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Bannwarth, S.
146
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Online (146)
Mediatypes
Articles (Online) (48)
OpenAccess-fulltext (98)
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english (134)
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1
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/..
?
2
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/..
?
3
Membrane impedance porometry:
Bannwarth, S.
;
Breisig, H.
;
Houben, V.
..
Journal of Membrane Science. 542 (2017) - p. 352-366 , 2017
Link:
https://doi.org/10.1016/..
?
4
Erfassung des Koaleszenz‐ und Sedimentationsverhaltens von ..:
Bednarz, A.
;
Schmidt, M.
;
Eggert, A.
...
Chemie Ingenieur Technik. 88 (2016) 9 - p. 1289-1289 , 2016
Link:
https://doi.org/10.1002/..
?
5
On-line monitoring of cake layer structure during fouling o..:
Bannwarth, S.
;
Trieu, T.
;
Oberschelp, C.
.
Journal of Membrane Science. 503 (2016) - p. 188-198 , 2016
Link:
https://doi.org/10.1016/..
?
6
Online monitoring of transient L/L phase separation using l..:
Bednarz, A.
;
Schmidt, M.
;
Bannwarth, S.
..
Chemical Engineering Research and Design. 115 (2016) - p. 251-259 , 2016
Link:
https://doi.org/10.1016/..
?
7
Mutation update and uncommon phenotypes in a French cohort ..:
Chaussenot, A.
;
Rouzier, C.
;
Quere, M.
...
Clinical Genetics. 87 (2014) 5 - p. 430-439 , 2014
Link:
https://doi.org/10.1111/..
?
8
Reply: MFN2, a new gene responsible for mitochondrial DNA d..:
Rouzier, C.
;
Serre, V.
;
Chaussenot, A.
...
Brain. 135 (2012) 8 - p. e224-e224 , 2012
Link:
https://doi.org/10.1093/..
?
9
Reply: MFN2 mutations cause compensatory mitochondrial DNA ..:
Rouzier, C.
;
Bannwarth, S.
;
Chaussenot, A.
...
Brain. 135 (2012) 8 - p. e220-e220 , 2012
Link:
https://doi.org/10.1093/..
?
10
The MFN2 gene is responsible for mitochondrial DNA instabil..:
Rouzier, C.
;
Bannwarth, S.
;
Chaussenot, A.
...
Brain. 135 (2011) 1 - p. 23-34 , 2011
Link:
https://doi.org/10.1093/..
?
11
O12 Étude des manifestations neurologiques et des aspects I..:
Chaussenot, A.
;
Bannwarth, S.
;
Vialettes, B.
...
Diabetes & Metabolism. 36 (2010) - p. A4 , 2010
Link:
https://doi.org/10.1016/..
?
12
O11 La cartographie des SNP du gène WFS1 révèle son rôle da..:
Ait El Mkadem, S.
;
Bannwarth, S.
;
Attaoua, R.
...
Diabetes & Metabolism. 36 (2010) - p. A3 , 2010
Link:
https://doi.org/10.1016/..
?
13
P203 Association diabète et surdité secondaire à une nouvel..:
Abbassi, M.
;
Bannwarth, S.
;
Fragaki, K.
...
Diabetes & Metabolism. 36 (2010) - p. A86-A87 , 2010
Link:
https://doi.org/10.1016/..
?
14
Autosomal dominant transmission of diabetes and congenital ..:
Valro, R.
;
Bannwarth, S.
;
Roman, S.
..
Diabetic Medicine. 25 (2008) 6 - p. 657-661 , 2008
Link:
https://doi.org/10.1111/..
?
15
Rapid identification of mitochondrial DNA (mtDNA) mutations..:
Bannwarth, S.
;
Procaccio, V.
;
Rouzier, C.
...
Mitochondrion. 8 (2008) 2 - p. 136-145 , 2008
Link:
https://doi.org/10.1016/..
1-15