Estournet B - Search Results

1

[Familial mitochondrial encephalopathy. A clinicopathologic study].

Estournet B, Duyckaerts C, Marsac C, Chabbi N, Bataille J, Barois A, Hauw JJ, Goulon M. Estournet B, et al. Rev Neurol (Paris). 1991;147(6-7):491-6. Rev Neurol (Paris). 1991. PMID: 1660181 French.

2

[Infantile spinal muscular atrophy].

Barois A, Estournet B, Duval-Beaupère G, Bataille J, Leclair-Richard D. Barois A, et al. Among authors: estournet b. Rev Neurol (Paris). 1989;145(4):299-304. Rev Neurol (Paris). 1989. PMID: 2660222 French.

3

[Pathological anatomy of the heart in myopathies and infantile muscular atrophies].

Bataille J, Guillon F, Urtizberea A, Estournet B, Richard S, Barois A. Bataille J, et al. Among authors: estournet b. Ann Med Interne (Paris). 1991;142(1):5-8. Ann Med Interne (Paris). 1991. PMID: 2048876 Review. French.

4

[Myasthenia in children: long-term course].

Descamps H, Bataille J, Estournet B, Barois A. Descamps H, et al. Among authors: estournet b. Ann Med Interne (Paris). 1987;138(8):615-9. Ann Med Interne (Paris). 1987. PMID: 3450209 French.

5

[Myasthenia and pernicious anemia or Biermer's (author's transl)].

Goulon M, Zittoun J, Tulliez M, Estournet B. Goulon M, et al. Among authors: estournet b. Rev Neurol (Paris). 1979 Oct;135(8-9):605-14. Rev Neurol (Paris). 1979. PMID: 394262 French.

6

Ondine's curse: a discussion of five cases.

Commare MC, François B, Estournet B, Barois A. Commare MC, et al. Among authors: estournet b. Neuropediatrics. 1993 Dec;24(6):313-8. doi: 10.1055/s-2008-1071563. Neuropediatrics. 1993. PMID: 8133976

7

Congenital muscular dystrophy: use of brain MR imaging findings to predict merosin deficiency.

Lamer S, Carlier RY, Pinard JM, Mompoint D, Bagard C, Burdairon E, Estournet B, Barois A, Vallée C. Lamer S, et al. Among authors: estournet b. Radiology. 1998 Mar;206(3):811-6. doi: 10.1148/radiology.206.3.9494506. Radiology. 1998. PMID: 9494506

8

[Oxygen therapy and assisted ventilation in children at home].

Estournet B, Barois A. Estournet B, et al. Rev Prat. 1989 Sep 21;39(21):1861-6. Rev Prat. 1989. PMID: 2814269 French.

9

[Congenital muscular dystrophy with merosin deficiency: clinical, histopathological, immunocytochemical and genetic analysis].

Fardeau M, Tomé FM, Helbling-Leclerc A, Evangelista T, Ottolini A, Chevallay M, Barois A, Estournet B, Harpey JP, Fauré S, Guicheney P, Hillaire D. Fardeau M, et al. Among authors: estournet b. Rev Neurol (Paris). 1996 Jan;152(1):11-9. Rev Neurol (Paris). 1996. PMID: 8729391 French.

10

[A neonatal case of immunoallergic acute interstitial nephritis].

Essid A, Allani-Essid N, Rubinsztajn R, Estournet B, Bataille J. Essid A, et al. Among authors: estournet b. Arch Pediatr. 2010 Nov;17(11):1559-61. doi: 10.1016/j.arcped.2010.08.014. Epub 2010 Sep 28. Arch Pediatr. 2010. PMID: 20880680 French.

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