Literature DB >> 11442328

Progressive spastic paraparesis: hereditary spastic paraplegia and its relation to primary and amyotrophic lateral sclerosis.

J K Fink1.   

Abstract

The syndrome of insidiously progressive spastic weakness of both legs occurs in a number of etiologically distinct disorders including hereditary spastic paraplegia (HSP), primary lateral sclerosis (PLS), and sometimes in amyotrophic lateral sclerosis (ALS). This review summarizes the clinical and pathologic relationship between these disorders.

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Year:  2001        PMID： 11442328     DOI： 10.1055/s-2001-15265

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


  12 in total

1.  White matter alterations differ in primary lateral sclerosis and amyotrophic lateral sclerosis.

Authors:  Nobue K Iwata; Justin Y Kwan; Laura E Danielian; John A Butman; Fernanda Tovar-Moll; Elham Bayat; Mary Kay Floeter
Journal:  Brain       Date:  2011-07-28       Impact factor: 13.501

2.  Iron-sensitive MR imaging of the primary motor cortex to differentiate hereditary spastic paraplegia from other motor neuron diseases.

Authors:  Mirco Cosottini; Graziella Donatelli; Ivana Ricca; Francesca Bianchi; Daniela Frosini; Vincenzo Montano; Gianmichele Migaleddu; Eleonora Del Prete; Alessandra Tessa; Paolo Cecchi; Claudio D'Amelio; Gabriele Siciliano; Michelangelo Mancuso; Filippo Maria Santorelli
Journal:  Eur Radiol       Date:  2022-05-20       Impact factor: 7.034

3.  SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis.

Authors:  Antonio Orlacchio; Carla Babalini; Antonella Borreca; Clarice Patrono; Roberto Massa; Sarenur Basaran; Renato P Munhoz; Ekaterina A Rogaeva; Peter H St George-Hyslop; Giorgio Bernardi; Toshitaka Kawarai
Journal:  Brain       Date:  2010-01-28       Impact factor: 13.501

Review 4.  Hereditary spastic paraplegia.

Authors:  John K Fink
Journal:  Curr Neurol Neurosci Rep       Date:  2006-01       Impact factor: 5.081

5.  Seipin/BSCL2 mutation screening in sporadic adult-onset upper motor neuron syndromes.

Authors:  Frans Brugman; Hans Scheffer; H Jurgen Schelhaas; Willy M Nillesen; John H J Wokke; Bart P C van de Warrenburg; Leonard H van den Berg
Journal:  J Neurol       Date:  2009-03-01       Impact factor: 4.849

6.  Description of combined ARHSP/JALS phenotype in some patients with SPG11 mutations.

Authors:  Marzieh Khani; Hosein Shamshiri; Farzad Fatehi; Mohammad Rohani; Bahram Haghi Ashtiani; Fahimeh Haji Akhoundi; Afagh Alavi; Hamidreza Moazzeni; Hanieh Taheri; Mina Tolou Ghani; Leila Javanparast; Seyyed Saleh Hashemi; Ramona Haji-Seyed-Javadi; Matineh Heidari; Shahriar Nafissi; Elahe Elahi
Journal:  Mol Genet Genomic Med       Date:  2020-05-08       Impact factor: 2.183

Review 7.  Complexity of Generating Mouse Models to Study the Upper Motor Neurons: Let Us Shift Focus from Mice to Neurons.

Authors:  Baris Genc; Oge Gozutok; P Hande Ozdinler
Journal:  Int J Mol Sci       Date:  2019-08-07       Impact factor: 5.923

8.  Primary lateral sclerosis: consensus diagnostic criteria.

Authors:  Martin R Turner; Richard J Barohn; Philippe Corcia; John K Fink; Matthew B Harms; Matthew C Kiernan; John Ravits; Vincenzo Silani; Zachary Simmons; Jeffrey Statland; Leonard H van den Berg; Hiroshi Mitsumoto
Journal:  J Neurol Neurosurg Psychiatry       Date:  2020-02-06       Impact factor: 10.154

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

Review 10.  Retrograde labeling, transduction, and genetic targeting allow cellular analysis of corticospinal motor neurons: implications in health and disease.

Authors:  Javier H Jara; Barış Genç; Jodi L Klessner; P Hande Ozdinler
Journal:  Front Neuroanat       Date:  2014-03-26       Impact factor: 3.856
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