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Bannwarth, S.
146  results:
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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