WOS: 000220339800007PubMed ID: 15094651A 5-year-old boy is reported with genetically confirmed Pelizaeus-Merzbacher disease. On chemical-shift spectroscopic imaging choline (Cho) peaks were prominently decreased in the white matter resulting. in markedly high NAA/Cho ratios, and low Cho/Cr ratios, compared to five control cases. Low Cho levels could be indicative of the dysmyelinating disorder in the disease. On b = 1000 s/mm(2) images of diffusion MRI, a tigroid pattern was evident, and there was no apparent signal abnormality. However, on ADC maps high signal and high ADC values were evident in the white matter ranging from 1.16 to 1.52 X 10(-3) mm(2)/s, compared to the ADC values of nine control cases, consistent with some disintegration...
PubMed ID: 15891499In a 5-month-old boy with tyrosinemia, computed tomography revealed diffuse hypod...
WOS: 000229458400008PubMed ID: 15891499In a 5-month-old boy with tyrosinemia, computed tomography re...
Background: Classic Pelizaeus-Merzbacher disease is a rare x-linked disorder of proteolipid protein ...
Pelizaeus-Merzbacher disease is a rare disease of infants and young children in which there is an ar...
BACKGROUND AND PURPOSE: Pelizeaus-Merzbacher disease (PMD) is a clinically and molecularly heterogen...
MR imaging was performed in five members of a family afflicted with Pelizaeus-Merzbacher disease. Th...
WOS: 000183962100015PubMed ID: 12846696Metachromatic leukodystrophy is characterized by dysmyelinati...
PubMed ID: 12846696Metachromatic leukodystrophy is characterized by dysmyelination caused by a defic...
In questo articolo vengono discussi gli aspetti clinici , evolutivi, genetici e neuroradiologici del...
Background: Classic Pelizaeus-Merzbacher disease is a rare x-linked disorder of proteolipid protein ...
WOS: 000178052100030PubMed ID: 12223391Herein the case of a 10-month-old boy, with metachromatic leu...
WOS: 000178252300011PubMed ID: 12380485An 8-year-old boy with the intermediate variant of maple syru...
WOS: 000184528200015PubMed ID: 12886139We report about a boy with nonketotic hyperglycinemia who was...
Summary: Herein the case of a 10-month-old boy with metachromatic leukodystrophy is reported. Diffus...
PubMed ID: 12886139We report about a boy with nonketotic hyperglycinemia who was studied at 15 days ...
PubMed ID: 15891499In a 5-month-old boy with tyrosinemia, computed tomography revealed diffuse hypod...
WOS: 000229458400008PubMed ID: 15891499In a 5-month-old boy with tyrosinemia, computed tomography re...
Background: Classic Pelizaeus-Merzbacher disease is a rare x-linked disorder of proteolipid protein ...
Pelizaeus-Merzbacher disease is a rare disease of infants and young children in which there is an ar...
BACKGROUND AND PURPOSE: Pelizeaus-Merzbacher disease (PMD) is a clinically and molecularly heterogen...
MR imaging was performed in five members of a family afflicted with Pelizaeus-Merzbacher disease. Th...
WOS: 000183962100015PubMed ID: 12846696Metachromatic leukodystrophy is characterized by dysmyelinati...
PubMed ID: 12846696Metachromatic leukodystrophy is characterized by dysmyelination caused by a defic...
In questo articolo vengono discussi gli aspetti clinici , evolutivi, genetici e neuroradiologici del...
Background: Classic Pelizaeus-Merzbacher disease is a rare x-linked disorder of proteolipid protein ...
WOS: 000178052100030PubMed ID: 12223391Herein the case of a 10-month-old boy, with metachromatic leu...
WOS: 000178252300011PubMed ID: 12380485An 8-year-old boy with the intermediate variant of maple syru...
WOS: 000184528200015PubMed ID: 12886139We report about a boy with nonketotic hyperglycinemia who was...
Summary: Herein the case of a 10-month-old boy with metachromatic leukodystrophy is reported. Diffus...
PubMed ID: 12886139We report about a boy with nonketotic hyperglycinemia who was studied at 15 days ...
PubMed ID: 15891499In a 5-month-old boy with tyrosinemia, computed tomography revealed diffuse hypod...
WOS: 000229458400008PubMed ID: 15891499In a 5-month-old boy with tyrosinemia, computed tomography re...
Background: Classic Pelizaeus-Merzbacher disease is a rare x-linked disorder of proteolipid protein ...