Gerstmann–Sträussler–Scheinker syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Gerstmann–Sträussler–Scheinker syndrome" in English language version.

refsWebsite

Global rank English rank

19nih.gov

4^th place

14doi.org

2^nd place

7semanticscholar.org

11^th place

8^th place

1whonamedit.com

2,888^th place

2,730^th place

1web.archive.org

1^st place

1merckmanuals.com

3,097^th place

2,317^th place

1harvard.edu

18^th place

17^th place

doi.org

Liberski PP (2012). "Gerstmann-Sträussler-Scheinker Disease". Neurodegenerative Diseases. Advances in Experimental Medicine and Biology. Vol. 724. pp. 128–37. doi:10.1007/978-1-4614-0653-2_10. ISBN 978-1-4614-0652-5. PMID 22411239.
Gerstmann J, Sträussler E, Scheinker I (1936). "Über eine eigenartige hereditär-familiäre Erkrankung des Zentralnervensystems. Zugleich ein Beitrag zur Frage des vorzeitigen lokalen Alterns". Zeitschrift für die gesamte Neurologie und Psychiatrie. 154: 736–762. doi:10.1007/bf02865827. S2CID 86904496.
De Michele G, Pocchiari M, Petraroli R, Manfredi M, Caneve G, Coppola G, et al. (August 2003). "Variable phenotype in a P102L Gerstmann-Sträussler-Scheinker Italian family". The Canadian Journal of Neurological Sciences. 30 (3): 233–6. doi:10.1017/S0317167100002651. PMID 12945948.
Farlow MR, Yee RD, Dlouhy SR, Conneally PM, Azzarelli B, Ghetti B (November 1989). "Gerstmann-Sträussler-Scheinker disease. I. Extending the clinical spectrum". Neurology. 39 (11): 1446–52. doi:10.1212/wnl.39.11.1446. PMID 2812321. S2CID 23716392.
Collins S, McLean CA, Masters CL (September 2001). "Gerstmann-Sträussler-Scheinker syndrome,fatal familial insomnia, and kuru: a review of these less common human transmissible spongiform encephalopathies". Journal of Clinical Neuroscience. 8 (5): 387–97. doi:10.1054/jocn.2001.0919. PMID 11535002. S2CID 31976428.
Tesar A, Matej R, Kukal J, Johanidesova S, Rektorova I, Vyhnalek M, Keller J, Eliasova I, Parobkova E, Smetakova M, Musova Z, Rusina R (November 2019). "Clinical Variability in P102L Gerstmann-Sträussler-Scheinker Syndrome". Annals of Neurology. 86 (5): 643–652. doi:10.1002/ana.25579. PMID 31397917. S2CID 199504473.
Poggiolini I, Saverioni D, Parchi P (2013). "Prion protein misfolding, strains, and neurotoxicity: an update from studies on Mammalian prions". International Journal of Cell Biology. 2013: 910314. doi:10.1155/2013/910314. PMC 3884631. PMID 24454379.
Arata H, Takashima H, Hirano R, Tomimitsu H, Machigashira K, Izumi K, et al. (June 2006). "Early clinical signs and imaging findings in Gerstmann-Sträussler-Scheinker syndrome (Pro102Leu)". Neurology. 66 (11): 1672–8. doi:10.1212/01.wnl.0000218211.85675.18. PMID 16769939. S2CID 26013402.
Umeh CC, Kalakoti P, Greenberg MK, Notari S, Cohen Y, Gambetti P, et al. (2016-02-18). "Clinicopathological Correlates in a PRNP P102L Mutation Carrier with Rapidly Progressing Parkinsonism-dystonia". Movement Disorders Clinical Practice. 3 (4): 355–358. doi:10.1002/mdc3.12307. PMC 5015693. PMID 27617269.
Ghetti B, Piccardo P, Frangione B, Bugiani O, Giaccone G, Young K, et al. (April 1996). "Prion protein amyloidosis". Brain Pathology. 6 (2): 127–45. doi:10.1111/j.1750-3639.1996.tb00796.x. PMID 8737929. S2CID 10240829.
Hsiao K, Baker HF, Crow TJ, Poulter M, Owen F, Terwilliger JD, et al. (March 1989). "Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome". Nature. 338 (6213): 342–5. Bibcode:1989Natur.338..342H. doi:10.1038/338342a0. PMID 2564168. S2CID 4319741.
Zou WQ, Gambetti P, Xiao X, Yuan J, Langeveld J, Pirisinu L (July 2013). "Prions in variably protease-sensitive prionopathy: an update". Pathogens. 2 (3): 457–71. doi:10.3390/pathogens2030457. PMC 4235694. PMID 25437202.
Gambetti P (March 2013). "Creationism and evolutionism in prions". The American Journal of Pathology. 182 (3): 623–7. doi:10.1016/j.ajpath.2012.12.016. PMC 3590995. PMID 23380581.
Ghetti B, Tagliavini F, Takao M, Bugiani O, Piccardo P (March 2003). "Hereditary prion protein amyloidoses". Clinics in Laboratory Medicine. 23 (1): 65–85, viii. doi:10.1016/s0272-2712(02)00064-1. PMID 12733425.

harvard.edu

ui.adsabs.harvard.edu

Hsiao K, Baker HF, Crow TJ, Poulter M, Owen F, Terwilliger JD, et al. (March 1989). "Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome". Nature. 338 (6213): 342–5. Bibcode:1989Natur.338..342H. doi:10.1038/338342a0. PMID 2564168. S2CID 4319741.

merckmanuals.com

Gambetti P. "Gerstmann–Sträussler–Scheinker Disease". The Merck Manuals: Online Medical Library. Archived from the original on February 22, 2011. Retrieved April 6, 2011.

nih.gov

pubmed.ncbi.nlm.nih.gov

Liberski PP (2012). "Gerstmann-Sträussler-Scheinker Disease". Neurodegenerative Diseases. Advances in Experimental Medicine and Biology. Vol. 724. pp. 128–37. doi:10.1007/978-1-4614-0653-2_10. ISBN 978-1-4614-0652-5. PMID 22411239.
De Michele G, Pocchiari M, Petraroli R, Manfredi M, Caneve G, Coppola G, et al. (August 2003). "Variable phenotype in a P102L Gerstmann-Sträussler-Scheinker Italian family". The Canadian Journal of Neurological Sciences. 30 (3): 233–6. doi:10.1017/S0317167100002651. PMID 12945948.
Farlow MR, Yee RD, Dlouhy SR, Conneally PM, Azzarelli B, Ghetti B (November 1989). "Gerstmann-Sträussler-Scheinker disease. I. Extending the clinical spectrum". Neurology. 39 (11): 1446–52. doi:10.1212/wnl.39.11.1446. PMID 2812321. S2CID 23716392.
Collins S, McLean CA, Masters CL (September 2001). "Gerstmann-Sträussler-Scheinker syndrome,fatal familial insomnia, and kuru: a review of these less common human transmissible spongiform encephalopathies". Journal of Clinical Neuroscience. 8 (5): 387–97. doi:10.1054/jocn.2001.0919. PMID 11535002. S2CID 31976428.
Tesar A, Matej R, Kukal J, Johanidesova S, Rektorova I, Vyhnalek M, Keller J, Eliasova I, Parobkova E, Smetakova M, Musova Z, Rusina R (November 2019). "Clinical Variability in P102L Gerstmann-Sträussler-Scheinker Syndrome". Annals of Neurology. 86 (5): 643–652. doi:10.1002/ana.25579. PMID 31397917. S2CID 199504473.
Poggiolini I, Saverioni D, Parchi P (2013). "Prion protein misfolding, strains, and neurotoxicity: an update from studies on Mammalian prions". International Journal of Cell Biology. 2013: 910314. doi:10.1155/2013/910314. PMC 3884631. PMID 24454379.
Arata H, Takashima H, Hirano R, Tomimitsu H, Machigashira K, Izumi K, et al. (June 2006). "Early clinical signs and imaging findings in Gerstmann-Sträussler-Scheinker syndrome (Pro102Leu)". Neurology. 66 (11): 1672–8. doi:10.1212/01.wnl.0000218211.85675.18. PMID 16769939. S2CID 26013402.
Umeh CC, Kalakoti P, Greenberg MK, Notari S, Cohen Y, Gambetti P, et al. (2016-02-18). "Clinicopathological Correlates in a PRNP P102L Mutation Carrier with Rapidly Progressing Parkinsonism-dystonia". Movement Disorders Clinical Practice. 3 (4): 355–358. doi:10.1002/mdc3.12307. PMC 5015693. PMID 27617269.
Ghetti B, Piccardo P, Frangione B, Bugiani O, Giaccone G, Young K, et al. (April 1996). "Prion protein amyloidosis". Brain Pathology. 6 (2): 127–45. doi:10.1111/j.1750-3639.1996.tb00796.x. PMID 8737929. S2CID 10240829.
Hsiao K, Baker HF, Crow TJ, Poulter M, Owen F, Terwilliger JD, et al. (March 1989). "Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome". Nature. 338 (6213): 342–5. Bibcode:1989Natur.338..342H. doi:10.1038/338342a0. PMID 2564168. S2CID 4319741.
Zou WQ, Gambetti P, Xiao X, Yuan J, Langeveld J, Pirisinu L (July 2013). "Prions in variably protease-sensitive prionopathy: an update". Pathogens. 2 (3): 457–71. doi:10.3390/pathogens2030457. PMC 4235694. PMID 25437202.
Gambetti P (March 2013). "Creationism and evolutionism in prions". The American Journal of Pathology. 182 (3): 623–7. doi:10.1016/j.ajpath.2012.12.016. PMC 3590995. PMID 23380581.
Ghetti B, Tagliavini F, Takao M, Bugiani O, Piccardo P (March 2003). "Hereditary prion protein amyloidoses". Clinics in Laboratory Medicine. 23 (1): 65–85, viii. doi:10.1016/s0272-2712(02)00064-1. PMID 12733425.

ncbi.nlm.nih.gov

Poggiolini I, Saverioni D, Parchi P (2013). "Prion protein misfolding, strains, and neurotoxicity: an update from studies on Mammalian prions". International Journal of Cell Biology. 2013: 910314. doi:10.1155/2013/910314. PMC 3884631. PMID 24454379.
Umeh CC, Kalakoti P, Greenberg MK, Notari S, Cohen Y, Gambetti P, et al. (2016-02-18). "Clinicopathological Correlates in a PRNP P102L Mutation Carrier with Rapidly Progressing Parkinsonism-dystonia". Movement Disorders Clinical Practice. 3 (4): 355–358. doi:10.1002/mdc3.12307. PMC 5015693. PMID 27617269.
Zou WQ, Gambetti P, Xiao X, Yuan J, Langeveld J, Pirisinu L (July 2013). "Prions in variably protease-sensitive prionopathy: an update". Pathogens. 2 (3): 457–71. doi:10.3390/pathogens2030457. PMC 4235694. PMID 25437202.
Gambetti P (March 2013). "Creationism and evolutionism in prions". The American Journal of Pathology. 182 (3): 623–7. doi:10.1016/j.ajpath.2012.12.016. PMC 3590995. PMID 23380581.

ninds.nih.gov

"Gerstmann-Straussler-Scheinker Disease Information Page". National Institute of Neurological Disorders and Stroke. U.S. Department of Health & Human Services. Retrieved 2021-04-18.
"Gerstmann-Straussler-Scheinker Disease". National Institute of Neurological Disorders and Stroke. Retrieved 27 February 2023.

semanticscholar.org

api.semanticscholar.org

Gerstmann J, Sträussler E, Scheinker I (1936). "Über eine eigenartige hereditär-familiäre Erkrankung des Zentralnervensystems. Zugleich ein Beitrag zur Frage des vorzeitigen lokalen Alterns". Zeitschrift für die gesamte Neurologie und Psychiatrie. 154: 736–762. doi:10.1007/bf02865827. S2CID 86904496.
Farlow MR, Yee RD, Dlouhy SR, Conneally PM, Azzarelli B, Ghetti B (November 1989). "Gerstmann-Sträussler-Scheinker disease. I. Extending the clinical spectrum". Neurology. 39 (11): 1446–52. doi:10.1212/wnl.39.11.1446. PMID 2812321. S2CID 23716392.
Collins S, McLean CA, Masters CL (September 2001). "Gerstmann-Sträussler-Scheinker syndrome,fatal familial insomnia, and kuru: a review of these less common human transmissible spongiform encephalopathies". Journal of Clinical Neuroscience. 8 (5): 387–97. doi:10.1054/jocn.2001.0919. PMID 11535002. S2CID 31976428.
Tesar A, Matej R, Kukal J, Johanidesova S, Rektorova I, Vyhnalek M, Keller J, Eliasova I, Parobkova E, Smetakova M, Musova Z, Rusina R (November 2019). "Clinical Variability in P102L Gerstmann-Sträussler-Scheinker Syndrome". Annals of Neurology. 86 (5): 643–652. doi:10.1002/ana.25579. PMID 31397917. S2CID 199504473.
Arata H, Takashima H, Hirano R, Tomimitsu H, Machigashira K, Izumi K, et al. (June 2006). "Early clinical signs and imaging findings in Gerstmann-Sträussler-Scheinker syndrome (Pro102Leu)". Neurology. 66 (11): 1672–8. doi:10.1212/01.wnl.0000218211.85675.18. PMID 16769939. S2CID 26013402.
Ghetti B, Piccardo P, Frangione B, Bugiani O, Giaccone G, Young K, et al. (April 1996). "Prion protein amyloidosis". Brain Pathology. 6 (2): 127–45. doi:10.1111/j.1750-3639.1996.tb00796.x. PMID 8737929. S2CID 10240829.
Hsiao K, Baker HF, Crow TJ, Poulter M, Owen F, Terwilliger JD, et al. (March 1989). "Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome". Nature. 338 (6213): 342–5. Bibcode:1989Natur.338..342H. doi:10.1038/338342a0. PMID 2564168. S2CID 4319741.

web.archive.org

Gambetti P. "Gerstmann–Sträussler–Scheinker Disease". The Merck Manuals: Online Medical Library. Archived from the original on February 22, 2011. Retrieved April 6, 2011.

whonamedit.com

synd/2269 at Whonamedit?