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Mitochondrial disease and pelvic organ dysfunction: an under-recognised but treatable clinical association
by
Poole, O.V
,
Panicker, J
,
Emmanuel, A
,
Hanna, M.G
,
Pitceathly, R.D.S
Published in
Neuromuscular disorders : NMD
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Service evaluation exploring the incidence of vestibular and balance dysfunction in people with mitochondrial disease
by
Holmes, S
,
Male, A
,
Ramdharry, G.M
,
Quinlivan, R
,
Bugiardini, E
,
Poole, O.V
,
James, N
,
Hanna, M.G
Published in
Neuromuscular disorders : NMD
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TPK1 mutations: unmasking a potentially treatable cause of Leigh-like syndrome
by
Bugiardini, E
,
Poole, O.V
,
Pittman, A
,
Woodward, C.E
,
Sweeney, M.G
,
Heales, S
,
Houlden, H
,
Hanna, M.G
,
Pitceathly, R.D.S
Published in
Neuromuscular disorders : NMD
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Cause of death in a cohort of mitochondrial patients
by
Skorupinska, I
,
Bugiardini, E
,
Ng, Y.S
,
Horga, A
,
Poole, O.V
,
McFarland, R
,
Pitceathly, R.D.S
,
Turnbull, D.M
,
Hanna, M.G
Published in
Neuromuscular disorders : NMD
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M16 - Mitochondrial disease and pelvic organ dysfunction: an under-recognised but treatable clinical association
by
Poole, O.V.
,
Panicker, J.
,
Emmanuel, A.
,
Hanna, M.G.
,
Pitceathly, R.D.S.
Published in
Neuromuscular disorders : NMD
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M11 - The “hidden” mitochondrial genome: a novel bioinformatic approach for extracting and analysing mitochondrial DNA from nuclear genomic NGS sequence data at the Institute of Ne...
by
Poole, O.V.
,
Murphy, D.
,
Woodward, C.
,
Bugiardini, E.
,
Hardy, J.
,
Houlden, H.
,
Hanna, M.G.
,
Pittman, A.
,
Pitceathly, R.D.S.
Published in
Neuromuscular disorders : NMD
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The “hidden” mitochondrial genome: a novel bioinformatic approach for extracting and analysing mitochondrial DNA from nuclear genomic NGS sequence data at the Institute of Neurolog...
by
Poole, O.V.
,
Murphy, D.
,
Woodward, C.
,
Bugiardini, E.
,
Hardy, J.
,
Houlden, H.
,
Hanna, M.G.
,
Pittman, A.
,
Pitceathly, R.D.S.
Published in
Neuromuscular disorders : NMD
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M18 - Service evaluation exploring the incidence of vestibular and balance dysfunction in people with mitochondrial disease
by
Holmes, S.
,
Male, A.
,
Ramdharry, G.M.
,
Quinlivan, R.
,
Bugiardini, E.
,
Poole, O.V.
,
James, N.
,
Hanna, M.G.
Published in
Neuromuscular disorders : NMD
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Article
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9
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M19 - TPK1 mutations: unmasking a potentially treatable cause of Leigh-like syndrome
by
Bugiardini, E.
,
Poole, O.V.
,
Pittman, A.
,
Woodward, C.E.
,
Sweeney, M.G.
,
Heales, S.
,
Houlden, H.
,
Hanna, M.G.
,
Pitceathly, R.D.S.
Published in
Neuromuscular disorders : NMD
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Article
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10
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M05 - Cause of death in a cohort of mitochondrial patients
by
Skorupinska, I.
,
Bugiardini, E.
,
Ng, Y.S.
,
Horga, A.
,
Poole, O.V.
,
McFarland, R.
,
Pitceathly, R.D.S.
,
Turnbull, D.M.
,
Hanna, M.G.
Published in
Neuromuscular disorders : NMD
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Decaborane beam from ITEP Bernas ion source
by
Kulevoy, T. V.
,
Petrenko, S. V.
,
Kuibeda, R. P.
,
Batalin, V. A.
,
Pershin, V. I.
,
Koslov, A. V.
,
Stasevich, Yu. B.
,
Hershcovitch, A.
,
Johnson, B. M.
,
Oks, E. M.
,
Gushenets, V. I.
,
Poole, H. J.
,
Storozhenko, P. A.
,
Gurkova, E. L.
,
Alexeyenko, O. V.
Published in
Review of scientific instruments
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