Warner TT - Search Results

1

Hereditary spastic paraplegia: from diagnosis to emerging therapeutic approaches.

Shribman S, Reid E, Crosby AH, Houlden H, Warner TT. Shribman S, et al. Among authors: warner tt. 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.

2

The Silver syndrome variant of hereditary spastic paraplegia maps to chromosome 11q12-q14, with evidence for genetic heterogeneity within this subtype.

Patel H, Hart PE, Warner TT, Houlston RS, Patton MA, Jeffery S, Crosby AH. Patel H, et al. Among authors: warner tt. Am J Hum Genet. 2001 Jul;69(1):209-15. doi: 10.1086/321267. Epub 2001 May 25. Am J Hum Genet. 2001. PMID: 11389484 Free PMC article.

3

Silver syndrome is not linked to any of the previously established autosomal dominant hereditary spastic paraplegia loci.

Patel H, Hart PE, Warner T, Allen I, Phillimore HE, Silver JR, Wood NW, Jeffery S, Patton MA, Crosby AH. Patel H, et al. Am J Med Genet. 2001 Jul 22;102(1):68-72. doi: 10.1002/1096-8628(20010722)102:1<68::aid-ajmg1411>3.0.co;2-r. Am J Med Genet. 2001. PMID: 11471175

4

A large family with hereditary spastic paraparesis due to a frame shift mutation of the spastin (SPG4) gene: association with multiple sclerosis in two affected siblings and epilepsy in other affected family members.

Mead SH, Proukakis C, Wood N, Crosby AH, Plant GT, Warner TT. Mead SH, et al. Among authors: warner tt. J Neurol Neurosurg Psychiatry. 2001 Dec;71(6):788-91. doi: 10.1136/jnnp.71.6.788. J Neurol Neurosurg Psychiatry. 2001. PMID: 11723204 Free PMC article.

5

Three novel spastin (SPG4) mutations in families with autosomal dominant hereditary spastic paraplegia.

Proukakis C, Hart PE, Cornish A, Warner TT, Crosby AH. Proukakis C, et al. Among authors: warner tt. J Neurol Sci. 2002 Sep 15;201(1-2):65-9. doi: 10.1016/s0022-510x(02)00192-2. J Neurol Sci. 2002. PMID: 12163196

6

Screening of patients with hereditary spastic paraplegia reveals seven novel mutations in the SPG4 (Spastin) gene.

Proukakis C, Auer-Grumbach M, Wagner K, Wilkinson PA, Reid E, Patton MA, Warner TT, Crosby AH. Proukakis C, et al. Among authors: warner tt. Hum Mutat. 2003 Feb;21(2):170. doi: 10.1002/humu.9108. Hum Mutat. 2003. PMID: 12552568

7

A clinical and genetic study of SPG5A linked autosomal recessive hereditary spastic paraplegia.

Wilkinson PA, Crosby AH, Turner C, Patel H, Wood NW, Schapira AH, Warner TT. Wilkinson PA, et al. Among authors: warner tt. Neurology. 2003 Jul 22;61(2):235-8. doi: 10.1212/01.wnl.0000069920.42968.8d. Neurology. 2003. PMID: 12874406

8

No association with common Caucasian genotypes in exons 8, 13 and 14 of the human cytoplasmic dynein heavy chain gene (DNCHC1) and familial motor neuron disorders.

Ahmad-Annuar A, Shah P, Hafezparast M, Hummerich H, Witherden AS, Morrison KE, Shaw PJ, Kirby J, Warner TT, Crosby A, Proukakis C, Wilkinson P, Orrell RW, Bradley L, Martin JE, Fisher EM. Ahmad-Annuar A, et al. Among authors: warner tt. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003 Sep;4(3):150-7. doi: 10.1080/14660820310011737. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003. PMID: 13129801

9

SPG3A mutation screening in English families with early onset autosomal dominant hereditary spastic paraplegia.

Wilkinson PA, Hart PE, Patel H, Warner TT, Crosby AH. Wilkinson PA, et al. Among authors: warner tt. J Neurol Sci. 2003 Dec 15;216(1):43-5. doi: 10.1016/s0022-510x(03)00210-7. J Neurol Sci. 2003. PMID: 14607301

10

Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome.

Windpassinger C, Auer-Grumbach M, Irobi J, Patel H, Petek E, Hörl G, Malli R, Reed JA, Dierick I, Verpoorten N, Warner TT, Proukakis C, Van den Bergh P, Verellen C, Van Maldergem L, Merlini L, De Jonghe P, Timmerman V, Crosby AH, Wagner K. Windpassinger C, et al. Among authors: warner tt. Nat Genet. 2004 Mar;36(3):271-6. doi: 10.1038/ng1313. Epub 2004 Feb 22. Nat Genet. 2004. PMID: 14981520

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