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福岡・大牟田の浸水4mに、防災科研解析…「線状降水帯」相次いで発生 (読売新聞)

防災科学技術研究所(茨城県つくば市)は6日夜、九州北部の大雨で、福岡県大牟田市では浸水の深さが少なくとも4メートルに達したとの解析結果を発表した。 防災科研は、...

  1. [企業] Dragonfly社が5500...
  2. コロナ 3か月以上闘病の米 俳優が死去
  3. 障害者雇用に関する優良な中小事業主に対す...
  4. 新型コロナウイルスに関連した患者等の発生...

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「"Salsano E "[Author]」の検索結果

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Asymptomatic adrenoleukodystrophy in elderly males.

Severe worsening of adult-onset Alexander disease after minor head trauma: Report of two patients and review of the literature.

-related disease is associated with central pontine calcifications and atypical parkinsonism.

Triheptanoin Supplementation Does not Affect Nutritional Status: A Case Report of Two Siblings With Adult Polyglucosan Body Disease.

The first case of the p.G294V mutation in a homozygous state: is a single pathogenic allele sufficient to cause ALS?

RARS1-related hypomyelinating leukodystrophy: Expanding the spectrum.

Leukoencephalopathy With Predominant Infratentorial Involvement Caused by a Novel ABCD1 Mutation: Does the Spinocerebellar Variant of Adrenoleukodystrophy Exist?

From congenital microcephaly to adult onset cerebellar ataxia: Distinct and overlapping phenotypes in patients with PNKP gene mutations.

Novel mutations in SLC16A2 associated with a less severe phenotype of MCT8 deficiency.

Saposin B deficiency as a cause of adult-onset metachromatic leukodystrophy.

Neuropsychological features of adult form of Alexander disease.

Longitudinal quantitative MRI in adrenomyeloneuropathy.

Biopsy-proven primary angiitis of the central nervous system mimicking leukodystrophy: A case report and review of the literature.

Spinal cord involvement in adult-onset metabolic and genetic diseases.

Primary brain calcification: an international study reporting novel variants and associated phenotypes.

Metachromatic Leukodystrophy: Too Frequent (Mis)Diagnosis?

Frontotemporal Dementia and Chorea associated with a Compound Heterozygous TREM2 Mutation.

Adult leukoencephalopathies with prominent infratentorial involvement can be caused by Erdheim-Chester disease.

Posterior column ataxia with retinitis pigmentosa coexisting with sensory-autonomic neuropathy and leukemia due to the homozygous p.Pro221Ser FLVCR1 mutation.

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