SCOPUS 정보 검색 플랫폼

Journal of Neurology

Volumn 249, Issue 12, 2002, Pages 1740-1741

Early and persistent sensory-psychiatric symptoms in an inherited prion disease with a PrP P105L mutation [4]

(3) Shiraishi, Atsushi a Mizusawa, Hidehiro a Yamada, Masahito b

a TOKYO MEDICAL AND DENTAL UNIVERSITY (Japan)

b KANAZAWA UNIVERSITY GRADUATE SCHOOL OF MEDICAL SCIENCE (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIDEPRESSANT AGENT;

ADULT; ALLELE; ANXIETY; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CLINICAL FEATURE; CODON; CONTROLLED STUDY; CREUTZFELDT JAKOB DISEASE; DISEASE COURSE; FAMILY HISTORY; FEMALE; HUMAN; LETTER; MEDICAL EXAMINATION; MENTAL DISEASE; MISSENSE MUTATION; MYOMA; NEUROLOGIC EXAMINATION; PAIN; PATIENT REFERRAL; PRION DISEASE; PRIORITY JOURNAL; SYMPTOM;

FEMALE; HUMANS; LEUCINE; MALE; MIDDLE AGED; MUTATION; PEDIGREE; PRION DISEASES; PRIONS; PROLINE;

EID: 0037004912 PISSN: 03405354 EISSN: None Source Type: Journal
DOI: 10.1007/s00415-002-0907-x Document Type: Letter

Times cited : (8)

References (4)

1
- 0033551458
- An inherited prion disease with a PrP P105L mutation. Clinicopathologic and PrP heterogeneity
- Yamada M, Itoh Y, Inaba A, Wada Y, Takashima M, Kamata T, Okeda R, Kayano T, Suematsu N, Kitamoto T, Otomo E, Matsushita M, Mizusawa H (1999) An inherited prion disease with a PrP P105L mutation. Clinicopathologic and PrP heterogeneity. Neurology 53:181-188
- (1999) Neurology , vol.53 , pp. 181-188
- Yamada, M.¹ Itoh, Y.² Inaba, A.³ Wada, Y.⁴ Takashima, M.⁵ Kamata, T.⁶ Okeda, R.⁷ Kayano, T.⁸ Suematsu, N.⁹ Kitamoto, T.¹⁰ Otomo, E.¹¹ Matsushita, M.¹² Mizusawa, H.¹³

2
- 0033228346
- Variant Gerstmann-Sträussler syndrome with the P105L prion gene mutation: An unusual case with nigral degeneration and widespread neurofibrillary tangles
- Yamazaki M, Oyanagi K, Mori O, Kitamura S, Ohyama M, Terashi A, Kitamoto T, Katayama Y (1999) Variant Gerstmann-Sträussler syndrome with the P105L prion gene mutation: an unusual case with nigral degeneration and widespread neurofibrillary tangles. Acta Neuropathol (Berl) 98:506-511
- (1999) Acta Neuropathol (Berl) , vol.98 , pp. 506-511
- Yamazaki, M.¹ Oyanagi, K.² Mori, O.³ Kitamura, S.⁴ Ohyama, M.⁵ Terashi, A.⁶ Kitamoto, T.⁷ Katayama, Y.⁸

3
- 0031588170
- New variant Creutzfeldt-Jakob disease: Psychiatric features
- Zeidler M, Johnstone EC, Bamber RWK, Dickens CM, Fisher CJ, Francis AF, Goldbeck R, Higgo R, Johnson-Sabine EC, Lodge GJ, McGarry P, Mitchell S, Tario L, Turner M, Ryley P, Will RG (1997) New variant Creutzfeldt-Jakob disease: psychiatric features. Lancet 350:908-910
- (1997) Lancet , vol.350 , pp. 908-910
- Zeidler, M.¹ Johnstone, E.C.² Bamber, R.W.K.³ Dickens, C.M.⁴ Fisher, C.J.⁵ Francis, A.F.⁶ Goldbeck, R.⁷ Higgo, R.⁸ Johnson-Sabine, E.C.⁹ Lodge, G.J.¹⁰ McGarry, P.¹¹ Mitchell, S.¹² Tario, L.¹³ Turner, M.¹⁴ Ryley, P.¹⁵ Will, R.G.¹⁶

4
- 0042422345
- Diagnosis of new variant Creutzfeldt-Jakob disease
- Will RG, Zeidler M, Stewart GE, Macleod MA, Ironside JW, Cousens SN, Stat DM, Mackenzie J, Estibeiro K, Green AJE, Knight RSG (2000) Diagnosis of new variant Creutzfeldt-Jakob disease. Ann Neurol 47:575-582
- (2000) Ann Neurol , vol.47 , pp. 575-582
- Will, R.G.¹ Zeidler, M.² Stewart, G.E.³ Macleod, M.A.⁴ Ironside, J.W.⁵ Cousens, S.N.⁶ Stat, D.M.⁷ Mackenzie, J.⁸ Estibeiro, K.⁹ Green, A.J.E.¹⁰ Knight, R.S.G.¹¹

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.