Native state stabilization by NSAIDs inhibits transthyretin amyloidogenesis from the most common familial disease variantsMILLER, Sean R; SEKIJIMA, Yoshiki; KELLY, Jeffery W et al.Laboratory investigation. 2004, Vol 84, Num 5, pp 545-552, issn 0023-6837, 8 p.Article

CPPD crystal deposition disease of the cervical spine: A common cause of acute neck pain encountered in the neurology departmentSEKIJIMA, Yoshiki; YOSHIDA, Takuhiro; IKEDA, Shu-Ichi et al.Journal of the neurological sciences. 2010, Vol 296, Num 1-2, pp 79-82, issn 0022-510X, 4 p.Article

Successful Pregnancy and Lactation Outcome in a Patient With Gaucher Disease Receiving Enzyme Replacement Therapy, and the Subsequent Distribution and Excretion of Imiglucerase in Human Breast MilkSEKIJIMA, Yoshiki; OHASHI, Toya; OHIRA, Satoshi et al.Clinical therapeutics. 2010, Vol 32, Num 12, pp 2048-2052, issn 0149-2918, 5 p.Article

Pathogenesis of and Therapeutic Strategies to Ameliorate the Transthyretin AmyloidosesSEKIJIMA, Yoshiki; KELLY, Jeffery W; IKEDA, Shu-Ichi et al.Current pharmaceutical design (Print). 2008, Vol 14, Num 30, pp 3219-3230, issn 1381-6128, 12 p.Article

AMYLOIDOGENIC TRANSTHYRETIN Val30Met HOMOZYGOTE SHOWING UNUSUALLY EARLY-ONSET FAMILIAL AMYLOID POLYNEUROPATHYTOJO, Kana; SEKIJIMA, Yoshiki; MACHIDA, Kazuko et al.Muscle & nerve. 2008, Vol 37, Num 6, pp 796-803, issn 0148-639X, 8 p.Article

A novel nonsense mutation in the TITF-1 gene in a Japanese family with benign hereditary choreaNAKAMURA, Katsuya; SEKIJIMA, Yoshiki; NAGAMATSU, Kiyoshiro et al.Journal of the neurological sciences. 2012, Vol 313, Num 1-2, pp 189-192, issn 0022-510X, 4 p.Article

Wild-type transthyretin significantly contributes to the formation of amyloid fibrils in familial amyloid polyneuropathy patients with amyloidogenic transthyretin Val30MetTSUCHIYA-SUZUKI, Ayako; YAZAKI, Masahide; KAMETANI, Fuyuki et al.Human pathology. 2011, Vol 42, Num 2, pp 236-243, issn 0046-8177, 8 p.Article

Neutropenia as a complication of high-dose intravenous immunoglobulin therapy in adult patients with neuroimmunologic disordersMATSUDA, Masayuki; HOSODA, Waki; SEKIJIMA, Yoshiki et al.Clinical neuropharmacology. 2003, Vol 26, Num 6, pp 306-311, issn 0362-5664, 6 p.Article

SELDI-TOF Mass Spectrometry Evaluation of Variant Transthyretins for Diagnosis and Pathogenesis of Familial Amyloidotic PolyneuropathyUEDA, Mitsuharu; MISUMI, Yohei; SUHR, Ole B et al.Clinical chemistry (Baltimore, Md.). 2009, Vol 55, Num 6, pp 1223-1227, issn 0009-9147, 5 p.Article

Soluble Aβ homeostasis in AD and DS: impairment of anti-amyloidogenic protection by lipoproteinsMATSUBARA, Etsuro; SEKIJIMA, Yoshiki; IKEDA, Shu-Ichi et al.Neurobiology of aging. 2004, Vol 25, Num 7, pp 833-841, issn 0197-4580, 9 p.Article

Severe generalized dystonia as a presentation of a patient with aprataxin gene mutationSEKIJIMA, Yoshiki; HASHIMOTO, Takao; ONODERA, Osam et al.Movement disorders. 2003, Vol 18, Num 10, pp 1198-1200, issn 0885-3185, 3 p.Article

Energetic characteristics of the new Transthyretin variant A25T may explain its atypical central nervous system pathologySEKIJIMA, Yoshiki; HAMMARSTRÖM, Per; MATSUMURA, Miyuki et al.Laboratory investigation. 2003, Vol 83, Num 3, pp 409-417, issn 0023-6837, 9 p.Article

Dystonia, mental deterioration, and dyschromatosis symmetrica hereditaria in a family with ADAR1 mutationTOJO, Kana; SEKIJIMA, Yoshiki; SUZUKI, Tamio et al.Movement disorders. 2006, Vol 21, Num 9, pp 1510-1513, issn 0885-3185, 4 p.Article

Increase in incidence of elderly-onset patients with myasthenia gravis in nagano prefecture, JapanMATSUDA, Masayuki; DOHI-IIJIMA, Naoko; IKEDA, Shu-Ichi et al.Internal medicine (Tokyo. 1992). 2005, Vol 44, Num 6, pp 572-577, issn 0918-2918, 6 p.Article

Hepatocellular carcinoma in a case of adult-onset type II citrullinemiaHAGIWARA, Naoki; SEKIJIMA, Yoshiki; TAKEI, Yo-Ichi et al.Internal medicine (Tokyo. 1992). 2003, Vol 42, Num 10, pp 978-982, issn 0918-2918, 5 p.Article

Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily geneDATE, Hidetoshi; ONODERA, Osamu; SAKAI, Tetsuo et al.Nature genetics. 2001, Vol 29, Num 2, pp 184-188, issn 1061-4036Article

Three patients with isolated adrenocorticotropin deficiency presenting with neuroleptic malignant syndrome-like symptomsSEKIJIMA, Yoshiki; HOSHI, Ken-Ichi; KASAI, Hiroki et al.Internal medicine (Tokyo. 1992). 2001, Vol 40, Num 6, pp 510-514, issn 0918-2918Article

Repurposing Diflunisal for Familial Amyloid Polyneuropathy: A Randomized Clinical TrialBERK, John L; SUHR, Ole B; NORDH, Erik et al.JAMA, the journal of the American Medical Association. 2013, Vol 310, Num 24, pp 2658-2667, issn 0098-7484, 10 p.Article

Genotype-phenotype correlations in early onset ataxia with ocular motor apraxia and hypoalbuminaemiaYOKOSEKI, Akio; ISHIHARA, Tomohiko; SATO, Tatsuya et al.Brain. 2011, Vol 134, pp 1387-1399, issn 0006-8950, 13 p., 5Article

High prevalence of wild-type transthyretin deposition in patients with idiopathic carpal tunnel syndrome: a common cause of carpal tunnel syndrome in the elderlySEKIJIMA, Yoshiki; UCHIYAMA, Shigeharu; TOJO, Kana et al.Human pathology. 2011, Vol 42, Num 11, pp 1785-1791, issn 0046-8177, 7 p.Article

Retrospective analyses of clinical features and therapeutic outcomes in thymectomized patients with myasthenia gravis at Shinshu universityDOHI-IIJIMA, Naoko; SEKIJIMA, Yoshiki; NAKAMURA, Akinori et al.Internal medicine (Tokyo. 1992). 2004, Vol 43, Num 3, pp 189-193, issn 0918-2918, 5 p.Article

Japanese family with an autosomal dominant chromosome instability syndrome : A new neurodegenerative disease?ISHIKAWA, Shozo; ISHIKAWA, Masayo; SHIGETA, Hiroaki et al.American journal of medical genetics. 2000, Vol 94, Num 4, pp 265-270, issn 0148-7299Article