Rivier F - Search Results

1

Infantile bilateral striatal necrosis following measles.

Cambonie G, Houdon L, Rivier F, Bongrand AF, Echenne B. Cambonie G, et al. Among authors: rivier f. Brain Dev. 2000 Jun;22(4):221-3. doi: 10.1016/s0387-7604(00)00105-4. Brain Dev. 2000. PMID: 10838107

2

Dominantly inherited hypoplasia of the vermis.

Rivier F, Echenne B. Rivier F, et al. Neuropediatrics. 1992 Aug;23(4):206-8. doi: 10.1055/s-2008-1071342. Neuropediatrics. 1992. PMID: 1407388

3

Epileptic electroencephalographic abnormalities and developmental dysphasias: a study of 32 patients.

Echenne B, Cheminal R, Rivier F, Negre C, Touchon J, Billiard M. Echenne B, et al. Among authors: rivier f. Brain Dev. 1992 Jul;14(4):216-25. doi: 10.1016/s0387-7604(12)80233-6. Brain Dev. 1992. PMID: 1443399

4

Benign paroxysmal tonic upward gaze.

Echenne B, Rivier F. Echenne B, et al. Among authors: rivier f. Pediatr Neurol. 1992 Mar-Apr;8(2):154-5. doi: 10.1016/0887-8994(92)90041-v. Pediatr Neurol. 1992. PMID: 1580962

5

Benign infantile epilepsy with autosomal dominant inheritance.

Echenne B, Humbertclaude V, Rivier F, Malafosse A, Cheminal R. Echenne B, et al. Among authors: rivier f. Brain Dev. 1994 Mar-Apr;16(2):108-11. doi: 10.1016/0387-7604(94)90044-2. Brain Dev. 1994. PMID: 8048696

6

Treatment with vigabatrin may mimic alpha-aminoadipic aciduria.

Vallat C, Rivier F, Bellet H, Magnan de Bornier B, Mion H, Echenne B. Vallat C, et al. Among authors: rivier f. Epilepsia. 1996 Aug;37(8):803-5. doi: 10.1111/j.1528-1157.1996.tb00655.x. Epilepsia. 1996. PMID: 8764822

7

Linkage mapping of benign familial infantile convulsions (BFIC) to chromosome 19q.

Guipponi M, Rivier F, Vigevano F, Beck C, Crespel A, Echenne B, Lucchini P, Sebastianelli R, Baldy-Moulinier M, Malafosse A. Guipponi M, et al. Among authors: rivier f. Hum Mol Genet. 1997 Mar;6(3):473-7. doi: 10.1093/hmg/6.3.473. Hum Mol Genet. 1997. PMID: 9147652

8

Merosin positive congenital muscular dystrophy with mental deficiency, epilepsy and MRI changes in the cerebral white matter.

Echenne B, Rivier F, Jellali AJ, Azais M, Mornet D, Pons F. Echenne B, et al. Among authors: rivier f. Neuromuscul Disord. 1997 May;7(3):187-90. doi: 10.1016/s0960-8966(97)00452-5. Neuromuscul Disord. 1997. PMID: 9185183

9

Congenital muscular dystrophy and cerebellar atrophy.

Echenne B, Rivier F, Tardieu M, Brive M, Robert A, Pages AM, Pons F, Mornet D. Echenne B, et al. Among authors: rivier f. Neurology. 1998 May;50(5):1477-80. doi: 10.1212/wnl.50.5.1477. Neurology. 1998. PMID: 9596013

10

Mosaic expression of two dystrophins in a boy with progressive muscular dystrophy.

Rivier F, Tuffery S, Jellali AJ, Echenne B, Mornet D, Pons F. Rivier F, et al. Muscle Nerve. 1998 Oct;21(10):1317-20. doi: 10.1002/(sici)1097-4598(199810)21:10<1317::aid-mus11>3.0.co;2-z. Muscle Nerve. 1998. PMID: 9736061

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