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         Leukodystrophy:     more books (21)
  1. The Official Parent's Sourcebook on Leukodystrophy: Directory for the Internet Age by Icon Health Publications, 2005-01-31
  2. Leukodystrophy - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References by ICON Health Publications, 2004-10-21
  3. The Official Parent's Sourcebook on Metachromatic Leukodystrophy: A Revised and Updated Directory for the Internet Age by Icon Health Publications, 2002-09-11
  4. Leukodystrophy: Webster's Timeline History, 1954 - 2007 by Icon Group International, 2010-05-14
  5. Leukodystrophy: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Ken Wells, 2005
  6. 21st Century Complete Medical Guide to Leukodystrophies: Authoritative Government Documents, Clinical References, and Practical Information for Patients and Physicians by PM Medical Health News, 2004-05
  7. 21st Century Ultimate Medical Guide to Leukodystrophies - Authoritative Clinical Information for Physicians and Patients (Two CD-ROM Set) by PM Medical Health News, 2009-05-21
  8. Leukodystrophies: Adrenoleukodystrophy, Canavan Disease, Pelizaeus-Merzbacher Disease, Metachromatic Leukodystrophy, Krabbe Disease
  9. Metachromatic leukodystrophy: An entry from Thomson Gale's <i>Gale Encyclopedia of Neurological Disorders</i> by Igor, MD, PhD Medica, 2005
  10. Leukodystrophy: An entry from Thomson Gale's <i>Gale Encyclopedia of Neurological Disorders</i> by Scott, MS, CGC Polzin, 2005
  11. 21st Century Complete Medical Guide to Degenerative Nerve Diseases, Adrenoleukodystrophy, Leukodystrophy, Rett Syndrome, Canavan Disease, Ataxias, Authoritative ... for Patients and Physicians (CD-ROM) by PM Medical Health News, 2004-04-01
  12. Gale Encyclopedia of Medicine: Lipidoses by Altha Roberts Edgren, 2002-01-01
  13. Krabbe disease: An entry from Thomson Gale's <i>Gale Encyclopedia of Neurological Disorders</i> by Amie, MS Stanley, Rosalyn, MD Carson-DeWitt, 2005
  14. Lipidoses: An entry from Gale's <i>Gale Encyclopedia of Medicine, 3rd ed.</i> by Altha Edgren, 2006

61. ScienceDaily -- Browse Topics: Health/Conditions_and_Diseases/Neurological_Disor
News about leukodystrophy More news about leukodystrophy . Books about leukodystrophy More books about leukodystrophy . Links about leukodystrophy
http://www.sciencedaily.com/directory/Health/Conditions_and_Diseases/Neurologica
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Real Estate Lookup Front Page Today's Digest Week in Review Email Updates ... Demyelinating Diseases Leukodystrophy (32 links) See Also: News about Leukodystrophy (October 29, 1998) full story [ More news about Leukodystrophy Books about Leukodystrophy [ More books about Leukodystrophy Links about Leukodystrophy
  • Call Again Soon - Directed at making life better for people affected by Leukodystrophy and those who know and love them. United Leukodystrophy Foundation - Nonprofit, voluntary health organization dedicated to providing patients and their families with information about their disease and assistance in their health.

62. ScienceDaily -- Browse Topics: Health/Conditions_and_Diseases/Neurological_Disor
News about Metachromatic leukodystrophy More news about Metachromatic leukodystrophy . Books about Metachromatic leukodystrophy
http://www.sciencedaily.com/directory/Health/Conditions_and_Diseases/Neurologica
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Real Estate Lookup Front Page Today's Digest Week in Review Email Updates ... Leukodystrophy Metachromatic Leukodystrophy (5 links) News about Metachromatic Leukodystrophy Brain Cell Transplants Potential Treatment For Multiple Sclerosis (November 1, 1999) full story (October 29, 1998) full story [ More news about Metachromatic Leukodystrophy Books about Metachromatic Leukodystrophy [ More books about Metachromatic Leukodystrophy Links about Metachromatic Leukodystrophy

63. Virtual Hospital: Radiology Resident Case Of The Week: Adrenal Leukodystrophy (A
1996. Adrenal leukodystrophy (ALD). underway. Adrenal leukodystrophy can be subdivided into classic Xlinked ALD and infantile ALD.
http://www.vh.org/pediatric/provider/radiology/PedRadSecTF/012696/
Radiology Resident Case of the Week: January 26, 1996
Adrenal Leukodystrophy (ALD)
Mike Rubin, M.D.
Peer Review Status: Internally Peer Reviewed Clinical Sx:
The disease usually presents in males age 5-10 years old with a gradual disturbance in gait and slight intellectual impairment. There is usually rapid progression with hypotension, seizures, visual complaints, and difficulty in swallowing appearing with time. Abnormal skin pigmentation or other signs and symptoms of adrenal insufficiency may become apparent before CNS symptoms. In some cases, adrenal symptoms never appear. Etiology/Pathophysiology:
Classic ALD and the adult variant adrenomyeloneuropathy (AMN) are X-linked diseases in which there is deficiency of lignoceroyl-CoA ligase, a perioxisomal enxyme needed for the degradation of very long chain fatty acids (VLCFA). Pathology:
White matter diseases are usually classified as demyelinating or dysmyelinating diseases. Dysmyelinating diseases such as ALD are inherited enzymatic deficiencies that cause abnormal formation or increased breakdown of myelin. Demyelinating diseases result in the loss of normally formed myelin by processes such as infection, chemotherapy, radiation, and autoimmune disorders such as multiple sclerosis. The diagnosis of ALD is made by the assay of plasma, red cells, or cultured fibroblasts for increased amounts of VLCFA.

64. Westie Health Concerns - Globoid Cell Leukodystrophy (GCL)
Globoid Cell leukodystrophy (synonym Krabbe s disease) is a degenerative disease......Globoid Cell leukodystrophy (GCL).
http://www.westieclubamerica.com/health/gcl.html
Globoid Cell Leukodystrophy (GCL)
Description: Globoid Cell Leukodystrophy (synonym: Krabbe's disease) is a degenerative disease of the white matter of the brain and spinal cord. Segmental degeneration of some peripheral nerves may also occur. It is the result of a genetic deficiency of an enzyme (galactocerebroside b-galactosidase) that is involved in the breakdown of certain lipids (fats) in the brain and spinal cord. Clinical signs begin early in life and progress rapidly. Lack of coordination, weakness, stumbling, loss of control of the hindquarters, and tail tremors may be observed. Then the dog will develop a wide stance, incoordination, and posterior or total limb paralysis. The dog may become blind or fail to recognize familiar individuals. The response to painful stimuli is generally unaffected. Age of Onset: The disease may occur as early as 4 weeks of age and nearly always before 5 - 6 months of age. Diagnosis: The typical clinical signs along with characteristic histopathologic findings at autopsy in appropriate breeds are diagnostic. In addition, antemortem (before death) diagnosis can be made by measuring the mean galactocerebroside b-galactosidase enzyme activity in white blood cells. Furthermore, heterozygotes can be identified, since affected dogs have about 18% and carriers about 51% of the mean activity found in the cells of normal dogs. Treatment: There is no treatment, and the disease is invariably fatal.

65. Metachromatic Leukodystrophy
Metachromatic leukodystrophy. Definition Metachromatic Treatment At present, there is no treatment for metachromatic leukodystrophy itself. Symptomatic
http://www.shands.org/health/information/article/001205.htm
Disease Injury Nutrition Poison ... Z
Metachromatic leukodystrophy
Definition: Metachromatic leukodystrophy is an inherited disease characterized by the absence of the enzyme arylsulfatase A, which causes a material called cerebroside sulfate to accumulate in cells. This is toxic to the cell, especially neurons (the cells of the nervous system) and causes the problems of the disease. MLD is a member of a class of diseases called lysosomal storage disorders. In these diseases, patients lack a protein needed to metabolize the food we eat.
Alternative Names: MLD; Arylsulfatase A deficiency
Causes, incidence, and risk factors: Metachromatic leukodystrophy (MLD) is transmitted as an autosomal recessive trait, which means that a person must inherit the defective gene from both parents to be affected. MLD has a wide range of symptoms. As with many other storage diseases, there are forms of early and delayed onset (late infant, juvenile, and adult types). The most common and most severe form is the late infant onset form, which has symptoms such as irritability decreased muscle tone muscle wasting , and the loss of the ability to walk in babies who have started walking. The disease progresses to

66. Leukodystrophy - Medical Dictionary Definitions Of Popular Medical Terms
leukodystrophy A disorder of the white matter of the brain, the part of the brain that contains myelinated nerve fibers. The white
http://www.medterms.com/script/main/art.asp?articlekey=4148

67. Healthfinder® - Leukodystrophy
Carefully selected government and nonprofit health information on leukodystrophy. healthfinder® home page, United leukodystrophy Foundation.
http://www.healthfinder.gov/Scripts/SearchContext.asp?topic=492

68. Leukodystrophy
Back Home Next. leukodystrophy. DrKoop.com Adrenoleukodystrophy. leukodystrophy - CHORUS document on the different types of leukodystrophy. A little technical.
http://www.ability.org.uk/Leukodystrophy.html
Our Aims Services Stats ... Z Leukodystrophy Alexander disease mini information sheet - From the National Institutes of Health (USA) The Amn-Ald Community Pages - Support site for families dealing with the diseases Leukodystrophies). Canavan Foundation Canavan Research Fund - The Canavan Research Fund is a not-for-profit organization dedicated to pioneering research Cockayne Syndrome treatment, prevention and much more DrKoop.com - Adrenoleukodystrophy Leukodystrophy - CHORUS document on the different types of Leukodystrophy. A little technical. Metachromatic Leukodystrophy (MLD) - Infomration from the Duke University for Patients and their families. United Leukodystrophy Foundation Webmaster . Site Design by Ability "see the ability, not the disability" Acknowledgments

69. The Vest Airway Clearance System - Airway Clearance Indications Of Leukodystroph
physicians. •, Reimbursed by more than 1,100 health plans nationwide. Airway Clearance Indications of leukodystrophy. Print Version. The
http://www.thevest.com/conditions/factsheets/leuko.asp?gs=patients

70. Neurological Disorders, Demyelinating Diseases, Leukodystrophy
Sponsored leukodystrophy Sites. Submit Your Site to the leukodystrophy category. Sponsored Results. Health Spotlight. List Your Site Here Today!
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Epilepsy Book Store At WellnessBooks.com

Comprehensive source to books on Epilepsy. Includes community boards and chat, book reviews and online ordering.
Neurological Disorders Due To An Imbalance?
Do you have a neurological disorder? This may be due to an imbalance. Check the balance of your system and get natural recommendations for restoring balance.
  • Aicardi-Goutieres Syndrome - News, descriptions, contacts, and other information concerning this leukodystrophy.
  • Alexander Disease - Information sheet compiled by NINDS, the National Institute of Neurological Disorders and Stroke.
  • Call Again Soon - Directed at making life better for people affected by Leukodystrophy and those who know and love them.
  • Devoted to Brianna - Medical experiences and terminology helpful for parents to understand and cope with genetic disorders. One little girl's story, concerning Canavan Leukodystrophy offers help and hope to many.

71. Metachromatic Leukodystrophy
More Metachromatic leukodystrophy Categories » Submit Your Site to the Metachromatic leukodystrophy category. Sponsored Metachromatic leukodystrophy Sites.
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Guide On Adrenoleukodystrophy

"This book has been created for patients who have decided to make education and research an integral part of the treatment process."

72. Leukodystrophy, Metachromatic
leukodystrophy, Metachromatic. impairment leading to blindness. Metachromatic leukodystrophy is inherited as an autosomal recessive trait.
http://www.meritcare.com/hwdb/showTopic.asp?pd_hwid=nord212

73. Leukodystrophy Connections
Martinez Foundation. leukodystrophy definition. Source for DeafBlind Information. leukodystrophy Info from FamilyVillage. United leukodystrophy Foundation.
http://www.joejohnson.net/leukodystrophy_connections.htm
Call Again Soon
Joey has neonatal adrenoleukodystrophy. It stole all of his sight and most of his hearing by the time he was eighteen months old. Joey is 17 years old now. The Call Again Soon is dedicated to Joey. Martinez Foundation Leukodystrophy definition Source for Deaf-Blind Information Download zip file of some searches ... NORD-National Organization of Rare Diseases Leave E-Mail for Joe Johnson

74. BrainTalk Communities - Leukodystrophy
Post New Thread. Threads in Forum leukodystrophy, Forum Tools, Search this Forum. Views 3,655 Announcement Donations to BrainTalk
http://brain.hastypastry.net/forums/forumdisplay.php?f=157

75. ► Metachromatic Leukodystrophy
Metachromatic leukodystrophy. Causes, incidence, and risk factors Metachromatic leukodystrophy (MLD) is transmitted as an autosomal recessive trait.
http://www.umm.edu/ency/article/001205.htm
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Metachromatic leukodystrophy
Overview Symptoms Treatment Prevention Definition: Metachromatic leukodystrophy is an inherited metabolic storage disease characterized by the absence of the enzyme arylsulfatase A and increased storage of sulfatide.
Alternative Names: MLD; Arylsulfatase A deficiency
Causes, incidence, and risk factors: Metachromatic leukodystrophy (MLD) is transmitted as an autosomal recessive trait. MLD has a wide range of symptoms. As with many other storage diseases, there are forms of early and delayed onset (late infant, juvenile and adult types). The most common (and the most severe form) is the late infant onset form, which has symptoms such as irritability decreased muscle tone muscle wasting , the loss of the ability to walk. Debility is progressive with blindness seizures , and partial paralysis . Death occurs usually before age 10.
Both the juvenile and adult forms have later onset but similar symptoms. In the adult and juvenile forms, psychosis and emotional disturbances are an important part of the illness. The juvenile form is fatal within a few years of diagnosis. The adult form may be drawn out over many years.

76. NEJM -- Hematopoietic Stem-Cell Transplantation In Globoid-Cell Leukodystrophy
Original Article from The New England Journal of Medicine Hematopoietic StemCell Transplantation in Globoid-Cell leukodystrophy.
http://content.nejm.org/cgi/content/short/338/16/1119
HOME SEARCH CURRENT ISSUE PAST ISSUES ... HELP Please sign in for full text and personal services Previous Volume 338:1119-1127 April 16, 1998 Number 16 Next Hematopoietic Stem-Cell Transplantation in Globoid-Cell Leukodystrophy
William Krivit, M.D., Ph.D., Elsa G. Shapiro, Ph.D., Charles Peters, M.D., John E. Wagner, M.D., Guy Cornu, M.D., Joanne Kurtzberg, M.D., David A. Wenger, Ph.D., Edwin H. Kolodny, M.D., Marie T. Vanier, M.D., Ph.D., Daniel J. Loes, M.D., Kathryn Dusenbery, M.D., and Lawrence A. Lockman, M.D.
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ABSTRACT Background Globoid-cell leukodystrophy is caused by a deficiency of galactocerebrosidase, which results in progressive central nervous system deterioration. We investigated whether allogeneic hematopoietic stem-cell transplantation can provide a source of leukocyte galactocerebrosidase and thereby prevent the decline of central nervous system function in patients with the disease. Methods Five children with globoid-cell leukodystrophy (one with the infantile type and four with late-onset disease) were treated with allogeneic hematopoietic stem-cell transplantation.

77. Leukodystrophy
Call Again Soon Directed at making life better for people affected by leukodystrophy and those who know and love them. United
http://www.thenewhealthfind.com/Health/ConditionsandDiseases/NeurologicalDisorde
Directory Home Health Conditions and Diseases Neurological Disorders ... Demyelinating Diseases : Leukodystrophy (31)

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78. CCHS Clinical Digital Library
Metachromatic leukodystrophy Clinical Resources. Online Mendelian Inheritance in Man Homepage Metachromatic leukodystrophy Access document;
http://cchs-dl.slis.ua.edu/clinical/metabolism/inborn/lysosomalstorage/sphingoli
Clinical Resources by Topic: Metabolic Disorders
Metachromatic Leukodystrophy Clinical Resources
Pediatrics Radiology Pathology Genetics ... Miscellaneous Resources See also:

79. CCHS Clinical Digital Library
Metachromatic leukodystrophy Patient/Family Resources. Metachromatic leukodystrophy Access document. United leukodystrophy FoundationAccess document
http://cchs-dl.slis.ua.edu/patientinfo/metabolism/inborn/lysosomalstorage/sphing
Patient/Family Resources by Topic: Metabolic Disorders
Metachromatic Leukodystrophy Patient/Family Resources
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80. Adreno-leukodystrophy
Home. Health Wellness Information. Adult Metabolic Diseases. Find Out About a Specific Disease. Adrenoleukodystrophy. Cystinuria. Galactosemia. Gaucher Disease.
http://www.vanhosp.bc.ca/html/wellness_amdc_findout_adrenoleukodystrophy.html

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