P. Hart

发表

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

A. Crosby, T. Warner, H. Patel, 2003, Journal of the Neurological Sciences.

Control of development and motility in the spermatozoids of lower plants.

V. Klink, C. Tsai, S. M. Wolniak, 2000, Gravitational and space biology bulletin : publication of the American Society for Gravitational and Space Biology.

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

M. Patton, N. Wood, A. Crosby, 2001, American journal of medical genetics.

Spermiogenesis in Marsilea vestita: a temporal correlation between centrin expression and blepharoplast differentiation.

S. M. Wolniak, P. Hart, Peter E. Hart, 1998, Cell motility and the cytoskeleton.

Coenzyme Q10 and vitamin E deficiency in Friedreich’s ataxia: predictor of efficacy of vitamin E and coenzyme Q10 therapy

J. Cooper, J. Bradley, A. Schapira, 2008, European journal of neurology.

Antioxidant treatment of patients with Friedreich ataxia: four-year follow-up.

A. Blamire, D. Manners, P. Styles, 2005, Archives of neurology.

Characterization of the X-linked murine centrin Cetn2 gene.

J. Salisbury, G. Poynter, S. Barrett, 2001, Gene.

Testis-specific murine centrin, Cetn1: genomic characterization and evidence for retroposition of a gene encoding a centrosome protein.

J. Salisbury, G. Poynter, J. D. Orth, 1999, Genomics.

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

R. Houlston, M. Patton, A. Crosby, 2001, American journal of human genetics.

Mitochondria: Aspects for neuroprotection

A. Schapira, P. Hart, 1999 .

Posterior reversible encephalopathy syndrome associated with use of Atezolizumab for the treatment of relapsed triple negative breast cancer.

S. McGrath, K. Downey, N. Senthivel, 2022, Cancer treatment and research communications.

MELAS mitochondrial DNA mutation A3243G reduces glutamate transport in cybrids cell lines

J. Cooper, L. Tremolizzo, C. Ferrarese, 2008, Experimental Neurology.

Molecular cloning of a centrin homolog from Marsilea vestita and evidence for its translational control during spermiogenesis.

S. M. Wolniak, P. Hart, Peter E. Hart, 1999, Biochemistry and cell biology = Biochimie et biologie cellulaire.

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

A. Crosby, T. Warner, C. Proukakis, 2002, Journal of the Neurological Sciences.

Mitochondrial dysfunction and free radical damage in the Huntington R6/2 transgenic mouse

A H Schapira, S. Tabrizi, J. Cooper, 2000, Annals of neurology.

Antioxidant treatment improves in vivo cardiac and skeletal muscle bioenergetics in patients with Friedreich's ataxia

A H Schapira, A. Blamire, D. Manners, 2001, Annals of neurology.

Role of Oxidative Damage in Friedreich's Ataxia

J. Cooper, J. Bradley, A. Schapira, 2004, Neurochemical Research.

International cooperative ataxia rating scale (ICARS): Appropriate for studies of Friedreich's ataxia?

J. Hobart, J. Cooper, S. Cano, 2005, Movement disorders : official journal of the Movement Disorder Society.