Roubertie A - Search Results

1

FGF14-related episodic ataxia: delineating the phenotype of Episodic Ataxia type 9.

Piarroux J, Riant F, Humbertclaude V, Remerand G, Hadjadj J, Rejou F, Coubes C, Pinson L, Meyer P, Roubertie A. Piarroux J, et al. Among authors: roubertie a. Ann Clin Transl Neurol. 2020 Apr;7(4):565-572. doi: 10.1002/acn3.51005. Epub 2020 Mar 12. Ann Clin Transl Neurol. 2020. PMID: 32162847 Free PMC article.

2

[Ectopic intraspinal extradural anaplastic ependymoma in an infant].

Roubertie A, Coubes P, Humbertclaude V, Cheminal R, Margueritte G, Double CM, Frerebeau P, Echenne B. Roubertie A, et al. Arch Pediatr. 1997 Mar;4(3):255-9. doi: 10.1016/s0929-693x(97)87243-0. Arch Pediatr. 1997. PMID: 9181020 French.

3

[Benign familial infantile convulsions].

Echenne B, Rivier F, Humbertclaude V, Roubertie A, Cheminal R, Malafosse A. Echenne B, et al. Among authors: roubertie a. Arch Pediatr. 1999 Jan;6(1):54-8. doi: 10.1016/S0929-693X(99)80075-X. Arch Pediatr. 1999. PMID: 9974098 French.

4

[Treatment of early-onset generalized dystonia by chronic bilateral stimulation of the internal globus pallidus. Apropos of a case].

Coubes P, Echenne B, Roubertie A, Vayssière N, Tuffery S, Humbertclaude V, Cambonie G, Claustres M, Frerebeau P. Coubes P, et al. Among authors: roubertie a. Neurochirurgie. 1999 May;45(2):139-44. Neurochirurgie. 1999. PMID: 10448655 French.

5

Recurrent episodes of coma: an unusual phenotype of familial hemiplegic migraine with linkage to chromosome 1.

Echenne B, Ducros A, Rivier F, Joutel A, Humbertclaude V, Roubertie A, Azaïs M, Bousser MG, Tournier-Lasserve E. Echenne B, et al. Among authors: roubertie a. Neuropediatrics. 1999 Aug;30(4):214-7. doi: 10.1055/s-2007-973493. Neuropediatrics. 1999. PMID: 10569214

6

[Acute myelitis of an unusual cause in a child: the lymphocytic choriomeningitis virus].

Humbertclaude V, Tourtet S, Semprino M, Roubertie A, Rivier F, Leboucq N, Astruc J, Echenne B. Humbertclaude V, et al. Among authors: roubertie a. Arch Pediatr. 2001 Mar;8(3):282-5. doi: 10.1016/s0929-693x(00)00196-2. Arch Pediatr. 2001. PMID: 11270252 French.

7

Is hyperprolinemia type I actually a benign trait? Report of a case with severe neurologic involvement and vigabatrin intolerance.

Humbertclaude V, Rivier F, Roubertie A, Echenne B, Bellet H, Vallat C, Morin D. Humbertclaude V, et al. Among authors: roubertie a. J Child Neurol. 2001 Aug;16(8):622-3. doi: 10.1177/088307380101600820. J Child Neurol. 2001. PMID: 11510941

8

Neurological presentation of three patients with 22q11 deletion (CATCH 22 syndrome).

Roubertie A, Semprino M, Chaze AM, Rivier F, Humbertclaude V, Cheminal R, Lefort G, Echenne B. Roubertie A, et al. Brain Dev. 2001 Dec;23(8):810-4. doi: 10.1016/s0387-7604(01)00258-3. Brain Dev. 2001. PMID: 11720799

9

[The varied etiologies of childhood-onset dystonia].

Roubertie A, Rivier F, Humbertclaude V, Tuffery S, Cavalier L, Cheminal R, Coubes P, Echenne B. Roubertie A, et al. Rev Neurol (Paris). 2002 Apr;158(4):413-24. Rev Neurol (Paris). 2002. PMID: 11984483 Review. French.

10

[Mitochondrial myopathies: their clinical, biological, morphological and molecular aspects].

Echenne B, Rivier F, Bellet H, Humbertclaude V, Roubertie A. Echenne B, et al. Among authors: roubertie a. Arch Pediatr. 2002 May;9 Suppl 2:179s-182s. doi: 10.1016/s0929-693x(01)00880-6. Arch Pediatr. 2002. PMID: 12108260 Review. French. No abstract available.

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