E-LIB Suche - Ergebnisse für: Brachet, Cécile

1

Childhood craniopharyngioma: a retrospective study of child..:

Magerman, Clémentine ; Boros, Emese ; Preziosi, Marco...
Frontiers in Endocrinology. 15 (2024) - p. , 2024

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

2

Growth response of syndromic versus non-syndromic children ..:

Becker, Marianne ; Thomas, Muriel ; Brachet, Cécile...
Frontiers in Endocrinology. 14 (2023) - p. , 2023

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

3

Efficacy and safety of a 4-year combination therapy of grow..:

Dotremont, Hilde ; France, Annick ; Heinrichs, Claudine...
Frontiers in Endocrinology. 14 (2023) - p. , 2023

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

4

Six Novel Variants in the MKRN3 Gene Causing Central Precoc..:

Gernay, Caroline ; Brachet, Cécile ; Boros, Emese...
Journal of the Endocrine Society. 7 (2022) 1 - p. , 2022

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

5

The Retina in Patients With Triple A Syndrome: A Window Int..:

Ulgiati, Fiorenza ; Lhoir, Sophie ; Balikova, Irina...
Frontiers in Endocrinology. 12 (2021) - p. , 2021

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

6

SRY‐negative 46,XX testicular/ovotesticular DSD: Long‐term ..:

Lambert, Sophie ; Peycelon, Matthieu ; Samara‐Boustani, Dinane...
Clinical Endocrinology. 94 (2020) 4 - p. 667-676 , 2020

Link: https://doi.org/10.1111/..

7

A novel approach in the intraoperative management of ovotes..:

Delforge, Xavier ; Brachet, Cécile ; Damry, Nasroola...
Journal of Pediatric Urology. 16 (2020) 6 - p. 768-770 , 2020

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

8

Truncating RAX Mutations: Anophthalmia, Hypopituitarism, Di..:

Brachet, Cécile ; Kozhemyakina, Elena A ; Boros, Emese...
The Journal of Clinical Endocrinology & Metabolism. 104 (2019) 7 - p. 2925-2930 , 2019

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

9

Delayed diagnosis of congenital hypopituitarism associated ..:

Boros, Emese ; Casimir, Madeleine ; Heinrichs, Claudine.
European Journal of Pediatrics. 179 (2019) 1 - p. 151-155 , 2019

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

10

Contribution of functionally assessedGHRHRmutations to idio..:

Cohen, Enzo ; Belkacem, Sabrina ; Fedala, Soumeya...
Human Mutation. 40 (2019) 11 - p. 2033-2043 , 2019

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

11

Acrodysostose de type 1 ou iPPSD4 ( inactivating PTH/PTHrP ..:

Azzi, Anne-Sophie ; Driessens, Natacha ; Linglart, Agnès...
Annales d'Endocrinologie. 78 (2017) 2 - p. 137 , 2017

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

12

Isolated and Syndromic Retinal Dystrophy Caused by Bialleli..:

Coppieters, Frauke ; Ascari, Giulia ; Dannhausen, Katharina...
The American Journal of Human Genetics. 99 (2016) 2 - p. 470-480 , 2016

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

13

Live birth after autograft of ovarian tissue cryopreserved ..:

Demeestere, Isabelle ; Simon, Philippe ; Dedeken, Laurence...
Human Reproduction. 30 (2015) 9 - p. 2107-2109 , 2015

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

14

Complex Tissue-Specific Epigenotypes in Russell-Silver Synd..:

Azzi, Salah ; Blaise, Annick ; Steunou, Virginie...
Human Mutation. 35 (2014) 10 - p. 1211-1220 , 2014

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

15

Haematopoietic stem cell transplantation for severe sickle ..:

Dedeken, Laurence ; Lê, Phu Q. ; Azzi, Nadira...
British Journal of Haematology. 165 (2014) 3 - p. 402-408 , 2014

Link: https://doi.org/10.1111/..