Albert SM. Projecting Neurologic Disease Burden: Difficult but Critical. Neurology

2007

Albert SM. Projecting neurologic disease burden: Difficult but critical. Neurology 2007;68:322-323.

Baldereschi M, Inzitari M, Di Carlo A, Farchi G, Scafato E, Inzitari, D. For The ILSA Working Group, Epidemiology of distal symmetrical neuropathies in the Italian elderly. Neurology 2007; 68: 1460-1467.

Beghi E, Millul, A, Micheli, A, Vitelli E, Logroscino G. for the SLALOM Group,
Incidence of ALS in Lombardy, Italy. Neurology 2007; 68: 141-145.

Borenstein A R, Mortimer JA, Schofield E, et al. Cycad exposure and risk of dementia, MCI, and PDC in the Chamorro population of Guam. Neurology 2007; 68: 1764-1771.

Bower JH, Asmera J, Zebenigus M, Sandroni P, Bower SM, Zenebe G. The burden of inpatient neurologic disease in two Ethiopian Hospitals. Neurology 2007;68:338-342.

Dahodwala N. Neurology education and global health: My rotation in Botswana. Neurology 2007;68:E15-E16.

DasSK, Bose P, Biswas A, et al. An epidemiologic study of mild cognitive impairment in Kolkata, India. Neurology 2007; 68: 2019-2026.

Debouverie EM, Lebrun C, Jeannin S, Pittion-Vouyovitch S, Roederer T, Vespignani H.
More severe disability of North Africans vs Europeans with multiple sclerosis in France
Neurology 2007;68:29-32.

Di Carlo A, Lamassa M, Baldereschi M, et al For the Italian Longitudinal Study on Aging Working Group, CIND and MCI in the Italian elderly: Frequency, vascular risk factors, progression to dementia.Neurology 2007; 68: 1909-1916.

Dorsey ER, Constantinescu R, Thompson JP et al. Projected number of people with Parkinson disease in the most populous nations, 2005 through 2030. Neurology 2007;68:384-386.

Fuchs J, Nilsson C, Kachergus J, et al.Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplication. Neurology 2007; 68: 916-922.

Galasko D, Salmon D, Gamst A et al. Prevalence of dementia in Chamorros on Guam: Relationship to age, gender, education, and APOE. Neurology 2007; 68: 1772-1781.

Gamst A, Olichney J, Thal L J, et al. Cycad exposure and risk of dementia, MCI, and PDC in the Chamorro population of Guam. Neurology 2007; 68: 1764-1771.

Hirtz D, Thurman DJ, Gwinn-Hardy K, Mohamed M, Chaudhuri AR, Zalutsky R. How common are the “common” neurologic disorders. Neurology 2007;68:326-337.

Kaye JA, Moore MM, Galasko D, CraigUK, Adonay R, Silbert LC. Brain volumes in Guam dementia vs Parkinson dementia complex vs aging Chamorro adults. Neurology 2007;69:196-199.

Murata M, Hasegawa K, Kanazawa I for the The Japan Zonisamide on PD Study Group. Zonisamide improves motor function in Parkinson disease: A randomized, double-blind study.Neurology 2007; 68: 45-50.

Noguchi-Shinohara M, Hamaguchi T, Kitamoto T, et al. Clinical features and diagnosis of dura mater graft associated Creutzfeldt Jakob disease. Neurology 2007; 69: 360-367.

van der Kooi A J, Frankhuizen WS, Barth PG, et al. Limb-girdle muscular dystrophy in the Netherlands: Gene defect identified in half the families. Neurology 2007; 68: 2125-2128.

WongKS, Huang YN, Yang HB, et al. A door-to-door survey of intracranial atherosclerosis in Liangbei County, China. Neurology 2007; 68: 2031-2034.

Wong MH, Robertson K, Nakasujja N, et al. Frequency of and risk factors for HIV dementia in an HIV clinic in sub-Saharan Africa. Neurology 2007; 68: 350-355.

2006

Alter M, Kahana E, Zilber N, Miller A for the Israeli MS Study Group. Multiple sclerosis frequency in Israel’s diverse populations. Neurology 2006; 66: 1061 - 1066.

Ekbom K, Svensson DA, Pedersen NL, Waldenlind E. Lifetime prevalence and concordance risk of cluster headache in the Swedish twin population. Neurology 2006;67:798-803.

Hague S, Klaffke S, Clarimon J, et al. Lack of association with TorsinA haplotype in German patients with sporadic dystonia.Neurology 2006;66:951-952.

Hall K, Murrell J, Ogunniyi A, Deeg M, et al. Cholesterol, APOE genotype, and Alzheimer disease: An epidemiologic study of Nigerian Yoruba.Neurology 2006; 66: 223-227.

Kim Y, Choi EJ, Choi CG, et al. Characteristics of CADASIL in Korea: A novel cysteine-sparing Notch3 mutation. Neurology 2006; 66: 1511 - 1516.

Kumar N, Orenstein R, Uslan DZ, Berbari E F, Klein CJ, Windebank AJ. Melarsoprol-associated multifocal inflammatory CNS illness in African trypanosomiasis. Neurology 2006; 66: 1120-1121.

Ling G, Maher C. U.S. neurologists in Iraq: Personal perspective. Neurology 2006;67:14 - 17.

Lopez-Bastida J, Serrano-Aguilar P, Perestelo-Perez L, Oliva-Moreno J. Social-economic costs and quality of life of Alzheimer disease in the Canary Islands, Spain.Neurology 2006; 67: 2186-2191.

Ng H-Y, Lin S-H, Hsu CY, Tsai YZ, Chen HC, Lee C-T. Hypokalemic paralysis due to Gitelman syndrome: A family study.Neurology 2006; 67: 1080-1082.

Onodera Y, Aoki M, Mizuno H, Warita H, Shiga Y, Itoyama Y. Clinical features of chromosome 16q22.1 linked autosomal dominant cerebellar ataxia in Japanese.Neurology 2006; 67: 1300-1302.

Rajshekhar V, Venkat Raghava M, Prabhakaran V, Oommen A, Muliyil J. Active epilepsy as an index of burden of neurocysticercosis in Vellore district, India.Neurology 2006; 67: 2135-2139.

Sacktor N, Nakasujja N, Skolasky R, et al. Antiretroviral therapy improves cognitive impairment in HIV+ individuals in sub-Saharan Africa.Neurology 2006; 67: 311-314.

Toft M, Pielsticker L, Ross OA, Aasly JO, Farrer MJ. Glucocerebrosidase gene mutations and Parkinson disease in the Norwegian population. Neurology 2006; 66: 415 - 417.

Ty AU, See SJ, Rao, JP, Khoo JBK, Wong MC. Oligodendroglial tumor chemotherapy using "decreased-dose-intensity" PCV: A Singapore experience.Neurology 2006; 66: 247-249.

Yang C-Y, Chang C-C, Kuo H-W, Chiu, H-F. Parity and risk of death from subarachnoid hemorrhage in women: Evidence from a cohort in Taiwan.Neurology 2006; 67:514-515.

Zabetian CP, Morino H, Ujike H, et al. Identification and haplotype analysis of LRRK2 G2019S in Japanese patients with Parkinson disease.Neurology 2006;67:697-699.

2005

Benito-Leon J, Bermejo-Pareja F, Louis ED for the Neurological Disorders in Central Spain (NEDICES) Study Group. Incidence of essential tremor in three elderly populations of central Spain. Neurology 2005; 64: 1721-1725.

Bower JH, Zenebe G. Neurologic services in the nations of Africa. Neurology 2005;64:412-415.

Engelter ST, Reichhart M, Sekoranja Let al. Thrombolysis in stroke patients aged 80 years and older: Swiss survey of IV thrombolysis.Neurology 2005; 65: 1795-1798.

Gorter RW, Butorac M, Cobian EP, van der Sluis W. Medical use of cannabis in the Netherlands
Neurology 2005; 64: 917-919.

Kovács GG, László L, Bakos A et al. Increased incidence of genetic human prion disease in Hungary. Neurology 2005; 65: 1666 - 1669.

Ladogana A, Puopolo M, Croes EA, et al. Mortality from Creutzfeldt-Jakob disease and related disorders in Europe, Australia, and Canada. Neurology 2005;64: 1586-1591.

Ladogana A, Puopolo M, Poleggi, Aet al. High incidence of genetic human transmissible spongiform encephalopathies in Italy.Neurology 2005; 64: 1592-1597.

Lin MT, Simon DK, Pedersen, NL et al. No evidence for heritability of Parkinson disease in Swedish twins. Neurology 2005; 64: 932.

Majoor-Krakauer D, Mulder PGH, Rowland LP, Ottman R. A link between ALS and short residence on Guam. Neurology 2005; 64: 1819-1820.

Montano SM, Villaran MV, Ylquimiche L, et al for the Cysticercosis Working Group in Peru. Neurocysticercosis: Association between seizures, serology, and brain CT in rural Peru.
Neurology 2005; 65: 229 - 233.

Patel VB, Sacoor Z, Francis P, Bill PLA, Bhigjee AI, Connolly C. Ischemic stroke in young HIV-positive patients in Kwazulu-Natal, South Africa. Neurology 2005; 65: 759-761.

Ravaglia G, Forti P, Maioli F, et al. Incidence and etiology of dementia in a large elderly Italian population. Neurology 2005; 64: 1525-1530.

Torelli P, Beghi E, Manzoni, GC. Cluster headache prevalence in the Italian general population. Neurology 2005; 64: 469-474.

Tremlett H, Paty, D, Devonshire V. The natural history of primary progressive MS in British Columbia, Canada. Neurology 2005; 65: 1919-1923.

Wong VCN, Lam C-W, Fung CW. Stiff child syndrome with mutation of DYT1 gene
Neurology 2005; 65: 1465-1466.

2004

Amouri R, Moreira M-C, Zouari M, et al. Aprataxin gene mutations in Tunisian families. Neurology 2004;63:928-929.

Benito-Leon J, Bermejo-Pareja F, Morales-Gonzalez JM, et al. Incidence of Parkinson disease and parkinsonism in three elderly populations of central Spain. Neurology 2004;62:734-741.

Bian L, Yang JD, Guo TW, et al. Insulin-degrading enzyme and Alzheimer disease: A genetic association study in the Han Chinese. Neurology 2004;63:241-245.

Bissar-Tadmouri N, Nelis E, Zuchner S, et al. Absence of KIF1B mutation in a large Turkish CMT2A family suggests involvement of a second gene. Neurology 2004;62:1522-1525.

Burk K, Zuhlke C, Konig IR, et al. Spinocerebellar ataxia type 5: Clinical and molecular genetic features of a German kindred. Neurology 2004;62:327-329.

Cree AC, Khan O, Bourdette D, et al. Clinical characteristics of African Americans vs Caucasian Americans with multiple sclerosis. Neurology 2004;63:2039-2045.

Criscuolo C, Banfi S, Orio M, et al. A novel mutation in SACS gene in a family from southern Italy. Neurology 2004;62:100-102.

Criscuolo C, Mancini P, Sacca F, et al. Ataxia with oculomotor apraxia type 1 in Southern Italy: Late onset and variable phenotype. Neurology 2004;63:2173-2175.

Del Brutto OH, Idrovo L, Mosquera A, et al. Stroke in rural Ecuador: A three-phase, door-to-door survey. Neurology 2004;63:1974-1975.

Healy DG, Abou-Sleiman PM, Gibson JM, et al. PINK1 (PARK6) associated Parkinson disease in Ireland. Neurology 2004;63:1486-1488.

Koike H, Misu K, Sugiura M, et al. Pathology of early- vs late-onset TTR Met30 familial amyloid polyneuropathy. Neurology 2004;63:129-138.

Kokubo Y, Kuzuhara S. Neurofibrillary tangles in ALS and parkinsonism-dementia complex focus in Kii, Japan. Neurology 2004;63:2399-2401.

Li J, Johansen C, Brønnum–Hansen H, Stenager E, Koch–Henriksen N, Olsen J. The risk of multiple sclerosis in bereaved parents: A nationwide cohort study in Denmark. Neurology 2004;62:726-729.

Linsell L, Cousens SN, Smith PG, et al. A case-control study of sporadic Creutzfeldt-Jakob disease in the United Kingdom: Analysis of clustering. Neurology 2004;63:2077-2083.

Ma SL, Tang NLS, Lam LCW, Chiu HFK. Association between tumor necrosis factor-α promoter polymorphism and Alzheimer's disease. Neurology 2004;62:307-309.

Martinez A, Rubio A, Urcelay E, et al. TNF-376A marks susceptibility to MS in the Spanish population: A replication study. Neurology 2004;62:809-810.

Okun MS, Thommi N. Americo Negrette (1924 to 2003): Diagnosing Huntington disease in Venezuela. Neurology 2004;63:340-343.

Rose MR, Sharief MK, Priddin J, et al. Evaluation of neuromuscular symptoms in UK Gulf War veterans: A controlled study. Neurology 2004;63:1681-1687.

Tan LCS, Venketasubramanian N, Hong CY, et al. Prevalence of Parkinson disease in Singapore: Chinese vs Malays vs Indians. Neurology 2004;62:1999-2004.

Tsai CH, Chang FC, Su YC, et al. Two novel mutations of the glycine receptor gene in a Taiwanese hyperekplexia family. Neurology 2004;63:893-896.

Wirdefeldt K, Gatz M, Schalling M, Pedersen NL. No evidence for heritability of Parkinson disease in Swedish twins. Neurology 2004;63:305-311.

Wirtz PW, van Dijk JG, van Doorn PA, et al. The epidemiology of the Lambert-Eaton myasthenic syndrome in the Netherlands. Neurology 2004;63:397-398.

Wu Z-Y, Wang Z-Q, Murong S-X, Wang N. FSHD in Chinese population: Characteristics of translocation and genotype-phenotype correlation. Neurology 2004;63:581-583.

Ya-Ping J, Gatz M, Johansson B, Pedersen NL. Sensitivity and specificity of dementia coding in two Swedish disease registries. Neurology 2004;63:739-741.

Yeh J-H, Chen W-H, Chiu H-C, Vincent A. Low frequency of MuSK antibody in generalized seronegative myasthenia gravis among Chinese. Neurology 2004;62:2131-2132.

2003

Argov Z, Eisenberg I, Grabov–Nardini et al. Hereditary inclusion body myopathy: The Middle Eastern genetic cluster. Neurology 2003;60:1519-1523.

Banack SA, Cox PA. Biomagnification of cycad neurotoxins in flying foxes: Implications for ALS-PDC in Guam. Neurology 2003;61:387-389.

Chan DKY, Lam MKP, Wong R, Hung WT, Wilcken DEL. Strong association between N-acetyltransferase 2 genotype and PD in Hong Kong Chinese. Neurology 2003;60:1002-1005.

Kikuchi S, Fukazawa T, Niino M, et al. HLA-related subpopulations of MS in Japanese with and without oligoclonal IgG bands. Neurology 2003;60:647-651.

Kokubo Y, Kunio I, Kuzuhara S. Ophthalmomyiasis-like pigmentary retinopathy in ALS/PDC in the Kii peninsula of Japan. Neurology 2003;60:1725-1726.

Mandrioli J, Faglioni P, Merelli E, Sola P. The epidemiology of ALS in Modena, Italy. Neurology 2003;60:683-689.

Mrissa N, Belal S, Hamida CB, et al. Prevalence of essential tremor: Door-to-door neurologic exams in Mersin Province, Turkey. Neurology 2003;61:1804-1806.

Sevim S, Dogu O, Camdeviren H, et al. Unexpectedly low prevalence and unusual characteristics of RLS in Mersin, Turkey. Neurology 2003;61:1562-1569.

Swerdlow AJ, Higgins CD, Adlard P, Jones ME, Preece MA. Creutzfeldt-Jakob disease in United Kingdom patients treated with human pituitary growth hormone. Neurology 2003;61:783-791.

2002

Arboleda–Velasquez JF, Lopera F, Lopez E, et al. C455R notch3 mutation in a Colombian CADASIL kindred with early onset of stroke. Neurology 2002; 59: 277-279.

Broccolini A, Pescatori M, D'Amico A, et al. An Italian family with autosomal recessive inclusion-body myopathy and mutations in the GNE gene. Neurology 2002; 59: 1808-1809.

Collins S, Boyd A, Lee JS, et al. Creutzfeldt-Jakob disease in Australia 1970-1999. Neurology 2002; 59: 1365-1371.

Cox PA, Sacks OW. Cycad neurotoxins, consumption of flying foxes, and ALS-PDC disease in Guam. Neurology 2002; 58: 956-959.

Galasko D, Salmon DP, Craig U-K, Thal L J, Schellenberg G, Wiederholt W. Clinical features and changing patterns of neurodegenerative disorders on Guam, 1997-2000.Neurology 2002; 58: 90-97.

Gamez J, Ferreiro C, Accarino ML, et al. Phenotypic variability in a Spanish family with MNGIE. Neurology 2002; 59: 455-457.

Hardy J, Gwinn-Hardy K, McGeer P, et al. Clinical features and changing patterns of neurodegenerative disorders on Guam, 1997-2000.Neurology 2002; 59: 1121.

Henry P, Auray JP, Gaudin AF, et al. Prevalence and clinical characteristics of migraine in France. Neurology 2002; 59: 232-237.

Ikeda S, Nakazato M, Ando Y, Sobue G. Familial transthyretin-type amyloid polyneuropathy in Japan: Clinical and genetic heterogeneity. Neurology 2002; 58: 1001-1007.

Ito M, Aiba H, Hashimoto K, et al. Low-dose ACTH therapy for West syndrome: Initial effects and long-term outcome. Neurology 2002; 58: 110-114.

Kis B, Schrag A, Ben-Shlomo Y, et al. Novel three-stage ascertainment method: Prevalence of PD and parkinsonism in South Tyrol, Italy. Neurology 2002; 58: 1820-1825.

Klein C, Hedrich K, Kabakci K et al.Exon deletions in the GCHI gene in two of four Turkish families with dopa-responsive dystonia. Neurology 2002; 59: 1783-1786.

Matsuura T, Ranum LPW, Volpini Vet al. Spinocerebellar ataxia type 10 is rare in populations other than Mexicans.Neurology 2002;58:983.

Nicoletti A, Bartoloni A, Reggio F,et al. Epilepsy, cysticercosis, and toxocariasis: A population-based case-control study in rural Bolivia. Neurology 2002; 58:1256-1261.

Plato CC, Galasko D, Garruto RM, et al. ALS and PDC of Guam: Forty-year follow-up. Neurology 2002; 58: 765-773.

Sharief MK, Priddin J, Delamont RS et al. Neurophysiologic analysis of neuromuscular symptoms in UK Gulf War veterans: A controlled study. Neurology 2002; 59: 1518 - 1525.

Swash M, Beresford R. Brain death: Still-unresolved issues worldwide. Neurology 2002;58:9-10.

Tsuboi Y, Baker M, Hutton ML,et al. Clinical and genetic studies of families with the tau N279K mutation (FTDP-17). Neurology 2002;59:1791-1793.

van de Warrenburg BPC, Sinke RJ, Verschuuren-Bemelmans CC, et al. Spinocerebellar ataxias in the Netherlands: Prevalence and age at onset variance analysis. Neurology 2002; 58: 702-708.

Vilensky JA, Robertson WM, Gilman S. Denny-Brown, Wilson's disease, and BAL (British antilewisite [2,3-dimercaptopropanol]). Neurology 2002; 59: 914-916.

Wijdicks EFM. Brain death worldwide: Accepted fact but no global consensus in diagnostic criteria. Neurology 2002;58:20-25.

Zappia M, Cittadella R, Manna I, et al. Genetic association of {alpha}2-macroglobulin polymorphisms with AD in southern Italy. Neurology 2002; 59: 756-758.

2001

Aiba H, Mochizuki M, Kimura M, Hojo H. Predictive value of serum interleukin-6 level in influenza virus-associated encephalopathy. Neurology 2001;57:295-299.

Ausems MGEM. Wokke JHJ, Reuser AJJ, et al. Juvenile and adult-onset acid maltase deficiency in France: Genotype-phenotype correlation. Neurology 2001;57:1938.

Bhigjee AI, Madurai S, Bill PLA, et al. Spectrum of myelopathies in HIV seropositive South African patients.
Neurology 2001;57: 348-351.

Cabre P, Heinzlef O, Merle H, et al. MS and neuromyelitis optica in Martinique (French West Indies). Neurology 2001; 56:507-514.

Chandra V, Pandav R, Dodge HH, et al.Incidence of Alzheimer's disease in a rural community in India: The Indo-US Study. Neurology 2001;57:985-989.

Chen RC, Chang SF, Su CL, et al. Prevalence, incidence, and mortality of PD: A door-to-door survey in Ilan County, Taiwan.Neurology 2001;57:1679-1686.

Chiò A for Piemonte and Valle d’Aosta Register for Amyotrophic Lateral Sclerosis (PARALS). Incidence of ALS in Italy: Evidence for a uniform frequency in Western countries. Neurology 2001;56:239-244.

Dauvilliers Y, Montplaisir J, Molinari N, et al.Age at onset of narcolepsy in two large populations of patients in France and Quebec. Neurology 2001;57:2029-2033.

Defazio G, Livrea P, De Salvia R, et al. Prevalence of primary blepharospasm in a community of Puglia region, Southern Italy. Neurology 2001;56:1579-1581.

Grimaldi LME, Salemi G, Grimaldi G, et al. High incidence and increasing prevalence of MS in Enna (Sicily), southern Italy. Neurology 2001;57:1891-1893.

Hou L, Osei-Hyiaman D, Yu H, et al.Association of a 27-bp repeat polymorphism in ecNOS gene with ischemic stroke in Chinese patients. Neurology 2001;56:490-496.

Ikeda M, Hokoishi K, Maki N, et al. Increased prevalence of vascular dementia in Japan: A community-based epidemiological study. Neurology 2001;57:839-844.

Lee B-C, Hwang S-H, Bae J-C, Kwon S-B.Brainstem infarction following Korean viper bite . Neurology 2001;56:1244-1245.

Mazarib A, Xiong L, Neufeld MY, et al.Unverricht–Lundborg disease in a five-generation Arab family: Instability of dodecamer repeats.Neurology 2001;57:1050-1054.

Muglia M, Zappia M, Timmerman V, et al. Clinical and genetic study of a large Charcot-Marie-Tooth type 2A family from southern Italy. Neurology 2001;56:100-103.

Nicoletti A, Lo Bartolo ML, Lo Fermo S, et al. Prevalence and incidence of multiple sclerosis in Catania, Sicily.Neurology2001;56:62-66.

Perini P, Tagliaferri C, Belloni M, Biasi G, Gallo P. The HLA-DR13 haplotype is associated with "benign" multiple sclerosis in northeast Italy. Neurology 2001;57:158-159.

Worth PF, Wood NW.Spinocerebellar ataxia type 12 is rare in the United Kingdom.Neurology 2001;56:419-420.

Wu RM, Cheng CW, Chen KH, et al.The COMT L allele modifies the association between MAOB polymorphism and PD in Taiwanese.Neurology 2001;56:375-382.

2000

Alvarado-de la Barrera C, Zuniga-Ramos J, Ruiz-Morales JA, Estanol B, Granados J, Llorente L.
HLA class II genotypes in Mexican Mestizos with familial and nonfamilial multiple sclerosis. Neurology 2000;55:1897-1900.

Badrising UA, Maat-Schieman M, van Duinen SG, et al. Epidemiology of inclusion body myositis in the Netherlands: A nationwide study. Neurology 2000;55:1385-1388.

Blumen SC, Korczyn AD, Lavoie H, et al.Oculopharyngeal MD among Bukhara Jews is due to a founder (GCG)9 mutation in the PABP2 gene. Neurology 2000;55:1267-1270.

Brown HC, Chau TTH, Mai NTH, et al. Blood–brain barrier function in cerebral malaria and CNS infections in Vietnam. Neurology 2000;55:104-111.

Brown P, Preece M, Brandel J-P, et al.Iatrogenic Creutzfeldt-Jakob disease at the millennium. Neurology 2000;55:1075-1081.

Coeytaux A, Jallon P, Galobardes B, Morabia A.Incidence of status epilepticus in French-speaking Switzerland: (EPISTAR).Neurology 2000;55:693-697.

Gouider-Khouja N, Belal S, Hamida M Ben, Hentati F. Clinical and genetic study of familial Parkinson's disease in Tunisia. Neurology 2000;54:1603-1609.

Gwinn-Hardy K, Chen JY, Liu H-C, et al.Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese. Neurology 2000;55:800-805.

Hackett ML, Anderson CS. Health outcomes 1 year after subarachnoid hemorrhage: An international population-based study. Neurology 2000;55:658-662.

Hoshi K, Yoshino H, Urata J, Nakamura Y, Yanagawa H, Sato T. Creutzfeldt-Jakob disease associated with cadaveric dura mater grafts in Japan. Neurology 2000;55:718-721.

Ikeda Y, Shizuka M, Watanabe M, Okamoto K, Shoji M.Molecular and clinical analyses of spinocerebellar ataxia type 8 in Japan. Neurology 2000;54:950-955.

Laforet P, Nicolino M, Eymard B, et al.Juvenile and adult-onset acid maltase deficiency in France: Genotype-phenotype correlation. Neurology 2000;55:1122-1128.

Mirabella M, Silvestri G, de Rosa G, et al.GCG genetic expansions in Italian patients with oculopharyngeal muscular dystrophy. Neurology 2000;54:608.

Misu K, Hattori N, Ando Y, Ikeda S, Sobue G. Anticipation in early- but not late-onset familial amyloid polyneuropathy (TTR Met 30) in Japan. Neurology 2000;55:451-452.

Mrissa N, Belal S, Ben Hamida C, et al. Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family.Neurology 2000;54:1408-1414.

Pulst SM, Filla A.Ataxias on the march from Quebec to Tunisia. Neurology 2000;54:1400-1401.

Van Koningsveld R, Van Doorn PA, Schmitz PIM, Ang CW, Van der Meche FGA. Mild forms of Guillain-Barre syndrome in an epidemiologic survey in the Netherlands. Neurology 2000;54:620.

Wang S-J, Fuh J-L, Lu S-R, et al.Chronic daily headache in Chinese elderly: Prevalence, risk factors, and biannual follow-up. Neurology 2000;54:314.

Yamakawa K, Kuroda H, Fujihara K, et al. Familial neuromyelitis optica (Devic's syndrome) with late onset in Japan. Neurology 2000;55:318-320.