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Corbett Alastair
75
results:
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Online (75)
Mediatypes
Articles (Online) (46)
OpenAccess-fulltext (29)
Sorted by: Relevance
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1
Genome and RNA sequencing boost neuromuscular diagnoses to ..:
Marchant, Rhett G.
;
Bryen, Samantha J.
;
Bahlo, Melanie
...
Annals of Clinical and Translational Neurology. 11 (2024) 5 - p. 1250-1266 , 2024
Link:
https://doi.org/10.1002/..
?
2
The facioscapulohumeral muscular dystrophy Rasch‐built over..:
Mul, Karlien
;
Hamadeh, Tatiana
;
Horlings, Corinne G. C.
...
European Journal of Neurology. 28 (2021) 7 - p. 2339-2348 , 2021
Link:
https://doi.org/10.1111/..
?
3
Facioscapulohumeral muscular dystrophy type 2: an update on..:
Jia, Fangzhi Frank
;
Drew, Alexander P.
;
Nicholson, Garth Alexander
..
Neuromuscular Disorders. 31 (2021) 11 - p. 1101-1112 , 2021
Link:
https://doi.org/10.1016/..
?
4
Is it Pompe Disease? Australian diagnostic considerations:
Tchan, Michel
;
Henderson, Robert
;
Kornberg, Andrew
...
Neuromuscular Disorders. 30 (2020) 5 - p. 389-399 , 2020
Link:
https://doi.org/10.1016/..
?
5
What Does Good Green Infrastructure Planning Policy Look Li..:
Hislop, Max
;
Scott, Alister J.
;
Corbett, Alastair
Planning Theory & Practice. 20 (2019) 5 - p. 633-655 , 2019
Link:
https://doi.org/10.1080/..
?
6
Enhanced serum immunoglobulin G clearance in myotonic dystr..:
Sasson, Sarah C.
;
Corbett, Alastair
;
McLachlan, Andrew J.
...
Journal of Medical Case Reports. 13 (2019) 1 - p. , 2019
Link:
https://doi.org/10.1186/..
?
7
Recessive DES cardio/myopathy without myofibrillar aggregat..:
Riley, Lisa G.
;
Waddell, Leigh B.
;
Ghaoui, Roula
...
European Journal of Human Genetics. 27 (2019) 8 - p. 1267-1273 , 2019
Link:
https://doi.org/10.1038/..
?
8
Congenital Titinopathy: Comprehensive characterization and ..:
Oates, Emily C.
;
Jones, Kristi J.
;
Donkervoort, Sandra
...
Annals of Neurology. 83 (2018) 6 - p. 1105-1124 , 2018
Link:
https://doi.org/10.1002/..
?
9
Warts and all: Fingolimod and unusual HPV-associated lesion:
Triplett, James
;
Kermode, Allan G
;
Corbett, Alastair
.
Multiple Sclerosis Journal. 25 (2018) 11 - p. 1547-1550 , 2018
Link:
https://doi.org/10.1177/..
?
10
High Degree of Genetic Heterogeneity for Hereditary Cerebel..:
Kang, Ce
;
Liang, Christina
;
Ahmad, Kate E.
...
The Cerebellum. 18 (2018) 1 - p. 137-146 , 2018
Link:
https://doi.org/10.1007/..
?
11
Bone health in facioscapulohumeral muscular dystrophy: A cr..:
Chagarlamudi, Hema
;
Corbett, Alastair
;
Stoll, Marion
...
Muscle & Nerve. 56 (2017) 6 - p. 1108-1113 , 2017
Link:
https://doi.org/10.1002/..
?
12
Sarcolemmal excitability in the myotonic dystrophies:
Boland‐Freitas, Robert
;
Lee, James
;
Howells, James
...
Muscle & Nerve. 57 (2017) 4 - p. 595-602 , 2017
Link:
https://doi.org/10.1002/..
?
13
Mortality and Causes of Death in Patients with Sporadic Inc..:
Price, Mark A.
;
Barghout, Victoria
;
Benveniste, Olivier
...
Journal of Neuromuscular Diseases. 3 (2016) 1 - p. 67-75 , 2016
Link:
https://doi.org/10.3233/..
?
14
Expanding the phenotype of GMPPB mutations:
Cabrera-Serrano, Macarena
;
Ghaoui, Roula
;
Ravenscroft, Gianina
...
Brain. 138 (2015) 4 - p. 836-844 , 2015
Link:
https://doi.org/10.1093/..
?
15
Assessment of Mortality in Sporadic Inclusion Body Myositis..:
Barghout, Victoria
;
Price, Mark
;
Benveniste, Olivier
...
Neurology. 82 (2014) 10_supplement - p. , 2014
Link:
https://doi.org/10.1212/..
1-15