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Volumn 32, Issue 1, 2001, Pages 45-48
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MRI and proton spectroscopy in Lowe syndrome
a a a a a |
Author keywords
Lowe syndrome; Magnetic resonance spectroscopy; Metabolic disease; MRI; MRS; Myo inositol; OCRL; Oculocerebrorenal syndrome; Phosphatidylinositol 4,5 biphosphate; White matter disease
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Indexed keywords
PHOSPHATIDYLINOSITOL 4,5 BISPHOSPHATE;
ARTICLE;
BRAIN CYST;
CASE REPORT;
CATARACT EXTRACTION;
CLINICAL FEATURE;
CONGENITAL CATARACT;
DIAGNOSTIC IMAGING;
DIFFERENTIAL DIAGNOSIS;
DISEASE COURSE;
GROWTH RETARDATION;
HUMAN;
INFANT;
KIDNEY DISEASE;
LOWE SYNDROME;
MALE;
METABOLIC DISORDER;
NUCLEAR MAGNETIC RESONANCE IMAGING;
PRIORITY JOURNAL;
PROTEIN DEGRADATION;
PROTON NUCLEAR MAGNETIC RESONANCE;
PSYCHOMOTOR DEVELOPMENT;
SIGNAL DETECTION;
WHITE MATTER;
X CHROMOSOME RECESSIVE INHERITANCE;
BRAIN;
CEREBRAL VENTRICLES;
CHILD;
CHILD, PRESCHOOL;
CYSTS;
DIAGNOSIS, DIFFERENTIAL;
FOLLOW-UP STUDIES;
HUMANS;
INFANT;
INOSITOL;
LINKAGE (GENETICS);
MAGNETIC RESONANCE IMAGING;
MAGNETIC RESONANCE SPECTROSCOPY;
MALE;
OCULOCEREBRORENAL SYNDROME;
PHOSPHATIDYLINOSITOL 4,5-DIPHOSPHATE;
SEX CHROMOSOME ABERRATIONS;
X CHROMOSOME;
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EID: 0035072052
PISSN: 0174304X
EISSN: None
Source Type: Journal
DOI: 10.1055/s-2001-12221 Document Type: Article |
Times cited : (34)
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References (19)
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