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Jardel, C.
195
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Online (195)
Mediatypes
Articles (Online) (141)
Bookchapter (Online) (3)
OpenAccess-fulltext (51)
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1
Sensory motor ataxic neuropathy associated dysarthria and o..:
Rafai, M.A.
;
Khattab, H.
;
Jardel, C.
...
Revue Neurologique. 177 (2021) 1-2 - p. 144-146 , 2021
Link:
https://doi.org/10.1016/..
?
2
Life-threatening lactic acidosis occurring in adults with m..:
Brisset, M.
;
Béhin, A.
;
Pottier, C.
...
Revue Neurologique. 175 (2019) 9 - p. 564-567 , 2019
Link:
https://doi.org/10.1016/..
?
3
Myopathy with MTCYB mutation mimicking Multiple Acyl-CoA De..:
Kaphan, E.
;
Bou Ali, H.
;
Gastaldi, M.
...
Revue Neurologique. 174 (2018) 10 - p. 731-735 , 2018
Link:
https://doi.org/10.1016/..
?
4
A high prevalence of hypertension inpatients presenting wit..:
Chong-Nguyen, C.
;
Laforêt, P.
;
Goursot, Y.
...
Archives of Cardiovascular Diseases Supplements. 10 (2018) 1 - p. 35-36 , 2018
Link:
https://doi.org/10.1016/..
?
5
METABOLIC MYOPATHIES I:
Madsen, K.
;
Laforêt, P.
;
Buch, A.
...
Neuromuscular Disorders. 28 (2018) - p. S113-S114 , 2018
Link:
https://doi.org/10.1016/..
?
6
Homozygous p.R707W MFN2 mutation is associated with neuropa..:
Masingue, M.
;
Vatier, C.
;
Jéru, I.
...
Neuromuscular Disorders. 27 (2017) - p. S148 , 2017
Link:
https://doi.org/10.1016/..
?
7
Étude phénotypique des mutations rares responsables de diab..:
Decoux-Poullot, A.G.
;
Paquis, V.
;
Bannwarth, S.
...
Annales d'Endocrinologie. 78 (2017) 4 - p. 232 , 2017
Link:
https://doi.org/10.1016/..
?
8
Prediction of long‐term prognosis by heteroplasmy levels of..:
Fayssoil, A.
;
Laforêt, P.
;
Bougouin, W.
...
European Journal of Neurology. 24 (2016) 2 - p. 255-261 , 2016
Link:
https://doi.org/10.1111/..
?
9
Two new cases of mitochondrial myopathy with exercise intol..:
Tosserams, A.
;
Papadopoulos, C.
;
Jardel, C.
...
Neuromuscular Disorders. 26 (2016) - p. S176 , 2016
Link:
https://doi.org/10.1016/..
?
10
G.P.189:
Péréon, Y.
;
Magot, A.
;
Fayet, G.
...
Neuromuscular Disorders. 24 (2014) 9-10 - p. 866-867 , 2014
Link:
https://doi.org/10.1016/..
?
11
SFP P-051 – Syndrome MEGDEL avec polyurie et insuffisance r..:
Harbulot, C.
;
Dorboz, I.
;
Pichard, S.
...
Archives de Pédiatrie. 21 (2014) 5 - p. 761 , 2014
Link:
https://doi.org/10.1016/..
?
12
Altération du gène de la polymérase gamma de l'ADN mitochon..:
Tchikviladzé, M.
;
Gilleron, M.
;
Maisonobe, T.
...
Revue Neurologique. 169 (2013) - p. A20-A21 , 2013
Link:
https://doi.org/10.1016/..
?
13
P.17.15 Life-threatening lactic acidosis occurring in adult..:
Laforêt, P.
;
Pottier, C.
;
Behin, A.
...
Neuromuscular Disorders. 23 (2013) 9-10 - p. 830-831 , 2013
Link:
https://doi.org/10.1016/..
?
14
Hypersignal T2 des olives bulbaires à l'imagerie par résona..:
Lebedel, N.
;
Tilikete, C.
;
Anheim, M.
..
Revue Neurologique. 169 (2013) - p. A18 , 2013
Link:
https://doi.org/10.1016/..
?
15
Altération du gène de la polymérase gamma de l'ADN mitochon..:
Tchikviladzé, M.
;
Gilleron, M.
;
Maisonobe, T.
...
Revue Neurologique. 169 (2013) - p. A226 , 2013
Link:
https://doi.org/10.1016/..
1-15