Literature DB >> 26515619

Primary Lateral Sclerosis.

Jeffrey M Statland1, Richard J Barohn2, Mazen M Dimachkie2, Mary Kay Floeter3, Hiroshi Mitsumoto4.   

Abstract

Primary lateral sclerosis is characterized by insidious onset of progressive upper motor neuron dysfunction in the absence of clinical signs of lower motor neuron involvement. Patients experience stiffness; decreased balance and coordination; mild weakness; and, if the bulbar region is affected, difficulty speaking and swallowing, and emotional lability. The diagnosis is made based on clinical history, typical examination findings, and diagnostic testing negative for other causes of upper motor neuron dysfunction. Electromyogram is normal, or only shows mild neurogenic findings in a few muscles, not meeting El Escorial criteria. Treatment is largely supportive.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Motor neuron disease; Neuroimaging; Primary lateral sclerosis; Pseudobulbar affect; Spastic quadriparesis; Upper motor neuron disease

Mesh:

Year:  2015        PMID: 26515619      PMCID: PMC4628724          DOI: 10.1016/j.ncl.2015.07.007

Source DB:  PubMed          Journal:  Neurol Clin        ISSN: 0733-8619            Impact factor:   3.806


  45 in total

1.  Neuroanatomical patterns of cerebral white matter involvement in different motor neuron diseases as studied by diffusion tensor imaging analysis.

Authors:  Hans-Peter Müller; Alexander Unrath; Hans-Jürgen Huppertz; Albert C Ludolph; Jan Kassubek
Journal:  Amyotroph Lateral Scler       Date:  2012-03-13

Review 2.  Primary lateral sclerosis, hereditary spastic paraplegia, and mutations in the alsin gene: historical background for the first International Conference.

Authors:  Lewis P Rowland
Journal:  Amyotroph Lateral Scler Other Motor Neuron Disord       Date:  2005-06

3.  Primary lateral sclerosis: A heterogeneous disorder composed of different subtypes?

Authors:  P Zhai; F Pagan; J Statland; J A Butman; M K Floeter
Journal:  Neurology       Date:  2003-04-22       Impact factor: 9.910

4.  Motor neuron firing dysfunction in spastic patients with primary lateral sclerosis.

Authors:  Mary Kay Floeter; Ping Zhai; Rajiv Saigal; Yongkyun Kim; Jeffrey Statland
Journal:  J Neurophysiol       Date:  2005-04-13       Impact factor: 2.714

5.  Resting state functional connectivity alterations in primary lateral sclerosis.

Authors:  Federica Agosta; Elisa Canu; Alberto Inuggi; Adriano Chiò; Nilo Riva; Vincenzo Silani; Andrea Calvo; Stefano Messina; Andrea Falini; Giancarlo Comi; Massimo Filippi
Journal:  Neurobiol Aging       Date:  2013-10-12       Impact factor: 4.673

6.  Randomized double-blind study of botulinum toxin type B for sialorrhea in ALS patients.

Authors:  Carlayne E Jackson; Gary Gronseth; Jeffrey Rosenfeld; Richard J Barohn; Richard Dubinsky; C Blake Simpson; April McVey; Pamela P Kittrell; Ruth King; Laura Herbelin
Journal:  Muscle Nerve       Date:  2009-02       Impact factor: 3.217

7.  Progression in primary lateral sclerosis: a prospective analysis.

Authors:  Mary Kay Floeter; Reversa Mills
Journal:  Amyotroph Lateral Scler       Date:  2009 Oct-Dec

Review 8.  Hereditary spastic paraplegia: clinico-pathologic features and emerging molecular mechanisms.

Authors:  John K Fink
Journal:  Acta Neuropathol       Date:  2013-07-30       Impact factor: 17.088

9.  Beta-band intermuscular coherence: a novel biomarker of upper motor neuron dysfunction in motor neuron disease.

Authors:  Karen M Fisher; Boubker Zaaimi; Timothy L Williams; Stuart N Baker; Mark R Baker
Journal:  Brain       Date:  2012-06-22       Impact factor: 13.501

10.  Extramotor damage is associated with cognition in primary lateral sclerosis patients.

Authors:  Elisa Canu; Federica Agosta; Sebastiano Galantucci; Adriano Chiò; Nilo Riva; Vincenzo Silani; Andrea Falini; Giancarlo Comi; Massimo Filippi
Journal:  PLoS One       Date:  2013-12-05       Impact factor: 3.240

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  12 in total

1.  Extra-motor cerebral changes and manifestations in primary lateral sclerosis.

Authors:  Eoin Finegan; Stacey Li Hi Shing; Rangariroyashe H Chipika; Kai Ming Chang; Mary Clare McKenna; Mark A Doherty; Jennifer C Hengeveld; Alice Vajda; Niall Pender; Colette Donaghy; Siobhan Hutchinson; Russell L McLaughlin; Orla Hardiman; Peter Bede
Journal:  Brain Imaging Behav       Date:  2021-01-07       Impact factor: 3.978

2.  Better understanding the neurobiology of primary lateral sclerosis.

Authors:  P Hande Ozdinler; Mukesh Gautam; Oge Gozutok; Csaba Konrad; Giovanni Manfredi; Estela Area Gomez; Hiroshi Mitsumoto; Marcella L Erb; Zheng Tian; Georg Haase
Journal:  Amyotroph Lateral Scler Frontotemporal Degener       Date:  2020-11       Impact factor: 4.092

3.  FIG4 variants in central European patients with amyotrophic lateral sclerosis: a whole-exome and targeted sequencing study.

Authors:  Alma Osmanovic; Isolde Rangnau; Anne Kosfeld; Susanne Abdulla; Claas Janssen; Bernd Auber; Peter Raab; Matthias Preller; Susanne Petri; Ruthild G Weber
Journal:  Eur J Hum Genet       Date:  2017-01-04       Impact factor: 4.246

4.  Clinicopathologic correlations in a family with a TBK1 mutation presenting as primary progressive aphasia and primary lateral sclerosis.

Authors:  Veronica Hirsch-Reinshagen; Omar A Alfaify; Ging-Yuek R Hsiung; Cyril Pottier; Matt Baker; Ralph B Perkerson; Rosa Rademakers; Hanna Briemberg; Dean J Foti; Ian R Mackenzie
Journal:  Amyotroph Lateral Scler Frontotemporal Degener       Date:  2019-06-27       Impact factor: 4.092

5.  Mills' syndrome is a unique entity of upper motor neuron disease with N-shaped progression: Three case reports.

Authors:  Zhi-Yun Zhang; Zhi-Yuan Ouyang; Guo-Hua Zhao; Jia-Jia Fang
Journal:  World J Clin Cases       Date:  2022-07-06       Impact factor: 1.534

6.  Loss of functional connectivity is an early imaging marker in primary lateral sclerosis.

Authors:  Michael G Clark; Rachel Smallwood Shoukry; Caleb J Huang; Laura E Danielian; Devin Bageac; Mary Kay Floeter
Journal:  Amyotroph Lateral Scler Frontotemporal Degener       Date:  2018-10-09       Impact factor: 4.092

7.  Lipidomics study of plasma from patients suggest that ALS and PLS are part of a continuum of motor neuron disorders.

Authors:  Estela Area-Gomez; H Mitsumoto; D Larrea; T Yun; Y Xu; J Hupf; F Zandkarimi; R B Chan
Journal:  Sci Rep       Date:  2021-06-30       Impact factor: 4.379

8.  Longitudinal evaluation of upper motor neuron burden scales in primary lateral sclerosis.

Authors:  Mary Kay Floeter; Tianxia Wu
Journal:  Amyotroph Lateral Scler Frontotemporal Degener       Date:  2020-07-13       Impact factor: 4.092

Review 9.  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

10.  Initial Cerebellar Ataxia in Hereditary Adult-Onset Primary Lateral Sclerosis.

Authors:  José Gazulla; Silvia Izquierdo-Alvarez; Emilio Ruiz-Fernández; José Berciano
Journal:  Case Rep Neurol       Date:  2021-06-21
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