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Author/Creator Wilson, Matthew P

1. 15.09 Inherited peripheral neuropathies: analysis of PDXK gene identifies a new treatable disorder. Issue 12 (14th November 2019)

Authors:
Chelban, Viorica; Wilson, Matthew P; Chardon, Jodi Warman; Vandrovcova, Jana; Natalia Zanetti, M; Zamba-Papanicolaou, Eleni; Efthymiou, Stephanie; Pope, Simon; Conte, Maria R; Abis, Giancarlo; Liu, Yo-Tsen; Tribollet, Eloise; Haridy, Nourelhoda A; Botía, Juan A; Ryten, Mina; Nicolaou, Paschalis; ...
Journal:
Journal of neurology, neurosurgery and psychiatry
Issue:
Volume 90:Issue 12(2019)
Page Start:
e4
Record Type:
Journal Article
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2. CAMLG-CDG: a novel congenital disorder of glycosylation linked to defective membrane trafficking. Issue 15 (9th March 2022)

Authors:
Wilson, Matthew P; Durin, Zoé; Unal, Özlem; Ng, Bobby G; Marrecau, Thomas; Keldermans, Liesbeth; Souche, Erika; Rymen, Daisy; Gündüz, Mehmet; Köse, Gülşen; Sturiale, Luisa; Garozzo, Domenico; Freeze, Hudson H; Jaeken, Jaak; Foulquier, François; Matthijs, Gert
Journal:
Human molecular genetics
Issue:
Volume 31:Issue 15(2022)
Page Start:
2571
Record Type:
Journal Article
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3. Quality and stability of extemporaneous pyridoxal phosphate preparations used in the treatment of paediatric epilepsy. (21st February 2017)

Authors:
Mohamed-Ahmed, Abeer H A; Wilson, Matthew P; Albuera, Maedelyn; Chen, Ting; Mills, Philippa B; Footitt, Emma J; Clayton, Peter T; Tuleu, Catherine
Journal:
Journal of pharmacy and pharmacology
Issue:
Volume 69:Number 4(2017:Apr.)
Page Start:
480
Record Type:
Journal Article
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