E-LIB Suche - Ergebnisse für: Hamdi-Rozé, Houda

1

Non-invasive diagnosis and follow-up of hyperferritinaemia:

Bardou-Jacquet, Edouard ; Hamdi-Roze, Houda ; Paisant, Anita...
Clinics and Research in Hepatology and Gastroenterology. 46 (2022) 1 - p. 101762 , 2022

Link: https://doi.org/10.1016/..

2

A simple clinical score to promote and enhance ferroportin ..:

Landemaine, Amandine ; Hamdi-Roze, Houda ; Cunat, Séverine...
Journal of Hepatology. 76 (2022) 3 - p. 568-576 , 2022

Link: https://doi.org/10.1016/..

3

Disrupted Hypothalamo-Pituitary Axis in Association With Re..:

Hamdi-Rozé, Houda ; Ware, Michelle ; Guyodo, Hélène...
The Journal of Clinical Endocrinology & Metabolism. 105 (2020) 9 - p. e3183-e3196 , 2020

Link: https://doi.org/10.1210/..

4

Reduced phenotypic expression in genetic hemochromatosis wi..:

Deugnier, Yves ; Morcet, Jeff ; Lainé, Fabrice...
Journal of Hepatology. 70 (2019) 1 - p. 118-125 , 2019

Link: https://doi.org/10.1016/..

5

Variable expressivity of HJV related hemochromatosis: "Juve..:

Hamdi-Rozé, Houda ; Ben Ali, Zeineb ; Ropert, Martine...
Blood Cells, Molecules, and Diseases. 74 (2019) - p. 30-33 , 2019

Link: https://doi.org/10.1016/..

6

Twenty Years of Ferroportin Disease: A Review or An Update ..:

Vlasveld, L. Tom ; Janssen, Roel ; Bardou-Jacquet, Edouard...
Pharmaceuticals. 12 (2019) 3 - p. 132 , 2019

Link: https://doi.org/10.3390/..

7

Targeted panel sequencing establishes the implication of pl..:

Beaumont, Marie ; Akloul, Linda ; Carré, Wilfrid...
Human Genetics. 138 (2019) 4 - p. 363-374 , 2019

Link: https://doi.org/10.1007/..

8

Integrated clinical and omics approach to rare diseases: no..:

Kim, Artem ; Savary, Clara ; Dubourg, Christèle...
Brain. 142 (2018) 1 - p. 35-49 , 2018

Link: https://doi.org/10.1093/..

9

Mutational Landscape of DDR2 Gene in Lung Squamous Cell Car..:

Ricordel, Charles ; Lespagnol, Alexandra ; Llamas-Gutierrez, Francisco...
Clinical Lung Cancer. 19 (2018) 2 - p. 163-169.e4 , 2018

Link: https://doi.org/10.1016/..

10

Regulation of downstream neuronal genes by proneural transc..:

Ware, Michelle ; Hamdi-Rozé, Houda ; Le Friec, Julien..
Neural Development. 11 (2016) 1 - p. , 2016

Link: https://doi.org/10.1186/..

11

Array-CGH diagnosis in ovarian failure: identification of n..:

Jaillard, Sylvie ; Akloul, Linda ; Beaumont, Marion...
Journal of Ovarian Research. 9 (2016) 1 - p. , 2016

Link: https://doi.org/10.1186/..

12

Inversions autosomiques et troubles de la reproduction:

Beaumont, Marion ; Lucas, Josette ; Akloul, Linda...
Morphologie. 100 (2016) 330 - p. 161-162 , 2016

Link: https://doi.org/10.1016/..

13

Mutational Spectrum in Holoprosencephaly Shows That FGF is ..:

Dubourg, Christèle ; Carré, Wilfrid ; Hamdi-Rozé, Houda...
Human Mutation. 37 (2016) 12 - p. 1329-1339 , 2016

Link: https://doi.org/10.1002/..

14

Homozygous STIL Mutation Causes Holoprosencephaly and Micro..:

Mouden, Charlotte ; de Tayrac, Marie ; Dubourg, Christèle...
PLOS ONE. 10 (2015) 2 - p. e0117418 , 2015

Link: https://doi.org/10.1371/..

15

Notch signaling and proneural genes work together to contro..:

Ware, Michelle ; Hamdi-Rozé, Houda ; Dupé, Valérie
Frontiers in Neuroanatomy. 8 (2014) - p. , 2014

Link: https://doi.org/10.3389/..