Literature DB >> 22422211

Leukoencephalopathies in adulthood.

Jan-Mendelt Tillema1, Deborah L Renaud.   

Abstract

The understanding of the genetic basis of late-onset leukoencephalopathies has continued to increase in recent years. The most commonly presenting leukoencephalopathies in adulthood can be late-onset manifestations of metabolic pathways. The understanding of these diagnoses is crucial to the evaluation of adult patients presenting with leukoencephalopathies. The authors provide an overview of the common leukoencephalopathies in adulthood, the current understanding of the pathology, and genetics of these disorders with typical imaging findings. When available, treatment options will be discussed. Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

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Year:  2012        PMID: 22422211     DOI: 10.1055/s-0032-1306391

Source DB:  PubMed          Journal:  Semin Neurol        ISSN: 0271-8235            Impact factor:   3.420


  5 in total

Review 1.  Small vessel disease and memory loss: what the clinician needs to know to preserve patients' brain health.

Authors:  Christian Schenk; Timothy Wuerz; Alan J Lerner
Journal:  Curr Cardiol Rep       Date:  2013-12       Impact factor: 2.931

2.  Impaired information-processing speed and working memory in leukoencephalopathy with brainstem and spinal cord involvement and elevated lactate (LBSL) and DARS2 mutations: a report of three adult patients.

Authors:  Mika H Martikainen; Ulla Ellfolk; Kari Majamaa
Journal:  J Neurol       Date:  2013-05-08       Impact factor: 4.849

3.  Case records of the Massachusetts General Hospital. Case 9-2015. A 31-year-old man with personality changes and progressive neurologic decline.

Authors:  Bruce L Miller; Bradford C Dickerson; Diane E Lucente; Mykol Larvie; Matthew P Frosch
Journal:  N Engl J Med       Date:  2015-03-19       Impact factor: 91.245

Review 4.  A Clinical Approach to the Differential Diagnosis of Multiple Sclerosis.

Authors:  Michel Toledano; Brian G Weinshenker; Andrew J Solomon
Journal:  Curr Neurol Neurosci Rep       Date:  2015-08       Impact factor: 6.030

5.  Case Report: A Homozygous Mutation (p.Y62X) of Phospholipase D3 May Lead to a New Leukoencephalopathy Syndrome.

Authors:  Yi-Hui Liu; Hai-Feng Zhang; Jie-Yuan Jin; Yan-Qiu Wei; Chen-Yu Wang; Liang-Liang Fan; Lv Liu
Journal:  Front Aging Neurosci       Date:  2021-06-29       Impact factor: 5.750

  5 in total

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