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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1982 1
1983 1
1989 2
1990 2
1991 1
1992 1
1993 2
1994 4
1995 4
1996 3
1997 3
1998 1
1999 12
2000 6
2001 9
2002 7
2003 10
2004 9
2005 5
2006 12
2007 7
2008 6
2009 11
2010 10
2011 12
2012 18
2013 18
2014 20
2015 20
2016 14
2017 15
2018 19
2019 24
2020 19
2021 21
2022 22
2023 22

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324 results

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Page 1
Hereditary Spastic Paraplegia: An Update.
Meyyazhagan A, Orlacchio A. Meyyazhagan A, et al. Int J Mol Sci. 2022 Feb 1;23(3):1697. doi: 10.3390/ijms23031697. Int J Mol Sci. 2022. PMID: 35163618 Free PMC article. Review.
Hereditary spastic paraplegia (HSP) is a rare neurodegenerative disorder with the predominant clinical manifestation of spasticity in the lower extremities. ...
Hereditary spastic paraplegia (HSP) is a rare neurodegenerative disorder with the predominant clinical manifestation of …
Hereditary spastic paraplegia.
Murala S, Nagarajan E, Bollu PC. Murala S, et al. Neurol Sci. 2021 Mar;42(3):883-894. doi: 10.1007/s10072-020-04981-7. Epub 2021 Jan 13. Neurol Sci. 2021. PMID: 33439395 Review.
Hereditary spastic paraplegias (HSPs) are a group of neurodegenerative disorders which involve the corticospinal tracts and present with distinct spasticity and weakness of the lower extremities. ...
Hereditary spastic paraplegias (HSPs) are a group of neurodegenerative disorders which involve the corticospinal tracts and pr …
Hereditary spastic paraplegia: clinico-pathologic features and emerging molecular mechanisms.
Fink JK. Fink JK. Acta Neuropathol. 2013 Sep;126(3):307-28. doi: 10.1007/s00401-013-1115-8. Epub 2013 Jul 30. Acta Neuropathol. 2013. PMID: 23897027 Free PMC article. Review.
Hereditary spastic paraplegia (HSP) is a syndrome designation describing inherited disorders in which lower extremity weakness and spasticity are the predominant symptoms. ...SPG2/Proteolipid protein and SPG42/Connexin 47); (5) protein folding and ER-stress r …
Hereditary spastic paraplegia (HSP) is a syndrome designation describing inherited disorders in which lower extremity w …
The global epidemiology of hereditary ataxia and spastic paraplegia: a systematic review of prevalence studies.
Ruano L, Melo C, Silva MC, Coutinho P. Ruano L, et al. Neuroepidemiology. 2014;42(3):174-83. doi: 10.1159/000358801. Epub 2014 Mar 5. Neuroepidemiology. 2014. PMID: 24603320 Free article. Review.
BACKGROUND: Hereditary cerebellar ataxias (HCA) and hereditary spastic paraplegias (HSP) are two groups of neurodegenerative disorders that usually present with progressive gait impairment, often leading to permanent disability. ...The prevalence of autosomal …
BACKGROUND: Hereditary cerebellar ataxias (HCA) and hereditary spastic paraplegias (HSP) are two groups of neurodegener …
Hereditary spastic paraplegia: from diagnosis to emerging therapeutic approaches.
Shribman S, Reid E, Crosby AH, Houlden H, Warner TT. Shribman S, et al. Lancet Neurol. 2019 Dec;18(12):1136-1146. doi: 10.1016/S1474-4422(19)30235-2. Epub 2019 Jul 31. Lancet Neurol. 2019. PMID: 31377012 Review.
Hereditary spastic paraplegia (HSP) describes a heterogeneous group of genetic neurodegenerative diseases characterised by progressive spasticity of the lower limbs. ...
Hereditary spastic paraplegia (HSP) describes a heterogeneous group of genetic neurodegenerative diseases characterised …
Clinical and genetic update of hereditary spastic paraparesis.
Lallemant-Dudek P, Durr A. Lallemant-Dudek P, et al. Rev Neurol (Paris). 2021 May;177(5):550-556. doi: 10.1016/j.neurol.2020.07.001. Epub 2020 Aug 15. Rev Neurol (Paris). 2021. PMID: 32807405 Review.
Hereditary spastic paraparesis is a group of inherited neurological diseases characterized by underlying wide genetic heterogeneity. ...
Hereditary spastic paraparesis is a group of inherited neurological diseases characterized by underlying wide genetic heteroge …
A Diagnostic Approach to Spastic ataxia Syndromes.
Pedroso JL, Vale TC, França Junior MC, Kauffman MA, Teive H, Barsottini OGP, Munhoz RP. Pedroso JL, et al. Cerebellum. 2022 Dec;21(6):1073-1084. doi: 10.1007/s12311-021-01345-5. Epub 2021 Nov 15. Cerebellum. 2022. PMID: 34782953 Review.
Spastic ataxia is characterized by the combination of cerebellar ataxia with spasticity and other pyramidal features. It is the hallmark of some hereditary ataxias, but it can also occur in some spastic paraplegias and acquired conditions. ...
Spastic ataxia is characterized by the combination of cerebellar ataxia with spasticity and other pyramidal features. It is the hallm …
Protein Misfolding Diseases and Therapeutic Approaches.
Yadav K, Yadav A, Vashistha P, Pandey VP, Dwivedi UN. Yadav K, et al. Curr Protein Pept Sci. 2019;20(12):1226-1245. doi: 10.2174/1389203720666190610092840. Curr Protein Pept Sci. 2019. PMID: 31187709 Review.
Protein misfolding diseases caused due to defective mitochondrial PQC system include medium-chain acyl-CoA dehydrogenase (MCAD)/Short-chain Acyl-CoA Dehydrogenase (SCAD) deficiency diseases, hereditary spastic paraplegia. Among therapeutic approaches towards …
Protein misfolding diseases caused due to defective mitochondrial PQC system include medium-chain acyl-CoA dehydrogenase (MCAD)/Short-chain …
Genetic mimics of cerebral palsy.
Pearson TS, Pons R, Ghaoui R, Sue CM. Pearson TS, et al. Mov Disord. 2019 May;34(5):625-636. doi: 10.1002/mds.27655. Epub 2019 Mar 26. Mov Disord. 2019. PMID: 30913345 Review.
Hereditary spastic paraplegia.
Blackstone C. Blackstone C. Handb Clin Neurol. 2018;148:633-652. doi: 10.1016/B978-0-444-64076-5.00041-7. Handb Clin Neurol. 2018. PMID: 29478605 Review.
The hereditary spastic paraplegias (HSPs) are a heterogeneous group of neurologic disorders with the common feature of prominent lower-extremity spasticity, resulting from a length-dependent axonopathy of corticospinal upper motor neurons. ...
The hereditary spastic paraplegias (HSPs) are a heterogeneous group of neurologic disorders with the common feature of promine …
324 results