Literature DB >> 7608680

Motor neuron disease (amyotrophic lateral sclerosis) arising from longstanding primary lateral sclerosis.

R P Bruyn1, J H Koelman, D Troost, J M de Jong.   

Abstract

Three men were initially diagnosed as having primary lateral sclerosis (PLS), but eventually developed amyotrophic lateral sclerosis (ALS) after 7.5, 9, and at least 27 years. Non-familial ALS and PLS might be different manifestations of a single disease or constitute completely distinct entities. The clinical diagnosis of PLS predicts a median survival that is four to five times longer than in ALS.

Entities:  

Mesh：

Year:  1995        PMID： 7608680      PMCID： PMC1073559          DOI： 10.1136/jnnp.58.6.742

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN： 0022-3050            Impact factor:   10.154


  13 in total

1.  Encephalomyelitis induced by a white matter fraction.

Authors:  F HULCHER; E V SPUDIS; M G NETSKY
Journal:  Arch Neurol       Date:  1963-01

2.  Abnormal sensory evoked potentials in amyotrophic lateral sclerosis.

Authors:  R A Radtke; A Erwin; C W Erwin
Journal:  Neurology       Date:  1986-06       Impact factor: 9.910

3.  The central nervous system in motor neurone disease.

Authors:  B Brownell; D R Oppenheimer; J T Hughes
Journal:  J Neurol Neurosurg Psychiatry       Date:  1970-06       Impact factor: 10.154

4.  Primary lateral sclerosis. A clinical diagnosis reemerges.

Authors:  D S Younger; S Chou; A P Hays; D J Lange; R Emerson; M Brin; H Thompson; L P Rowland
Journal:  Arch Neurol       Date:  1988-12

5.  Pure spastic paralysis of corticospinal origin.

Authors:  C M Fisher
Journal:  Can J Neurol Sci       Date:  1977-11       Impact factor: 2.104

6.  Primary lateral sclerosis. Clinical features, neuropathology and diagnostic criteria.

Authors:  C E Pringle; A J Hudson; D G Munoz; J A Kiernan; W F Brown; G C Ebers
Journal:  Brain       Date:  1992-04       Impact factor: 13.501

7.  Detection of p53 overexpression in routinely paraffin-embedded tissue of human carcinomas using a novel target unmasking fluid.

Authors:  F M van den Berg; I O Baas; M M Polak; G J Offerhaus
Journal:  Am J Pathol       Date:  1993-02       Impact factor: 4.307

8.  Primary lateral sclerosis: a case report.

Authors:  M F Beal; E P Richardson
Journal:  Arch Neurol       Date:  1981-10

9.  Spastic paraplegia-paraparesis. A reappraisal.

Authors:  J Y Ungar-Sargon; R E Lovelace; J C Brust
Journal:  J Neurol Sci       Date:  1980-04       Impact factor: 3.181

10.  Duration of amyotrophic lateral sclerosis is age dependent.

Authors:  A Eisen; M Schulzer; M MacNeil; B Pant; E Mak
Journal:  Muscle Nerve       Date:  1993-01       Impact factor: 3.217
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  6 in total

1.  High T2 signal in primary lateral sclerosis supports the topographic distribution of fibers in the corpus callosum: assessing disease in the primary motor segment.

Authors:  S M Riad; H Hathout; J C Huang
Journal:  AJNR Am J Neuroradiol       Date:  2010-03-18       Impact factor: 3.825

Review 2.  Primary Lateral Sclerosis.

Authors:  Jeffrey M Statland; Richard J Barohn; Mazen M Dimachkie; Mary Kay Floeter; Hiroshi Mitsumoto
Journal:  Neurol Clin       Date:  2015-09-08       Impact factor: 3.806

3.  Primary lateral sclerosis: clinical, neurophysiological, and magnetic resonance findings.

Authors:  J Kuipers-Upmeijer; A E de Jager; J M Hew; J W Snoek; T W van Weerden
Journal:  J Neurol Neurosurg Psychiatry       Date:  2001-11       Impact factor: 10.154

4.  Natural History of "Pure" Primary Lateral Sclerosis.

Authors:  Anhar Hassan; Shivam Om Mittal; William T Hu; Keith A Josephs; Eric J Sorenson; J Eric Ahlskog
Journal:  Neurology       Date:  2021-02-26       Impact factor: 9.910

5.  Investigation of white matter pathology in ALS and PLS using tract-based spatial statistics.

Authors:  Olga Ciccarelli; Timothy E Behrens; Heidi Johansen-Berg; Kevin Talbot; Richard W Orrell; Robin S Howard; Rita G Nunes; David H Miller; Paul M Matthews; Alan J Thompson; Stephen M Smith
Journal:  Hum Brain Mapp       Date:  2009-02       Impact factor: 5.038

Review 6.  Upper Motor Neuron Disorders: Primary Lateral Sclerosis, Upper Motor Neuron Dominant Amyotrophic Lateral Sclerosis, and Hereditary Spastic Paraplegia.

Authors:  Timothy Fullam; Jeffrey Statland
Journal:  Brain Sci       Date:  2021-05-11
  6 in total

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