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Echaniz-Laguna, A.
334
results:
Search for persons
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Format
Online (334)
Mediatypes
Articles (Online) (167)
Bookchapter (Online) (1)
OpenAccess-fulltext (166)
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english (275)
french (55)
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1
Transthyretin amyloid polyneuropathy in France: A cross-sec..:
Adams, D.
;
Cintas, P.
;
Solé, G.
...
Revue Neurologique. , 2024
Link:
https://doi.org/10.1016/..
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2
Prediction of cardiac outcomes in 600 adult patients with m..:
Savvatis, K.
;
Vissing, C.
;
Klouvi, L.
...
Archives of Cardiovascular Diseases Supplements. 15 (2023) 1 - p. 30 , 2023
Link:
https://doi.org/10.1016/..
?
3
Treating hereditary transthyretin amyloidosis: Present & fu..:
Echaniz-Laguna, A.
;
Cauquil, C.
;
Labeyrie, C.
.
Revue Neurologique. 179 (2023) 1-2 - p. 30-34 , 2023
Link:
https://doi.org/10.1016/..
?
4
Parvovirus B19-related peripheral nerve necrotizing vasculi..:
Fargeot, G.
;
Périllaud-Dubois, C.
;
Deback, C.
...
Revue Neurologique. 178 (2022) 1-2 - p. 158-160 , 2022
Link:
https://doi.org/10.1016/..
?
5
French recommendations for the management of adult & pediat..:
Fargeot, G.
;
Gitiaux, C.
;
Magy, L.
...
Revue Neurologique. 178 (2022) 9 - p. 953-968 , 2022
Link:
https://doi.org/10.1016/..
?
6
Early detection of cardiac and skin amyloid deposits among ..:
Slama, M.
;
Piekarski, E.
;
Eliahou, L.
...
Archives of Cardiovascular Diseases Supplements. 13 (2021) 1 - p. 31 , 2021
Link:
https://doi.org/10.1016/..
?
7
Neuropathies périphériques associées aux syndromes lymphopr..:
Pacoureau, L.
;
Labeyrie, C.
;
Catalan, P.
...
La Revue de Médecine Interne. 42 (2021) 12 - p. 844-854 , 2021
Link:
https://doi.org/10.1016/..
?
8
RFC1 gene intronic repeat expansion and unexplained chronic..:
Fargeot, G.
;
Humbert, M.
;
Echaniz-Laguna, A.
Respiratory Medicine and Research. 80 (2021) - p. 100831 , 2021
Link:
https://doi.org/10.1016/..
?
9
O.5A new glycogen storage disorder caused by a dominant mut..:
Echaniz-Laguna, A.
;
Lornage, X.
;
Edelweiss, E.
...
Neuromuscular Disorders. 29 (2019) - p. S39 , 2019
Link:
https://doi.org/10.1016/..
?
10
P.114Clinical, histological, and genetic characterization o..:
Lornage, X.
;
Schartner, V.
;
Balbueno, I.
...
Neuromuscular Disorders. 29 (2019) - p. S82 , 2019
Link:
https://doi.org/10.1016/..
?
11
METABOLIC MYOPATHIES I:
Echaniz-Laguna, A.
;
Nadjar, Y.
;
Béhin, A.
...
Neuromuscular Disorders. 28 (2018) - p. S114 , 2018
Link:
https://doi.org/10.1016/..
?
12
Progressive encephalomyelitis with rigidity and myoclonus, ..:
Wirth, T.
;
Kaeuffer, C.
;
Chanson, J.B.
...
Revue Neurologique. 174 (2018) 5 - p. 343-346 , 2018
Link:
https://doi.org/10.1016/..
?
13
Comparing ataxias with oculomotor apraxia: a multimodal stu..:
Mariani, L. L.
;
Rivaud-Péchoux, S.
;
Charles, P.
...
Scientific Reports. 7 (2017) 1 - p. , 2017
Link:
https://doi.org/10.1038/..
?
14
Deciphering the causes of sporadic late-onset cerebellar at..:
Gebus, O.
;
Montaut, S.
;
Monga, B.
...
Journal of Neurology. 264 (2017) 6 - p. 1118-1126 , 2017
Link:
https://doi.org/10.1007/..
?
15
A novel mutation in HSPB8 causes dominant adult-onset axial..:
Echaniz-Laguna, A.
;
Lornage, X.
;
Lannes, B.
...
Neuromuscular Disorders. 27 (2017) - p. S120 , 2017
Link:
https://doi.org/10.1016/..
1-15