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13 in total

1. Complicated hereditary spastic paraplegia with thin corpus callosum: variation of phenotypic expression over time.

Authors: Anne-Dörte Sperfeld; Jan Kassubek; Andrew H Crosby; Beate Winner; Albert C Ludolph; Ingo Uttner; C Oliver Hanemann
Journal: J Neurol Date: 2004-10 Impact factor: 4.849

2. Interaction of two hereditary spastic paraplegia gene products, spastin and atlastin, suggests a common pathway for axonal maintenance.

Authors: Katia Evans; Christian Keller; Karen Pavur; Kristen Glasgow; Bryan Conn; Brett Lauring
Journal: Proc Natl Acad Sci U S A Date: 2006-06-30 Impact factor: 11.205

3. Corticospinal motor neurons and related subcerebral projection neurons undergo early and specific neurodegeneration in hSOD1G⁹³A transgenic ALS mice.

Authors: P Hande Ozdinler; Susanna Benn; Ted H Yamamoto; Mine Güzel; Robert H Brown; Jeffrey D Macklis
Journal: J Neurosci Date: 2011-03-16 Impact factor: 6.167

4. AAV2 mediated retrograde transduction of corticospinal motor neurons reveals initial and selective apical dendrite degeneration in ALS.

Authors: Javier H Jara; Stephanie R Villa; Nabil A Khan; Martha C Bohn; P Hande Ozdinler
Journal: Neurobiol Dis Date: 2012-04-11 Impact factor: 5.996

5. Intragenic modifiers of hereditary spastic paraplegia due to spastin gene mutations.

Authors: Ingrid K Svenson; Mark T Kloos; P Craig Gaskell; Martha A Nance; James Y Garbern; Shin-ichi Hisanaga; Margaret A Pericak-Vance; Allison E Ashley-Koch; Douglas A Marchuk
Journal: Neurogenetics Date: 2004-07-10 Impact factor: 2.660

6. NIPA1 gene mutations cause autosomal dominant hereditary spastic paraplegia (SPG6).

Authors: Shirley Rainier; Jing-Hua Chai; Debra Tokarz; Robert D Nicholls; John K Fink
Journal: Am J Hum Genet Date: 2003-09-23 Impact factor: 11.025

7. A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10).

Authors: Evan Reid; Mark Kloos; Allison Ashley-Koch; Lori Hughes; Simon Bevan; Ingrid K Svenson; Felicia Lennon Graham; Perry C Gaskell; Andrew Dearlove; Margaret A Pericak-Vance; David C Rubinsztein; Douglas A Marchuk
Journal: Am J Hum Genet Date: 2002-09-24 Impact factor: 11.025

8. Intramuscular viral delivery of paraplegin rescues peripheral axonopathy in a model of hereditary spastic paraplegia.

Authors: Marinella Pirozzi; Angelo Quattrini; Gennaro Andolfi; Giorgia Dina; Maria Chiara Malaguti; Alberto Auricchio; Elena I Rugarli
Journal: J Clin Invest Date: 2005-12-15 Impact factor: 14.808

9. An SPG3A whole gene deletion neither co-segregates with disease nor modifies phenotype in a hereditary spastic paraplegia family with a pathogenic SPG4 deletion.

Authors: Christian Beetz; Anders O H Nygren; Thomas Deufel; Evan Reid
Journal: Neurogenetics Date: 2007-07-27 Impact factor: 3.017

Review 10. Dealing with misfolded proteins: examining the neuroprotective role of molecular chaperones in neurodegeneration.

Authors: Yousuf O Ali; Brandon M Kitay; R Grace Zhai
Journal: Molecules Date: 2010-10-08 Impact factor: 4.411