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Volumn 32, Issue 1, 2012, Pages 3-8
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Inherited leukoencephalopathies
a
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Author keywords
[No Author keywords available]
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Indexed keywords
ABC TRANSPORTER;
ALDEHYDE DEHYDROGENASE;
ALPHA LEVO FUCOSIDASE;
ASPARTOACYLASE;
BETA GALACTOSIDASE;
BETA N ACETYLHEXOSAMINIDASE A;
BIOTINIDASE;
CEREBROSIDE SULFATASE;
CONNEXIN 43;
CONNEXIN 46;
DIHYDROXYACETONE PHOSPHATE ACYLTRANSFERASE;
DNA DIRECTED DNA POLYMERASE GAMMA;
FOLATE RECEPTOR 1;
FRAGILE X MENTAL RETARDATION PROTEIN;
GALACTOSYLCERAMIDASE;
GLIAL FIBRILLARY ACIDIC PROTEIN;
GLUTARYL COENZYME A DEHYDROGENASE;
NOTCH RECEPTOR;
PEROXIN;
PHENYLALANINE 4 MONOOXYGENASE;
SPECTRIN;
SPHINGOLIPID ACTIVATOR PROTEIN;
STEROL 27 HYDROXYLASE;
THYMIDINE PHOSPHORYLASE;
ADRENOLEUKODYSTROPHY;
AICARDI GOUTIERES SYNDROME;
ALEXANDER DISEASE;
AUTOSOMAL DOMINANT INHERITANCE;
AUTOSOMAL RECESSIVE INHERITANCE;
BIOTINIDASE DEFICIENCY;
CADASIL;
CANAVAN DISEASE;
CEREBROTENDINOUS XANTHOMATOSIS;
CHONDRODYSPLASIA PUNCTATA;
COCKAYNE SYNDROME;
DIFFERENTIAL DIAGNOSIS;
EDITORIAL;
FABRY DISEASE;
FOLIC ACID DEFICIENCY;
FRAGILE X SYNDROME;
FUCOSIDOSIS;
GENETIC DISORDER;
GLOBOID CELL LEUKODYSTROPHY;
GM1 GANGLIOSIDOSIS;
GM2 GANGLIOSIDOSIS;
HUMAN;
INHERITANCE;
KLINEFELTER SYNDROME;
LEUKOENCEPHALOPATHY;
MACROCEPHALY;
METACHROMATIC LEUKODYSTROPHY;
MNGIE SYNDROME;
MUCOLIPIDOSIS;
MULTIPLE ACYL COA DEHYDROGENASE DEFICIENCY;
MULTIPLE SULFATASE DEFICIENCY;
MYELINATION;
NUCLEAR MAGNETIC RESONANCE IMAGING;
OCULODENTODIGITAL SYNDROME;
PELIZAEUS MERZBACHER DISEASE;
PHENYLKETONURIA;
PRIORITY JOURNAL;
RESPIRATORY CHAIN;
SIALIC ACID STORAGE DISEASE;
SJOEGREN LARSSON SYNDROME;
SPASTIC PARAPLEGIA;
TAY SACHS DISEASE;
WEST SYNDROME;
WHITE MATTER;
X CHROMOSOMAL INHERITANCE;
ZELLWEGER SYNDROME;
BRAIN DISEASES, METABOLIC;
HEREDITARY CENTRAL NERVOUS SYSTEM DEMYELINATING DISEASES;
HUMANS;
LEUKOENCEPHALOPATHIES;
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EID: 84858126742
PISSN: 02718235
EISSN: 10989021
Source Type: Journal
DOI: 10.1055/s-0032-1306380 Document Type: Editorial |
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Times cited : (7)
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References (0)
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