Hallo! Tracked shipping to Austria with Delivery Duty Paid for just €3.99  

Ship to
Austria
0

My Account

  • argentina
  • chile
  • colombia
  • españa
  • méxico
  • perú
  • estados unidos
  • internacional

menu

Select your country

Americas

Europe

Rest of the world

portada Monoclonal Gammopathies and the Kidney
Type
Physical Book
Publisher
Author
Year
2010
Language
English
Pages
300
Format
Paperback
ISBN
9048161991
ISBN13
9789048161997
Categories

Monoclonal Gammopathies and the Kidney

Touchard, G. ; Aucouturier ; Hermine, O. (Author) · Springer · Paperback

Monoclonal Gammopathies and the Kidney - Touchard, G. ; Aucouturier ; Hermine, O.

Cheaper New Book Imported to Austria
Delivery: 01 Oct - 05 Oct Shipping: 15 to 16 business days.
188,28 €
Faster New Book Imported to Austria
Delivery: 29 Sep - 01 Oct Shipping: 13 to 14 business days.
219,43 €
Import costs and 10% VAT included in the price ✅
188,28 €

Choose the list to add your product or create one New List

Go to My Wishlists
Calculate shipping cost

Synopsis "Monoclonal Gammopathies and the Kidney"

Table 1 Comparison of MIDD and immunoglobulinic amyloidosis MIDD Amyloidosis Presentation Multivisceral or predominant involvement of an organ (kidney) Underlying disease Monoclonal immunoproliferative disorders, mostly myeloma. Monoclonal bone marrow plasma cell populations without overt malignancy. Possibility of 'non-secretory' forms. Deposits by EM (Granular) non-organized Fibrillar (13 pleated sheets) Spectrum LCDD: L chains, most K, either AL-amyloidosis: fragments (?)* of or apparently enlarged, normal-sized normal-sized or apparently enlarged or short. Frequent glycosylation L chains most A. Frequent and polymeration. glycosylation.Abnormal susceptibility to proteolysis. LHCDD: associated H chains Cases with associated short H chains (short by biosynthesis by biosynthesis experiments. experiments). HCDD: short H chains. AH-amyloidosis: short H chains. L chain isotypy V K IV predominance. VAVI C A3predominance. V region mutations Yes Yes *Found in necropsy material; whether they exist in vivo is doubtful. 3 After Preud'homme et al. AL-amyloidosis). Therefore, we believe' that the term MIDD should be restricted to this pathological entity, whatever the Ig content of the deposits, light 4 5 ) or both (LHCDD ). However, the chains (LCDD), heavy chains (HCDD New York group used the denomination MIDD for both Randall's disease and immunoglobulinic amyloidosis'S." The two processes have many features in common (Table I) and they can be associated in the same patients.

Customers reviews

More customer reviews
  • 0% (0)
  • 0% (0)
  • 0% (0)
  • 0% (0)
  • 0% (0)

Frequently Asked Questions about the Book

Is the book original?

All books in our catalog are Original.

In what language is the book written?

The book is written in English.

What is the format of this book?

The binding of this edition is Paperback.

Questions and Answers about the Book

Do you have a question about the book? Login to be able to add your own question.

Opinions about Bookdelivery

More customer reviews