WOS: 000183962100015PubMed ID: 12846696Metachromatic leukodystrophy is characterized by dysmyelination caused by a deficiency of arylsulfatase-A. In a 17-month-old boy with metachromatic leukodystrophy, an echo-planar diffusion MR sequence revealed a restricted diffusion pattern in the deep white matter, manifested by high-signal on b = 1000 s/mm(2) images, and low ADC values (0.56 x 10(-3) mm(2)/s). Proton MR spectroscopy revealed a marked decrease in choline, a metabolite related to myelin turnover. These observations consisting of a restricted diffusion pattern on diffusion MR imaging, and decreased choline peaks on proton spectroscopy, likely represented dysmyelination in metachromatic leukodystrophy
BACKGROUND AND PURPOSE: Sjogren-Larsson syndrome (SLS) is a neurocutaneous syndrome caused by a gene...
boy that was diagnosed when the patient was 34 months old. The patient presented clinically with meg...
We aimed to gain more insight into the pathomechanisms of metachromatic leukodystrophy (MLD), by com...
WOS: 000183962100015PubMed ID: 12846696Metachromatic leukodystrophy is characterized by dysmyelinati...
PubMed ID: 12846696Metachromatic leukodystrophy is characterized by dysmyelination caused by a defic...
WOS: 000178052100030PubMed ID: 12223391Herein the case of a 10-month-old boy, with metachromatic leu...
Summary: Herein the case of a 10-month-old boy with metachromatic leukodystrophy is reported. Diffus...
Leukodystrophies encompass a wide spectrum of inherited neurodegenerative disorders affecting white ...
WOS: 000220339800007PubMed ID: 15094651A 5-year-old boy is reported with genetically confirmed Peliz...
Dysmyelinating diseases, or leukodystrophies, encompass a wide spectrum of inherited neurodegenerati...
BACKGROUND AND PURPOSE: Childhood white matter disorders often show similar MR imaging signal-intens...
AbstractObjectiveTo analyze MR Spectroscopic findings and metabolite ratios in regions of abnormal s...
WOS: 000178252300011PubMed ID: 12380485An 8-year-old boy with the intermediate variant of maple syru...
BACKGROUND AND PURPOSE: Sjögren-Larsson syndrome (SLS) is a neurocutaneous syndrome caused by a gene...
BACKGROUND AND PURPOSE: Sjögren-Larsson syndrome (SLS) is a neurocutaneous syndrome caused by a gen...
BACKGROUND AND PURPOSE: Sjogren-Larsson syndrome (SLS) is a neurocutaneous syndrome caused by a gene...
boy that was diagnosed when the patient was 34 months old. The patient presented clinically with meg...
We aimed to gain more insight into the pathomechanisms of metachromatic leukodystrophy (MLD), by com...
WOS: 000183962100015PubMed ID: 12846696Metachromatic leukodystrophy is characterized by dysmyelinati...
PubMed ID: 12846696Metachromatic leukodystrophy is characterized by dysmyelination caused by a defic...
WOS: 000178052100030PubMed ID: 12223391Herein the case of a 10-month-old boy, with metachromatic leu...
Summary: Herein the case of a 10-month-old boy with metachromatic leukodystrophy is reported. Diffus...
Leukodystrophies encompass a wide spectrum of inherited neurodegenerative disorders affecting white ...
WOS: 000220339800007PubMed ID: 15094651A 5-year-old boy is reported with genetically confirmed Peliz...
Dysmyelinating diseases, or leukodystrophies, encompass a wide spectrum of inherited neurodegenerati...
BACKGROUND AND PURPOSE: Childhood white matter disorders often show similar MR imaging signal-intens...
AbstractObjectiveTo analyze MR Spectroscopic findings and metabolite ratios in regions of abnormal s...
WOS: 000178252300011PubMed ID: 12380485An 8-year-old boy with the intermediate variant of maple syru...
BACKGROUND AND PURPOSE: Sjögren-Larsson syndrome (SLS) is a neurocutaneous syndrome caused by a gene...
BACKGROUND AND PURPOSE: Sjögren-Larsson syndrome (SLS) is a neurocutaneous syndrome caused by a gen...
BACKGROUND AND PURPOSE: Sjogren-Larsson syndrome (SLS) is a neurocutaneous syndrome caused by a gene...
boy that was diagnosed when the patient was 34 months old. The patient presented clinically with meg...
We aimed to gain more insight into the pathomechanisms of metachromatic leukodystrophy (MLD), by com...