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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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「"Pareyson D "[Author]」の検索結果

256件中 1件~20件表示    検索結果をPubMedで見る PubMedで見る

Validation of the Italian version of the Charcot-Marie-Tooth Health Index.

Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes.

Validation of the Italian Version of the Charcot-Marie-Tooth disease Pediatric Scale.

Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes.

Charcot-Marie-Tooth Type 2B: A New Phenotype Associated with a Novel Mutation and Inhibited EGFR Degradation.

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.

ATPase domain AFG3L2 mutations alter OPA1 processing and cause Optic Neuropathy.

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

Discovering the Italian phenotype of cerebral amyloid angiopathy (CAA): the SENECA project.

A longitudinal study of CMT1A using Rasch analysis based CMT neuropathy and examination scores.

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

Treadmill training in people affected by Charcot-Marie-Tooth (CMT) neuropathy: results of a multicenter, prospective, randomized, single blind, controlled study.

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

Mutation update for myelin protein zero-related neuropathies and the increasing role of variants causing a late-onset phenotype.

Expanding the spectrum of genes responsible for hereditary motor neuropathies.

A multicentre retrospective study of Charcot-Marie-Tooth disease type 4B (CMT4B) due to mutations in Myotubularin-related proteins (MTMRs).

Neuropsychological features of adult form of Alexander disease.

Balance Impairment in Pediatric Charcot-Marie-Tooth Disease.

Hereditary neuropathy with liability to pressure palsies.

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