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au.\*:("HUDSON, Gavin")

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Mitochondrial DNA polymerase-γ and human diseaseHUDSON, Gavin; CHINNERY, Patrick F.Human molecular genetics (Print). 2006, Vol 15, issn 0964-6906, R244-R252, NS2Article

Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathyGIORDANO, Carla; LOMMARINI, Luisa; FANELLI, Francesca et al.Brain. 2014, Vol 137, pp 335-353, issn 0006-8950, 19 p., 2Article

Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathyHORVATH, Rita; KEMP, John P; KOLLBERG, Gittan et al.Brain. 2009, Vol 132, pp 3165-3174, issn 0006-8950, 10 p., 11Article

Characterizing mild cognitive impairment in incident Parkinson disease: The ICICLE-PD StudyYARNALL, Alison J; BREEN, David P; MOLLENHAUER, Brit et al.Neurology. 2014, Vol 82, Num 4, pp 308-316, issn 0028-3878, 9 p.Article

Genetic and Pathological Links Between Parkinson's Disease and the Lysosomal Disorder Sanfilippo SyndromeWINDER-RHODES, Sophie E; GARCIA-REITBÖCK, Pablo; BURN, David J et al.Movement disorders. 2012, Vol 27, Num 2, pp 312-315, issn 0885-3185, 4 p.Article

Quality of Life in Patients with Leber Hereditary Optic NeuropathyKIRKMAN, Matthew Anthony; KORSTEN, Alex; LEONHARDT, Miriam et al.Investigative ophthalmology & visual science. 2009, Vol 50, Num 7, pp 3112-3115, issn 0146-0404, 4 p.Article

Single-Cell Expression Profiling of Dopaminergic Neurons Combined with Association Analysis Identifies Pyridoxal Kinase as Parkinson's Disease GeneELSTNER, Matthias; MORRIS, Christopher M; GIOVANETTI, Alessandro et al.Annals of neurology. 2009, Vol 66, Num 6, pp 792-798, issn 0364-5134, 7 p.Article

Clinical expression of leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup backgroundHUDSON, Gavin; CARELLI, Valerio; VALENTINO, Maria Lucia et al.American journal of human genetics. 2007, Vol 81, Num 2, pp 228-233, issn 0002-9297, 6 p.Article

A New Phenotype of Brain Iron Accumulation with Dystonia, Optic Atrophy, and Peripheral NeuropathyHORVATH, Rita; HOLINSKI-FEDER, Elke; NURNBERG, Peter et al.Movement disorders. 2012, Vol 27, Num 6, pp 789-793, issn 0885-3185, 5 p.Article

Genetic variation of CHRNA4 does not modulate attention in Parkinson's diseaseHUDSON, Gavin; STUTT, Andrea; ECCLES, Martin et al.Neuroscience letters. 2010, Vol 479, Num 2, pp 123-125, issn 0304-3940, 3 p.Article

Mutation of OPAI causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions : a novel disorder of mtDNA maintenance. CommentaryZEVIANI, Massimo; HUDSON, Gavin; REYNIER, Pascal et al.Brain. 2008, Vol 131, issn 0006-8950, 314-317, 329-337 [13 p.], 2Article

POLG1 Mutations Manifesting as Autosomal Recessive Axonal Charcot-Marie-Tooth DiseaseHARROWER, Timothy; STEWART, Joanna D; HUDSON, Gavin et al.Archives of neurology (Chicago). 2008, Vol 65, Num 1, pp 133-136, issn 0003-9942, 4 p.Article

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