applebyb's phenotype [63 articles] Export

Recent papers added to applebyb's library classified by the tag phenotype. You can also see everyone's phenotype.

	A case of Creutzfeldt-Jakob disease with stroke-like episode as an initial symptom. [My Copy] Nippon Ronen Igakkai zasshi. Japanese journal of geriatrics, Vol. 46, No. 5. (2009), pp. 458-461. by Kenji Kamogawa, Takayuki Toi, Kensho Okamoto, Bungo Okuda posted to stroke phenotype creutzfeldt_jakob_disease clinical by applebyb on 2009-11-19 13:25:04 as
	Clinical-Genetic Correlations in Familial Alzheimer's Disease Caused by Presenilin 1 Mutations. [My Copy] Journal of Alzheimer's disease : JAD (17 November 2009) by Estrella G Mez-Tortosa, Sagrario Barquero, Manuel Barón, et al.Eulogio Gil-Neciga, Fernando Castellanos, Martín Zurdo, Sagrario Manzano, David G. Muñoz, Adolfo Jiménez-Huete, Alberto Rábano, M. José Sainz, Rosa Guerrero, Isabel Gobernado, Julián Pérez-Pérez, Adriano Jiménez-Escrig posted to ps-1 presenilin phenotype genetic familial_alzheimer clinical alzheimers_disease by applebyb on 2009-11-19 13:24:01 as
	Inherited CreutzfeldtâJakob disease in a Dutch patient with a novel five octapeptide repeat insertion and unusual cerebellar morphology [My Copy] Journal of Neurology, Neurosurgery & Psychiatry, Vol. 80, No. 12. (December 2009), pp. 1386-1389. by C. Jansen, J. C. van Swieten, S. Capellari, R. Strammiello, P. Parchi, A. J. M. Rozemuller posted to phenotype octapeptide genetics creutzfeldt_jakob_disease by applebyb on 2009-11-17 19:34:28 as
	Prion protein amyloidosis with divergent phenotype associated with two novel nonsense mutations in PRNP. [My Copy] Acta neuropathologica (13 November 2009) by Casper Jansen, Piero Parchi, Sabina Capellari, et al.Ad J. Vermeij, Patrizia Corrado, Frank Baas, Rosaria Strammiello, Willem A. van Gool, John C. van Swieten, Annemieke J. Rozemuller posted to prnp prion phenotype genetics amyloidosis by applebyb on 2009-11-17 19:25:57 as
	Clinical features of sporadic fatal insomnia. [My Copy] Reviews in neurological diseases, Vol. 6, No. 3. (2009) by Jed A. Barash posted to sporadic_fatal_insomnia phenotype clinical by applebyb on 2009-11-11 13:08:49 as
	Survival Profiles of Patients With Frontotemporal Dementia and Motor Neuron Disease [My Copy] Arch Neurol, Vol. 66, No. 11. (1 November 2009), pp. 1359-1364. by William T. Hu, Harro Seelaar, Keith A. Josephs, et al.David S. Knopman, Bradley F. Boeve, Eric J. Sorenson, Leo McCluskey, Lauren Elman, Helenius J. Schelhaas, Joseph E. Parisi, Benno Kuesters, Virginia M. Y. Lee, John Q. Trojanowski, Ronald C. Petersen, John C. van Swieten, Murray Grossman posted to survival phenotype motor_neuron_disease frontotemporal_dementia by applebyb on 2009-11-10 13:53:30 as
	Clinical syndromes associated with posterior atrophy: Early age at onset AD spectrum [My Copy] Neurology, Vol. 73, No. 19. (10 November 2009), pp. 1571-1578. by R. Migliaccio, F. Agosta, K. Rascovsky, et al.A. Karydas, S. Bonasera, G. D. Rabinovici, B. L. Miller, M. L. Gorno-Tempini posted to young_onset_dementia posterior_cortical_atrophy phenotype alzheimers_disease by applebyb on 2009-11-10 13:49:08 as
	Two distinct subtypes of right temporal variant frontotemporal dementia. [My Copy] Neurology, Vol. 73, No. 18. (3 November 2009), pp. 1443-1450. by K. A. Josephs, J. L. Whitwell, D. S. Knopman, et al.B. F. Boeve, P. Vemuri, M. L. Senjem, J. E. Parisi, R. J. Ivnik, D. W. Dickson, R. C. Petersen, C. R. Jack posted to variant right phenotype frontotemporal_dementia by applebyb on 2009-11-04 22:54:03 as
	The oldest old Creutzfeldt-Jakob disease case [My Copy] J Neurol Neurosurg Psychiatry, Vol. 80, No. 10. (1 October 2009), pp. 1140-1142. by M. Buganza, S. Ferrari, M. E. Cecchini, D. Orrico, S. Monaco, G. Zanusso posted to phenotype cjd age by applebyb on 2009-09-19 17:45:57 as
	Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics. [My Copy] Brain : a journal of neurology (4 September 2009) by Ignazio Cali, Rudolph Castellani, Amer Alshekhlee, et al.Yvonne Cohen, Janis Blevins, Jue Yuan, Jan P. Langeveld, Piero Parchi, Jiri G. Safar, Wen-Quan Q. Zou, Pierluigi Gambetti posted to prion phenotype genotype cjd by applebyb on 2009-09-08 14:17:01 as
	Movement disorders and Creutzfeldt-Jakob disease: A review [My Copy] Parkinsonism & Related Disorders, Vol. 12, No. 2. (March 2006), pp. 65-71. by D. Maltete, L. Guyantmarechal, B. Mihout, D. Hannequin posted to phenotype movement_disorders cjd by applebyb on 2009-09-07 13:56:40 as
	Incidence and spectrum of sporadic Creutzfeldt-Jakob disease variants with mixed phenotype and co-occurrence of PrP(Sc) types: an updated classification. [My Copy] Acta neuropathologica (29 August 2009) by Piero Parchi, Rosaria Strammiello, Silvio Notari, et al.Armin Giese, Jan P. Langeveld, Anna Ladogana, Inga Zerr, Federico Roncaroli, Patrich Cras, Bernardino Ghetti, Maurizio Pocchiari, Hans Kretzschmar, Sabina Capellari posted to phenotype neuropathology cjd by applebyb on 2009-09-01 17:21:30 as
	[Ophthalmological first manifestation of Creutzfeldt-Jacob disease] [My Copy] Klinische Monatsblätter für Augenheilkunde, Vol. 226, No. 5. (May 2009), pp. 436-437. by A-C C. Haller, B. Schroeder, W. Wiegand posted to phenotype cjd by applebyb on 2009-08-21 13:31:25 as
	Different prion conformers target the olfactory pathway in sporadic Creutzfeldt-Jakob disease. [My Copy] Annals of the New York Academy of Sciences, Vol. 1170 (July 2009), pp. 637-643. by Gianluigi Zanusso, Sergio Ferrari, Diego Benedetti, Marco Sbriccoli, Nicola Rizzuto, Salvatore Monaco posted to prion phenotype cjd by applebyb on 2009-08-20 17:51:06 as
	An atypical case of sporadic fatal insomnia [My Copy] J Neurol Neurosurg Psychiatry, Vol. 80, No. 8. (1 August 2009), pp. 924-927. by L. Priano, G. Giaccone, M. Mangieri, et al.G. Albani, L. Limido, A. Brioschi, L. Pradotto, L. Orsi, P. Mortara, P. Fociani, A. Mauro, F. Tagliavini posted to phenotype prion sfi by applebyb on 2009-07-17 02:02:55 as
	Cognitive and Noncognitive Neurological Features of Young-Onset Dementia [My Copy] posted to phenotype presentation yod by applebyb on 2009-07-17 01:57:05 as
	Creutzfeldt-Jakob disease with E200K PRNP mutation: a case report and revision of the literature. [My Copy] Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology (14 July 2009) by Michelangelo Mancuso, Gabriele Siciliano, Sabina Capellari, et al.Daniele Orsucci, Policarpo Moretti, Giuseppe D. Fede, Silvia Suardi, Rosaria Strammiello, Piero Parchi, Fabrizio Tagliavini, Luigi Murri posted to cjd genetics phenotype by applebyb on 2009-07-16 01:19:32 as
	Cognitive and Noncognitive Neurological Features of Young-Onset Dementia [My Copy] posted to phenotype presentation yod by applebyb on 2009-07-12 01:21:13 as
	Cathepsin D (C224T) Polymorphism in Sporadic and Genetic Creutzfeldt-Jakob Disease. [My Copy] Alzheimer disease and associated disorders (30 June 2009) by Gabor G. Kovacs, Pascual Sanchez-Juan, Thomas Ströbel, et al.Maaike Schuur, Anna Poleggi, Sara Nocentini, Claudia Giannattasio, Girma Belay, Matthew Bishop, Sabina Capellari, Piero Parchi, Ellen Gelpi, Aniko Gal, Agnes Bakos, Maria J. Molnar, Uta Heinemann, Inga Zerr, Richard S. Knight, Eva Mitrova, Cornelia van Duijn, Herbert Budka posted to cjd genetics phenotype polymorphism by applebyb on 2009-07-05 15:59:35 as
	A Case of Dementia With PRNP D178Ncis-129M and No Insomnia. [My Copy] Alzheimer disease and associated disorders (30 June 2009) by Rita J. Guerreiro, Tina Vaskov, Cynthia Crews, Andrew Singleton, John Hardy posted to ffi genetics phenotype by applebyb on 2009-07-05 15:55:21 as
	Species and strain glycosylation patterns of PrP. [My Copy] PLoS ONE, Vol. 4, No. 5. (2009) by K. Xanthopoulos, M. Polymenidou, S. J. Bellworthy, S. L. Benestad, T. Sklaviadis posted to phenotype prpsc by applebyb on 2009-05-25 21:36:09 as
	De novo generation of infectious prions in vitro produces a new disease phenotype. [My Copy] PLoS pathogens, Vol. 5, No. 5. (May 2009) by M. A. Barria, A. Mukherjee, D. Gonzalez-Romero, R. Morales, C. Soto posted to biology pathogenesis phenotype prion by applebyb on 2009-05-15 18:26:10 as
	Combined magnetic resonance imaging and positron emission tomography brain imaging in behavioural variant frontotemporal degeneration: refining the clinical phenotype. [My Copy] Brain : a journal of neurology (4 May 2009) by C M M. Kipps, J R R. Hodges, T D D. Fryer, P J J. Nestor posted to diagnosis ftd mri neuroimaging phenotype by applebyb on 2009-05-08 14:37:22 as
	Survival in Frontotemporal Lobar Degeneration and Related Disorders: Latent Class Predictors and Brain Functional Correlates. [My Copy] Rejuvenation research (23 February 2009) by B Borroni, M Grassi, C Agosti, et al.E Premi, A Alberici, B Paghera, S Lucchini, M Di D. Luca, D Perani, A Padovani posted to clinical ftld neuroimaging phenotype prediction survival symptoms by applebyb on 2009-03-02 12:45:25 as along with 1 person belljar
	Creutzfeldt-Jacob disease presenting as severe depression: a case report. [My Copy] Cases journal, Vol. 2, No. 1. (4 February 2009) by Ethan U. Cumbler, Kristin Furfari, Jeannette Guerrasio posted to cjd depression phenotype presentation prion by applebyb on 2009-02-07 01:12:58 as
	The effect of onset age on the clinical features of Parkinson's disease. [My Copy] European journal of neurology : the official journal of the European Federation of Neurological Societies (27 January 2009) by M M M. Wickremaratchi, Y Ben-Shlomo, H R R. Morris posted to pd phenotype yod by applebyb on 2009-02-06 19:33:00 as
	A quantitative study of the pathological changes in the cerebellum in 15 cases of variant CreutzfeldtJakob disease (vCJD) [My Copy] Neuropathology & Applied Neurobiology, Vol. 35, No. 1., pp. 36-45. by R. A. Armstrong, J. W. Ironside, P. L. Lantos, N. J. Cairns posted to neuropathology phenotype prion vcjd by applebyb on 2009-02-06 19:30:55 as
	Electroretinograms in three cases of Creutzfeldt-Jakob disease with visual disturbances [My Copy] Japanese Journal of Ophthalmology, Vol. 53, No. 1. (1 January 2009), pp. 31-34. by Akira Ishikawa, Atsuhiro Tanikawa, Yoshiaki Shimada, Tatsuro Mutoh, Hiroko Yamamoto, Masayuki Horiguchi posted to cjd phenotype prion_disease by applebyb on 2009-02-06 19:24:41 as
	Presymptomatic Signs in Healthy CJD Mutation Carriers [My Copy] posted to cjd gcjd genetics phenotype presentation by applebyb on 2009-01-28 21:11:56 as
	'Agrypnia excitata' in a case of sporadic Creutzfeldt-Jakob disease VV2 [My Copy] J Neurol Neurosurg Psychiatry, Vol. 80, No. 2. (1 February 2009), pp. 244-246. by C. La Morgia, P. Parchi, S. Capellari, et al.R. Lodi, C. Tonon, R. Rinaldi, S. Mondini, F. Cirignotta posted to genetics phenotype prion scjd by applebyb on 2009-01-17 01:10:48 as
	A Patient With Creutzfeldt-Jakob Disease With an Insertion of 7 Octa-Repeats in the PRNP Gene: Molecular Characteristics and Clinical Features. [My Copy] The American journal of the medical sciences, Vol. 336, No. 6. (December 2008), pp. 519-523. by Yan-Jun J. Guo, Xiao-Fan F. Wang, Jun Han, et al.Bao-Yun Y. Zhang, Wei-Qin Q. Zhao, Qi Shi, Yan-Zhen Z. Wan, Chen Gao, Ji-Mei M. Li, DE-Xin X. Wang, Xiao-Ping P. Dong posted to cjd genetics phenotype prion prnp by applebyb on 2009-01-02 14:39:13 as
	Phenotypic heterogeneity and genetic modifiers in prion disease caused by a Pro102Leu mutation in the PRNP gene. [My Copy] Nature clinical practice. Neurology (17 December 2008) by Manuela Neumann posted to gcjd genetics phenotype prion prnp by applebyb on 2009-01-02 14:36:48 as
	Strain-specific viral properties of variant Creutzfeldt-Jakob disease (vCJD) are encoded by the agent and not by host prion protein. [My Copy] Journal of cellular biochemistry (18 December 2008) by Laura Manuelidis, Ying Liu, Brian Mullins posted to cjd phenotype prion strain vcjd by applebyb on 2009-01-02 14:36:00 as
	The Montgomery-Asberg Depression Rating Scale and the Cornell Scale for Depression in Dementia: a validation study with patients exhibiting early-onset dementia. [My Copy] The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry, Vol. 17, No. 1. (January 2009), pp. 56-64. by R. Leontjevas, S. van Hooren, A. Mulders posted to dementia depression phenotype presentation by applebyb on 2009-01-02 14:31:33 as
	Cognitive Function and Psychiatric Symptoms in Early- and Late-Onset Frontotemporal Dementia [My Copy] posted to age ftd phenotype symptoms by applebyb on 2008-12-28 18:23:12 as
	A novel presenilin 1 mutation (V261L) associated with presenile Alzheimers disease and spastic paraparesis [My Copy] European Journal of Neurology, Vol. 15, No. 9. (September 2008), pp. 991-994. by Jimenez Caballero, P. E., De D. Boguna, et al. C., Martin Correa, E., Servia Candela, M., Marsal Alonso, C. posted to ad genetics phenotype ps-1 by applebyb on 2008-12-25 00:41:32 as
	Panencephalopathic Creutzfeldt-Jakob disease in the Netherlands and UK: clinical and pathological characteristics of nine patients. [My Copy] Neuropathology and applied neurobiology (1 December 2008) by C Jansen, M W W. Head, A J M J. Rozemuller, J W W. Ironside posted to cjd phenotype prion by applebyb on 2008-12-13 15:00:01 as
	Is early-onset clinically different from late-onset frontotemporal dementia? [My Copy] European Journal of Neurology, Vol. 15, No. 12. (December 2008), pp. 1412-1415. by B. Borroni, C. Agosti, G. Bellelli, A. Padovani posted to age ftd ftld phenotype presentation yod by applebyb on 2008-12-06 11:16:40 as along with 1 person belljar
	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 [My Copy] Neurological Sciences by Anna Giovagnoli, Giuseppe Di Fede, Anna Aresi, Fabiola Reati, Giacomina Rossi, Fabrizio Tagliavini posted to ftd genetics gss phenotype prion by applebyb on 2008-11-27 14:59:46 as
	The anatomic correlate of prosopagnosia in semantic dementia [My Copy] Neurology, Vol. 71, No. 20. (11 November 2008), pp. 1628-1633. by K. A. Josephs, J. L. Whitwell, P. Vemuri, et al.M. L. Senjem, B. F. Boeve, D. S. Knopman, G. E. Smith, R. J. Ivnik, R. C. Petersen, C. R. Jack posted to agnosia ftld mri neuroimaging phenotype sd symptoms by applebyb on 2008-11-22 20:37:56 as along with 2 people nishiokov belljar
	Poor attentional function predicts cognitive decline in patients with non-demented Parkinson's disease independent of motor phenotype [My Copy] J Neurol Neurosurg Psychiatry, Vol. 79, No. 12. (1 December 2008), pp. 1318-1323. by J. P. Taylor, E. N. Rowan, D. Lett, J. T. O'Brien, I. G. Mckeith, D. J. Burn posted to attention cognition dementia pd phenotype by applebyb on 2008-11-22 20:15:56 as
	Familial Creutzfeldt-Jakob disease presenting as epilepsia partialis continua. [My Copy] Epileptic disorders : international epilepsy journal with videotape, Vol. 10, No. 4. (18 November 2008), pp. 271-275. by Max R R. Lowden, Kevin Scott, Milind J J. Kothari posted to cjd diagnosis gcjd genetics phenotype prion_disease by applebyb on 2008-11-21 14:45:47 as
	Heightened incidence of sporadic Creutzfeldt-Jakob disease is associated with a shift in clinicopathological profiles [My Copy] Journal of Neurology, Vol. 255, No. 10. (1 October 2008), pp. 1464-1472. by Katharina Stoeck, Klaus Hess, Lorenz Amsler, et al.Tobias Eckert, Dieter Zimmermann, Adriano Aguzzi, Markus Glatzel posted to cjd phenotype prion_disease scjd by applebyb on 2008-11-21 14:37:22 as
	An unusually presenting case of sCJD-The VV1 subtype. [My Copy] Clinical neurology and neurosurgery (6 November 2008) by Kaloyan S S. Tanev, Mimi Yilma posted to cjd molecular_subtype phenotype prion_disease scjd vv1 by applebyb on 2008-11-21 14:33:03 as
	Creutzfeldt-Jakob disease presenting with visual manifestations. [My Copy] Canadian journal of ophthalmology. Journal canadien d'ophtalmologie, Vol. 43, No. 5. (October 2008), pp. 591-595. by A. A. Proulx, M. J. Strong, D. A. Nicolle posted to cjd heidenhain phenotype prion_disease by applebyb on 2008-11-21 14:25:47 as
	Effects of human PrPSc type and PRNP genotype in an in-vitro conversion assay. [My Copy] Neuroreport (24 October 2008) by Michael Jones, Alexander H. Peden, Darren Wight, et al.Christopher Prowse, Ian Macgregor, Jean Manson, Marc Turner, James W. Ironside, Mark W. Head posted to phenotype prion_disease prnp protein prpsc by applebyb on 2008-11-21 14:16:55 as
	Creutzfeldt-Jakob's disease presenting with ataxia and a movement disorder. [My Copy] Movement disorders : official journal of the Movement Disorder Society, Vol. 6, No. 2. (1991), pp. 157-162. by K. D. Sethi, D. C. Hess posted to ataxia cjd movement_disorder oppenheimer_brownell phenotype prion by applebyb on 2008-10-22 20:27:10 as
	Review. The neuropathology of kuru and variant Creutzfeldt-Jakob disease. [My Copy] Philosophical transactions of the Royal Society of London. Series B, Biological sciences, Vol. 363, No. 1510. (27 November 2008), pp. 3685-3687. by C. A. McLean posted to cjd codon129 genetics incubation kuru phenotype prion vcjd by applebyb on 2008-10-20 00:07:40 as
	A clinical study of kuru patients with long incubation periods at the end of the epidemic in Papua New Guinea. [My Copy] 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, et al.A. Frosh, S. Mead, A. F. Hill, S. Brandner, D. Thomas, M. P. Alpers posted to age genetics incubation kuru phenotype prion risk by applebyb on 2008-10-20 00:01:37 as
	Review. The origin of the prion agent of kuru: molecular and biological strain typing. [My Copy] Philosophical transactions of the Royal Society of London. Series B, Biological sciences, Vol. 363, No. 1510. (27 November 2008), pp. 3747-3753. by Jonathan D. Wadsworth, Susan Joiner, Jacqueline M. Linehan, Emmanuel A. Asante, Sebastian Brandner, John Collinge posted to cjd icjd kuru phenotype prion prpsc scjd strain by applebyb on 2008-10-19 23:57:27 as along with 1 person bmezmer

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prion	272
cjd	149
ad	132
genetics	96
academics	77
treatment	76
dementia	65
phenotype	63
prion_diseases	62
risk	62
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ftld	32
prpc	31
vcjd	31
dx	29
dz	29
human	29
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of	29
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tau	25
protein	22
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psychosurgery	18
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amyloid	16
caregiver	16
icjd	16
prnp	16
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kuru	15
neuroethics	15
parkinsons_disease	15
review	15
als	14
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data	13
gcjd	13
pd	13
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geriatric_psychiatry	11
prpsc	11
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tdp-43	11
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apoe	10
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leukoencephalopathy	1
limibic_encephalitis	1
lipid	1
lipid_rafts	1
liposomes	1
logopenia	1
lymphoreticular	1
major_depression	1
major_depressive_disorder	1
management	1
manganese	1
medication_regimens	1
medication_trials	1
medicine	1
mentoring	1
metadata	1
metal	1
mice	1
misdiagnosis	1
misfolding	1
mixed_dementia	1
mm1	1
mmse	1
mood	1
motor_neuron_disease	1
mrna	1
msa	1
muscle	1
mutation	1
network_structure	1
neural_circuits	1
neuroanatomy	1
neuroimagin	1
neurology	1
neuropath	1
neuroradiology	1
neurostimulation	1
neurotoxicity	1
nms	1
npi	1
nucleation	1
nucleic_acid	1
nucleus_accumbens	1
octapeptide	1
onset	1
oppenheimer_brownell	1
p102l	1
palliative_care	1
paraneoplastic_syndrome	1
parity	1
parkinsonism	1
peptides	1
ph	1
pharmacology	1
physiology	1
pib	1
plaques	1
plasminogen	1
polymorphisms	1
posterior_cortical_atrophy	1
ppar-gamma	1
preclinical	1
pregnancy	1
prevalence	1
primary	1
progressive_supranuclear_palsy	1
protective	1
prusiner	1
ps2	1
ps-2	1
pseudodementia	1
psychiatriy	1
psychosocial	1
psychotherapy	1
psychotropics	1
ptau	1
public_health	1
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rapidly_progressive_dementia	1
redox	1
remission_rates	1
right	1
role	1
rpd	1
rtms	1
science	1
scientist	1
sd-ftd	1
sd-nft	1
serotonin	1
sertraline	1
simvastatin	1
snps	1
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srage	1
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stard	1
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stem_cells	1
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stimulant	1
stimulants	1
stimulation	1
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telomeres	1
thalamus	1
theory	1
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tissue	1
transient_global_amnesia	1
traumatic_brain_injury	1
trea	1
treamtent	1
treatment_alternatives	1
treatment_outcome	1
trisomy_21	1
ttau	1
ubiquitination	1
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vad	1
variant	1
verbal_fluency	1
vpa	1
vv1	1
weblab	1
weight	1
wernicke_encephalopathy	1
wilsons_disease	1

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