Subclinical multisystem neurologic disease in "pure" OPA1 autosomal dominant optic atrophy
Baker, M R, Fisher, K M, Whittaker, R G, Griffiths, P G, Yu-Wai-Man, P, Chinnery, P F
Published in Neurology (27.09.2011)
Published in Neurology (27.09.2011)
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Journal Article
Prevalence and progression of diabetes in mitochondrial disease
Whittaker, R. G, Schaefer, A. M, McFarland, R, Taylor, R. W, Walker, M, Turnbull, D. M
Published in Diabetologia (01.10.2007)
Published in Diabetologia (01.10.2007)
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Journal Article
Myotonic dystrophy: practical issues relating to assessment of strength
Whittaker, R G, Ferenczi, E, Hilton-Jones, D
Published in Journal of neurology, neurosurgery and psychiatry (01.11.2006)
Published in Journal of neurology, neurosurgery and psychiatry (01.11.2006)
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Journal Article
VIRAL ENTRY INTO THE NUCLEUS
Whittaker, Gary R, Kann, Michael, Helenius, Ari
Published in Annual review of cell and developmental biology (01.01.2000)
Published in Annual review of cell and developmental biology (01.01.2000)
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Journal Article
Estimating motor unit numbers from a CMAP scan: Repeatability study on three muscles at 15 centres
Sørensen, D.M., Bostock, H., Abrahao, A., Alaamel, A., Alaydin, H.C., Ballegaard, M., Boran, E., Cengiz, B., de Carvalho, M., Dunker, Ø., Fuglsang-Frederiksen, A., Graffe, C.C., Jones, K.E., Kallio, M., Kalra, S., Krarup, C., Krøigård, T., Liguori, R., Lupescu, T., Maitland, S., Matamala, J.M., Moldovan, M., Moreno-Roco, J., Nilsen, K.B., Phung, L., Santos, M.O., Themistocleous, A.C., Uysal, H., Vacchiano, V., Whittaker, R.G., Zinman, L., Tankisi, H.
Published in Clinical neurophysiology (01.07.2023)
Published in Clinical neurophysiology (01.07.2023)
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Journal Article
Mitochondrial disease in pregnancy: a systematic review
Say, R E, Whittaker, R G, Turnbull, H E, McFarland, R, Taylor, R W, Turnbull, D M
Published in Obstetric Medicine (01.09.2011)
Published in Obstetric Medicine (01.09.2011)
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Book Review
Journal Article
Urine heteroplasmy is the best predictor of clinical outcome in the m.3243A>G mtDNA mutation
Whittaker, R G, Blackwood, J K, Alston, C L, Blakely, E L, Elson, J L, McFarland, R, Chinnery, P F, Turnbull, D M, Taylor, R W
Published in Neurology (10.02.2009)
Published in Neurology (10.02.2009)
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Journal Article
Substrate preference profiles of proteases released by allergenic pollens
WIDMER, F, HAYES, P. J, WHITTAKER, R. G, KUMAR, R. K
Published in Clinical and experimental allergy (01.04.2000)
Published in Clinical and experimental allergy (01.04.2000)
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Journal Article
Correction: Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy–like disease
Boczonadi, V., King, M.S., Smith, A.C., Olahova, M., Bansagi, B., Roos, A., Eyassu, F., Borchers, C., Ramesh, V., Lochmüller, H., Polvikoski, T., Whittaker, R.G., Pyle, A., Griffin, H., Taylor, R.W., Chinnery, P.F., Robinson, A.J., Kunji, E.R.S., Horvath, R.
Published in Genetics in medicine (01.09.2019)
Published in Genetics in medicine (01.09.2019)
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Journal Article
Testing the neuromuscular junction: what neurophysiology can offer the neurologist
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Journal Article
Book Review
Role of clathrin-mediated endocytosis during vesicular stomatitis virus entry into host cells
Sun, Xiangjie, Yau, Vivian K., Briggs, Benjamin J., Whittaker, Gary R.
Published in Virology (New York, N.Y.) (20.07.2005)
Published in Virology (New York, N.Y.) (20.07.2005)
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Journal Article