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Ged, Cécile
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1

Severe Perinatal Presentations of Günther's Disease: Series..:

Goudet, Claire ; Ged, Cécile ; Petit, Audrey...
Life.  14 (2024)  1 - p. 130 , 2024
Link: https://doi.org/10.3390/..
 
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2

Acquired glucose 6‐phosphate dehydrogenase (G6PD) deficienc..:

Naville, Anne‐Sophie ; Lazaro, Estibaliz ; Boutin, Julian...
British Journal of Haematology.  197 (2022)  4 - p. , 2022
Link: https://doi.org/10.1111/..
 
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3

Homozygosity for the hyperunstable hemoglobin variant Hb Ag..:

Szepetowski, Sarah ; Berger, Claire ; Joly, Philippe...
American Journal of Hematology.  97 (2022)  11 - p. , 2022
Link: https://doi.org/10.1002/..
 
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4

Phenotypic and genotypic characterization of familial hyper..:

Fourgeaud, Mélanie ; Lebreton, Louis ; Belabbas, Khaldia...
Journal of Clinical Lipidology.  16 (2022)  3 - p. 298-305 , 2022
Link: https://doi.org/10.1016/..
 
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5

Identification of novel UROS mutations in a patient with co..:

Blouin, Jean-Marc ; Ged, Cécile ; Bernardo-Seisdedos, Ganeko...
Molecular Genetics and Metabolism Reports.  27 (2021)  - p. 100722 , 2021
Link: https://doi.org/10.1016/..
 
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6

Xeroderma Pigmentosum C (XPC) Mutations in Primary Fibrobla..:

Fayyad, Nour ; Kobaisi, Farah ; Beal, David...
Frontiers in Genetics.  11 (2020)  - p. , 2020
Link: https://doi.org/10.3389/..
 
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7

Bone Marrow Transplantation in Congenital Erythropoietic Po..:

Besnard, Caroline ; Schmitt, Caroline ; Galmiche-Rolland, Louise...
Biology of Blood and Marrow Transplantation.  26 (2020)  4 - p. 704-711 , 2020
Link: https://doi.org/10.1016/..
 
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8

Genetic background influences hepcidin response to iron imb..:

Lefebvre, Thibaud ; Millot, Sarah ; Richard, Emmanuel...
Biochemical and Biophysical Research Communications.  520 (2019)  2 - p. 297-303 , 2019
Link: https://doi.org/10.1016/..
 
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9

CRISPR-Cas9 genome editing induces megabase-scale chromosom..:

Cullot, Grégoire ; Boutin, Julian ; Toutain, Jérôme...
Nature Communications.  10 (2019)  1 - p. , 2019
Link: https://doi.org/10.1038/..
 
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10

Pigmentation abnormalities in nucleotide excision repair di..:

Kasraian, Zeinab ; Trompezinski, Sandra ; Cario‐André, Muriel...
Pigment Cell & Melanoma Research.  32 (2018)  1 - p. 25-40 , 2018
Link: https://doi.org/10.1111/..
 
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11

Missense UROS mutations causing congenital erythropoietic p..:

Blouin, Jean-Marc ; Bernardo-Seisdedos, Ganeko ; Sasso, Emma...
Human Molecular Genetics.  26 (2017)  8 - p. 1565-1576 , 2017
Link: https://doi.org/10.1093/..
 
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12

Diagnosis of Xeroderma pigmentosum variant in a young patie..:

De Palma, Armando ; Morren, Marie‐Anne ; Ged, Cécile...
American Journal of Medical Genetics Part A.  173 (2017)  9 - p. 2511-2516 , 2017
Link: https://doi.org/10.1002/..
 
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13

UGT1A1 genotype and irinotecan therapy: general review and ..:

Etienne‐Grimaldi, Marie‐Christine ; Boyer, Jean‐Christophe ; Thomas, Fabienne...
Fundamental & Clinical Pharmacology.  29 (2015)  3 - p. 219-237 , 2015
Link: https://doi.org/10.1111/..
 
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14

Inaugural Cerebral Sinovenous Thrombosis Revealing Homocyst..:

Saboul, Cécile ; Darteyre, Stéphane ; Ged, Cécile...
Journal of Child Neurology.  30 (2014)  1 - p. 107-112 , 2014
Link: https://doi.org/10.1177/..
 
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15

Therapeutic potential of proteasome inhibitors in congenita..:

Blouin, Jean-Marc ; Duchartre, Yann ; Costet, Pierre...
Proceedings of the National Academy of Sciences of the United States of America.  110 (2013)  45 - p. 18238-18243 , 2013
Link: https://www.jstor.org/st..
 
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