Resultados de Procura por Autor

1

Clinical and genetic characterization of families with triple A (Allgrove) syndrome por Henry Houlden

Publicado 2002

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2

Mutations in the 5' region of the myotubularin-related protein 2 (MTMR2) gene in autosomal recessive hereditary neuropathy with focally folded myelin por Henry Houlden

Publicado 2001

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3

The genetics and neuropathology of Parkinson’s disease por Henry Houlden, Andrew Singleton

Publicado 2012

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4

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

Publicado 2018

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5

The inherited ataxias: Genetic heterogeneity, mutation databases, and future directions in research and clinical diagnostics por Joshua Hersheson, Andrea Haworth, Henry Houlden

Publicado 2012

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6

DNA repair in the trinucleotide repeat disorders por Lesley Jones, Henry Houlden, Sarah J. Tabrizi

Publicado 2016

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7

Somatic alpha‐synuclein mutations in Parkinson's disease: Hypothesis and preliminary data por Christos Proukakis, Henry Houlden, Anthony H.V. Schapira

Publicado 2013

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8

Review: Insights into molecular mechanisms of disease in neurodegeneration with brain iron accumulation: unifying theories por Charles Arber, A. Li, Henry Houlden, Selina Wray

Publicado 2015

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9

An update on the genetics, clinical presentation, and pathomechanisms of human riboflavin transporter deficiency por Benjamin O’Callaghan, Annet M. Bosch, Henry Houlden

Publicado 2019

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10

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

Publicado 2020

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11

Familial PRRT2 mutation with heterogeneous paroxysmal disorders including paroxysmal torticollis and hemiplegic migraine por Russell C. Dale, A. Gardiner, Jayne Antony, Henry Houlden

Publicado 2012

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12

Towards a complete resolution of the genetic architecture of disease por Andrew Singleton, John Hardy, Bryan J. Traynor, Henry Houlden

Publicado 2010

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13

Genetic risk factors for intracranial aneurysms por Varinder S. Alg, Reecha Sofat, Henry Houlden, David J. Werring

Publicado 2013

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14

Spinocerebellar ataxia: an update por Roisin Sullivan, Wai Yan Yau, Emer O’Connor, Henry Houlden

Publicado 2018

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15

CSF1R -Related Disorder por Charles Wade, Kyle Runeckles, Jeremy Chataway, Henry Houlden, David S. Lynch

Publicado 2024

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16

Hereditary spastic paraplegia: from diagnosis to emerging therapeutic approaches por Samuel Shribman, Evan Reid, Andrew H. Crosby, Henry Houlden, Thomas T. Warner

Publicado 2019

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17

SPG11 mutations are common in familial cases of complicated hereditary spastic paraplegia por Coro Paisán‐Ruíz, Okan Doğu, Ayça Dilara Yılmaz, Henry Houlden, Andrew Singleton

Publicado 2008

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18

Human ataxias: a genetic dissection of inositol triphosphate receptor (ITPR1)-dependent signaling por Stéphanie Schorge, Joyce van de Leemput, Andrew Singleton, Henry Houlden, John Hardy

Publicado 2010

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19

Riboflavin Responsive Mitochondrial Dysfunction in Neurodegenerative Diseases por Tamilarasan Udhayabanu, Andreea Manole, Mohan Rajeshwari, Perumal Varalakshmi, Henry Houlden, Balasubramaniem Ashokkumar

Publicado 2017

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20

α-Synuclein mutations cluster around a putative protein loop por Eleanna Kara, Patrick A. Lewis, Helen Ling, Christos Proukakis, Henry Houlden, John Hardy

Publicado 2013

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Clinical and genetic characterization of families with triple A (Allgrove) syndrome por Henry Houlden

Mutations in the 5' region of the myotubularin-related protein 2 (MTMR2) gene in autosomal recessive hereditary neuropathy with focally folded myelin por Henry Houlden

The genetics and neuropathology of Parkinson’s disease por Henry Houlden, Andrew Singleton

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

The inherited ataxias: Genetic heterogeneity, mutation databases, and future directions in research and clinical diagnostics por Joshua Hersheson, Andrea Haworth, Henry Houlden

DNA repair in the trinucleotide repeat disorders por Lesley Jones, Henry Houlden, Sarah J. Tabrizi

Somatic alpha‐synuclein mutations in Parkinson's disease: Hypothesis and preliminary data por Christos Proukakis, Henry Houlden, Anthony H.V. Schapira

Review: Insights into molecular mechanisms of disease in neurodegeneration with brain iron accumulation: unifying theories por Charles Arber, A. Li, Henry Houlden, Selina Wray

An update on the genetics, clinical presentation, and pathomechanisms of human riboflavin transporter deficiency por Benjamin O’Callaghan, Annet M. Bosch, Henry Houlden

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

Familial <i>PRRT2</i> mutation with heterogeneous paroxysmal disorders including paroxysmal torticollis and hemiplegic migraine por Russell C. Dale, A. Gardiner, Jayne Antony, Henry Houlden

Towards a complete resolution of the genetic architecture of disease por Andrew Singleton, John Hardy, Bryan J. Traynor, Henry Houlden

Genetic risk factors for intracranial aneurysms por Varinder S. Alg, Reecha Sofat, Henry Houlden, David J. Werring

Spinocerebellar ataxia: an update por Roisin Sullivan, Wai Yan Yau, Emer O’Connor, Henry Houlden

<i>CSF1R</i> -Related Disorder por Charles Wade, Kyle Runeckles, Jeremy Chataway, Henry Houlden, David S. Lynch

Hereditary spastic paraplegia: from diagnosis to emerging therapeutic approaches por Samuel Shribman, Evan Reid, Andrew H. Crosby, Henry Houlden, Thomas T. Warner

<i>SPG11</i> mutations are common in familial cases of complicated hereditary spastic paraplegia por Coro Paisán‐Ruíz, Okan Doğu, Ayça Dilara Yılmaz, Henry Houlden, Andrew Singleton

Human ataxias: a genetic dissection of inositol triphosphate receptor (ITPR1)-dependent signaling por Stéphanie Schorge, Joyce van de Leemput, Andrew Singleton, Henry Houlden, John Hardy

Riboflavin Responsive Mitochondrial Dysfunction in Neurodegenerative Diseases por Tamilarasan Udhayabanu, Andreea Manole, Mohan Rajeshwari, Perumal Varalakshmi, Henry Houlden, Balasubramaniem Ashokkumar

α-Synuclein mutations cluster around a putative protein loop por Eleanna Kara, Patrick A. Lewis, Helen Ling, Christos Proukakis, Henry Houlden, John Hardy

Resultados de procura - Henry Houlden

Clinical and genetic characterization of families with triple A (Allgrove) syndrome por Henry Houlden

Mutations in the 5' region of the myotubularin-related protein 2 (MTMR2) gene in autosomal recessive hereditary neuropathy with focally folded myelin por Henry Houlden

The genetics and neuropathology of Parkinson’s disease por Henry Houlden, Andrew Singleton

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

The inherited ataxias: Genetic heterogeneity, mutation databases, and future directions in research and clinical diagnostics por Joshua Hersheson, Andrea Haworth, Henry Houlden

DNA repair in the trinucleotide repeat disorders por Lesley Jones, Henry Houlden, Sarah J. Tabrizi

Somatic alpha‐synuclein mutations in Parkinson's disease: Hypothesis and preliminary data por Christos Proukakis, Henry Houlden, Anthony H.V. Schapira

Review: Insights into molecular mechanisms of disease in neurodegeneration with brain iron accumulation: unifying theories por Charles Arber, A. Li, Henry Houlden, Selina Wray

An update on the genetics, clinical presentation, and pathomechanisms of human riboflavin transporter deficiency por Benjamin O’Callaghan, Annet M. Bosch, Henry Houlden

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

Familial <i>PRRT2</i> mutation with heterogeneous paroxysmal disorders including paroxysmal torticollis and hemiplegic migraine por Russell C. Dale, A. Gardiner, Jayne Antony, Henry Houlden

Towards a complete resolution of the genetic architecture of disease por Andrew Singleton, John Hardy, Bryan J. Traynor, Henry Houlden

Genetic risk factors for intracranial aneurysms por Varinder S. Alg, Reecha Sofat, Henry Houlden, David J. Werring

Spinocerebellar ataxia: an update por Roisin Sullivan, Wai Yan Yau, Emer O’Connor, Henry Houlden

<i>CSF1R</i> -Related Disorder por Charles Wade, Kyle Runeckles, Jeremy Chataway, Henry Houlden, David S. Lynch

Hereditary spastic paraplegia: from diagnosis to emerging therapeutic approaches por Samuel Shribman, Evan Reid, Andrew H. Crosby, Henry Houlden, Thomas T. Warner

<i>SPG11</i> mutations are common in familial cases of complicated hereditary spastic paraplegia por Coro Paisán‐Ruíz, Okan Doğu, Ayça Dilara Yılmaz, Henry Houlden, Andrew Singleton

Human ataxias: a genetic dissection of inositol triphosphate receptor (ITPR1)-dependent signaling por Stéphanie Schorge, Joyce van de Leemput, Andrew Singleton, Henry Houlden, John Hardy

Riboflavin Responsive Mitochondrial Dysfunction in Neurodegenerative Diseases por Tamilarasan Udhayabanu, Andreea Manole, Mohan Rajeshwari, Perumal Varalakshmi, Henry Houlden, Balasubramaniem Ashokkumar

α-Synuclein mutations cluster around a putative protein loop por Eleanna Kara, Patrick A. Lewis, Helen Ling, Christos Proukakis, Henry Houlden, John Hardy

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