E-LIB Suche - Ergebnisse für: Baujat, G

1

CO32 Heterotopic Ossification in Palovarotene-Treated and U..:

Al Mukaddam, M. ; Baujat, G. ; Cheung, A.M....
Value in Health. 26 (2023) 6 - p. S20 , 2023

2

Audiological phenotyping evaluation in KBG syndrome: Descri..:

Rhamati, L. ; Marcolla, A. ; Guerrot, A.M....
International Journal of Pediatric Otorhinolaryngology. 171 (2023) - p. 111606 , 2023

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

3

Unequal Impact of COL1A1 and COL1A2 Variants on Dentinogene..:

Yamaguti, P.M. ; de La Dure-Molla, M. ; Monnot, S....
Journal of Dental Research. , 2023

Link: https://doi.org/10.1177/..

4

POSC373 Use of Aids, Assistive Devices and Adaptations by I..:

Al Mukaddam, M ; Baujat, G ; Houchard, A...
Value in Health. 25 (2022) 1 - p. S245-S246 , 2022

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

5

Les mutations d'EPHX1 sont responsables de diabète lipoatro..:

Gautheron, J. ; Morisseau, C. ; Chung, W....
Annales d'Endocrinologie. 82 (2021) 5 - p. 266 , 2021

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

6

S3-17 SESSION 3: FACIOCRANIOSYNOSTOSIS – PART I FRONTO-FACI..:

Khonsari, R. H. ; Haber, S. ; Paternoster, G....
Plastic and Reconstructive Surgery - Global Open. 7 (2019) 8S-2 - p. 40-40 , 2019

Link: https://doi.org/10.1097/..

7

Craniosynostosis and metabolic bone disorder. A review:

Di Rocco, F. ; Rothenbuhler, A. ; Cormier Daire, V....
Neurochirurgie. 65 (2019) 5 - p. 258-263 , 2019

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

8

Gnathodiaphyseal dysplasia with a novel R597I mutation of A..:

Marechal, G. ; Schouman, T. ; Mauprivez, C....
Journal of Stomatology, Oral and Maxillofacial Surgery. 120 (2019) 5 - p. 428-431 , 2019

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

9

P6497Loeys-Dietz syndrome-5: phenotypic spectrum of TGFB3 m..:

Marsili, L ; Overwater, E ; Hanna, N...
European Heart Journal. 40 (2019) Supplement_1 - p. , 2019

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

10

IL11RA‐related Crouzon‐like autosomal recessive craniosynos..:

Brischoux‐Boucher, E. ; Trimouille, A. ; Baujat, G....
Clinical Genetics. 94 (2018) 3-4 - p. 373-380 , 2018

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

11

Enzyme-replacement therapy in perinatal hypophosphatasia: C..:

Rougier, H. ; Desrumaux, A. ; Bouchon, N....
Archives de Pédiatrie. 25 (2018) 7 - p. 442-447 , 2018

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

12

Rachitisme hypophosphatémique : complication rare du syndro..:

Welfringer-Morin, A. ; Pinto, G. ; Baujat, G....
Annales de Dermatologie et de Vénéréologie. 145 (2018) 12 - p. S207 , 2018

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

13

Chondrodysplasia with multiple dislocations: comprehensive ..:

Ranza, E. ; Huber, C. ; Levin, N....
Clinical Genetics. 91 (2017) 6 - p. 868-880 , 2017

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

14

Perinatal and infantile hypophosphatasia: clinical features..:

Baujat, G. ; Michot, C. ; Le Quan Sang, K.H..
Archives de Pédiatrie. 24 (2017) 5 - p. 5S61-5S65 , 2017

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

15

Craniosynostosis and hypophosphatasia:

Di Rocco, F. ; Baujat, G. ; Cormier-Daire, V...
Archives de Pédiatrie. 24 (2017) 5 - p. 5S89-5S92 , 2017

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