H. Mundy
发表
K. Bhattacharya,
F. Maillot,
H. Mundy,
2015,
Orphanet Journal of Rare Diseases.
D. Pennell,
R. Mohiaddin,
J. Moon,
2003,
Circulation.
J. Abdenur,
M. Tassini,
N. Dorison,
2018,
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
P. Hindmarsh,
D. Matthews,
J. Leonard,
2003,
Clinical endocrinology.
K. Hussain,
A. Aynsley-Green,
H. Mundy,
2002,
European Journal of Pediatrics.
M. Baumgartner,
B. Seifert,
H. Blom,
2018,
Journal of Inherited Metabolic Disease.
A. Cousins,
H. Mundy,
Philip J. Lee,
2002,
The Lancet.
J. Leonard,
P. Georgiadou,
A. Cousins,
2005,
The Journal of clinical endocrinology and metabolism.
Natural history of epilepsy in argininosuccinic aciduria provides new insights into pathophysiology.
Rishi Sharma,
P. Gissen,
S. Santra,
2022,
medRxiv.
Robert W. Taylor,
N. Lax,
D. Turnbull,
2018,
EBioMedicine.
P. Lee,
H. Mundy,
2002,
Medical hypotheses.
H. Mizumoto,
S. Wortmann,
S. Grünert,
2022,
Genetics in medicine : official journal of the American College of Medical Genetics.
C. Ellaway,
P. Lee,
H. Mundy,
2001,
Journal of Inherited Metabolic Disease.
M. Baumgartner,
B. Seifert,
H. Blom,
2019,
Journal of inherited metabolic disease.
N. Heaton,
G. Mieli-Vergani,
N. Hadžić,
2011,
Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society.
M. Tarnopolsky,
C. Wusthoff,
J. Christodoulou,
2016,
Molecular genetics and metabolism.
Robert W. Taylor,
M. Minczuk,
T. Wieland,
2013,
American journal of human genetics.
S. Eaton,
P. Lee,
H. Mundy,
2007,
Journal of Inherited Metabolic Disease.
Robert W. Taylor,
H. Prokisch,
M. Simpson,
2015,
Brain : a journal of neurology.
B. Weschke,
M. Verbeek,
G. Mancini,
2010,
Brain : a journal of neurology.
Rachel L. Taylor,
Mark T. Handley,
J. Clayton-Smith,
2017,
Investigative ophthalmology & visual science.
Rachel L. Taylor,
Mark T. Handley,
J. Clayton-Smith,
2017
.
C. Marelli,
P. Gissen,
Ç. Kasapkara,
2022,
Life.
M. Deheragoda,
N. Hadžić,
H. Mundy,
2020,
Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver.
R. Lachmann,
A. Broomfield,
E. Jameson,
2017,
Journal of Inherited Metabolic Disease.
P. Fallon,
H. Mundy,
N. Ismayilova,
2019,
JIMD reports.
R. Dalton,
H. Mundy,
C. Turner,
2022,
Orphanet Journal of Rare Diseases.
John J. Mitchell,
Irene J. Hoogeveen,
F. de Boer,
2018,
Molecular genetics and metabolism.
S. Santra,
M. McSweeney,
B. Schwahn,
2021,
JIMD reports.
U. Seedorf,
J. Burn,
P. Clayton,
2001,
European Journal of Human Genetics.
E. Christensen,
N. Dorison,
A. Lund,
2014,
Human mutation.
C. Hendriksz,
J. Guest,
E. Murphy,
2018,
PloS one.
Robert W. Taylor,
R. Horvath,
S. Heales,
2010,
Neuromuscular Disorders.
M. Samuel,
T. Harrower,
J. Moriarty,
2013,
Movement disorders : official journal of the Movement Disorder Society.
Robert W. Taylor,
A. Bender,
R. Horvath,
2010,
Neuromuscular Disorders.
S. Burford,
H. Mundy,
A. Wong,
2008,
The journal of nutrition, health & aging.
A. Cousins,
P. Lee,
H. Mundy,
2006,
Journal of Inherited Metabolic Disease.
M. Baumgartner,
H. Blom,
F. Mochel,
2022,
Journal of inherited metabolic disease.
M. Fewtrell,
P. Lee,
H. Mundy,
2008,
Journal of Inherited Metabolic Disease.
A. Siddiqui,
H. Jungbluth,
A. Marinaki,
2010,
Pediatric neurology.
R. Lachmann,
H. Mundy,
2009
.
J. Hobart,
M. Hanna,
S. Jones,
2003,
Neurology.
E. Christensen,
N. Dorison,
A. Lund,
2014,
Human mutation.
Rishi Sharma,
P. Gissen,
A. Chakrapani,
2023,
Epilepsia.