis with predominant involvement of the heart and gastrointestinal tract
6. Primary palpebral amyloidosis
7. The clinical significance of serum free light chain in primary systemic amyloidosis
8. 18F-FDG PET/CT in primary AL hepatic amyloidosis associated with multiple myeloma.
9. A case of isolated primary amyloidosis in the medial rectus muscle.
10. A new c.1845A→T of oncostatin M receptor-β mutation and slightly enhanced oncostatin M receptor-β expression in a Chinese family with primary localized cutaneous amyloidosis.
11. A rare case of primary systemic amyloidosis presenting with hepatic failure.
12. Case of primary localized cutaneous amyloidosis with protean clinical manifestations: Lichen, poikiloderma-like, dyschromic and bullous variants.
13. Changes in serum-free light chain rather than intact monoclonal immunoglobulin levels predicts outcome following therapy in primary amyloidosis.
14. Characterization of the response of primary cells relevant to dialysis-related amyloidosis to β2-microglobulin monomer and fibrils.
15. Concurrent systemic AA amyloidosis can discriminate primary sclerosing cholangitis from IgG4-associated cholangitis.
16. CT features of primary systemic pulmonary amyloidosis mimicking pulmonary sarcoidosis.
17. Dimethyl sulphoxide does not contribute to renal failure in patients undergoing stem cell transplant for multiple myeloma and primary amyloidosis.
18. Double autologous bone marrow transplantation and orthotopic liver transplantation in a patient with primary light chain (AL) amyloidosis.
19. Dramatic improvement of primary cutaneous amyloidosis with thalidomide.
20. Formation of immunoglobulin light chain amyloid oligomers in primary cutaneous nodular amyloidosis.
21. How to manage primary amyloidosis.
22. Kappa L-chain primary nodular lung amyloidosis: a case report.
23. Left atrial size is an independent predictor of overall survival in patients with primary systemic amyloidosis.
24. Localized primary AL amyloidosis of the colon without other GI involvement.
25. Localized Primary Cutaneous Nodular Amyloidosis in a Patient With Paraproteinemia.
26. Localized primary cutaneous nodular amyloidosis: case report.
27. Localized primary ureteral amyloidosis.
28. Long standing polyneuropathy as a form of presentation of primary systemic amyloidosis.
29. Nodular localized primary cutaneous amyloidosis and primary marginal zone B-cell lymphoma on the nose: treatment with microscopically controlled surgery.
30. On primary pulmonary amyloidosis.
31. Primary amyloidosis involving mesenteric lymph nodes: diagnosis by fine-needle aspiration cytology.
32. Primary amyloidosis presenting as "dropped head syndrome".
33. Primary cutaneous amyloidosis of the external ear: a clinicopathological and immunohistochemical study of 17 cases.
34. Primary gastroduodenal amyloidosis.
35. Primary hepatic amyloidosis: report of an unusual case presenting as a mass.
36. Primary localized amyloidosis of the nose.
37. Primary localized amyloidosis of the ureter.
38. Primary localized amyloidosis presenting as diffuse amorphous calcified mass in both orbits: case report.
39. Primary localized cutaneous nodular amyloidosis following local trauma.
40. Primary localized cutaneous nodular amyloidosis that appeared in a patient with severe atopic dermatitis.
41. Primary sjögren syndrome manifested as localized cutaneous nodular amyloidosis.
42. Primary systemic amyloidosis presenting as constrictive pericarditis.
43. Radiological findings of primary localized amyloidosis of the ureter.
44. Radiology quiz case 3. Primary tracheal amyloidosis.
45. Renal failure due to primary amyloidosis: a case report and literature review.
46. Role of oligomers in the amyloidogenesis of primary cutaneous amyloidosis.
47. Surgical removal of amyloid-laden lymph nodes: a possible therapeutic approach in a primary systemic AL amyloidosis patient with focal lymphadenopathy.
48. Tracheobronchial FDG uptake in primary amyloidosis detected by PET/CT.
49. Treatment of immunoglobulin light chain (primary or AL) amyloidosis.
50. Unusual primary cutaneous amyloidosis with an incontinentia pigmenti-like pattern.