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$3.10
1. Gale Encyclopedia of Medicine:
$28.95
2. Alport Syndrome - A Bibliography
 
$112.57
3. The Molecular Genetics of X-Linked
$184.26
4. Molecular Pathology and Genetics
 
5. Hereditary nephropathy with hearing
 
6. Hereditary hearing loss with nephropathy
 
$3.95
7. Familial nephritis: An entry from

1. Gale Encyclopedia of Medicine: Alport syndrome
by Carol A. Turkington
 Digital: Pages (2002-01-01)
list price: US$3.10 -- used & new: US$3.10
(price subject to change: see help)
Asin: B00075UU7Q
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Editorial Review

Book Description
The article is excerpted fromGale Encyclopedia of Medicine.

Consult the second edition of this authoritative, comprehensive, in-depth medical guide for information on more than 1,700 medical topics in language accessible to adult laypersons. Presented in a single alphabetical sequence, articles range in length from one or two paragraphs for minor topics, to several pages or more for major topics. Disease/disorder articles typically cover definition; description; causes and symptoms; diagnosis; treatments; prevention; and more. Test/treatment articles typically cover definition; purposes; precautions; preparation; risks; normal and abnormal results; and much more. This second edition includes more than 200 new entries, 300 updated entries, approximately 650 color images and illustrations, and a comprehensive subject index. New features include biographical and historical sidebars throughout the text.

Disease/disorder articles contain some or all of the following sections:

  • Definitions -- brief dictionary-style definition of the disorder
  • Descriptions -- overview of the disorder; who gets it and why
  • Causes & symptoms -- process, substance or organism that produces the condition; any risk factors that increase susceptibility to the condition; signs and symptoms of the disease
  • Diagnosis -- overview of procedures and tests used to diagnose the condition; how the test is done; who should be tested and when; time required; cost; whether it's typically covered by insurance
  • Treatments -- overview of conventional methods of care or management of the condition, such as drugs, surgeries, physical therapy, etc.
  • Alternative treatments -- overview of alternative/complementary therapies that may be used to treat the condition
  • Prognosis -- probable outcome of the disease
  • Preventions -- what actions can be taken to prevent the condition from occurring

Test/treatment articles contain some or all of the following sections:

  • Definitions -- brief dictionary-style definition of the test/treatment
  • Purposes -- why and when this test/treatment is prescribed
  • Precautions -- when this test/treatment should not be prescribed
  • Descriptions -- overview of the test/treatment including cost, length of time required, procedures followed, whether typically covered by insurance
  • Preparation -- pre-test treatment procedures, if any
  • Aftercare -- post-test treatment procedures, if any
  • Risks -- any complications/side effects commonly associated with the test/treatment
  • Normal results -- for tests, describes the normal values; for treatments, describes the anticipated outcomes
  • Abnormal results -- defines abnormal test values

Published/Released: December 2001

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2. Alport Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers
by Philip M. Parker
Paperback: 174 Pages (2007-07-19)
list price: US$28.95 -- used & new: US$28.95
(price subject to change: see help)
Asin: 0497113236
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Editorial Review

Product Description
In March 2001, the National Institutes of Health issued the following warning: "The number of Web sites offering health-related resources grows every day. Many sites provide valuable information, while others may have information that is unreliable or misleading." Furthermore, because of the rapid increase in Internet-based information, many hours can be wasted searching, selecting, and printing. Since only the smallest fraction of information dealing with Alport syndrome is indexed in search engines, such as www.google.com or others, a non-systematic approach to Internet research can be not only time consuming, but also incomplete. This book was created for medical professionals, students, and members of the general public who want to conduct medical research using the most advanced tools available and spending the least amount of time doing so. ... Read more


3. The Molecular Genetics of X-Linked Alport Syndrome (Acta Biomedica Lovaniensia , No 109)
by Caiying Guo
 Paperback: 86 Pages (1995-11)
list price: US$39.50 -- used & new: US$112.57
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Asin: 9061866812
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4. Molecular Pathology and Genetics of Alport Syndrome (Contributions to Nephrology)
Hardcover: 204 Pages (1996-02)
list price: US$184.50 -- used & new: US$184.26
(price subject to change: see help)
Asin: 3805561938
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5. Hereditary nephropathy with hearing loss: "Alport's syndrome" (Acta paediatrica Scandinavica : Supplement)
by Ulla Marianne Iversen
 Unknown Binding: 23 Pages (1974)

Asin: B0007AJO2S
Canada | United Kingdom | Germany | France | Japan

6. Hereditary hearing loss with nephropathy (Alport's syndrome); (Acta oto-laryngologica. Supplement[um])
by John Sidney Turner
 Unknown Binding: 26 Pages (1970)

Asin: B0006C6LT6
Canada | United Kingdom | Germany | France | Japan

7. Familial nephritis: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i>
by Maria, PhD Basile
 Digital: 6 Pages (2005)
list price: US$3.95 -- used & new: US$3.95
(price subject to change: see help)
Asin: B000M5B160
Canada | United Kingdom | Germany | France | Japan
Editorial Review

Book Description

Information on many genetic disorders, and the frequent new findings on them, has been extremely difficult to come byuntil now. The Gale Encyclopedia of Genetic Disorders addresses the need for current, hard-to-find facts on emerging discoveries. The two-volume Encyclopedia, presented in a single alphabetical sequence, provides clear, complete information on genetic disorders, including conditions, tests, procedures, treatments and therapies, in articles that are both comprehensive and easy to understand, in language accessible to laypersons. The articles are arranged in a standardized format for quick comparison and ease of use, while non-disorder topics are covered in detail with extended entries. Students will want to consult the Gale Encyclopedia of Genetic Disorders for useful information on a range of well known disorders, including Down Syndrome, Trisomy, Hemophilia and Tourette Syndrome, and rarely seen diseases such as Meckel Syndrome, Neuraminidase Deficiency and Phenylketonuria.

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