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applebybs prion [140 articles]

Neue Publikationen in applebybs Bibliothek eingetragen unter dem Bezeichner: prion. You can also see everyone's prion.
  • Atypical frontotemporal dementia as a new clinical phenotype of Gerstmann-Straussler-Scheinker disease with the PrP-P102L mutation. Description of a previously unreported Italian family
    Neurological Sciences
    by Anna Giovagnoli, Giuseppe Di Fede, Anna Aresi, Fabiola Reati, Giacomina Rossi, Fabrizio Tagliavini
    posted to prion phenotype gss genetics ftd by applebyb on 2008-11-27 14:59:46 as ****
  • Cryo-Immunogold Electron Microscopy for Prions: Toward Identification of a Conversion Site.
    The Journal of neuroscience : the official journal of the Society for Neuroscience, Vol. 28, No. 47. (19 November 2008), pp. 12489-12499.
    by Susan F F Godsave, Holger Wille, Pekka Kujala, Diane Latawiec, Stephen J J Dearmond, Ana Serban, Stanley B B Prusiner, Peter J J Peters
    posted to prpsc prion by applebyb on 2008-11-22 19:57:20 as ****
  • A miRNA Signature of Prion Induced Neurodegeneration
    PLoS ONE, Vol. 3, No. 11. (6 November 2008), e3652.
    by Reuben Saba, Chelsey D Goodman, Rhiannon L Huzarewich, Catherine Robertson, Stephanie A Booth
    posted to rnai prion neurodegeneration mrna by applebyb on 2008-11-21 14:32:13 as ***** along with 1 person moleopard
  • Human platelets as a substrate source for the in vitro amplification of the abnormal prion protein (PrP) associated with variant Creutzfeldt-Jakob disease.
    Transfusion (29 October 2008)
    by Michael Jones, Alexander H H Peden, Helen Yull, Darren Wight, Matthew T T Bishop, Chris V V Prowse, Marc L L Turner, James W W Ironside, Ian R R Macgregor, Mark W W Head
    posted to prion_disease prion platelets cjd by applebyb on 2008-11-21 14:26:20 as ****
  • A novel PRNP-P105S mutation associated with atypical prion disease and a rare PrPSc conformation
    Neurology, Vol. 71, No. 18. (28 October 2008), pp. 1431-1438.
    by E Tunnell, R Wollman, S Mallik, CJ Cortes, SJ Dearmond, JA Mastrianni
    posted to prpsc prion gss genetics by applebyb on 2008-10-28 00:37:31 as ****
  • Clinical findings in Creutzfeldt-Jakob disease mimicking dementia with Lewy bodies.
    Arquivos de neuro-psiquiatria, Vol. 66, No. 3b. (2008), pp. 741-743.
    by Luís Fabiano F Marin, André Carvalho C Felício, Denis Bernardi B Bichuetti, William Adolfo Celso Dos A Santos, Lia Raquel Rodrigues R Borges, Renata Parissi P Buainain, Henrique Ballalai B Ferraz
    posted to symptoms prion dlb diagnosis cjd by applebyb on 2008-10-26 22:52:27 as *****
  • Diffusion tensor imaging in patients with Creutzfeldt-Jakob disease.
    Journal of neurology, neurosurgery, and psychiatry, Vol. 79, No. 11. (November 2008), pp. 1304-1306.
    by K Fujita, S Nakane, M Harada, Y Izumi, R Kaji
    posted to prion neuroimaging mri cjd by applebyb on 2008-10-25 01:43:49 as ****
  • Immune-Directed Gene Therapeutic Development for Alzheimer's, Prion, and Parkinson's Diseases.
    Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology (18 October 2008)
    by Kathleen A Maguire-Zeiss, Howard J Federoff
    posted to therapy prion pd genetics ad by applebyb on 2008-10-25 01:30:34 as ****
  • Surveillance for Creutzfeldt-Jakob disease in China from 2006 to 2007
    BMC Public Health, Vol. 8 (18 October 2008), 360.
    by Qi Shi, Chen Gao, Wei Zhou, Baoyun Zhang, Jianming Chen, Chan Tian, Huiying Jiang, Jun Han, Nijuan Xiang, Xiaofang Wang, Yongjun Gao, Xiaoping Dong
    posted to prion epidemiology cjd by applebyb on 2008-10-25 01:27:34 as ****
  • Creutzfeldt-Jakob's disease presenting with ataxia and a movement disorder.
    Movement disorders : official journal of the Movement Disorder Society, Vol. 6, No. 2. (1991), pp. 157-162.
    by KD Sethi, DC Hess
    posted to prion phenotype oppenheimer_brownell movement_disorder cjd ataxia by applebyb on 2008-10-22 20:27:10 as *****
  • Central nervous system amyloidoses: A comparison of Alzheimer's disease and Creutzfeldt-Jakob disease
    Neurology, Vol. 39, No. 8. (1 August 1989), 1103.
    by Paul Brown
    posted to proteinopathy protein prion cjd amyloid ad by applebyb on 2008-10-22 19:37:06 as ****
  • A genetic human prion disease with G114V mutation in PRNP and epidemiological studies in a Chinese family: a case series.
    Journal of medical case reports, Vol. 2, No. 1. (17 October 2008)
    by Jing Ye, Jun Han, Qi Shi, Bao-Yun Y Zhang, Gui-Rong R Wang, Chan Tian, Chen Gao, Jian-Ming M Chen, Cun-Jiang J Li, Zheng Lui, Xian-Zhang Z Li, Lai-Zhong Z Zhang, Xiao-Ping P Dong
    posted to prion gcjd g114v by applebyb on 2008-10-20 00:16:50 as ****
  • Review. The neuropathology of kuru and variant Creutzfeldt-Jakob disease.
    Philosophical transactions of the Royal Society of London. Series B, Biological sciences, Vol. 363, No. 1510. (27 November 2008), pp. 3685-3687.
    by CA McLean
    posted to vcjd prion phenotype kuru incubation genetics codon129 cjd by applebyb on 2008-10-20 00:07:40 as *****
  • Review. Lessons of kuru research: background to recent studies with some personal reflections.
    Philosophical transactions of the Royal Society of London. Series B, Biological sciences, Vol. 363, No. 1510. (27 November 2008), pp. 3689-3696.
    by J Collinge
    posted to risk prion kuru incubation cjd by applebyb on 2008-10-20 00:06:22 as ****
  • Review. Kuru and its contribution to medicine.
    Philosophical transactions of the Royal Society of London. Series B, Biological sciences, Vol. 363, No. 1510. (27 November 2008), pp. 3697-3700.
    by DC Gajdusek
    posted to review prion kuru cjd by applebyb on 2008-10-20 00:05:11 as ****
  • Review. The epidemiology of kuru: monitoring the epidemic from its peak to its end.
    Philosophical transactions of the Royal Society of London. Series B, Biological sciences, Vol. 363, No. 1510. (27 November 2008), pp. 3707-3713.
    by MP Alpers
    posted to transmission review prion kuru by applebyb on 2008-10-20 00:03:32 as ****
  • A clinical study of kuru patients with long incubation periods at the end of the epidemic in Papua New Guinea.
    Philosophical transactions of the Royal Society of London. Series B, Biological sciences, Vol. 363, No. 1510. (27 November 2008), pp. 3725-3739.
    by J Collinge, J Whitfield, E McKintosh, A Frosh, S Mead, AF Hill, S Brandner, D Thomas, MP Alpers
    posted to risk prion phenotype kuru incubation genetics age by applebyb on 2008-10-20 00:01:37 as *****
  • Genetic susceptibility, evolution and the kuru epidemic.
    Philosophical transactions of the Royal Society of London. Series B, Biological sciences, Vol. 363, No. 1510. (27 November 2008), pp. 3741-3746.
    by S Mead, J Whitfield, M Poulter, P Shah, J Uphill, J Beck, T Campbell, H Al-Dujaily, H Hummerich, MP Alpers, J Collinge
    posted to risk prion kuru genetics codon129 anthropology by applebyb on 2008-10-19 23:59:39 as *****
  • Review. The origin of the prion agent of kuru: molecular and biological strain typing.
    Philosophical transactions of the Royal Society of London. Series B, Biological sciences, Vol. 363, No. 1510. (27 November 2008), pp. 3747-3753.
    by JD Wadsworth, S Joiner, JM Linehan, EA Asante, S Brandner, J Collinge
    posted to strain scjd prpsc prion phenotype kuru icjd cjd by applebyb on 2008-10-19 23:57:27 as ****
  • Central and peripheral pathology of kuru: pathological analysis of a recent case and comparison with other forms of human prion disease.
    Philosophical transactions of the Royal Society of London. Series B, Biological sciences, Vol. 363, No. 1510. (27 November 2008), pp. 3755-3763.
    by S Brandner, J Whitfield, K Boone, A Puwa, C O'Malley, JM Linehan, S Joiner, F Scaravilli, I Calder, M P Alpers, JD Wadsworth, J Collinge
    posted to transmission risk prion neuropathology kuru cjd by applebyb on 2008-10-19 23:55:53 as ****
  • Chemistry: Prion progress
    Nature, Vol. 455, No. 7215. (16 October 2008), pp. 838-838.
    posted to prion by applebyb on 2008-10-18 20:47:56 as **** along with 1 person reyez
  • Amyloids, prions and the inherent infectious nature of misfolded protein aggregates
    Trends in Biochemical Sciences, Vol. 31, No. 3. (March 2006), pp. 150-155.
    by C Soto, L Estrada, J Castilla
    posted to transmission proteinopathy protein prion amyloid by applebyb on 2008-10-17 17:25:32 as *****
  • Arch Neurol -- Download Directly to Citation Manager
    posted to prion pet neuroimaging gcjd disease diagnosis cjd by applebyb on 2008-10-15 01:41:25 as ****
  • Surgery and Risk of Sporadic Creutzfeldt-Jakob Disease in Denmark and Sweden: Registry-Based Case-Control Studies.
    Neuroepidemiology, Vol. 31, No. 4. (9 October 2008), pp. 229-240.
    by Ignacio Mahillo-Fernandez, Jesús de Pedro-Cuesta, Maria José J Bleda, Mabel Cruz, Kåre Mølbak, Henning Laursen, Gerhard Falkenhorst, Pablo Martínez-Martín, Ake Siden
    posted to surgery risk prion icjd by applebyb on 2008-10-12 04:00:12 as *****
  • Surgery and Risk of Sporadic Creutzfeldt-Jakob Disease.
    Neuroepidemiology, Vol. 31, No. 4. (9 October 2008), pp. 241-242.
    by Hester J T J Ward, Richard S G S Knight
    posted to surgery risk prion icjd by applebyb on 2008-10-12 03:59:10 as *****
  • Wernicke's encephalopathy mimicking variant Creutzfeldt-Jakob disease.
    Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia (29 September 2008)
    by Richard Stone, John S S Archer, Matthew Kiernan
    posted to wernicke_encephalopathy prion diagnosis cjd by applebyb on 2008-10-05 01:40:10 as *****
  • Brain biopsy in patients with suspected Creutzfeldt-Jakob disease.
    Journal of neurosurgery, Vol. 109, No. 4. (October 2008), pp. 735-741.
    by Uta Heinemann, Anna Krasnianski, Bettina Meissner, Kai Kallenberg, Hans A A Kretzschmar, Walter Schulz-Schaeffer, Inga Zerr
    posted to surgery risk prion diagnosis cjd brain_biopsy by applebyb on 2008-10-03 14:50:06 as *****
  • The behavioural features of fatal familial insomnia: A new Italian case with pathological verification.
    Sleep medicine (26 September 2008)
    by Alberto Raggi, Daniela Perani, Giorgio Giaccone, Sandro Iannaccone, Mauro Manconi, Marco Zucconi, Valentina Garibotto, Alessandra Marcone, Michele Zamboni, Lucia Limido, Fabrizio Tagliavini, Luigi Ferini-Strambi, Stefano F F Cappa
    posted to symptoms prion phenotype ffi by applebyb on 2008-10-03 14:46:53 as *****
  • MRI of sporadic Creutzfeldt-Jakob disease.
    Journal of medical imaging and radiation oncology, Vol. 52, No. 4. (August 2008), pp. 318-324.
    by A Kong, T Kleinig, A Van der Vliet, P Bergin, C Coscia, S Ring, R Brooder
    posted to prion neuroimaging mri diagnosis cjd by applebyb on 2008-10-03 14:38:39 as ****
  • Management of a CJD case. Part 2. The patient with CJD in the operating theatre.
    British journal of perioperative nursing : the journal of the National Association of Theatre Nurses, Vol. 14, No. 5. (May 2004), pp. 223-226.
    by B McNeil
    posted to surgery prion cjd by applebyb on 2008-09-27 02:00:17 as ****
  • Management of a CJD case. Part 1. Preoperative organisation of the case.
    British journal of perioperative nursing : the journal of the National Association of Theatre Nurses, Vol. 14, No. 4. (April 2004)
    by B McNeil
    posted to surgery prion cjd by applebyb on 2008-09-27 01:59:50 as ****
  • Care management of Creutzfeldt-Jakob Disease within the United Kingdom
    Journal of Nursing Management, Vol. 13, No. 2. (March 2005), pp. 111-118.
    by Fiona ARNETT Barnett, Gordon Mclean
    posted to prion nursing cjd caregiver by applebyb on 2008-09-27 01:58:58 as ****
  • Creutzfeldt-Jakob disease: diagnosis and nursing care issues.
    Nursing times, Vol. 101, No. 20. (3 2005), pp. 52-53.
    by B Smith-Bathgate
    posted to prion nursing cjd caregiver by applebyb on 2008-09-27 01:57:58 as ****
  • The clinical picture in Creutzfeldt-Jakob disease.
    Transactions of the American Neurological Association, Vol. 85 (1960), pp. 147-150.
    by CM FISHER
    posted to symptoms prion phenotype cjd by applebyb on 2008-09-26 01:56:44 as *****
  • Insulin resistance to both glucose and aminoacid metabolism in a patient with Fatal Familial Insomnia.
    Nutrition, metabolism, and cardiovascular diseases : NMCD (15 September 2008)
    by Stefano Benedini, Pietro Cortelli, Andrea Caumo, Ileana Terruzzi, Manolo Beelke, Gianluca Perseghin, Pasquale Montagna, Elio Lugaresi, Livio Luzi
    posted to prion insulin ffi by applebyb on 2008-09-26 01:29:36 as ****
  • The role of calorie restriction and SIRT1 in prion-mediated neurodegeneration.
    Experimental gerontology (30 August 2008)
    by Danica Chen, Andrew D D Steele, Gregor Hutter, Joanne Bruno, Arvind Govindarajan, Erin Easlon, Su-Ju J Lin, Adriano Aguzzi, Susan Lindquist, Leonard Guarente
    posted to prion neurodegeneration geriatrics calorie_restriction by applebyb on 2008-09-26 01:26:24 as ****
  • Endoplasmic reticulum stress, PrP trafficking, and neurodegeneration.
    Developmental cell, Vol. 15, No. 3. (September 2008), pp. 339-341.
    by C Soto
    posted to prion neurodegeneration er by applebyb on 2008-09-26 01:11:12 as ****
  • Relationship between clinical course and Diffusion-weighted MRI findings in sporadic Creutzfeldt-Jakob Disease.
    Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, Vol. 29, No. 4. (September 2008), pp. 251-255.
    by SH Yi, KC Park, SS Yoon, EJ Kim, WC Shin
    posted to prion prediction neuroimaging mri cjd by applebyb on 2008-09-26 01:07:11 as ****
  • Creutzfeldt-Jakob disease: extending palliative care nursing knowledge.
    International journal of palliative nursing, Vol. 6, No. 3. (March 2000), pp. 131-139.
    by B Bailey, S Aranda, K Quinn, H Kean
    posted to treatment prion cjd caregiver by applebyb on 2008-09-18 01:30:42 as *****
  • Transmissible agent in the amyotrophic form of Creutzfeldt-Jakob disease.
    Journal of neurology, neurosurgery, and psychiatry, Vol. 51, No. 11. (November 1988), pp. 1459-1460.
    by JH Connolly, IV Allen, E Dermott
    posted to survival prion phenotype cjd by applebyb on 2008-09-18 01:26:37 as *****
  • The ubiquitin-proteasome system in spongiform degenerative disorders.
    Biochimica et biophysica acta (23 August 2008)
    by Brandi R R Whatley, Lian Li, Lih-Shen S Chin
    posted to ubiquitination tse proteasome prion by applebyb on 2008-09-18 00:43:12 as ****
  • Creutzfeldt-Jacob Disease: a case report.
    Cases journal, Vol. 1, No. 1. (9 September 2008)
    by Eren Gozke, Nursel Erdal, Muge Unal
    posted to prion phenotype neuroimaging mri diagnosis dementia cjd by applebyb on 2008-09-14 15:10:05 as read
  • The ataxic (cerebellar) form of Creutzfeldt-Jakob disease.
    Journal of neurology, Vol. 207, No. 4. (1974), pp. 289-305.
    by K Jellinger, WD Heiss, E Deisenhammer
    posted to prion phenotype oppenheimer-brownell cjd by applebyb on 2008-09-08 02:50:45 as read
  • The ataxic form of Creutzfeldt-Jakob disease.
    Archives of neurology, Vol. 29, No. 5. (November 1973), pp. 318-323.
    by AJ Gomori, MJ Partnow, DS Horoupian, A Hirano
    posted to prion phenotype oppenheimer-brownell cjd by applebyb on 2008-09-08 02:50:13 as read
  • Homonymous field defect as the first manifestation of Creutzfeldt-Jakob disease.
    American journal of ophthalmology, Vol. 119, No. 4. (April 1995), pp. 497-504.
    by ME Vargas, MJ Kupersmith, PJ Savino, F Petito, LP Frohman, FA Warren
    posted to prion phenotype heidenhain cjd by applebyb on 2008-09-08 02:48:07 as read
  • Surveillance of Creutzfeldt-Jakob disease in Australia: 2008.
    Communicable diseases intelligence, Vol. 32, No. 2. (June 2008), pp. 232-236.
    by GM Klug, A Boyd, V Lewis, AR McGlade, H Roberts, SL Douglass, CL Masters, SJ Collins
    posted to prion epidemiology cjd by applebyb on 2008-09-06 19:51:56 as ****
  • Prion disease causes less severe lesions in human hippocampus than other parts of brain
    Psychiatry and Clinical Neurosciences, Vol. 62, No. 3. (June 2008), pp. 264-270.
    by Kaneko, Minoru, Sugiyama, Nobuhiro, Sasayama, Daimei, Yamaoka, Keiko, Miyakawa, Tomohiro, Arima, Kunimasa, Tsuchiya, Kuniaki, Hasegawa, Kazuko, Washizuka, Shinsuke, Hanihara, Tokisi, Amano, Naoji, Yagishita, Saburo
    posted to prion hippocampus by applebyb on 2008-09-06 19:42:08 as ****
  • Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series.
    Brain : a journal of neurology (1 September 2008)
    by T E F E Webb, M Poulter, J Beck, J Uphill, G Adamson, T Campbell, J Linehan, C Powell, S Brandner, S Pal, D Siddique, J D D Wadsworth, S Joiner, K Alner, C Petersen, S Hampson, C Rhymes, C Treacy, E Storey, M D D Geschwind, A H H Nemeth, S Wroe, J Collinge, S Mead
    posted to prion phenotype p102l gss by applebyb on 2008-09-06 19:32:41 as ****
  • Excretion of transmissible spongiform encephalopathy infectivity in urine.
    Emerging infectious diseases, Vol. 14, No. 9. (September 2008), pp. 1406-1412.
    by L Gregori, GG Kovacs, I Alexeeva, H Budka, RG Rohwer
    posted to urine tse risk prion by applebyb on 2008-09-06 19:26:38 as ****
  • Prion disease transmission: can we apply standard precautions to prevent or reduce risks?
    Journal of perioperative practice, Vol. 18, No. 7. (July 2008), pp. 298-304.
    by G McDonnell
    posted to icjd prion surgery by applebyb on 2008-08-26 02:22:44 as *****
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