E-LIB Suche - Ergebnisse für: Hewamadduma, Channa

1

Conformational fingerprinting with Raman spectroscopy revea..:

Alix, James J. P. ; Plesia, Maria ; Dudgeon, Alexander P....
The Analyst. 149 (2024) 9 - p. 2738-2746 , 2024

Link: https://doi.org/10.1039/..

2

Male Reproduction in Spinal Muscular Atrophy (SMA) and the ..:

Bar-Chama, Natan ; Elsheikh, Bakri ; Hewamadduma, Channa...
Neurology and Therapy. , 2024

Link: https://doi.org/10.1007/..

3

Long-term safety and efficacy of zilucoplan in patients wit..:

Howard Jr, James F. ; Bresch, Saskia ; Farmakidis, Constantine...
Therapeutic Advances in Neurological Disorders. 17 (2024) - p. , 2024

Link: https://doi.org/10.1177/..

4

A Single-Sensor Approach to Quantify Gait in Patients with ..:

van Gelder, Linda M. A. ; Bonci, Tecla ; Buckley, Ellen E....
Sensors. 23 (2023) 14 - p. 6563 , 2023

Link: https://doi.org/10.3390/..

5

Long-term safety, efficacy & self-injection satisfaction wi..:

Genge, Angela ; Leite, M. Isabel ; Bresch, Saskia...
Journal of the Neurological Sciences. 455 (2023) - p. 122025 , 2023

Link: https://doi.org/10.1016/..

6

Subgroup outcomes from RAISE: A randomized, Phase 3 trial o..:

Weiss, Michael D. ; Bresch, Saskia ; Freimer, Miriam...
Neurology. 100 (2023) 17_supplement_2 - p. , 2023

Link: https://doi.org/10.1212/..

7

Multi-Centre Audit Of Myotonic Dystrophy In the UK: How Can..:

Hewamadduma, Channa ; Lilleker, James ; Kelly, Phillip...
Neurology. 100 (2023) 17_supplement_2 - p. , 2023

Link: https://doi.org/10.1212/..

8

Heterozygous UCHL1 loss-of-function variants cause a neurod..:

Park, Joohyun ; Tucci, Arianna ; Cipriani, Valentina...
Genetics in Medicine. 25 (2023) 10 - p. 100961 , 2023

Link: https://doi.org/10.1016/..

9

Mutant TRIAP1 causes impaired mitochondrial bioenergetics a..:

Falabella, Micol ; Tabara, Luis Carlos ; Poole, Olivia V....
Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1863 (2022) - p. 148844 , 2022

Link: https://doi.org/10.1016/..

10

Rapid identification of human muscle disease with fibre opt..:

Alix, James J. P. ; Plesia, Maria ; Lloyd, Gavin R....
The Analyst. 147 (2022) 11 - p. 2533-2540 , 2022

Link: https://doi.org/10.1039/..

11

Heterozygous UCHL1 loss-of-function variants cause a neurod..:

Park, Joohyun ; Tucci, Arianna ; Cipriani, Valentina...
Genetics in Medicine. 24 (2022) 10 - p. 2079-2090 , 2022

Link: https://doi.org/10.1016/..

12

Value of systematic genetic screening of patients with amyo..:

Shepheard, Stephanie R ; Parker, Matthew D ; Cooper-Knock, Johnathan...
Journal of Neurology, Neurosurgery & Psychiatry. 92 (2021) 5 - p. 510-518 , 2021

Link: https://doi.org/10.1136/..

13

The utility of thermal threshold tests in the management of..:

Wijekoon, Tharindri ; McTigh, Aimee ; Hewamadduma, Channa
Clinical Medicine. 19 (2019) 2 - p. s43 , 2019

Link: https://doi.org/10.7861/..

14

Chronic idiopathic axonal polyneuropathy: Prevalence of pai..:

Zis, Panagiotis ; Sarrigiannis, Ptolemaios G. ; Rao, Dasappaiah G...
Brain and Behavior. 9 (2018) 1 - p. , 2018

Link: https://doi.org/10.1002/..

15

Chronic idiopathic axonal polyneuropathy: a systematic revi..:

Zis, Panagiotis ; Sarrigiannis, Ptolemaios Georgios ; Rao, Dasappaiah Ganesh..
Journal of Neurology. 263 (2016) 10 - p. 1903-1910 , 2016

Link: https://doi.org/10.1007/..