Anheim M - Search Results

1

Highlighting the Dystonic Phenotype Related to GNAO1.

Wirth T, Garone G, Kurian MA, Piton A, Millan F, Telegrafi A, Drouot N, Rudolf G, Chelly J, Marks W, Burglen L, Demailly D, Coubes P, Castro-Jimenez M, Joriot S, Ghoumid J, Belin J, Faucheux JM, Blumkin L, Hull M, Parnes M, Ravelli C, Poulen G, Calmels N, Nemeth AH, Smith M, Barnicoat A, Ewenczyk C, Méneret A, Roze E, Keren B, Mignot C, Beroud C, Acosta F Jr, Nowak C, Wilson WG, Steel D, Capuano A, Vidailhet M, Lin JP, Tranchant C, Cif L, Doummar D, Anheim M. Wirth T, et al. Among authors: anheim m. Mov Disord. 2022 Jul;37(7):1547-1554. doi: 10.1002/mds.29074. Epub 2022 Jun 20. Mov Disord. 2022. PMID: 35722775 Free PMC article.

2

[Acute relapse in Charcot-Marie-Tooth 1B neuropathy: can protein P0 behave like an autoantigen?].

Fleury M, Anheim M, Tranchant C, Warter JM. Fleury M, et al. Among authors: anheim m. Rev Neurol (Paris). 2004 Sep;160(8-9):839-42. doi: 10.1016/s0035-3787(04)71042-5. Rev Neurol (Paris). 2004. PMID: 15454874 French.

3

[Hereditary neuropathy with liability to pressure palsy presenting with an acute inflammatory demyelinating polyneuropathy].

Degos B, Echaniz-Laguna A, Latour P, Vandenberghe A, Anheim M, Talmant V, Tranchant C. Degos B, et al. Among authors: anheim m. Rev Neurol (Paris). 2004 Dec;160(12):1203-6. doi: 10.1016/s0035-3787(04)71168-6. Rev Neurol (Paris). 2004. PMID: 15602369 French.

4

A family with early-onset and rapidly progressive X-linked spinal and bulbar muscular atrophy.

Echaniz-Laguna A, Rousso E, Anheim M, Cossée M, Tranchant C. Echaniz-Laguna A, et al. Among authors: anheim m. Neurology. 2005 Apr 26;64(8):1458-60. doi: 10.1212/01.WNL.0000158617.41819.F3. Neurology. 2005. PMID: 15851746

5

[Pure trigeminal motor neuropathy presenting with temporo-mandibular joint dysfunction in a patient with HIV and HCV infections].

Anheim M, Echaniz-Laguna A, Rey D, Tranchant C. Anheim M, et al. Rev Neurol (Paris). 2006 Jan;162(1):92-4. doi: 10.1016/s0035-3787(06)74987-6. Rev Neurol (Paris). 2006. PMID: 16446628 French.

6

Subthalamic nucleus stimulation is efficacious in patients with Parkinsonism and LRRK2 mutations.

Schüpbach M, Lohmann E, Anheim M, Lesage S, Czernecki V, Yaici S, Worbe Y, Charles P, Welter ML, Pollak P, Dürr A, Agid Y, Brice A. Schüpbach M, et al. Among authors: anheim m. Mov Disord. 2007 Jan;22(1):119-22. doi: 10.1002/mds.21178. Mov Disord. 2007. PMID: 17080443 Clinical Trial.

7

[Motor and sensory deficit in the limbs].

Anheim M, Tranchant C. Anheim M, et al. Rev Prat. 2007 Sep 15;57(13):1481-6; quiz 1486. Rev Prat. 2007. PMID: 18018548 French. No abstract available.

8

ADCK3, an ancestral kinase, is mutated in a form of recessive ataxia associated with coenzyme Q10 deficiency.

Lagier-Tourenne C, Tazir M, López LC, Quinzii CM, Assoum M, Drouot N, Busso C, Makri S, Ali-Pacha L, Benhassine T, Anheim M, Lynch DR, Thibault C, Plewniak F, Bianchetti L, Tranchant C, Poch O, DiMauro S, Mandel JL, Barros MH, Hirano M, Koenig M. Lagier-Tourenne C, et al. Among authors: anheim m. Am J Hum Genet. 2008 Mar;82(3):661-72. doi: 10.1016/j.ajhg.2007.12.024. Am J Hum Genet. 2008. PMID: 18319074 Free PMC article.

9

[Severe generalized dystonia due to postradiotherapy cerebral calcifications].

Chanson JB, Anheim M, Lagha-Boukbiza O, Fleury M, Sellal F, Tranchant C. Chanson JB, et al. Among authors: anheim m. Rev Neurol (Paris). 2008 May;164(5):477-80. doi: 10.1016/j.neurol.2008.02.030. Epub 2008 Apr 1. Rev Neurol (Paris). 2008. PMID: 18555882 French.

10

Clinical and molecular findings of ataxia with oculomotor apraxia type 2 in 4 families.

Anheim M, Fleury MC, Franques J, Moreira MC, Delaunoy JP, Stoppa-Lyonnet D, Koenig M, Tranchant C. Anheim M, et al. Arch Neurol. 2008 Jul;65(7):958-62. doi: 10.1001/archneur.65.7.958. Arch Neurol. 2008. PMID: 18625865

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