Resultados da pesquisa - Houlden, Henry

The small, spastic, and furrowed tongue of Allgrove syndrome Por Houlden, Henry

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Extending the clinical spectrum of pain channelopathies Por Houlden, Henry

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Defective N-linked protein glycosylation pathway in congenital myasthenic syndromes Por Houlden, Henry

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C9orf72 and its Relevance in Parkinsonism and Movement Disorders: A Comprehensive Review of the Literature Por Bourinaris, Thomas, Houlden, Henry

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The genetics and neuropathology of Parkinson’s disease Por Houlden, Henry, Singleton, Andrew B.

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Neurology and orthopaedics Por Houlden, Henry, Charlton, Paul, Singh, Dishan

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The pallidopyramidal syndromes: nosology, aetiology and pathogenesis Por Kara, Eleanna, Hardy, John, Houlden, Henry

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Reply to: No evidence supports genetic heterogeneity of neuronal intranuclear inclusion disease Por Chen, Zhongbo, Ryten, Mina, Houlden, Henry

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Thinning of the Corpus Callosum and Cerebellar Atrophy is Correlated with Phenotypic Severity in a Family with Spastic Paraplegia Type 11 Por Rajakulendran, Sanjeev, Paisán-Ruiz, Coro, Houlden, Henry

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Somatic Alpha-Synuclein Mutations in Parkinson's Disease: Hypothesis and Preliminary Data Por Proukakis, Christos, Houlden, Henry, Schapira, Anthony H

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Late-onset Lafora disease with prominent parkinsonism due to a rare mutation in EPM2A Por Lynch, David S., Wood, Nicholas W., Houlden, Henry

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DRPLA: understanding the natural history and developing biomarkers to accelerate therapeutic trials in a globally rare repeat expansion disorder Por Chaudhry, Aiysha, Anthanasiou-Fragkouli, Alkyoni, Houlden, Henry

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Whole-genome sequencing Por Morris, Huw R, Houlden, Henry, Polke, James

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Madras motor neuron disease (MMND) is distinct from the riboflavin transporter genetic defects that cause Brown–Vialetto–Van Laere syndrome Por Nalini, Atchayaram, Pandraud, Amelie, Mok, Kin, Houlden, Henry

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Multiple system atrophy: genetic risks and alpha-synuclein mutations Por Whittaker, Heather T, Qui, Yichen, Bettencourt, Conceição, Houlden, Henry

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Paroxysmal Movement Disorder and Epilepsy Caused by a De Novo Truncating Mutation in KAT6A Por Efthymiou, Stephanie, Salpietro, Vincenzo, Bettencourt, Conceicao, Houlden, Henry

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A Review of Copy Number Variants in Inherited Neuropathies Por Salpietro, Vincenzo, Manole, Andreea, Efthymiou, Stephanie, Houlden, Henry

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Advances in the Genetics of Parkinson's Disease: A Guide for the Clinician Por Sheerin, Una‐Marie, Houlden, Henry, Wood, Nicholas W.

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The genetics of intellectual disability: advancing technology and gene editing Por Ilyas, Muhammad, Mir, Asif, Efthymiou, Stephanie, Houlden, Henry

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Editorial: Multifaceted Genes in Amyotrophic Lateral Sclerosis-Frontotemporal Dementia Por Conforti, Francesca Luisa, Renton, Alan Edward, Houlden, Henry

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