Estournet-Mathiaud B - Search Results

1

Congenital myasthenic syndrome due to rapsyn deficiency: three cases with arthrogryposis and bulbar symptoms.

Ioos C, Barois A, Richard P, Eymard B, Hantaï D, Estournet-Mathiaud B. Ioos C, et al. Neuropediatrics. 2004 Aug;35(4):246-9. doi: 10.1055/s-2004-820993. Neuropediatrics. 2004. PMID: 15328566

2

Respiratory capacity course in patients with infantile spinal muscular atrophy.

Ioos C, Leclair-Richard D, Mrad S, Barois A, Estournet-Mathiaud B. Ioos C, et al. Chest. 2004 Sep;126(3):831-7. doi: 10.1378/chest.126.3.831. Chest. 2004. PMID: 15364763

3

[Jeune'disease (asphyxiating thoracic dystrophy) and respiratory failure: importance of early respiratory management with periodic hyperinsufflation].

Do Ngoc Thanh C, Barois A, Estournet-Mathiaud B, Bataille J, Ioos C. Do Ngoc Thanh C, et al. Among authors: estournet mathiaud b. Bull Acad Natl Med. 2007 Oct;191(7):1411-29; discussion 1429-32. Bull Acad Natl Med. 2007. PMID: 18447062 French.

4

Respiratory problems in spinal muscular atrophies.

Barois A, Estournet-Mathiaud B. Barois A, et al. Pediatr Pulmonol Suppl. 1997;16:140-1. doi: 10.1002/ppul.1950230875. Pediatr Pulmonol Suppl. 1997. PMID: 9443243 Review. No abstract available.

5

Sleep disorders caused by brainstem tumor: case report.

Ioos C, Estournet-Mathiaud B, Pinard JM, Cheliout-Héraut F. Ioos C, et al. J Child Neurol. 2001 Oct;16(10):767-70. doi: 10.1177/088307380101601012. J Child Neurol. 2001. PMID: 11669353

6

Evoked potentials in spinal muscular atrophy.

Cheliout-Heraut F, Barois A, Urtizberea A, Viollet L, Estournet-Mathiaud B. Cheliout-Heraut F, et al. J Child Neurol. 2003 Jun;18(6):383-90. doi: 10.1177/08830738030180061101. J Child Neurol. 2003. PMID: 12886971

7

Congenital muscular dystrophy with primary partial laminin alpha2 chain deficiency: molecular study.

He Y, Jones KJ, Vignier N, Morgan G, Chevallay M, Barois A, Estournet-Mathiaud B, Hori H, Mizuta T, Tomé FM, North KN, Guicheney P. He Y, et al. Neurology. 2001 Oct 9;57(7):1319-22. doi: 10.1212/wnl.57.7.1319. Neurology. 2001. PMID: 11591858

8

[Spinal muscular atrophy. A 4-year prospective, multicenter, longitudinal study (168 cases)].

Barois A, Mayer M, Desguerre I, Chabrol B, Berard C, Cuisset JM, Leclair-Richard D, Visconti-Lougovoy J, Hatton F, Estournet-Mathiaud B. Barois A, et al. Among authors: estournet mathiaud b. Bull Acad Natl Med. 2005 Jun;189(6):1181-98; discussion 1198-9. Bull Acad Natl Med. 2005. PMID: 16433443 French.

9

Clinical correlations and long-term follow-up in 100 patients with sarcoglycanopathies.

Guimarães-Costa R, Fernández-Eulate G, Wahbi K, Leturcq F, Malfatti E, Behin A, Leonard-Louis S, Desguerre I, Barnerias C, Nougues MC, Isapof A, Estournet-Mathiaud B, Quijano-Roy S, Fayssoil A, Orlikowski D, Fauroux B, Richard I, Semplicini C, Romero NB, Querin G, Eymard B, Laforêt P, Stojkovic T. Guimarães-Costa R, et al. Among authors: estournet mathiaud b. Eur J Neurol. 2021 Feb;28(2):660-669. doi: 10.1111/ene.14592. Epub 2020 Nov 21. Eur J Neurol. 2021. PMID: 33051934 Free article.

10

Jeune syndrome and liver disease: report of three cases treated with ursodeoxycholic acid.

Labrune P, Fabre M, Trioche P, Estournet-Mathiaud B, Grangeponte MC, Rambaud C, Maurage C, Bernard O. Labrune P, et al. Am J Med Genet. 1999 Dec 3;87(4):324-8. doi: 10.1002/(sici)1096-8628(19991203)87:4<324::aid-ajmg8>3.0.co;2-u. Am J Med Genet. 1999. PMID: 10588838

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