I agree that this site is using cookies. You can find further informations here.
X
Mine, Manuele
22  results:
Search for persons X
?
1

Further refinement of COL4A1 and COL4A2 related cortical ma..:

Cavallin, Mara ; Mine, Manuele ; Philbert, Marion...
European Journal of Medical Genetics.  61 (2018)  12 - p. 765-772 , 2018
Link: https://doi.org/10.1016/..
 
?
2

Amyloid imaging by 18F-florbetaben PET in a patient with is..:

Renard, Dimitri ; Jacob, Melissa ; Miné, Manuele...
Acta Neurologica Belgica.  116 (2015)  4 - p. 623-625 , 2015
Link: https://doi.org/10.1007/..
 
?
3

Cerebral small-vessel disease associated withCOL4A1andCOL4A..:

Renard, Dimitri ; Miné, Manuele ; Pipiras, Eva...
Neurology.  83 (2014)  11 - p. 1029-1031 , 2014
Link: https://doi.org/10.1212/..
 
?
4

COL4A2 mutation causing adult onset recurrent intracerebral..:

Gunda, Bence ; Mine, Manuele ; Kovács, Tibor...
Journal of Neurology.  261 (2014)  3 - p. 500-503 , 2014
Link: https://doi.org/10.1007/..
 
?
5

A novel hereditary extensive vascular leukoencephalopathy m..:

Hervé, Dominique ; Chabriat, Hugues ; Rigal, Mélanie...
Neurology.  79 (2012)  23 - p. 2283-2287 , 2012
Link: https://doi.org/10.1212/..
 
?
6

A cortical form of CADASIL with cerebral Aβ amyloidosis:

Paquet, Claire ; Jouvent, Eric ; Mine, Manuèle...
Acta Neuropathologica.  120 (2010)  6 - p. 813-820 , 2010
Link: https://doi.org/10.1007/..
 
?
7

Intracerebral hemorrhage and COL4A1 mutations, from preterm..:

Mine, Manuele ; Tournier‐Lasserve, Elisabeth
Annals of Neurology.  65 (2009)  1 - p. 1-2 , 2009
Link: https://doi.org/10.1002/..
 
?
8

Activating NOTCH3 mutation in a patient with small-vessel-d..:

Fouillade, Charles ; Chabriat, Hugues ; Riant, Florence...
Human Mutation.  29 (2008)  3 - p. 452-452 , 2008
Link: https://doi.org/10.1002/..
 
?
9

A large genomic deletion in thePDHX gene caused by the retr..:

Miné, Manuèle ; Chen, Jian-Min ; Brivet, Michèle...
Human Mutation.  28 (2007)  2 - p. 137-142 , 2007
Link: https://doi.org/10.1002/..
 
?
10

Corrections:

Schiff, Manuel ; Miné, Manuele ; Brivet, Michèle...
Annals of Neurology.  59 (2006)  6 - p. 990-990 , 2006
Link: https://doi.org/10.1002/..
 
?
11

Leigh's disease due to a new mutation in the PDHX gene:

Schiff, Manuel ; Miné, Manuele ; Brivet, Michèle...
Annals of Neurology.  59 (2006)  4 - p. 709-714 , 2006
Link: https://doi.org/10.1002/..
 
?
12

First characterization of a large deletion of the PDHA1 gen:

Brivet, Michèle ; Moutard, Marie-Laure ; Zater, Mokhtar...
Molecular Genetics and Metabolism.  86 (2005)  4 - p. 456-461 , 2005
Link: https://doi.org/10.1016/..
 
?
13

Splicing Error in E1α Pyruvate Dehydrogenase mRNA Caused by..:

Miné, Manuèle ; Brivet, Michèle ; Touati, Guy...
Journal of Biological Chemistry.  278 (2003)  14 - p. 11768-11772 , 2003
Link: https://doi.org/10.1074/..
 
?
14

A new case of pyruvate dehydrogenase deficiency due to a no..:

Dey, Runu ; Mine, Manuele ; Desguerre, Isabelle...
Annals of Neurology.  53 (2003)  2 - p. 273-277 , 2003
Link: https://doi.org/10.1002/..
 
?
15

Proteomic Consequences of a Human Mitochondrial tRNA Mutati..:

Tryoen-Tóth, Petra ; Richert, Sophie ; Sohm, Bénédicte...
Journal of Biological Chemistry.  278 (2003)  27 - p. 24314-24323 , 2003
Link: https://doi.org/10.1074/..
 
1-15