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Journal articles on the topic 'Gerstmann'

Author: Grafiati

Published: 4 June 2021

Last updated: 15 February 2022

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1

Pyrtek, Sylwia, Arkadiusz Badziński, Monika Adamczyk-Sowa, and Maria Pąchalska. "DOES GERSTMANN SYNDROME EXIST?" Acta Neuropsychologica 18, no. 2 (2020): 259–84. http://dx.doi.org/10.5604/01.3001.0014.1425.

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The aim of the study is to present Gerstmann syndrome, manifested as a neuropsychological deficit resulting from the damage to the parietal lobe of the left hemisphere. Here it is discussed based on the studies conducted mainly since the 1950’s when it attracted considerable interest, as well as and controversy at the same time. The classic symptoms are briefly described, including the clinical tasks useful in any the diagnosis for during the neuropsychological assessment. The paper also presents recent studies and a alternative different proposal for the understanding of this clinical syndrom

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2

Colucci, Monica, Francisco J. Moleres, Zhi-Liang Xie, et al. "Gerstmann-Sträussler-Scheinker." Journal of Neuropathology and Experimental Neurology 65, no. 7 (2006): 642–51. http://dx.doi.org/10.1097/01.jnen.0000228198.81797.4d.

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3

PeBENITO, RHANDY. "Developmental Gerstmann Syndrome." Journal of Developmental & Behavioral Pediatrics 8, no. 4 (1987): 229???232. http://dx.doi.org/10.1097/00004703-198708000-00008.

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4

Kleinschmidt, Andreas, and Elena Rusconi. "Gerstmann Meets Geschwind." Neuroscientist 17, no. 6 (2011): 633–44. http://dx.doi.org/10.1177/1073858411402093.

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That disconnection causes clinical symptoms is a very influential concept in behavioral neurology. Criteria for subcortical disconnection usually are symptoms that are distinct from those following cortical lesions and damage to a single, long-range fiber tract. Yet, a recent study combining functional magnetic resonance imaging and fiber tracking concluded that a focal lesion in left parietal white matter provides the only tenable explanation for pure Gerstmann’s syndrome, an enigmatic tetrad of acalculia, agraphia, finger agnosia, and left-right disorientation. Such a lesion would affect not

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5

Ebert, Anne D., Juliane Wendt, and Manfred Herrmann. "Das «Gerstmann-Syndrom» und sein Stellenwert für die Neuropsychologie." Zeitschrift für Neuropsychologie 10, no. 3 (1999): 129–38. http://dx.doi.org/10.1024//1016-264x.10.3.129.

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Zusammenfassung: Wir berichten über einen Patienten, welcher nach einer fokalen ischämischen Infarzierung im linksseitigen temporo-parietalen Übergangsgebiet unter Einschluß der Gyri angularis und supramarginalis ein «Gerstmann-Syndrom» mit «Fingeragnosie», Agraphie, Akalkulie und Störung der Rechts-Links-Diskrimination präsentierte. Während der neuropsychologischen Untersuchungen zeigte der Patient weder Zeichen einer Aphasie noch visuo-perzeptive, visuo-konstruktive oder apraktische Störungen. Nach einer kurzen Einführung in die historische Debatte um das «Gerstmann-Syndrom» diskutieren wir

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6

Wimberger, Daniela, Konrad Uranitsch, Erwin Schindler, and Josef Kramer. "Gerstmann-Strässler-Scheinker Syndrome." Journal of Computer Assisted Tomography 17, no. 2 (1993): 326–27. http://dx.doi.org/10.1097/00004728-199303000-00030.

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7

Triarhou, Lazaros C. "Josef Gerstmann (1887–1969)." Journal of Neurology 255, no. 4 (2007): 614–15. http://dx.doi.org/10.1007/s00415-008-0851-5.

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8

Millichap, J. Gordon. "Functional Anatomy of Gerstmann Syndrome." Pediatric Neurology Briefs 24, no. 1 (2010): 5. http://dx.doi.org/10.15844/pedneurbriefs-24-1-6.

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9

Mazzoni, M., L. Pardossi, R. Cantini, V. Giorgetti, and R. Arena. "Gerstmann Syndrome: A Case Report." Cortex 26, no. 3 (1990): 459–67. http://dx.doi.org/10.1016/s0010-9452(13)80096-2.

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10

Tucha, O., A. Steup, C. Smely, and K. W. Lange. "Toe agnosia in Gerstmann syndrome." Journal of Neurology, Neurosurgery & Psychiatry 63, no. 3 (1997): 399–403. http://dx.doi.org/10.1136/jnnp.63.3.399.

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11

Benke, Thomas. "Zur Lehre vom «Gerstmann-Syndrom»." Zeitschrift für Neuropsychologie 10, no. 3 (1999): 148–49. http://dx.doi.org/10.1024//1016-264x.10.3.148.

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12

Garty, Ben-Zion, Yehezkel Waisman, and Raphael Weitz. "Gerstmann tetrad in Leopard syndrome." Pediatric Neurology 5, no. 6 (1989): 391–92. http://dx.doi.org/10.1016/0887-8994(89)90057-x.

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13

Dimitrov, Iv, S. Atanasova, A. Kaprelyan, et al. "Gerstmann syndrome in a young man: a case report." Trakia Journal of Sciences 16, no. 3 (2018): 239–41. http://dx.doi.org/10.15547/tjs.2018.03.011.

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Gerstmann syndrome is a classical cerebral syndrome in neurology, named after Joseph Gerstmann, a Jewish Austrian-born American neurologist. Patients present with a tetrad of cognitive symptoms, including agraphia, acalculia, finger agnosia and left-right disorientation. The syndrome is known to result from a lesion of the posterior portion of the dominant parietal lobe and is usually due to stroke or to developmental problems. We describe the case of a 35-year-old man whose illness debuted about 9 months before the initial presentation to the neurology clinic, with memory complaints, anxiety,

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14

Tunç, Abdulkadir, and Yonca Ünlübaş. "Aleksinin Eşlik Ettiği Gerstmann Sendromu Olgusu." Sakarya Medical Journal 8, no. 4 (2018): 869–73. http://dx.doi.org/10.31832/smj.477465.

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15

Wingard, E. M. "The Gerstmann syndrome in Alzheimer's disease." Journal of Neurology, Neurosurgery & Psychiatry 72, no. 3 (2002): 403–5. http://dx.doi.org/10.1136/jnnp.72.3.403.

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16

&NA;. "GERSTMANN-STRÄUSSLER-SCHEINKER (GSS) DISEASE (P102L)." Journal of Neuropathology and Experimental Neurology 54, no. 3 (1995): 448. http://dx.doi.org/10.1097/00005072-199505000-00165.

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17

Gonzalez, S., C. Rousselle, and N. Badinand. "Le syndrome de Gerstmann: perspective développementale." Archives de Pédiatrie 2, no. 9 (1995): 911–12. http://dx.doi.org/10.1016/0929-693x(95)90469-j.

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18

Vaddiparti, Aparna, Hari McGrath, Christopher F. A. Benjamin, et al. "Gerstmann Syndrome Deconstructed by Cortical Stimulation." Neurology 97, no. 9 (2021): 420–22. http://dx.doi.org/10.1212/wnl.0000000000012441.

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19

Bhattacharyya, S., X. Cai, and J. P. Klein. "Dyscalculia, Dysgraphia, and Left-Right Confusion from a Left Posterior Peri-Insular Infarct." Behavioural Neurology 2014 (2014): 1–4. http://dx.doi.org/10.1155/2014/823591.

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The Gerstmann syndrome of dyscalculia, dysgraphia, left-right confusion, and finger agnosia is generally attributed to lesions near the angular gyrus of the dominant hemisphere. A 68-year-old right-handed woman presented with sudden difficulty completing a Sudoku grid and was found to have dyscalculia, dysgraphia, and left-right confusion. Magnetic resonance imaging (MRI) showed a focus of abnormal reduced diffusivity in the left posterior insula and temporoparietal operculum consistent with acute infarct. Gerstmann syndrome from an insular or peri-insular lesion has not been described in the

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20

IRISAWA, Momoko, Makoto AMANUMA, Eito KOZAWA, Fumiko KIMURA, and Nobuo ARAKI. "A Case of Gerstmann-Sträussler-Scheinker Syndrome." Magnetic Resonance in Medical Sciences 6, no. 1 (2007): 53–57. http://dx.doi.org/10.2463/mrms.6.53.

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21

Tekgol Uzuner, Gulnur, Ahmet Ubur, Murat Erten, and Nevzat Uzuner. "A Rare Clinical Antity; Pure Gerstmann Syndrome." Journal of Stroke and Cerebrovascular Diseases 29, no. 10 (2020): 105161. http://dx.doi.org/10.1016/j.jstrokecerebrovasdis.2020.105161.

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22

Karmon, Yuval, Arielle Kurzweil, Eric Lindzen, Tomas Holmlund, and Bianca Weinstock-Guttman. "Gerstmann–Sträussler–Scheinker syndrome masquerading multiple sclerosis." Journal of the Neurological Sciences 309, no. 1-2 (2011): 55–57. http://dx.doi.org/10.1016/j.jns.2011.07.028.

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23

Zhao, Ming-Ming, Liang-Shu Feng, Shuai Hou, Ping-Ping Shen, Li Cui, and Jia-Chun Feng. "Gerstmann-Sträussler-Scheinker disease: A case report." World Journal of Clinical Cases 7, no. 3 (2019): 389–95. http://dx.doi.org/10.12998/wjcc.v7.i3.389.

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24

Bugiani, Orso, Giorgio Giaccone, Pedro Piccardo, Michela Morbin, Fabrizio Tagliavini, and Bernardino Ghetti. "Neuropathology of Gerstmann-Str�ussler-Scheinker disease." Microscopy Research and Technique 50, no. 1 (2000): 10–15. http://dx.doi.org/10.1002/1097-0029(20000701)50:1<10::aid-jemt3>3.0.co;2-6.

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25

Park, Min Jeong, Hee Young Jo, Sang-Myung Cheon, Sun Seob Choi, Yong-Sun Kim, and Jae Woo Kim. "A Case of Gerstmann-Sträussler-Scheinker Disease." Journal of Clinical Neurology 6, no. 1 (2010): 46. http://dx.doi.org/10.3988/jcn.2010.6.1.46.

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26

Zeidman, Lawrence A., Matthias Georg Ziller, and Michael Shevell. "Ilya Mark Scheinker: Controversial Neuroscientist and Refugee From National Socialist Europe." Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 43, no. 2 (2016): 334–44. http://dx.doi.org/10.1017/cjn.2015.359.

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AbstractRussian-born, Vienna-trained neurologist and neuropathologist Ilya Mark Scheinker collaborated with Josef Gerstmann and Ernst Sträussler in 1936 to describe the familial prion disorder now known as Gerstmann-Sträussler-Scheinker disease. Because of Nazi persecution following the annexation of Austria by Nazi Germany, Scheinker fled from Vienna to Paris, then after the German invasion of France, to New York. With the help of neurologist Tracy Putnam, Scheinker ended up at the University of Cincinnati, although his position was never guaranteed. He more than doubled his prior publication

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27

Smid, Jerusa, Adalberto Studart Neto, Michele Christine Landemberger, et al. "High phenotypic variability in Gerstmann-Sträussler-Scheinker disease." Arquivos de Neuro-Psiquiatria 75, no. 6 (2017): 331–38. http://dx.doi.org/10.1590/0004-282x20170049.

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ABSTRACT Gerstmann-Sträussler-Scheinker is a genetic prion disease and the most common mutation is p.Pro102Leu. We report clinical, molecular and neuropathological data of seven individuals, belonging to two unrelated Brazilian kindreds, carrying the p.Pro102Leu. Marked differences among patients were observed regarding age at onset, disease duration and clinical presentation. In the first kindred, two patients had rapidly progressive dementia and three exhibited predominantly ataxic phenotypes with variable ages of onset and disease duration. In this family, age at disease onset in the mother

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28

Liberski, Pawel P., and Herbert Budka. "Ultra Structural Pathology of Gerstmann-Sträussler-Scheinker Disease." Ultrastructural Pathology 19, no. 1 (1995): 23–36. http://dx.doi.org/10.3109/01913129509014600.

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29

Lang, Ch. "Die Agraphie des Gerstmann-Syndroms -Versuch einer Charakterisierung." Fortschritte der Neurologie · Psychiatrie 62, no. 05 (1994): 155–63. http://dx.doi.org/10.1055/s-2007-996667.

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30

Stretz, Christoph, Amanda Mook, Janhavi M. Modak, Jose M. Rodriguez, and Amre M. Nouh. "Gerstmann Syndrome in a Patient With Aggressive Mucormycosis." Neurohospitalist 7, no. 2 (2016): 102–3. http://dx.doi.org/10.1177/1941874416663282.

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31

Hamasaki, Shinji, Susumu Shirabe, Ryouichi Tsuda, Toshiro Yoshimura, Tatsufumi Nakamura, and Katsumi Eguchi. "Discordant Gerstmann-Sträussler-Scheinker disease in monozygotic twins." Lancet 352, no. 9137 (1998): 1358–59. http://dx.doi.org/10.1016/s0140-6736(05)60749-0.

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32

Yee, Robert D. "Abnormal Eye Movements in Gerstmann-Sträussler-Scheinker Disease." Archives of Ophthalmology 110, no. 1 (1992): 68. http://dx.doi.org/10.1001/archopht.1992.01080130070028.

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33

Tateishi, June, Tetsuyuki Kitamoto, Hideyuki Hashiguchi, and Hirofumi Shii. "Gerstmann-Sträussler-Scheinker disease: Immunohistological and experimental studies." Annals of Neurology 24, no. 1 (1988): 35–40. http://dx.doi.org/10.1002/ana.410240108.

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34

Sherrill, Kenneth. "Same-Sex Marriage and the Constitutionby Evan Gerstmann." Political Science Quarterly 119, no. 4 (2004): 696–97. http://dx.doi.org/10.1002/j.1538-165x.2004.tb01302.x.

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35

Tesar, Adam, Radoslav Matej, Jaromir Kukal, et al. "Clinical Variability in P102L Gerstmann–Sträussler–Scheinker Syndrome." Annals of Neurology 86, no. 5 (2019): 643–52. http://dx.doi.org/10.1002/ana.25579.

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36

Ghetti, Bernardino, Stephen R. Dlouhy, Giorgio Giaccone, et al. "Gerstmann-Sträussler-Scheinker Disease and the Indiana Kindred." Brain Pathology 5, no. 1 (1995): 61–75. http://dx.doi.org/10.1111/j.1750-3639.1995.tb00578.x.

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37

Young, K., P. Piccardo, S. R. Dlouhy, H. B. Clark, and B. Ghetti. "GERSTMANN-STRÄUSSLER-SCHEINKER (GSS) DISEASE WITH SPINAL ATROPHY." Journal of Neuropathology and Experimental Neurology 54, no. 3 (1995): 448. http://dx.doi.org/10.1097/00005072-199505000-00166.

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38

Aralasmak, Ayse, Barbara J. Crain, Wen-Quan Zou, and David M. Yousem. "A Prion Disease-Possible Gerstmann-Straussler-Scheinker Disease." Journal of Computer Assisted Tomography 30, no. 1 (2006): 135–39. http://dx.doi.org/10.1097/01.rct.0000193816.42051.1a.

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39

Jiang, Aiyang Allen, Katherine Longardner, Dennis Dickson, and Rebecca Sell. "Gerstmann-Sträussler-Scheinker syndrome misdiagnosed as conversion disorder." BMJ Case Reports 12, no. 8 (2019): e229729. http://dx.doi.org/10.1136/bcr-2019-229729.

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Gerstmann-Sträussler-Scheinker syndrome (GSS) is a rare cause of genetic prion disease. Overlapping neurological, cognitive and psychiatric symptoms make GSS difficult to diagnose based on clinical features alone. We present a 40-year-old man without relevant medical or family history who developed progressive neurocognitive and behavioural symptoms over 3 years. Initial extensive diagnostic workup of his variable motor symptoms was unrevealing and he was diagnosed with conversion disorder. This diagnosis persisted for over 2 years, despite progressive neurocognitive symptoms. He eventually de

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40

Jang, Albert, Tameka A. Smith, Steven Trainor, and Peter C. Caldwell. "Manifestation of metastatic lung adenocarcinoma as Gerstmann syndrome." BMJ Case Reports 13, no. 10 (2020): e238098. http://dx.doi.org/10.1136/bcr-2020-238098.

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41

Liberski, Pawel P., and H. Budka. "Tubulovesicular structures in Gerstmann-Str�ussler-Scheinker disease." Acta Neuropathologica 88, no. 5 (1994): 491–92. http://dx.doi.org/10.1007/bf00389506.

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42

Ghetti, Bernardino, F. Tagliavini, G. Giaccone, et al. "Familial Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles." Molecular Neurobiology 8, no. 1 (1994): 41–48. http://dx.doi.org/10.1007/bf02778006.

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43

Long, Nina, Satnaam Bassi, Don Pepito, and Hossein Akhondi. "Gerstmann syndrome complicating polycythemia secondary to anabolic steroid use." BMJ Case Reports 12, no. 6 (2019): e229004. http://dx.doi.org/10.1136/bcr-2018-229004.

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Anabolic steroid use is prevalent among athletes and bodybuilders. There are known cardiovascular, reproductive, musculoskeletal and neuropsychiatric risks associated with their prolonged use. Although there have been very few documented cases of strokes associated with anabolic steroid use, cardiomyopathy and secondary erythropoiesis can increase the risk of strokes in users with no other risk factors. We present a 49-year-old man with left parietal ischaemic stroke with haemorrhagic conversion resulting in Gerstmann syndrome secondary to a hypercoagulable state from chronic anabolic steroid

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44

Calvo Romero, José María, Juan Carlos Buero Dacal, and Juan Lucio Ramos Salado. "Síndrome de Gerstmann causado por ictus isquémico parietal derecho." Revista de Neurología 30, no. 04 (2000): 398. http://dx.doi.org/10.33588/rn.3004.99278.

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45

Fournier del Castillo, María Concepción, Juan José García Peñas, Luis González Gutiérrez-Solana, and María Luz Ruiz-Falcó Rojas. "Síndrome de Gerstmann en un varón de 9 años." Revista de Neurología 30, no. 08 (2000): 731. http://dx.doi.org/10.33588/rn.3008.99454.

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46

Farlow, M. R., R. D. Yee, S. R. Dlouhy, P. M. Conneally, B. Azzarelli, and B. Ghetti. "Gerstmann-Straussler-Scheinker disease. I. Extending the clinical spectrum." Neurology 39, no. 11 (1989): 1446. http://dx.doi.org/10.1212/wnl.39.11.1446.

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47

Salmona, Mario, Michela Morbin, Tania Massignan, et al. "Structural Properties of Gerstmann-Sträussler-Scheinker Disease Amyloid Protein." Journal of Biological Chemistry 278, no. 48 (2003): 48146–53. http://dx.doi.org/10.1074/jbc.m307295200.

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48

Rusconi, Elena, Philippe Pinel, Evelyn Eger, et al. "A disconnection account of Gerstmann syndrome: Functional neuroanatomy evidence." Annals of Neurology 66, no. 5 (2009): 654–62. http://dx.doi.org/10.1002/ana.21776.

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49

De Bleser, Ria. "Die Neuropsychologie und ihr Stellenwert für das «Gerstmann-Syndrom»." Zeitschrift für Neuropsychologie 10, no. 3 (1999): 141–44. http://dx.doi.org/10.1024//1016-264x.10.3.141.

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50

Grigsby, James P., Melinda B. Kemper, and Randi J. Hagerman. "Developmental Gerstmann syndrome without aphasia in Fragile X syndrome." Neuropsychologia 25, no. 6 (1987): 881–91. http://dx.doi.org/10.1016/0028-3932(87)90093-5.

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