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         Krabbe Disease:     more detail
  1. Krabbe's Disease: A Medical Dictionary, Bibliography, And Annotated Research Guide To Internet References by Icon Health Publications, 2004-10-08
  2. Krabbe disease: An entry from Thomson Gale's <i>Gale Encyclopedia of Neurological Disorders</i> by Amie, MS Stanley, Rosalyn, MD Carson-DeWitt, 2005
  3. Krabbe Disease - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-18
  4. Krabbe disease: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Amie, MS Stanley, 2005
  5. Leukodystrophies: Adrenoleukodystrophy, Canavan Disease, Pelizaeus-Merzbacher Disease, Metachromatic Leukodystrophy, Krabbe Disease
  6. Neurology, lectures for medical students and general practitioners by Knud H Krabbe, 1941
  7. Urolithiasis in dogs and cats by Agnete Krabbe, 1949

41. Entrez PubMed
No abstract, Lysosomal diseases metachromatic leukodystrophy (adult), Krabbe s disease (adult) Nippon Rinsho. No abstract, Infantile krabbe disease.
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=PureSearch&db=PubMed&details_t

42. Short Description Of Cell Lines. Pathology: Krabbe Disease *245200
Version 4.200205, Short description of cell lines. Pathology krabbe disease *245200 OMIM record. By selecting the cell line name
http://www.biotech.ist.unige.it/cldb/pat105.html
Version
Short description of cell lines.
Pathology: Krabbe disease
OMIM record
By selecting the cell line name , you will receive the detailed description of the cell line
By selecting one of the terms between parentheses, you will receive the list of all relevant cell lines
You can search any term of the list by using the 'Find' utility of your browser
human, Caucasian
amnion GEIMM
human, Caucasian
...
By Beatrice...

43. Malattia Di Krabbe Krabbe Disease Bambi
Malattia di Krabbe krabbe disease. http//digilander.libero.it/ailu/krabbe.htm http//www.ninds.nih.gov/health_and_medical/disorders
http://antares.fastnet.it/enti/bambi/malattia-krabbe.htm
Malattia di Krabbe Krabbe Disease http://digilander.libero.it/ailu/krabbe.htm
http://www.ninds.nih.gov/health_and_medical/disorders/krabbe_doc.htm
http://www.1uphealth.com/health/krabbe_disease_info.html
http://www.healthcyclopedia.com/krabbe_disease.html
http://www.emedicine.com/ped/topic2892.htm
http://www.nlm.nih.gov/medlineplus/ency/article/001198.htm
http://www.geneclinics.org/profiles/krabbe/
http://members.aol.com/TOMDIA22/
http://www.krabbes.com/
http://healthlink.mcw.edu/article/921771775.html
http://www.mielina.org http://www.krabbes.net/ http://www.biotech.ist.unige.it/cldb/pat105.html http://accessible.ninds.nih.gov/health_and_medical/disorders/krabbe_doc.htm http://www.medlina.com/krabbe_disease.htm http://www.whonamedit.com/synd.cfm/1457.html http://www.disabilityresources.org/KRABBES.html http://www.drkoop.com/ency/article/001198.htm http://members.aol.com/GETINMERRY/krabbes.html

44. Krabbe Disease
Selected medical images OMIM krabbe disease. krabbe disease Clinical profile; Sources Indian Pediatrics. Print this page. Edited by Aldo Campana, August 13, 2003.
http://www.gfmer.ch/Genetic_diseases/Krabbe_disease/Krabbe_disease.htm
Selected medical images
OMIM

Krabbe disease Sources
Print this page
Edited by Aldo Campana, August 13, 2003

45. Krabbe('s) Disease (Globoid Cell Leukodystrophy)
Galactosylceramidosis). Krabbe s Family Network; Krabbes Disease Homepage (CJ s page); Krabbes Disease; krabbe disease; krabbe disease; krabbe disease. HOME.
http://www.bdid.com/krabbe.htm

HOME
Krabbe('s) Disease (Globoid Cell Leukodystrophy, Galactosylceramidosis)

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46. Krabbe Disease
krabbe disease PubMed Medline search on krabbe disease krabbe disease factsheet National Institute for Neurological Disorders and Stroke.
http://www.ion.ucl.ac.uk/library/patient/krabbe.htm
Krabbe Disease PubMed Medline search on Krabbe Disease
Krabbe Disease
factsheet: National Institute for Neurological Disorders and Stroke
see also leukodystrophy page
Support Groups
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The Quadrangle, Crewe Hall, Weston Road, Crewe, Cheshire CW1 6UR
Tel: 01270 250221 (information, advice and support to parents and professionals involved with metabolic diseases). The office is open 9.00am - 5.00pm Mondays to Fridays.
Fax: 01270 250244
A national umbrella organisation working on behalf of children, young people and families affected by metabolic disease. Offers a telephone helpline for information, counselling and support; written information by post (detailed information only available following confirmed diagnosis, appropriate professional counselling and telephone contact); details of other agencies and sources of help; information about the latest research and whom to contact for specialist advice etc.

47. Disease - Krabbe Disease - Hartford, Connecticut , Saint Francis Care
Disease krabbe disease - courtesy of Saint Francis Care of Hartford, Connecticut, contemporary medicine with major clinical concentrations in heart disease
http://www.saintfranciscare.com/12419.cfm
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Disease - Krabbe disease
Definition: Krabbe disease is an inherited disorder characterized by a deficiency of the enzyme galactocerebroside beta-galactosidase (galactosylcereamidase). It results in destruction of myelin , a fatty material that surrounds and insulates many of the nerves. Alternative Names: Globoid cell leukodystrophy; Galactosylcerebrosidase deficiency; Galactosylcereamidase deficiency Causes And Risk: Krabbe disease is inherited as an autosomal recessive trait. It is most common among people of Scandinavian descent, but it generally affects about 1 in 150,000 infants. Absence of the enzyme galactocerebroside beta-galactosidase causes increasing destruction of myelin. This results in progressive destruction of the nervous system.
Krabbe disease has an early onset form and a late onset form. In the early form, symptoms begin in the first months of life with feeding problems and failure to thrive , unexplained fevers, and vomiting.

48. Krabbe Disease
krabbe disease. Alternative Names Causes, incidence, and risk factors krabbe disease is inherited as an autosomal recessive trait.
http://lebonheur.adam.com/pages/content.asp?genId=001198&proj=1&lang=en

49. ClinicalTrials.gov - Information On Clinical Trials And Human Research Studies:
Search results for krabbe disease ALLFIELDS are shown below. Include trials that are no longer recruiting patients. 1 study was found.
http://www.clinicaltrials.gov/search/term=Krabbe Disease
Home Search Browse Resources ... About Search results for Krabbe Disease [ALL-FIELDS] are shown below.
Include trials that are no longer recruiting patients.
1 study was found. Recruiting Phase II Study of Allogeneic Bone Marrow or Umbilical Cord Blood Transplantation in Patients With Lysosomal or Peroxisomal Inborn Errors of Metabolism
Conditions: Graft Versus Host Disease; Lysosomal Storage Diseases; Peroxisomal Disorders U.S. National Library of Medicine Contact NLM Customer Service National Institutes of Health Privacy ... Freedom of Information Act

50. Krabbe Disease
krabbe disease. This response submitted by PF Jennings on 1/14/99. Email Address jennings@cyberport.com Title Twenty five years
http://neuro-www.mgh.harvard.edu/forum/MitochondrialDis.F/Krabbedisease.html
Krabbe disease
This response submitted by P.F. Jennings on 1/14/99.
Email Address: jennings@cyberport.com
Title Twenty five years of the "psychosine hypothesis":
a personal perspective of its history and present status
Author Suzuki K
Addr Neuroscience Ctr, Dept of Neurology/Psychiatry, Univ of No Carolina School of Medicine, Chapel Hill
Source Neurochem Res, 1998 Mar, 23:3, 251-9 Abstract
Language of Publication English
Unique Identifier 98141341 Title The inherited leukodystrophies: a clinical overview.
Author Aicardi J
Addr Hôpital des Enfants Malades, Paris, France. Source J Inherit Metab Dis, 1993, 16:4, 733-43 Abstract Language of Publication English Unique Identifier 94017594 Previous Article Return to original Article Click HERE to return to the main Neurology WebForum Homepage. These forums are maintained by the Department of Neurology at Massachusetts General Hospital John Lester - Webspinner

51. Krabbe Disease
adults. krabbe disease A short information sheet compiled by NINDS, the National Institute of Neurological Disorders and Stroke.
http://www.thenewhealthfind.com/Health/ConditionsandDiseases/NeurologicalDisorde
Directory Home Health Conditions and Diseases Neurological Disorders ... Leukodystrophy : Krabbe Disease (3)
    Krabbe's Family Network - The area most affected by this is the central nervous system. The CNS controls such things as Breathing, body temperature, and all other automatic body functions are controlled by the CNS. There are two types of Krabbe's. Most common is the infantile form. The second type affects children and adults. Krabbe Disease - A short information sheet compiled by NINDS, the National Institute of Neurological Disorders and Stroke. Hunter's Hope - Was formed in September 1997, after their infant son, Hunter, was diagnosed with Krabbe disease (Globoid-Cell Leukodystrophy). To date they have raised over two million dollars to further research on Krabbes and other Leukodystrophies.

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52. What Do You All Know About Krabbe Disease - Allnurses.com - Nursing Discussion B
ashleigh. Registered User. Join Date Mar 2004. Age 32. Posts 3. What do you all know about krabbe disease. Infants with krabbe disease are normal at birth.
http://allnurses.com/forums/showthread.php?t=62243

53. Krabbe Disease - A Medical Reference Article
krabbe disease. A Medical Article Maryland Medical Center. A resource with information on over 10,000 medical topics including krabbe disease.
http://www.mcadd.net/dwp/004040.htm
Krabbe disease
A Medical Article provided by University of Maryland Medical Center A resource with information on over 10,000 medical topics including: Krabbe disease Previous Next

54. Krabbe Disease
krabbe disease. This disease (also called globoid cell leucodystrophy) has an onset of 36 months with vague signs of irritability
http://www.sas-centre.org/genetic/genpages/lysstodiskrabbedisease.htm
Krabbe Disease This disease (also called globoid cell leucodystrophy) has an onset of 3-6 months with vague signs of irritability, hypersensitivity to slight stimuli and some joint stiffness. There is then rapid neurological degeneration with hypertonicity and, later, hypotonicity, blindness and deafness. A peripheral neuropathy is usually present. Symptoms are confined to the nervous system, there being no visceromegaly or skeletal changes. Patients with the classical presentation rarely survive beyond two years, but later onset cases with a more prolonged course are not uncommon. ENZYME TESTS : Deficiency of galactocerebrosidase is the primary defect.

55. NINDS Krabbe Disease Information Page
More about NINDS krabbe disease Information Page. Content for this page. NINDS krabbe disease Information Page. Synonym(s) Globoid Cell Leukodystrophy.
http://accessible.ninds.nih.gov/health_and_medical/disorders/krabbe_doc.htm
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    Synonym(s): Globoid Cell Leukodystrophy Reviewed 12-01-2003 Get Web page suited for printing
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    Table of Contents (click to jump to sections)
    What is Krabbe Disease?

    Is there any treatment?

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    What is Krabbe Disease?
    Is there any treatment?

    56. :: Ez2Find :: Krabbe Disease
    Guide krabbe disease, Global Metasearch Any Language Guides, krabbe disease. ez2Find Home Directory Health
    http://ez2find.com/cgi-bin/directory/meta/search.pl/Health/Conditions_and_Diseas
    Guide : Krabbe Disease Global Metasearch
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    ez2Find Home Directory Health Conditions and Diseases ... Leukodystrophy : Krabbe Disease
    Web Sites
    • Hunter's Hope Foundation [Site Info] [Translate] [Open New Window]
    • Formed in honor of infant son, Hunter, who was diagnosed with Krabbe disease (Globoid-Cell Leukodystrophy). Supports research on this and other leukodystrophies. Includes disease information, family registry, and other resources. URL: http://www.huntershope.org/

    57. The Health Library — Nutritional & Metabolic
    krabbe disease. krabbe diseaseNINDS. krabbe disease (Globoid Cell Leukodystrophy)United Leukodystrophy Foundation. krabbe diseaseHunter s Hope Foundation.
    http://healthlibrary.stanford.edu/resources/internet/bodysystems/nutrition5.html
    Diseases and Disorders
    Page 1
    Page 2 Page 3 Page 4 ... Page 7 Use these links to jump directly to your topic of interest: Nutrition: General Nutrition Caffeine Carbohydrates Fats ... Water Balance Nutritional Disease: Malnutrition Obesity Metabolic Disease: General Metabolic Disease A-F G-L M-O ... P-Z Metabolic Diseases (G - L) (Jump to: A B C D E F G H I J K L M N ... P Q R S T U V W X Y Z Galactosemia What Is Galactosemia:Parents of Galactosemic Children Galactosemia Information (Diet and Complications):Parents of Galactosemic Children Galactose-1-Phosphate Uridyltransferase Deficiency (Galactosemia):eMedicine Galactosemia:Save Babies Through Screening ... Galactosemia Survival Kit:Adult Metabolic Transition Project [for Young Adults] Galactosemia:Genetics Home Reference, NLM Galactosemia:GeneReviews Gaucher's Disease What is Gaucher Disease:National Gaucher Foundation Gaucher's Disease:Jewish Genetic Diseases Gaucher's Disease:NINDS Gaucher Disease Treatment Program:Mt. Sinai School of Medicine ... Gaucher Disease: Diagnosis and Treatment:University of Pittsburgh [PDF] Gaucher Disease:Genetics Home Reference, NLM

    58. Krabbe Disease And Leukodystrophies
    krabbe disease AND LEUKODYSTROPHIES HUNTER’S HOPE FOUNDATION. Hunter’s Hope Foundation supports research directly related to
    http://vpr2.admin.arizona.edu/rso/02020107.htm
    • Postdoctoral Fellowships - for investigators who are within 5 years of having received their doctoral degrees. Awards are $40,000 to $60,000 per year for 2 years.
      Pilot Studies - for the testing of new concepts or ideas. Awards are up to $30,000.
      Major Research Grants - for senior investigators conducting major research studies. Awards are up to $100,000 per year for 1 to 3 years.
    Contact: suzanne@huntershope.org Web: http://www.huntershope.org/ Deadline: 15 April, 15 September 2002. RSO Reference No.:

    59. WFTV.com - Health - Mother Helps Families Fight Krabbe Disease
    Mother Helps Families Fight krabbe disease. She lost her son, David, when he was 15 months old to a genetic disorder called krabbe disease.
    http://www.wftv.com/health/2075049/detail.html
    Search Make wftv.com Your Homepage Contact WFTV Sign up for E-News Local Experts ... Health Email This Story Print This Story // Set DC ad position if(typeof dcadposition == 'undefined')dcadposition = 1; else dcadposition++; document.write("");
    Mother Helps Families Fight Krabbe Disease
    Stem-Cell Transplants Offer Hope For Affected Children
    UPDATED: 12:52 p.m. EST March 31, 2003
    DURHAM, N.C. A mother who lost her son to a rare disease is on a mission to help other children have a chance at life. Kelly Brown's work is helping families all around the world. She lost her son, David, when he was 15 months old to a genetic disorder called Krabbe disease. The average lifespan for Krabbe patients is 13 months, doctors told Brown. David was diagnosed at 6 months old. "I knew it was a terminal illness, but didn't know much about it," said Brown. Children with Krabbe disease do not have an enzyme needed for brain development, which destroys their nervous systems. About 1 in 150,000 infants are diagnosed with the disease, according to the National Institutes of Health. Since her son's death, Brown has started working with Hunter's Hope, a foundation started by former NFL quarterback Jim Kelly, whose son, Hunter, also has Krabbe disease.

    60. Article : KRABBE DISEASE ; Author : H Singh ; Co-Author(s) : V Khanna, V Maurya,
    Letter to the Editor krabbe disease. Sir,. Finelli DA, Tarr RW, Sawyer RN. Deceptively normal MR in early infantile krabbe disease, AJNR 1994;15167171.
    http://www.ijri.org/articles/archives/2002-12-2/letter_298.htm
    Letter to the Editor
    KRABBE DISEASE

    Sir, Inherited leukodystrophies are neurodegenerative disorders that primarily involve the brain white matter. They are caused by genetic defects that result in the abnormal synthesis, maintenance or catabolism of CNS myelin. Those with an early infantile onset include Krabbe disease (KD) or globoid cell leukodystrophy (GLD), Pelizaeus Merzbacher disease, Canavan disease and Alexander disease. KD is a rare autosomal recessive disorder resulting from the deficiency of the lysosomal enzyme galactocerebrosidase (GALC) [1]. Diagnostic protocol in these cases includes cerebro-spinal fluid analysis, nerve conduction studies, neuroimaging and GALC assay in peripheral blood leukocytes or cultured skin fibroblasts. Fig.1 : Axial CT section at the level of the lateral ventricles shows symmetrical hyperdensities involving the caudate, thalami and optic radiation Fig.2: CT section at a higher ventricular level shows periventricular hyperdensities

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