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1

Pletz, C. "Steele-Richardson-Olszewski-Syndrom." Klinische Monatsblätter für Augenheilkunde 224, no. 12 (2007): 939–42. http://dx.doi.org/10.1055/s-2007-963603.

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2

Koop, G., and M. Gräf. "Steele-Richardson-Olszewski-Syndrom - Darstellung eines selten erkannten Krankheitsbildes anhand zweier Fallberichte." Klinische Monatsblätter für Augenheilkunde 224, no. 10 (2007): 799–803. http://dx.doi.org/10.1055/s-2007-963605.

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3

Klimke, A., and R. Larisch. "Zur klinischen Wertigkeit der zerebralen Dopamin-D2-Rezeptorszintigraphie." Nuklearmedizin 37, no. 07 (1998): 245–50. http://dx.doi.org/10.1055/s-0038-1632342.

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ZusammenfassungDie vorliegende Arbeit gibt eine Übersicht über Befunde und klinische Indikationen zur Dopamin-D2-Rezeptorszintigraphie. Methoden zur Untersuchung der D2-Rezeptoren sind die Positronen-Emissions-Tomographie (PET) mit 11C- oder 18F-markierten Butyrophenonen oder Benza- miden oder die Einzelphotonen-Emissions-Tomographie (SPECT) mit 123l-lodobenzamid (IBZM). Die wichtigste neurologische Indikation ist die Differentialdiagnose des Parkinsonismus: In frühen Stadien des Morbus Parkinson findet sich eine Erhöhung der Striatalen D2-Rezeptorbin- dung (D2-RB) im Vergleich zu gesunden Nor
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4

Steele, J. C. "IN31-TU-04 PSP Steele-Richardson-Olszewski syndrome Richardson's disease." Journal of the Neurological Sciences 285 (October 2009): S25. http://dx.doi.org/10.1016/s0022-510x(09)70122-4.

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5

Gokhale, VijayashreeS, Zubin Sharma, and Neha Chaudhari. "Steele Richardson Olszewski syndrome." Medical Journal of Dr. D.Y. Patil University 6, no. 3 (2013): 342. http://dx.doi.org/10.4103/0975-2870.114671.

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6

LEENDERS, K. L., R. S. J. FRACKOWIAK, and A. J. LEES. "STEELE-RICHARDSON-OLSZEWSKI SYNDROME." Brain 111, no. 3 (1988): 615–30. http://dx.doi.org/10.1093/brain/111.3.615.

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7

Fehlow, P., and F. Walther. "Richards-Rundle-Syndrom." Klinische Pädiatrie 203, no. 03 (1991): 184–86. http://dx.doi.org/10.1055/s-2007-1025427.

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8

Richardson, Ruth. "Improving awareness of myalgic encephalomyelitis among healthcare professionals." British Journal of Healthcare Management 27, no. 8 (2021): 1–3. http://dx.doi.org/10.12968/bjhc.2021.0095.

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Myalgic encephalomyelitis, or chronic fatigue syndrome, represents a significant human and economic health burden. Ruth Richardson of UK charity Action for ME discusses the need to increase awareness of this condition among healthcare professionals and shares resources to help with this.
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9

Kouri, Naomi, Melissa E. Murray, Anhar Hassan, et al. "Neuropathological features of corticobasal degeneration presenting as corticobasal syndrome or Richardson syndrome." Brain 134, no. 11 (2011): 3264–75. http://dx.doi.org/10.1093/brain/awr234.

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10

Davie, Charles A., Gareth J. Barker, Christine Machado, David H. Miller, and Andrew J. Lees. "Proton magnetic resonance spectroscopy in steele-richardson-olszewski syndrome." Movement Disorders 12, no. 5 (1997): 767–71. http://dx.doi.org/10.1002/mds.870120525.

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11

Seliverstov, Yu A., Yu A. Shpilyukova, and S. N. Illarioshkin. "Are Some Eponyms in Neurology Used Correctly?" Russian neurological journal 25, no. 3 (2020): 45–50. http://dx.doi.org/10.30629/2658-7947-2020-25-3-45-50.

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The article analyzes the origin and competence of using several eponyms widely known in neurology. It is shown that some of them are not used correctly. So, the alternates “Jakob–Creutzfeldt disease” and “Arnold– Chiari malformation” are more correct. The eponym “Steele–Richardson–Olszewski syndrome” should not be used as a synonym for progressive supranuclear palsy syndrome. The historical aspects and correct variants of the use of a number of other neurological eponyms are highlighted in the article.
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12

Nath, U., and D. J. Burn. "The epidemiology of progressive supranuclear palsy (Steele–Richardson–Olszewski syndrome)." Parkinsonism & Related Disorders 6, no. 3 (2000): 145–53. http://dx.doi.org/10.1016/s1353-8020(00)00011-0.

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13

Patgiri, Priyanka R. "A Case of Progressive Supranuclear Palsy/Steele—Richardson—Olszewski Syndrome." MGM Journal of Medical Sciences 4, no. 2 (2017): 102–4. http://dx.doi.org/10.5005/jp-journals-10036-1149.

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14

Lopez, G., K. Bayulkem, and M. Hallett. "Progressive supranuclear palsy (PSP): Richardson syndrome and other PSP variants." Acta Neurologica Scandinavica 134, no. 4 (2016): 242–49. http://dx.doi.org/10.1111/ane.12546.

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15

Maher, E. R., E. M. Smith, and A. J. Lees. "Cognitive deficits in the Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy)." Journal of Neurology, Neurosurgery & Psychiatry 48, no. 12 (1985): 1234–39. http://dx.doi.org/10.1136/jnnp.48.12.1234.

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16

Sonthalia, N., and S. Ray. "The Hummingbird sign: a diagnostic clue for Steele-Richardson-Olszweski syndrome." Case Reports 2012, sep14 1 (2012): bcr2012006263. http://dx.doi.org/10.1136/bcr-2012-006263.

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17

Pearce, J. M. S. "Progressive Supranuclear Palsy (Steele-Richardson-Olszewski Syndrome): A Short Historical Review." Neurologist 13, no. 5 (2007): 302–4. http://dx.doi.org/10.1097/01.nrl.0000254743.69160.b3.

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18

Hardwick, A., J. C. Rucker, M. L. Cohen, et al. "EVOLUTION OF OCULOMOTOR AND CLINICAL FINDINGS IN AUTOPSY-PROVEN RICHARDSON SYNDROME." Neurology 73, no. 24 (2009): 2122–24. http://dx.doi.org/10.1212/wnl.0b013e3181c67ba2.

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19

Gliwa, Renata. "Speech and language disturbances in a patient with the clinical features of Steele‑Richardson‑Olszewski syndrome." Logopaedica Lodziensia, no. 1 (December 30, 2017): 43–61. http://dx.doi.org/10.18778/2544-7238.01.05.

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Steele‑Richardson‑Olszewski syndrome also known as progressive supranuclear palsy (PSP) is a neurodegenerative disease of the central nervous system of extrapyramidal type of neuropathy of unknown etiology. This chapter describes the case of 62 patients diagnosed with PSP, the changes they observe are related to selective linguistic dysfunction resulting from subcortical dementia and executive and motor dysfunction, and the functioning of the subject is significantly determined by emotional disturbance.
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20

Bayram, Ece, Dennis W. Dickson, Stephen G. Reich, and Irene Litvan. "Pathology‐Proven Corticobasal Degeneration Presenting as Richardson's Syndrome." Movement Disorders Clinical Practice 7, no. 3 (2020): 267–72. http://dx.doi.org/10.1002/mdc3.12900.

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21

Adam, A. M., and D. O. Orinda. "Focal paroxysmal kinesigenic choreoathetosis preceding the development of Steele-Richardson-Olszewski syndrome." Journal of Neurology, Neurosurgery & Psychiatry 49, no. 8 (1986): 957–59. http://dx.doi.org/10.1136/jnnp.49.8.957-a.

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22

Hauw, J. J., S. E. Daniel, D. Dickson, et al. "Preliminary NINDS neuropathologic criteria for Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy)." Neurology 44, no. 11 (1994): 2015. http://dx.doi.org/10.1212/wnl.44.11.2015.

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23

Frank, Anika, Kevin Peikert, Jennifer Linn, Moritz D. Brandt, and Andreas Hermann. "MDS criteria for the diagnosis of progressive supranuclear palsy overemphasize Richardson syndrome." Annals of Clinical and Translational Neurology 7, no. 9 (2020): 1702–7. http://dx.doi.org/10.1002/acn3.51065.

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24

De Bruin, V. S., C. Machado, R. S. Howard, N. P. Hirsch, and A. J. Lees. "Nocturnal and respiratory disturbances in Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy)." Postgraduate Medical Journal 72, no. 847 (1996): 293–96. http://dx.doi.org/10.1136/pgmj.72.847.293.

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25

Ovsiew, F., and J. Schneider. "Schizophrenia and Atypical Motor Features in a Case of Progressive Supranuclear Palsy (The Steele-Richardson-Olszewski Syndrome)." Behavioural Neurology 6, no. 4 (1993): 243–47. http://dx.doi.org/10.1155/1993/206834.

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Mental manifestations are characteristic of the syndrome described by Steele, Richardson, and Olszewski as progressive supranuclear palsy (SRO). Discussions emphasize cognitive aspects, namely the “subcortical dementia” for which the disease is prototypical, but personality change has been mentioned beginning with the earliest accounts. Psychosis has been virtually absent from neuropsychiatric descriptions, perhaps curiously so in view of the association between subcortical disease and delusions. We report here a case of autopsy-proven SRO in which a schizophrenia-like psychosis was a central
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26

Fatterpekar, Girish M., August Dietrich, Patrizia Pantano, et al. "Cerebral Peduncle Angle: An Objective Criterion for Assessing Progressive Supranuclear Palsy Richardson Syndrome." American Journal of Roentgenology 205, no. 2 (2015): 386–91. http://dx.doi.org/10.2214/ajr.14.12724.

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27

VIDAILHET, M., J. C. ROTHWELLL, P. D. THOMPSON, A. J. LEES, and C. D. MARSDEN. "THE AUDITORY STARTLE RESPONSE IN THE STEELE-RICHARDSON-OLSZEWSKI SYNDROME AND PARKINSON'S DISEASE." Brain 115, no. 4 (1992): 1181–92. http://dx.doi.org/10.1093/brain/115.4.1181.

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28

Revesz, T., H. Sangha, and S. E. Daniel. "The nucleus raphe interpositus in the Steele--Richardson--Olszewski syndrome (progressive supranuclear palsy)." Brain 119, no. 4 (1996): 1137–43. http://dx.doi.org/10.1093/brain/119.4.1137.

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29

Nath, U. "The prevalence of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) in the UK." Brain 124, no. 7 (2001): 1438–49. http://dx.doi.org/10.1093/brain/124.7.1438.

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30

Will, R. G., A. J. Lees, W. Gibb, and R. O. Barnard. "A case of progressive subcortical gliosis presenting clinically as Steele-Richardson-Olszewski syndrome." Journal of Neurology, Neurosurgery & Psychiatry 51, no. 9 (1988): 1224–27. http://dx.doi.org/10.1136/jnnp.51.9.1224.

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31

de Bruin, V. M. S., and A. J. Lees. "The Clinical Features of 67 Patients with Clinically Definite Steele-Richardson-Olszewski Syndrome." Behavioural Neurology 5, no. 4 (1992): 229–32. http://dx.doi.org/10.1155/1992/545287.

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The clinical features of 67 patients with probable Steele-Richardson-Olszewski syndrome have been analysed. Bradykinesia was present in 92.5% of cases at the time of initial assessment and the two commonest presenting complaints were walking difficulties and stiffness. Only 11 patients had a supranuclear gaze palsy when first seen. Forty-nine patients developed cognitive impairment in the course of their illness based on neuropsychological testing. In addition to the classical clinical findings occasional other findings included focal dystonia, tonic inhibition of levator palpebrae and blephar
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32

Qureshi, Ihtesham A., Mohtashim A. Qureshi, and Alberto Maud. "A 72-year-old with eyelid opening apraxia in Steele-Richardson-Olszewski syndrome." Clinical Case Reports 5, no. 6 (2017): 1054–55. http://dx.doi.org/10.1002/ccr3.958.

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33

Tarı Cömert, Itır, Zerrin Pelin, Tolga Arıcak, and Saadet Yapan. "Validation of the Turkish Version of the Rapid Eye Movement Sleep Behavior Disorder Questionnaire." Behavioural Neurology 2016 (2016): 1–6. http://dx.doi.org/10.1155/2016/8341651.

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The aim of this study was to assess the validity and reliability of a Turkish version of the rapid eye movement sleep behavior disorder questionnaire (the RBDSQ-T) for identifying patients with rapid eye movement sleep behavior disorder (RBD) and to ensure that this tool can be applied in Turkish language. Three groups were enrolled to validate the RBDSQ-T: 78 healthy controls, 17 patients previously diagnosed with RBD, and 28 patients with obstructive sleep apnea syndrome (OSAS). Based on a cut-off score of five, the RBDSQ-T was able to discriminate RBD patients from healthy controls with sen
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34

Burn, D. J., J. O. Rinne, N. P. Quinn, A. J. Lees, C. D. Marsden, and D. J. Brooks. "Striatal opioid receptor binding in Parkinson's disease, striatonigral degeneration and Steele-Richardson-Olszewski syndrome." Brain 118, no. 4 (1995): 951–58. http://dx.doi.org/10.1093/brain/118.4.951.

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35

Revesz, T., G. M. Gibb, B. H. Anderton, and S. E. Daniel. "TAU-PATTERNS IN TYPICAL AND ATYPICAL CASES OF THE STEELE-RICHARDSON-OLSZEWSKI SYNDROME (SROS)." Journal of Neuropathology and Experimental Neurology 56, no. 5 (1997): 591. http://dx.doi.org/10.1097/00005072-199705000-00093.

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36

Schofield, Emma C., John R. Hodges, Thomas H. Bak, John H. Xuereb, and Glenda M. Halliday. "The relationship between clinical and pathological variables in Richardson’s syndrome." Journal of Neurology 259, no. 3 (2011): 482–90. http://dx.doi.org/10.1007/s00415-011-6205-8.

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37

Daniel, S. E., V. M. S. de Bruin, and A. J. Lees. "The clinical and pathological spectrum of Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy): a reappraisal." Brain 118, no. 3 (1995): 759–70. http://dx.doi.org/10.1093/brain/118.3.759.

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38

Litvan, I., Y. Agid, J. Jankovic, et al. "Accuracy of clinical criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome)." Neurology 46, no. 4 (1996): 922–30. http://dx.doi.org/10.1212/wnl.46.4.922.

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39

Maher, E. R., and A. J. Lees. "The clinical features and natural history of the Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy)." Neurology 36, no. 7 (1986): 1005. http://dx.doi.org/10.1212/wnl.36.7.1005.

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40

Ahn, Jong Hyeon, Minkyeong Kim, Ji Sun Kim, et al. "Midbrain atrophy in patients with presymptomatic progressive supranuclear palsy-Richardson's syndrome." Parkinsonism & Related Disorders 66 (September 2019): 80–86. http://dx.doi.org/10.1016/j.parkreldis.2019.07.009.

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41

Agosta, Federica, Michela Pievani, Marina Svetel, et al. "Diffusion tensor MRI contributes to differentiate Richardson's syndrome from PSP-parkinsonism." Neurobiology of Aging 33, no. 12 (2012): 2817–26. http://dx.doi.org/10.1016/j.neurobiolaging.2012.02.002.

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42

Srulijes, Karin, Grit Mallien, Sarah Bauer, et al. "In vivo comparison of Richardson’s syndrome and progressive supranuclear palsy-parkinsonism." Journal of Neural Transmission 118, no. 8 (2011): 1191–97. http://dx.doi.org/10.1007/s00702-010-0563-8.

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43

Morales, Blas, Armando Martínez, Isabel Gonzalo, et al. "Steele-Richardson-Olszewski syndrome in a patient with a single C212Y mutation in the parkin protein." Movement Disorders 17, no. 6 (2002): 1374–80. http://dx.doi.org/10.1002/mds.10264.

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44

Nath, U. "Population based mortality and quality of death certification in progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome)." Journal of Neurology, Neurosurgery & Psychiatry 76, no. 4 (2005): 498–502. http://dx.doi.org/10.1136/jnnp.2004.039370.

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45

Fowler, Clare J., and M. J. G. Harrison. "EEG changes in subcortical dementia: A study of 22 patients with Steele-Richardson-Olszewski (SRO) syndrome." Electroencephalography and Clinical Neurophysiology 64, no. 4 (1986): 301–3. http://dx.doi.org/10.1016/0013-4694(86)90153-7.

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46

Srulijes, Karin, Matthias Reimold, Rajka M. Liscic, et al. "Fluorodeoxyglucose positron emission tomography in Richardson's syndrome and progressive supranuclear palsy-parkinsonism." Movement Disorders 27, no. 1 (2011): 151–55. http://dx.doi.org/10.1002/mds.23975.

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47

Litvan, I. "Which clinical features differentiate progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) from related disorders? A clinicopathological study." Brain 120, no. 1 (1997): 65–74. http://dx.doi.org/10.1093/brain/120.1.65.

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48

Manolakis, Anastassios C., Mara Kardasi, Fotios D. Tsiopoulos, Andreas N. Kapsoritakis, Athanassios K. Psychos, and Spyros P. Potamianos. "Progressive Supranuclear Palsy (Steele-Richardson-Olszewski Syndrome) With Fatal Outcome, After the Manifestation of an Ampullary Adenocarcinoma." Pancreas 39, no. 5 (2010): 688–89. http://dx.doi.org/10.1097/mpa.0b013e3181c40596.

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49

Bisdorff, A. R., A. M. Bronstein, C. Wolsley, and A. J. Lees. "Torticollis due to disinhibition of the vestibulo-collic reflex in a patient with Steele-Richardson-Olszewski syndrome." Movement Disorders 12, no. 3 (1997): 328–36. http://dx.doi.org/10.1002/mds.870120311.

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50

Pouchot, Jacques, Philippe Vinceneux, Didier Bouccara, Olivier Sterkers, and Bernard Bodelet. "Methotrexate as a steroid-sparing agent in coganapos;s syndrome: comment on the concise communication by richardson." Arthritis & Rheumatism 38, no. 9 (1995): 1348. http://dx.doi.org/10.1002/art.1780380936.

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