Search

Author/Creator Beeson, David

2. Antagonistic postsynaptic and presynaptic actions of cyclohexanol on neuromuscular synaptic transmission and function. (26th November 2021)

Authors:
Dissanayake, Kosala N.; Margetiny, Filip; Whitmore, Charlotte L.; Chou, Robert C.‐C.; Roesl, Cornelia; Patel, Vishwendra; McArdle, Joseph J.; Webster, Richard; Beeson, David; Tattersall, John E.H.; Wyllie, David J. A.; Eddleston, Michael; Ribchester, Richard R.
Journal:
Journal of physiology
Issue:
Volume 599:Number 24(2021)
Page Start:
5417
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. Clinical features of congenital myasthenic syndrome due to mutations in DPAGT1. Issue 10 (27th February 2013)

Authors:
Finlayson, Sarah; Palace, Jacqueline; Belaya, Katsiaryna; Walls, Timothy J; Norwood, Fiona; Burke, Georgina; Holton, Janice L; Pascual-Pascual, Samuel I; Cossins, Judith; Beeson, David
Journal:
Journal of neurology, neurosurgery and psychiatry
Issue:
Volume 84:Issue 10(2013)
Page Start:
1119
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

5. Clinical features of the myasthenic syndrome arising from mutations in GMPPB. Issue 8 (4th May 2016)

Authors:
Rodríguez Cruz, Pedro M; Belaya, Katsiaryna; Basiri, Keivan; Sedghi, Maryam; Farrugia, Maria Elena; Holton, Janice L; Liu, Wei Wei; Maxwell, Susan; Petty, Richard; Walls, Timothy J; Kennett, Robin; Pitt, Matthew; Sarkozy, Anna; Parton, Matt; Lochmüller, Hanns; Muntoni, Francesco; Palace, Jacqueli...
Journal:
Journal of neurology, neurosurgery and psychiatry
Issue:
Volume 87:Issue 8(2016)
Page Start:
802
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

7. Congenital myasthenic syndrome due to a TOR1AIP1 mutation: a new disease pathway for impaired synaptic transmission. Issue 2 (18th October 2020)

Authors:
Cossins, Judith; Webster, Richard; Maxwell, Susan; Rodríguez Cruz, Pedro M; Knight, Ravi; Llewelyn, John Gareth; Shin, Ji-Yeon; Palace, Jacqueline; Beeson, David
Journal:
Brain communications
Issue:
Volume 2:Issue 2(2020)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

8. Congenital myasthenic syndrome due to mutations in MUSK suggests that the level of MuSK phosphorylation is crucial for governing synaptic structure. Issue 3 (25th November 2019)

Authors:
Rodríguez Cruz, Pedro M.; Cossins, Judith; Cheung, Jonathan; Maxwell, Susan; Jayawant, Sandeep; Herbst, Ruth; Waithe, Dominic; Kornev, Alexandr P.; Palace, Jacqueline; Beeson, David
Journal:
Human mutation
Issue:
Volume 41:Issue 3(2020)
Page Start:
619
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗