Kulshrestha R - Search Results

1

Neuromuscular diseases and advance care plans: traffic light system.

Willis TA, Macfarlane M, Vithlani R, Bassie C, Kulshrestha R, Willis D. Willis TA, et al. Among authors: kulshrestha r. BMJ Support Palliat Care. 2021 Mar;11(1):116. doi: 10.1136/bmjspcare-2020-002336. Epub 2020 Jun 8. BMJ Support Palliat Care. 2021. PMID: 32513680 No abstract available.

2

Charcot Marie Tooth disease type 2S with late onset diaphragmatic weakness: An atypical case.

Kulshrestha R, Forrester N, Antoniadi T, Willis T, Sethuraman SK, Samuels M. Kulshrestha R, et al. Neuromuscul Disord. 2018 Dec;28(12):1016-1021. doi: 10.1016/j.nmd.2018.09.008. Epub 2018 Oct 5. Neuromuscul Disord. 2018. PMID: 30409445

3

Healthcare utilisation in children with SMA type 1 treated with nusinersen: a single centre retrospective review.

Ali I, Gilchrist FJ, Carroll WD, Alexander J, Clayton S, Kulshrestha R, Willis T, Samuels M. Ali I, et al. Among authors: kulshrestha r. BMJ Paediatr Open. 2019 Dec 5;3(1):e000572. doi: 10.1136/bmjpo-2019-000572. eCollection 2019. BMJ Paediatr Open. 2019. PMID: 31909224 Free PMC article.

4

Evaluating the Feasibility and Reliability of Remotely Delivering and Scoring the North Star Ambulatory Assessment in Ambulant Patients with Duchenne Muscular Dystrophy.

Emery N, Strachan K, Kulshrestha R, Kuiper JH, Willis T. Emery N, et al. Among authors: kulshrestha r. Children (Basel). 2022 May 16;9(5):728. doi: 10.3390/children9050728. Children (Basel). 2022. PMID: 35626905 Free PMC article.

5

Upper Limb Rehabilitation in Facioscapulohumeral Muscular Dystrophy: A Patients' Perspective.

Faux-Nightingale A, Kulshrestha R, Emery N, Pandyan A, Willis T, Philp F. Faux-Nightingale A, et al. Among authors: kulshrestha r. Arch Rehabil Res Clin Transl. 2021 Sep 16;3(4):100157. doi: 10.1016/j.arrct.2021.100157. eCollection 2021 Dec. Arch Rehabil Res Clin Transl. 2021. PMID: 34977539 Free PMC article.

6

A pilot study of a single intermittent arm cycling exercise programme on people affected by Facioscapulohumeral dystrophy (FSHD).

Philp F, Kulshrestha R, Emery N, Arkesteijn M, Pandyan A, Willis T. Philp F, et al. Among authors: kulshrestha r. PLoS One. 2022 Jun 24;17(6):e0268990. doi: 10.1371/journal.pone.0268990. eCollection 2022. PLoS One. 2022. PMID: 35749388 Free PMC article.

7

A novel MYH2 mutation in family members presenting with congenital myopathy, ophthalmoplegia and facial weakness.

Willis T, Hedberg-Oldfors C, Alhaswani Z, Kulshrestha R, Sewry C, Oldfors A. Willis T, et al. Among authors: kulshrestha r. J Neurol. 2016 Jul;263(7):1427-33. doi: 10.1007/s00415-016-8154-8. Epub 2016 May 13. J Neurol. 2016. PMID: 27177998

8

Two Cases of Spinal Muscular Atrophy Type II with Eosinophilic Oesophagitis.

Fuller HR, Shorrock HK, Gillingwater TH, Pigott A, Smith V, Kulshrestha R, Sewry CS, Willis TA. Fuller HR, et al. Among authors: kulshrestha r. J Neuromuscul Dis. 2017;4(4):357-362. doi: 10.3233/JND-170260. J Neuromuscul Dis. 2017. PMID: 29172006

9

Deletion of P2 promoter of GJB1 gene a cause of Charcot-Marie-Tooth disease.

Kulshrestha R, Burton-Jones S, Antoniadi T, Rogers M, Jaunmuktane Z, Brandner S, Kiely N, Manuel R, Willis T. Kulshrestha R, et al. Neuromuscul Disord. 2017 Aug;27(8):766-770. doi: 10.1016/j.nmd.2017.05.001. Epub 2017 May 4. Neuromuscul Disord. 2017. PMID: 28601552

10

High-Throughput Digital Image Analysis Reveals Distinct Patterns of Dystrophin Expression in Dystrophinopathy Patients.

Torelli S, Scaglioni D, Sardone V, Ellis MJ, Domingos J, Jones A, Feng L, Chambers D, Eastwood DM, Leturcq F, Yaou RB, Urtizberea A, Sabouraud P, Barnerias C, Stojkovic T, Ricci E, Beuvin M, Bonne G, Sewry CA, Willis T, Kulshrestha R, Tasca G, Phadke R, Morgan JE, Muntoni F. Torelli S, et al. Among authors: kulshrestha r. J Neuropathol Exp Neurol. 2021 Oct 26;80(10):955-965. doi: 10.1093/jnen/nlab088. J Neuropathol Exp Neurol. 2021. PMID: 34498054 Free PMC article.

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