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         Neuronal Ceroid Lipofuscinosis:     more detail
  1. Lysosomal Storage Diseases: Tay-Sachs Disease, Canavan Disease, Sly Syndrome, Neuronal Ceroid Lipofuscinosis, Mucopolysaccharidosis
  2. The dissection of a degenerative disease: Proceedings of four round-table conferences on the pathogenesis of Batten's disease (neuronal ceroid-lipofuscinosis)
  3. Lipofuscin and Ceroid Pigments (Advances in Experimental Medicine and Biology)
  4. Batten Disease: Diagnosis, Treatment, and Research, Volume 45 (Advances in Genetics)
  5. The Official Parent's Sourcebook on Batten Disease: A Revised and Updated Directory for the Internet Age by Icon Health Publications, 2002-11-18
  6. Lipofuscin and Ceroid Pigments: State of the Art 1995 (Journal - Gerontology, , Vol 41, Suppl. 2) (Pt.2)
  7. Dogs help track down genes.(MEDICAL UPDATE: Cutting-edge news from a source you can trust)(Batten disease): An article from: Saturday Evening Post
  8. Batten disease: An entry from Thomson Gale's <i>Gale Encyclopedia of Neurological Disorders</i> by Michelle lee Brandt, Rosalyn, MD Carson-Dewitt, 2005
  9. Batten disease: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Michelle Brandt, 2005
  10. Batten disease (SuDoc HE 20.3502:B 32) by U.S. Dept of Health and Human Services, 1992

81. Short Description Of Cell Lines. Pathology: Neuronal Ceroid-lipofuscinosis Infan
Version 4.200205, Short description of cell lines. Pathology neuronal ceroidlipofuscinosis infantile Finnish type 256730 OMIM record.
http://www.biotech.ist.unige.it/cldb/pat134.html
Version
Short description of cell lines.
Pathology: neuronal ceroid-lipofuscinosis infantile Finnish type
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
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human, Caucasian
skin, fibroblast GEIMM
By Beatrice...

82. ORPHANET® Ceroid Lipofuscinosis, Neuronal
ORPHANET. Orphanet database access. ceroid lipofuscinosis, neuronal. Direct access to data Alias Batten disease, infantile (ceroid
http://www.orpha.net/static/GB/ceroidlipofuscinosis.html

83. Orthoguide.com Neuronal Ceroid-Lipofuscinosis
Search results for neuronal ceroidlipofuscinosis . NO MATCHES FOUND-Please select a different keyword or category OR. Search AltaVista
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84. NEURORETINAL
Juvenile neuronal ceroidlipofuscinosis, or Batten disease, is a form of neuronal ceroid-lipofuscinosis that is characterized by onset of neuroretinal symptoms
http://mind-brain.com/abstracts.php?qa=neuroretinal

85. REFINED GENETIC-MAPPING OF JUVENILE-ONSET NEURONAL CEROID-LIPOFUSCINOSIS ON CHRO
Detailed Record. Journal Title REFINED GENETICMAPPING OF JUVENILE-ONSET neuronal ceroid-lipofuscinosis ON CHROMOSOME-16. Author(s
http://www.genome.uci.edu/journalview.asp?num=65

86. The Neuronal Ceroid-Lipofuscinoses
The neuronal ceroidLipofuscinoses. Key Words Batten disease; Cell biology; Classification; Genetics; neuronal ceroid-lipofuscinosis; Pathogenesis; Pathology.
http://neur.allenpress.com/neuronline/?request=get-abstract&issn=0022-3069&volum

87. Entrez PubMed
neuronal ceroidlipofuscinoses in childhood. Child; Child, Preschool; Human; Infant; neuronal ceroid-lipofuscinosis/classification*;
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Abstra

88. OMIM - CEROID LIPOFUSCINOSIS, NEURONAL 8; CLN8

http://www3.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600143

89. The Neuronal Ceroid-Lipofuscinoses
The neuronal ceroidLipofuscinoses. Keywords Batten disease, Cell biology, Classification, Genetics, neuronal ceroid-lipofuscinosis, Pathogenesis, Pathology.
http://apt.allenpress.com/aptonline/?request=get-abstract&issn=0022-3069&volume=

90. Clinical Science (1986) 71, 57-60 - Marklund SL And Others - Superoxide Dismutas
It was recently shown that cerebrospinal fluid from patients with infantile and juvenile neuronal ceroidlipofuscinosis were less protective against superoxide
http://www.clinsci.org/cs/071/cs0710057.htm
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Clinical Science (1986) (Printed in Great Britain)
Superoxide dismutase isoenzymes in cerebrospinal fluid and plasma from patients with neuronal ceroid-lipofuscinoses. Marklund SL, Heiskala H, Westermarck T, Santavuori P
The neuronal ceroid-lipofuscinoses is a group of diseases characterized by a widespread accumulation in the body of pigments believed to be end-products of lipid-peroxidation damaged organelles. It was recently shown that cerebrospinal fluid from patients with infantile and juvenile neuronal ceroid-lipofuscinosis were less protective against superoxide radical-induced hydroxyl radical formation compared with controls. The content of superoxide dismutase isoenzymes in cerebrospinal fluid and in plasma from patients with different forms of neuronal ceroid-lipofuscinosis was analysed. No significant difference from controls could be demonstrated in samples from patients with juvenile neuronal ceroid-lipofuscinosis. The few samples from patients with infantile and late infantile neuronal ceroid-lipofuscinosis analysed all fell within the range defined by the controls.
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91. MedlinePlus Medical Encyclopedia: Neuronal Ceroid Lipofuscinoses (NCLS)
neuronal ceroid lipofuscinoses (NCLS). The neuronal ceroid lipofuscinoses (NCLS) are a group of rare, inherited neurodegenerative disorders.
http://www.nlm.nih.gov/medlineplus/ency/article/001613.htm
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Neuronal ceroid lipofuscinoses (NCLS)
Contents of this page: Alternative names Lipofuscinoses; Batten disease; Jansky-Bielschowsky; Kufs' disease; Spielmeyer-Vogt Definition Return to top The neuronal ceroid lipofuscinoses (NCLS) are a group of rare, inherited neurodegenerative disorders. They associated with the accumulation of an abnormal pigment in the brain called lipofuscin. These disorders can be associated with severe diseases including blindness, mental retardation, and early death. There are three main types, depending on the age it begins late infantile (Jansky-Bielschowsky), juvenile (Batten disease), and adult (Kufs or Parry's disease). Causes, incidence, and risk factors Return to top Lipofuscin is the generic name of an abnormal pigment that builds up in brain cells in this group of diseases. It is a consequence of, and marker for, the disease rather than the cause of the problem. The genetic bases of multiple types of this disease are now known, but evidence indicates that there are problems in the ability of brain cells to remove and recycle brain proteins. The disorder may be evident at birth. More commonly it is diagnosed some time after the second year of life, in the teens, or as an adult. Children develop muscle incoordination (

92. Redirect

http://www.ncbi.nlm.nih.gov/htbin-post/Omim/dispmim?204500

93. Redirect

http://www.ncbi.nlm.nih.gov/htbin-post/Omim/dispmim?204200

94. Deutsches Ärzteblatt: Archiv

http://www.aerzteblatt.de/v4/archiv/lit.asp?id=8614

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