1. A novel homozygous variant extending the peripheral myelin protein 22 by 9 amino acids causes early‐onset Charcot‐Marie‐Tooth disease with predominant severe sensory ataxia. Issue 3 (29th May 2020) Authors: Zambon, Alberto A.; Pitt, Matthew; Laurà, Matilde; Polke, James M.; Reilly, Mary M.; Muntoni, Francesco Journal: Journal of the peripheral nervous system Issue: Volume 25:Issue 3(2020) Page Start: 303 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Acquired neuromyotonia in children with CASPR2 and LGI1 antibodies. (6th February 2019) Authors: Surana, Snehal; Kumar, Ratna; Pitt, Matthew; Hafner, Patricia; Mclellan, Ailsa; Davidson, Joyce; Prabakhar, Prab; Vincent, Angela; Hacohen, Yael; Wright, Sukhvir Journal: Developmental medicine & child neurology Issue: Volume 61:Number 11(2019) Page Start: 1344 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Backpack palsy: A rare complication of backpack use in children and young adults – A new case report. (September 2016) Authors: Rose, Katy; Davies, Anne; Pitt, Matthew; Ratnasinghe, Didi; D'Argenzio, Luigi Journal: European journal of paediatric neurology Issue: Volume 20:Number 5(2016:Sep.) Page Start: 750 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. 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) ↗
5. Early electrodiagnosis in the management of neonatal brachial plexus palsy: A systematic review. Issue 5 (9th December 2019) Authors: van der Looven, Ruth; Le Roy, Laura; Tanghe, Emma; van den Broeck, Christine; de Muynck, Martine; Vingerhoets, Guy; Pitt, Matthew; Vanderstraeten, Guy Journal: Muscle & nerve Issue: Volume 61:Issue 5(2020) Page Start: 557 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Effects of fluoxetine on functional outcomes after acute stroke (FOCUS): a pragmatic, double-blind, randomised, controlled trial. Issue 10168 (19th January 2019) Authors: Dennis, Martin; Mead, Gillian; Forbes, John; Graham, Catriona; Hackett, Maree; Hankey, Graeme J; House, Allan; Lewis, Stephanie; Lundström, Erik; Sandercock, Peter; Innes, Karen; Williams, Carol; Drever, Jonathan; Mcgrath, Aileen; Deary, Ann; Fraser, Ruth; Anderson, Rosemary; Walker, Pauli; Perry... Journal: Lancet Issue: Volume 393:Issue 10168(2019) Page Start: 265 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Goldberg–Shprintzen megacolon syndrome with associated sensory motor axonal neuropathy. (2nd April 2015) Authors: Dafsari, Hormos Salimi; Byrne, Susan; Lin, Jean‐Pierre; Pitt, Matthew; Jongbloed, Jan DH; Flinter, Frances; Jungbluth, Heinz Journal: American journal of medical genetics Issue: Volume 167:Number 6(2015:Jun.) Page Start: 1300 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Guidelines for single fiber EMG. Issue 8 (August 2019) Authors: Sanders, Donald B.; Arimura, Kimiyoshi; Cui, LiYing; Ertaş, Mustafa; Farrugia, Maria Elena; Gilchrist, James; Kouyoumdjian, João Aris; Padua, Luca; Pitt, Matthew; Stålberg, Erik Journal: Clinical neurophysiology Issue: Volume 130:Issue 8(2019:Aug.) Page Start: 1417 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Homozygous mutations in VAMP1 cause a presynaptic congenital myasthenic syndrome. Issue 4 (29th March 2017) Authors: Salpietro, Vincenzo; Lin, Weichun; Vedove, Andrea Delle; Storbeck, Markus; Liu, Yun; Efthymiou, Stephanie; Manole, Andreea; Wiethoff, Sarah; Ye, Qiaohong; Saggar, Anand; McElreavey, Kenneth; Krishnakumar, Shyam S.; Pitt, Matthew; Bello, Oscar D.; Rothman, James E.; Basel‐Vanagaite, Lina; Hubshman... Journal: Annals of neurology Issue: Volume 81:Issue 4(2017) Page Start: 597 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Isolated bulbar palsy and dysphagia in children with respiratory symptoms. (2nd October 2021) Authors: Zimmels, Stacey; Balfour‐Lynn, Ian M; Christodoulou, Loucas; Pantazi, Mantha; Pavlidou, Efterpi; Pitt, Matthew; Kinali, Maria; Ismayilova, Naila Journal: Developmental medicine & child neurology Issue: Volume 64:Number 4(2022) Page Start: 518 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗