Degos B - Search Results

1

Relationship between Substantia Nigra Neuromelanin Imaging and Dual Alpha-Synuclein Labeling of Labial Minor in Salivary Glands in Isolated Rapid Eye Movement Sleep Behavior Disorder and Parkinson's Disease.

Mangone G, Houot M, Gaurav R, Boluda S, Pyatigorskaya N, Chalancon A, Seilhean D, Prigent A, Lehéricy S, Arnulf I, Corvol JC, Vidailhet M, Duyckaerts C, Degos B. Mangone G, et al. Among authors: degos b. Genes (Basel). 2022 Sep 24;13(10):1715. doi: 10.3390/genes13101715. Genes (Basel). 2022. PMID: 36292600 Free PMC article.

2

Biotin-responsive basal ganglia disease in ethnic Europeans with novel SLC19A3 mutations.

Debs R, Depienne C, Rastetter A, Bellanger A, Degos B, Galanaud D, Keren B, Lyon-Caen O, Brice A, Sedel F. Debs R, et al. Among authors: degos b. Arch Neurol. 2010 Jan;67(1):126-30. doi: 10.1001/archneurol.2009.293. Arch Neurol. 2010. PMID: 20065143

3

POLG mutations associated with remitting/relapsing neurological events.

Degos B, Laforêt P, Jardel C, Sedel F, Jossay-Winter M, Romero NB, Lyon-Caen O, Tourbah A. Degos B, et al. J Clin Neurosci. 2014 Jan;21(1):186-8. doi: 10.1016/j.jocn.2013.03.019. Epub 2013 Jul 2. J Clin Neurosci. 2014. PMID: 23830586

4

Blepharospasm as a new feature of cerebrotendinous xanthomatosis.

Lagarde J, Sedel F, Degos B. Lagarde J, et al. Among authors: degos b. Parkinsonism Relat Disord. 2013 Aug;19(8):764-5. doi: 10.1016/j.parkreldis.2013.04.003. Epub 2013 Apr 25. Parkinsonism Relat Disord. 2013. PMID: 23623195 No abstract available.

5

NDRG1-linked Charcot-Marie-Tooth disease (CMT4D) with central nervous system involvement.

Echaniz-Laguna A, Degos B, Bonnet C, Latour P, Hamadouche T, Lévy N, Leheup B. Echaniz-Laguna A, et al. Among authors: degos b. Neuromuscul Disord. 2007 Feb;17(2):163-8. doi: 10.1016/j.nmd.2006.10.002. Epub 2006 Dec 4. Neuromuscul Disord. 2007. PMID: 17142040

6

[Ataxia associated with gluten sensitivity, myth or reality?].

Anheim M, Degos B, Echaniz-Laguna A, Fleury M, Grucker M, Tranchant C. Anheim M, et al. Among authors: degos b. Rev Neurol (Paris). 2006 Feb;162(2):214-21. doi: 10.1016/s0035-3787(06)75002-0. Rev Neurol (Paris). 2006. PMID: 16518262 French.

7

[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. Rev Neurol (Paris). 2004 Dec;160(12):1203-6. doi: 10.1016/s0035-3787(04)71168-6. Rev Neurol (Paris). 2004. PMID: 15602369 French.

8

C2orf37 mutational spectrum in Woodhouse-Sakati syndrome patients.

Alazami AM, Schneider SA, Bonneau D, Pasquier L, Carecchio M, Kojovic M, Steindl K, de Kerdanet M, Nezarati MM, Bhatia KP, Degos B, Goh E, Alkuraya FS. Alazami AM, et al. Among authors: degos b. Clin Genet. 2010 Dec;78(6):585-90. doi: 10.1111/j.1399-0004.2010.01441.x. Clin Genet. 2010. PMID: 20507343

9

A study of three patients with amyotrophic lateral sclerosis and a polyneuropathy resembling CIDP.

Echaniz-Laguna A, Degos B, Mohr M, Kessler R, Urban-Kraemer E, Tranchant C. Echaniz-Laguna A, et al. Among authors: degos b. Muscle Nerve. 2006 Mar;33(3):356-62. doi: 10.1002/mus.20475. Muscle Nerve. 2006. PMID: 16320313

10

From anti-GAD to ataxia with ocular motor apraxia type 2: through the looking glass.

Mariani LL, Degos B, Honnorat J, Trouillas P, Rabin M, Koenig M, Anheim M. Mariani LL, et al. Among authors: degos b. J Neurol. 2013 Apr;260(4):1158-9. doi: 10.1007/s00415-013-6840-3. Epub 2013 Jan 31. J Neurol. 2013. PMID: 23370611 No abstract available.

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