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Year Number of Results
1998 2
1999 1
2000 1
2001 1
2004 2
2011 1
2013 1
2015 1
2016 5
2017 5
2019 3
2020 1
2021 1
2022 3
2023 3
2024 0

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30 results

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Page 1
Spinocerebellar ataxia-type 34: A case report and brief review of the literature.
Batheja V, Fish M, Balar AB, Hedge S, Hogg JP, Lakhani DA, Khan M. Batheja V, et al. Radiol Case Rep. 2023 Aug 30;18(11):3954-3958. doi: 10.1016/j.radcr.2023.08.055. eCollection 2023 Nov. Radiol Case Rep. 2023. PMID: 37680663 Free PMC article.
While multiple system atrophy has a higher prevalence of the HCBS than other neurodegenerative diseases, the sign has also been described with other neurodegenerative disorders such as spinocerebellar ataxia (SCA), and variant Creutzfeldt-Jakob disease. Here, we present a …
While multiple system atrophy has a higher prevalence of the HCBS than other neurodegenerative diseases, the sign has also been described wi …
EAACI Molecular Allergology User's Guide 2.0.
Dramburg S, Hilger C, Santos AF, de Las Vecillas L, Aalberse RC, Acevedo N, Aglas L, Altmann F, Arruda KL, Asero R, Ballmer-Weber B, Barber D, Beyer K, Biedermann T, Bilo MB, Blank S, Bosshard PP, Breiteneder H, Brough HA, Bublin M, Campbell D, Caraballo L, Caubet JC, Celi G, Chapman MD, Chruszcz M, Custovic A, Czolk R, Davies J, Douladiris N, Eberlein B, Ebisawa M, Ehlers A, Eigenmann P, Gadermaier G, Giovannini M, Gomez F, Grohman R, Guillet C, Hafner C, Hamilton RG, Hauser M, Hawranek T, Hoffmann HJ, Holzhauser T, Iizuka T, Jacquet A, Jakob T, Janssen-Weets B, Jappe U, Jutel M, Kalic T, Kamath S, Kespohl S, Kleine-Tebbe J, Knol E, Knulst A, Konradsen JR, Korošec P, Kuehn A, Lack G, Le TM, Lopata A, Luengo O, Mäkelä M, Marra AM, Mills C, Morisset M, Muraro A, Nowak-Wegrzyn A, Nugraha R, Ollert M, Palosuo K, Pastorello EA, Patil SU, Platts-Mills T, Pomés A, Poncet P, Potapova E, Poulsen LK, Radauer C, Radulovic S, Raulf M, Rougé P, Sastre J, Sato S, Scala E, Schmid JM, Schmid-Grendelmeier P, Schrama D, Sénéchal H, Traidl-Hoffmann C, Valverde-Monge M, van Hage M, van Ree R, Verhoeckx K, Vieths S, Wickman M, Zakzuk J, Matricardi PM, Hoffmann-Sommergruber K. Dramburg S, et al. Pediatr Allergy Immunol. 2023 Mar;34 Suppl 28:e13854. doi: 10.1111/pai.13854. Pediatr Allergy Immunol. 2023. PMID: 37186333
Incidence of premature battery depletion in subcutaneous cardioverter-defibrillator patients: insights from a multicenter registry.
Lüker J, Strik M, Andrade JG, Raymond-Paquin A, Elrefai MH, Roberts PR, Pérez ÓC, Kron J, Koneru J, Franqui-Rivera H, Sultan A, Ernst A, Schmitt J, Pott A, Veltmann C, Srinivasan NT, Collinson J, van Stipdonk AMW, Linz D, Fluschnik N, Tönnis T, Haeberlin A, Ploux S, Steven D. Lüker J, et al. J Interv Card Electrophysiol. 2023 Jan 18. doi: 10.1007/s10840-023-01468-1. Online ahead of print. J Interv Card Electrophysiol. 2023. PMID: 36652082 Free article.
Growth and Growth Hormone through the Ages: Art and Science.
Rogol AD, Reiter EO. Rogol AD, et al. Horm Res Paediatr. 2022;95(6):515-528. doi: 10.1159/000526440. Epub 2022 Nov 29. Horm Res Paediatr. 2022. PMID: 36446319 Free article. Review.
Human GH was prepared from cadaveric pituitaries and distributed by the NIH to treat children with GH deficiency, but there was never enough pituitary hGH for all of the children who required it. When Creutzfeldt-Jakob disease was found in some patients who received pituit …
Human GH was prepared from cadaveric pituitaries and distributed by the NIH to treat children with GH deficiency, but there was never enough …
Atypical Case of VV1 Creutzfeldt-Jakob Disease Subtype: Case Report.
Carrasco AE, Appleby BS, Cali I, Okhravi HR. Carrasco AE, et al. Front Neurol. 2022 May 9;13:875370. doi: 10.3389/fneur.2022.875370. eCollection 2022. Front Neurol. 2022. PMID: 35614914 Free PMC article.
Creutzfeldt-Jakob disease (CJD) is a rare form of rapidly progressive, neurodegenerative disease that results from the misfolding and accumulation of an aberrant, disease-associated prion protein (PrPD). ...
Creutzfeldt-Jakob disease (CJD) is a rare form of rapidly progressive, neurodegenerative disease that results from the misfolding and …
Examining Rural-Urban Differences in Fatalism and Information Overload: Data from 12 NCI-Designated Cancer Centers.
Jensen JD, Shannon J, Iachan R, Deng Y, Kim SJ, Demark-Wahnefried W, Faseru B, Paskett ED, Hu J, Vanderpool RC, Lazovich D, Mendoza JA, Shete S, Robertson LB, Balkrishnan R, Briant KJ, Haaland B, Haggstrom DA, Fuemmeler BF; Rural Workgroup of the Population Health Assessment in Cancer Center Catchment Areas Consortium. Jensen JD, et al. Cancer Epidemiol Biomarkers Prev. 2022 Feb;31(2):393-403. doi: 10.1158/1055-9965.EPI-21-0355. Epub 2022 Jan 28. Cancer Epidemiol Biomarkers Prev. 2022. PMID: 35091459 Free PMC article.
Using Catchment Population to Estimate Sporadic Creutzfeldt-Jakob Disease Incidence.
Neeley BC, Niazi FA, Ebbert MA, Forman AG, Hobbs GR, Riggs JE. Neeley BC, et al. Mil Med. 2021 Dec 4:usab510. doi: 10.1093/milmed/usab510. Online ahead of print. Mil Med. 2021. PMID: 34865142
A method using catchment population to estimate the incidence of sporadic Creutzfeldt-Jakob disease (sCJD) is described. MATERIALS AND METHODS: A cohort of nine consecutive patients diagnosed with sCJD, symptom onset spanning 26 months, were observed at a rural tertiary un …
A method using catchment population to estimate the incidence of sporadic Creutzfeldt-Jakob disease (sCJD) is described. MATERIALS AN …
Liver-specific deletion of Ngly1 causes abnormal nuclear morphology and lipid metabolism under food stress.
Fujihira H, Masahara-Negishi Y, Akimoto Y, Hirayama H, Lee HC, Story BA, Mueller WF, Jakob P, Clauder-Münster S, Steinmetz LM, Radhakrishnan SK, Kawakami H, Kamada Y, Miyoshi E, Yokomizo T, Suzuki T. Fujihira H, et al. Biochim Biophys Acta Mol Basis Dis. 2020 Mar 1;1866(3):165588. doi: 10.1016/j.bbadis.2019.165588. Epub 2019 Nov 13. Biochim Biophys Acta Mol Basis Dis. 2020. PMID: 31733337 Free article.
Rare Case of Anti-LGI1 Limbic Encephalitis with New Onset Epilepsy: A Case Report.
Kurukumbi M, Castillo JA, Shah T, Gupta R. Kurukumbi M, et al. Cureus. 2019 May 7;11(5):e4608. doi: 10.7759/cureus.4608. Cureus. 2019. PMID: 31309031 Free PMC article.
Cerebrospinal fluid 14-3-3 protein or neuron specific enolase is usually seen in Creutzfeldt-Jakob disease (CJD) with high sensitivities, but can also be positive in other paraneoplastic and autoimmune encephalitides, which can make diagnosis challenging. ...
Cerebrospinal fluid 14-3-3 protein or neuron specific enolase is usually seen in Creutzfeldt-Jakob disease (CJD) with high sensitivit …
Globally important islands where eradicating invasive mammals will benefit highly threatened vertebrates.
Holmes ND, Spatz DR, Oppel S, Tershy B, Croll DA, Keitt B, Genovesi P, Burfield IJ, Will DJ, Bond AL, Wegmann A, Aguirre-Muñoz A, Raine AF, Knapp CR, Hung CH, Wingate D, Hagen E, Méndez-Sánchez F, Rocamora G, Yuan HW, Fric J, Millett J, Russell J, Liske-Clark J, Vidal E, Jourdan H, Campbell K, Springer K, Swinnerton K, Gibbons-Decherong L, Langrand O, Brooke ML, McMinn M, Bunbury N, Oliveira N, Sposimo P, Geraldes P, McClelland P, Hodum P, Ryan PG, Borroto-Páez R, Pierce R, Griffiths R, Fisher RN, Wanless R, Pasachnik SA, Cranwell S, Micol T, Butchart SHM. Holmes ND, et al. PLoS One. 2019 Mar 27;14(3):e0212128. doi: 10.1371/journal.pone.0212128. eCollection 2019. PLoS One. 2019. PMID: 30917126 Free PMC article.
30 results