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X
Ogier, Pascale
29  Ergebnisse:
Personensuche X
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1

Les nuits de la pleine lune 

comédies et proverbes  Les films de ma vie
Rohmer, Eric ; Ogier, Pascale ; Karyo, Tcheky. , [ca. 1997]
Exemplar:  Zentrale/Mediathek: po 0710
 
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2

Moisture Influence on Reliability and Electrical Characteri..:

, In: 2019 IEEE International Integrated Reliability Workshop (IIRW),
Vidal-Dho, Matthias ; Hubert, Quentin ; Gonon, Patrice... - p. 1-4 , 2019
Link: https://doi.org/10.1109/..
 
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3

29 French adult patients with PMM2-congenital disorder of g..:

Monin, Marie-Lorraine ; Mignot, Cyril ; De Lonlay, Pascale...
Orphanet Journal of Rare Diseases.  9 (2014)  1 - p. , 2014
Link: https://doi.org/10.1186/..
 
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4

LPIN1 gene mutations: a major cause of severe rhabdomyolysi..:

Michot, Caroline ; Hubert, Laurence ; Brivet, Michèle...
Human Mutation.  31 (2010)  7 - p. E1564-E1573 , 2010
Link: https://doi.org/10.1002/..
 
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5

Biological studies of radiolabeled glucose analogues iodina..:

Perret, Pascale ; Ghezzi, Catherine ; Ogier, Lionel...
Nuclear Medicine and Biology.  31 (2004)  2 - p. 241-250 , 2004
Link: https://doi.org/10.1016/..
 
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6

Neurocognitive profiles in MSUD school‐age patients:

Bouchereau, Juliette ; Leduc‐Leballeur, Julie ; Pichard, Samia...
Journal of Inherited Metabolic Disease.  40 (2017)  3 - p. 377-383 , 2017
Link: https://doi.org/10.1007/..
 
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7

Mitochondrial acetoacetyl‐CoA thiolase deficiency: basal ga..:

Paquay, Stéphanie ; Bourillon, Agnès ; Pichard, Samia...
Journal of Inherited Metabolic Disease.  40 (2017)  3 - p. 415-422 , 2017
Link: https://doi.org/10.1007/..
 
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8

Wide clinical spectrum in ALG8-CDG: clues from molecular fi..:

Vuillaumier-Barrot, Sandrine ; Schiff, Manuel ; Mattioli, Francesca...
Pediatric Research.  85 (2018)  3 - p. 384-389 , 2018
Link: https://doi.org/10.1038/..
 
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9

29 French adult patients with PMM2-congenital disorder of g..:

Monin, Marie-Lorraine ; Mignot, Cyril ; de Lonlay, Pascale...
info:eu-repo/semantics/altIdentifier/doi/10.1186/s13023-014-0207-4.  , 2014
Link: https://hal.sorbonne-uni..
 
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10

29 French adult patients with PMM2-congenital disorder of g..:

Monin, Marie-Lorraine ; Mignot, Cyril ; de Lonlay, Pascale...
info:eu-repo/semantics/altIdentifier/doi/10.1186/s13023-014-0207-4.  , 2014
Link: https://hal.sorbonne-uni..
 
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11

29 French adult patients with PMM2-congenital disorder of g..:

Monin, Marie-Lorraine ; Mignot, Cyril ; de Lonlay, Pascale...
info:eu-repo/semantics/altIdentifier/doi/10.1186/s13023-014-0207-4.  , 2014
Link: https://hal.sorbonne-uni..
 
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12

29 French adult patients with PMM2-congenital disorder of g..:

Monin, Marie-Lorraine ; Mignot, Cyril ; De Lonlay, Pascale...
info:eu-repo/semantics/altIdentifier/doi/10.1186/s13023-014-0207-4.  , 2014
Link: https://hal.sorbonne-uni..
 
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13

29 French adult patients with PMM2-congenital disorder of g..:

Monin, Marie-Lorraine ; Mignot, Cyril ; de Lonlay, Pascale...
info:eu-repo/semantics/altIdentifier/doi/10.1186/s13023-014-0207-4.  , 2014
Link: https://hal.sorbonne-uni..
 
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14

29 French adult patients with PMM2-congenital disorder of g..:

Monin, Marie-Lorraine ; Mignot, Cyril ; De Lonlay, Pascale...
http://www.ojrd.com/content/9/1/207.  , 2014
Link: http://www.ojrd.com/cont..
 
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15

The Compartmentalisation of Phosphorylated Free Oligosaccha..:

Peric, Delphine ; Durrant-Arico, Christelle ; Delenda, Christophe...
PLoS ONE.  5 (2010)  7 - p. e11675 , 2010
Link: https://doi.org/10.1371/..
 
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