All papers authored by Philippa Mills
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2022
Apostolos Papandreou,
Ivan Doykov,
Justyna Spiewak,
Nikita Komarov,
Stephanie Habermann,
Manju A. Kurian,
Philippa B. Mills 
,
Kevin Mills,
Paul Gissen,
Wendy E. Heywood
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,
Kevin Mills,
Paul Gissen,
Wendy E. Heywood
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2020
Katharina Iwan ,
Robert Clayton,
Philippa Mills ,
Barbara Csanyi,
Paul Gissen,
Sara E. Mole ,
David N. Palmer,
Kevin Mills ,
Wendy E. Heywood
,
Robert Clayton,
Philippa Mills ,
Barbara Csanyi,
Paul Gissen,
Sara E. Mole ,
David N. Palmer,
Kevin Mills ,
Wendy E. Heywood
Urine Proteomics Analysis of Patients with Neuronal Ceroid Lipofuscinoses
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2019
Nina Patel,
Philippa Mills ,
James Davison ,
Maureen Cleary,
Paul Gissen ,
Blerida Banushi ,
Ivan Doykov ,
Megan Dorman,
Kevin Mills ,
Wendy E. Heywood
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,
James Davison ,
Maureen Cleary,
Paul Gissen ,
Blerida Banushi ,
Ivan Doykov ,
Megan Dorman,
Kevin Mills ,
Wendy E. Heywood
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Matthew P. Wilson,
Barbara Plecko,
Philippa B. Mills ,
Peter T. Clayton
,
Peter T. Clayton
Disorders affecting vitamin B6 metabolism
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2018
Julien Baruteau,
Dany P. Perocheau,
Joanna Hanley,
Maëlle Lorvellec,
Eridan Rocha-Ferreira,
Rajvinder Karda ,
Joanne Ng,
Natalie Suff,
Juan Antinao Diaz ,
Ahad A. Rahim,
Michael P. Hughes,
Blerida Banushi,
Helen Prunty ,
Mariya Hristova,
Deborah A. Ridout
and 7 other authors
,
Joanne Ng,
Natalie Suff,
Juan Antinao Diaz ,
Ahad A. Rahim,
Michael P. Hughes,
Blerida Banushi,
Helen Prunty ,
Mariya Hristova,
Deborah A. Ridout
and 7 other authors
Argininosuccinic aciduria fosters neuronal nitrosative stress reversed by Asl gene transfer
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Wendy E. Heywood,
Nina Patel,
Ivan Doykov,
Simon Heales,
Derek Burke,
Peter Clayton,
Philippa Mills ,
James Davison,
Maureen Cleary,
Tenni Ruggero,
Paul Gissen,
Kevin Mills
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,
James Davison,
Maureen Cleary,
Tenni Ruggero,
Paul Gissen,
Kevin Mills
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2017
Matthew P. Wilson ,
Emma J. Footitt,
Apostolos Papandreou,
Mari-Liis Uudelepp,
Ronit Pressler,
Danielle C. Stevenson,
Camila Gabriel,
Mel McSweeney,
Matthew Baggot,
Derek Burke,
Tommy Stödberg,
Kate Riney,
Manuel Schiff,
Simon J. R. Heales,
Kevin A. Mills
and 3 other authors
Download from pubs.acs.org
,
Emma J. Footitt,
Apostolos Papandreou,
Mari-Liis Uudelepp,
Ronit Pressler,
Danielle C. Stevenson,
Camila Gabriel,
Mel McSweeney,
Matthew Baggot,
Derek Burke,
Tommy Stödberg,
Kate Riney,
Manuel Schiff,
Simon J. R. Heales,
Kevin A. Mills
and 3 other authors
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R. L. P. de Rooy,
F. J. Halbertsma,
E. A. Struijs,
E. A. Struys,
F. J. van Spronsen,
R. J. Lunsing,
H. M. Schippers,
P. M. van Hasselt,
B. Plecko,
L. A. Bok,
G. Wohlrab,
S. Whalen,
S. Wahlen,
J. F. Benoist,
S. Valence
and 1 other authors
Pyridoxine dependent epilepsy: Is late onset a predictor for favorable outcome?
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Timothy A. Scott,
Leonor M. Quintaneiro,
Povilas Norvaisas,
Prudence P. Lui,
Matthew P. Wilson,
Kit-Yi Leung,
Lucia Herrera-Dominguez,
Sonia Sudiwala,
Alberto Pessia,
Peter T. Clayton,
Kevin Bryson,
Vidya Velagapudi,
Philippa B. Mills ,
Athanasios Typas,
Nicholas D. E. Greene
and 1 other authors
,
Athanasios Typas,
Nicholas D. E. Greene
and 1 other authors
Host-Microbe Co-metabolism Dictates Cancer Drug Efficacy in C. elegans
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Julien Baruteau ,
Elisabeth Jameson,
Andrew A. Morris,
Anupam Chakrapani,
Saikat Santra,
Suresh Vijay,
Huriye Kocadag,
Clare E. Beesley,
Stephanie Grunewald,
Elaine Murphy,
Maureen Cleary,
Helen Mundy,
Lara Abulhoul,
Alexander Broomfield,
Robin Lachmann
and 11 other authors
,
Elisabeth Jameson,
Andrew A. Morris,
Anupam Chakrapani,
Saikat Santra,
Suresh Vijay,
Huriye Kocadag,
Clare E. Beesley,
Stephanie Grunewald,
Elaine Murphy,
Maureen Cleary,
Helen Mundy,
Lara Abulhoul,
Alexander Broomfield,
Robin Lachmann
and 11 other authors
Expanding the phenotype in argininosuccinic aciduria: need for new therapies
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2016
Pb Mills ,
Niklas Darin,
Emma Reid,
Laurence Prunetti,
Lena Samuelsson,
Ra Husain,
Matthew Wilson,
Basma El Yacoubi,
Emma Footitt,
Wk K. Chong,
Lc Wilson,
Helen Prunty,
Simon Pope ,
Simon Heales,
Valérie de Crécy-Lagard
and 6 other authors
Download from discovery.ucl.ac.uk
,
Niklas Darin,
Emma Reid,
Laurence Prunetti,
Lena Samuelsson,
Ra Husain,
Matthew Wilson,
Basma El Yacoubi,
Emma Footitt,
Wk K. Chong,
Lc Wilson,
Helen Prunty,
Simon Pope ,
Simon Heales,
Valérie de Crécy-Lagard
and 6 other authors
Download from discovery.ucl.ac.uk
Leslie Matalonga,
Miren Bravo ,
Carla Serra-Peinado,
Elisabeth García-Pelegrí,
Olatz Ugarteburu,
Silvia Vidal,
Maria Llambrich,
Ester Quintana,
Pedro Fuster-Jorge,
Maria Nieves Gonzalez-Bravo,
Sergi Beltran,
Joaquin Dopazo,
Francisco Garcia-Garcia,
François Foulquier,
Gert Matthijs
and 6 other authors
,
Carla Serra-Peinado,
Elisabeth García-Pelegrí,
Olatz Ugarteburu,
Silvia Vidal,
Maria Llambrich,
Ester Quintana,
Pedro Fuster-Jorge,
Maria Nieves Gonzalez-Bravo,
Sergi Beltran,
Joaquin Dopazo,
Francisco Garcia-Garcia,
François Foulquier,
Gert Matthijs
and 6 other authors
Mutations inTRAPPC11are associated with a congenital disorder of glycosylation
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Khairunnisa Mukhtiar,
Shahnaz Ibrahim,
Karin Tuschl ,
Phillipa Mills
Download from discovery.ucl.ac.uk
,
Phillipa Mills
Download from discovery.ucl.ac.uk
Emma S. Reid,
Apostolos Papandreou,
Suzanne Drury,
Christopher Boustred,
Wyatt W. Yue,
Yehani Wedatilake,
Clare Beesley,
Thomas S. Jacques,
Glenn Anderson,
Lara Abulhoul,
Alex Broomfield,
Maureen Cleary,
Stephanie Grunewald,
Sophia M. Varadkar,
Nick Lench
and 4 other authors
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Yehani Wedatilake,
Rojeen Niazi,
Elisa Fassone,
Christopher A. Powell,
Sarah Pearce,
Vincent Plagnol,
José W. Saldanha,
Robert Kleta,
W. Kling Chong,
Emma Footitt,
Philippa B. Mills ,
Jan-Willem Taanman,
Michal Minczuk,
Peter T. Clayton,
Shamima Rahman
,
Jan-Willem Taanman,
Michal Minczuk,
Peter T. Clayton,
Shamima Rahman
TRNT1 deficiency: clinical, biochemical and molecular genetic features
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Wendy E. Heywood ,
Emily Bliss,
Philippa Mills ,
Jale Yuzugulen,
Gabriela Carreno,
Peter T. Clayton,
Francesco Muntoni,
Viki C. Worthington,
Silvia Torelli,
Neil J. Sebire,
Kevin Mills,
Stephanie Grunewald
Download from www.ncbi.nlm.nih.gov
,
Emily Bliss,
Philippa Mills ,
Jale Yuzugulen,
Gabriela Carreno,
Peter T. Clayton,
Francesco Muntoni,
Viki C. Worthington,
Silvia Torelli,
Neil J. Sebire,
Kevin Mills,
Stephanie Grunewald
Download from www.ncbi.nlm.nih.gov
Karin Tuschl ,
Esther Meyer,
Leonardo E. Valdivia,
Ningning Zhao,
Chris Dadswell,
Alaa Abdul-Sada,
Christina Y. Hung,
Michael A. Simpson,
W. K. Chong,
Thomas S. Jacques,
Randy L. Woltjer,
Simon Eaton,
Allison Gregory,
Lynn Sanford,
Eleanna Kara
and 25 other authors
,
Esther Meyer,
Leonardo E. Valdivia,
Ningning Zhao,
Chris Dadswell,
Alaa Abdul-Sada,
Christina Y. Hung,
Michael A. Simpson,
W. K. Chong,
Thomas S. Jacques,
Randy L. Woltjer,
Simon Eaton,
Allison Gregory,
Lynn Sanford,
Eleanna Kara
and 25 other authors
Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism–dystonia
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