Hearing profile and MRI myelination of auditory pathway in Pelizaeus-Merzbacher disease.

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Loss of central auditory processing in a mouse model of Canavan disease.Modeling the natural history of Pelizaeus-Merzbacher disease.

P2860

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P2860

Hearing profile and MRI myelination of auditory pathway in Pelizaeus-Merzbacher disease.

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2008 nî lūn-bûn

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2008年の論文

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年學術文章

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Hearing profile and MRI myelination of auditory pathway in Pelizaeus-Merzbacher disease.

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Hearing profile and MRI myelination of auditory pathway in Pelizaeus-Merzbacher disease.

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type

Item

label

Hearing profile and MRI myelination of auditory pathway in Pelizaeus-Merzbacher disease.

@en

Hearing profile and MRI myelination of auditory pathway in Pelizaeus-Merzbacher disease.

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Hearing profile and MRI myelination of auditory pathway in Pelizaeus-Merzbacher disease.

@en

Hearing profile and MRI myelination of auditory pathway in Pelizaeus-Merzbacher disease.

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P1476

Hearing profile and MRI myelination of auditory pathway in Pelizaeus-Merzbacher disease.

@en

P2093

Chen-Chieh Kuan

http://www.w3.org/2001/XMLSchema#string

Kazuo Kodama

http://www.w3.org/2001/XMLSchema#string

Kimitaka Kaga

http://www.w3.org/2001/XMLSchema#string

Mariko Kodama

http://www.w3.org/2001/XMLSchema#string

Masaki Sano

http://www.w3.org/2001/XMLSchema#string

P2860

A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.

Three young adult patients with Pelizaeus-Merzbacher disease who showed only waves I and II in auditory brainstem responses but had good auditory perception.

Developmental features of the brain in preterm and fullterm infants on MR imaging.

Evidence for neuroaxonal injury in patients with proteolipid protein gene mutations.

Normal maturation of the neonatal and infant brain: MR imaging at 1.5 T.

Absence of later auditory brain stem response components, congenital horizontal nystagmus, and hypotonia in male infants.

Unusual clinical and magnetic resonance imaging findings in a family with proteolipid protein gene mutation.

An MRI and MRS study of Pelizaeus-Merzbacher disease.

Neurophysiological study in Pelizaeus-Merzbacher disease.

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539-546

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scholarly article

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10.1080/00016480701258713

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English

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128

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2008-05-01T00:00:00Z

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P698

18421608

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Hearing profile and MRI myelination of auditory pathway in Pelizaeus-Merzbacher disease.

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P2860

P2860

Hearing profile and MRI myelination of auditory pathway in Pelizaeus-Merzbacher disease.

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P1433

P1476

P2093

P2860

P304

P31

P356

P407

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P478

P577

P698

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P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

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P698