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Items: 1 to 20 of 240

1.

Autopsy-proven progressive supranuclear palsy in two siblings.

Tetrud JW, Golbe LI, Forno LS, Farmer PM.

Neurology. 1996 Apr;46(4):931-4.

PMID:
8780066
2.

Familial progressive supranuclear palsy.

Gazeley S, Maguire JA.

Clin Neuropathol. 1996 Jul-Aug;15(4):215-20.

PMID:
8836606
3.

[A 65-year-old man with Parkinsonism, gaze palsy, and dementia].

Mizuno Y, Yokochi F, Ohta S, Mori H, Takubo H.

No To Shinkei. 1996 Apr;48(4):381-93. Japanese.

PMID:
8679336
4.
5.

[An autopsied case of progressive supranuclear palsy presenting with slow progression and unusually prolonged disease duration].

Iwasaki Y, Mori K, Ito M, Mimuro M, Yoshida M.

Rinsho Shinkeigaku. 2012;52(3):156-60. Japanese.

PMID:
22453039
6.

[A 65-year-old man with rigid-bradykinetic parkinsonism, vertical gaze palsy, difficulty of eye-lid opening, and marked pseudo-bulbar palsy].

Noda K, Kobayashi T, Matsuoka S, Takanashi M, Kanazawa A, Mizuno Y.

No To Shinkei. 2005 Jan;57(1):73-86. Japanese.

PMID:
15782604
7.

Natural history of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) and clinical predictors of survival: a clinicopathological study.

Litvan I, Mangone CA, McKee A, Verny M, Parsa A, Jellinger K, D'Olhaberriague L, Chaudhuri KR, Pearce RK.

J Neurol Neurosurg Psychiatry. 1996 Jun;60(6):615-20.

8.

[An autopsy case of progressive supranuclear palsy with central pontine myelinolysis].

Inagaki T, Hashizume Y, Nokura K, Yamamoto T, Niimi T, Mitake S, Ojika K, Yamamoto M.

Nihon Ronen Igakkai Zasshi. 1991 Mar;28(2):226-31. Japanese.

9.

Familial progressive supranuclear palsy. Description of a pedigree and review of the literature.

de YĆ©benes JG, Sarasa JL, Daniel SE, Lees AJ.

Brain. 1995 Oct;118 ( Pt 5):1095-103. Review.

PMID:
7496773
10.

Progressive supranuclear palsy presenting with primary progressive aphasia--clinicopathological report of an autopsy case.

Mochizuki A, Ueda Y, Komatsuzaki Y, Tsuchiya K, Arai T, Shoji S.

Acta Neuropathol. 2003 Jun;105(6):610-4. Epub 2003 Apr 1.

PMID:
12669238
11.

[A 85-year-old woman with the onset of progressive gait disturbance at 80 years of the age].

Yoritaka A, Hattori T, Hattori Y, Mori H, Matsuoka S, Shirai T, Kondo T, Mizuno Y.

No To Shinkei. 1997 Apr;49(4):379-89. Japanese.

PMID:
9125748
12.

Regional brain atrophy in progressive supranuclear palsy and Lewy body disease.

Cordato NJ, Halliday GM, Harding AJ, Hely MA, Morris JG.

Ann Neurol. 2000 Jun;47(6):718-28.

PMID:
10852537
13.

Early progressive supranuclear palsy: pathology and clinical presentation.

Kleinschmidt-DeMasters BK.

Clin Neuropathol. 1989 Mar-Apr;8(2):79-84.

PMID:
2721044
14.

Different tau pathology pattern in two clinical phenotypes of progressive supranuclear palsy.

Jellinger KA.

Neurodegener Dis. 2008;5(6):339-46. doi: 10.1159/000121388. Epub 2008 Mar 18.

PMID:
18349518
15.

[An autopsied case of progressive supranuclear palsy, initially diagnosed as spinocerebellar degeneration with severe olivopontocerebellar involvement].

Iwasaki Y, Mori K, Ito M, Mimuro M, Yoshida M.

Rinsho Shinkeigaku. 2011 Oct;51(10):756-60. Japanese.

PMID:
22019867
16.

Progressive supranuclear palsy-like syndrome in two siblings of a consanguineous marriage.

Ohara S, Kondo K, Morita H, Maruyama K, Ikeda S, Yanagisawa N.

Neurology. 1992 May;42(5):1009-14.

PMID:
1579223
17.

Progressive supranuclear palsy: pathology and genetics.

Dickson DW, Rademakers R, Hutton ML.

Brain Pathol. 2007 Jan;17(1):74-82. Review.

PMID:
17493041
18.

Pure akinesia manifested neuroleptic malignant syndrome: a clinical variant of progressive supranuclear palsy.

Yoshikawa H, Oda Y, Sakajiri K, Takamori M, Nakanishi I, Makifuchi T, Ide Y, Matsubara S, Mizushima N.

Acta Neuropathol. 1997 Mar;93(3):306-9.

PMID:
9083564
19.

Lewy bodies in progressive supranuclear palsy represent an independent disease process.

Uchikado H, DelleDonne A, Ahmed Z, Dickson DW.

J Neuropathol Exp Neurol. 2006 Apr;65(4):387-95.

PMID:
16691119
20.

Pallido-nigro-luysian atrophy, progressive supranuclear palsy and adult onset Hallervorden-Spatz disease: a case of akinesia as a predominant feature of parkinsonism.

Yamamoto T, Kawamura J, Hashimoto S, Nakamura M, Iwamoto H, Kobashi Y, Ichijima K.

J Neurol Sci. 1991 Jan;101(1):98-106.

PMID:
1709202

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