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Bonnet sign相关文献:
Chloropsia in the Charles Bonnet syndrome.
Bhatnagar A, Ishihara R, Pakravan M, Charoenkijkajorn C, Lee AG.
Am J Ophthalmol Case Rep. 2022 Sep 10;28:101703. doi: 10.1016/j.ajoc.2022.101703. eCollection 2022 Dec.
PMID:36133354
Visual hallucinations (Charles Bonnet syndrome) as the presenting sign of pituitary adenoma.
Hashemi N, Zhang J, Gelman R, Lee AG.
Can J Ophthalmol. 2012 Jun;47(3):e5-6. doi: 10.1016/j.jcjo.2012.03.029. Epub 2012 May 1.
PMID:22687320
Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19.
Matuozzo D, Talouarn E, Marchal A, Zhang P, Manry J, Seeleuthner Y, Zhang Y, Bolze A, Chaldebas M, Milisavljevic B, Gervais A, Bastard P, Asano T, Bizien L, Barzaghi F, Abolhassani H, Abou Tayoun A, Aiuti A, Alavi Darazam I, Allende LM, Alonso-Arias R, Arias AA, Aytekin G, Bergman P, Bondesan S, Bryceson YT, Bustos IG, Cabrera-Marante O, Carcel S, Carrera P, Casari G, Chaïbi K, Colobran R, Condino-Neto A, Covill LE, Delmonte OM, El Zein L, Flores C, Gregersen PK, Gut M, Haerynck F, Halwani R, Hancerli S, Hammarström L, Hatipoğlu N, Karbuz A, Keles S, Kyheng C, Leon-Lopez R, Franco JL, Mansouri D, Martinez-Picado J, Metin Akcan O, Migeotte I, Morange PE, Morelle G, Martin-Nalda A, Novelli G, Novelli A, Ozcelik T, Palabiyik F, Pan-Hammarström Q, de Diego RP, Planas-Serra L, Pleguezuelo DE, Prando C, Pujol A, Reyes LF, Rivière JG, Rodriguez-Gallego C, Rojas J, Rovere-Querini P, Schlüter A, Shahrooei M, Sobh A, Soler-Palacin P, Tandjaoui-Lambiotte Y, Tipu I, Tresoldi C, Troya J, van de Beek D, Zatz M, Zawadzki P, Al-Muhsen SZ, Alosaimi MF, Alsohime FM, Baris-Feldman H, Butte MJ, Constantinescu SN, Cooper MA, Dalgard CL, Fellay J, Heath JR, Lau YL, Lifton RP, Maniatis T, Mogensen TH, v…
Genome Med. 2023 Apr 5;15(1):22. doi: 10.1186/s13073-023-01173-8.
PMID:37020259
Re: visual hallucinations (Charles Bonnet syndrome) as the presenting sign of pituitary adenoma.
Li KZ, Ngo WK, Tan CS.
Can J Ophthalmol. 2012 Dec;47(6):509; author reply 510. doi: 10.1016/j.jcjo.2012.08.010.
PMID:23217505
Non-accidental injury or congenital infection?
Hérissé AL, Chiaverini C, Hubiche T, Tran A, Rondel J, Rosello O, Giovannini-Chami L, Haas H.
Arch Dis Child. 2017 Sep;102(9):852. doi: 10.1136/archdischild-2016-311692. Epub 2017 Jan 17.
PMID:28096106
Factors That Influence Susceptibility Vessel Sign in Patients With Acute Stroke Referred for Mechanical Thrombectomy.
Dillmann M, Bonnet L, Vuillier F, Moulin T, Biondi A, Charbonnier G.
Front Neurol. 2022 May 11;13:893060. doi: 10.3389/fneur.2022.893060. eCollection 2022.
PMID:35645960
Extreme thrombocytosis with an aggressive evolution harboring a novel variant of calreticulin (CALR) in exon 3.
Bonnet S, Carillo S, Legrand B, Burroni B, Lavabre-Bertrand T, Requirand G, Robert N, Fornero L, Al Mansoori A, Moreaux J, Cartron G, Gabellier L, Herbaux C.
Eur J Haematol. 2024 Mar;112(3):475-478. doi: 10.1111/ejh.14126. Epub 2023 Nov 2.
PMID:37918825
The Hyperdense Middle Cerebral Artery Sign in Drip-and-Ship Models of Acute Stroke Management.
Jodaitis L, Ligot N, Chapusette R, Bonnet T, Gaspard N, Naeije G.
Cerebrovasc Dis Extra. 2020;10(1):36-43. doi: 10.1159/000506971. Epub 2020 Apr 28.
PMID:32344421
[Acute myopic shift call sign of hantavirus infection].
Tilkin C, Bonnet S.
Rev Med Liege. 2018 Jul;73(7-8):425-427.
PMID:30113787
Correction: Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19.
Matuozzo D, Talouarn E, Marchal A, Zhang P, Manry J, Seeleuthner Y, Zhang Y, Bolze A, Chaldebas M, Milisavljevic B, Gervais A, Bastard P, Asano T, Bizien L, Barzaghi F, Abolhassani H, Tayoun AA, Aiuti A, Darazam IA, Allende LM, Alonso-Arias R, Arias AA, Aytekin G, Bergman P, Bondesan S, Bryceson YT, Bustos IG, Cabrera-Marante O, Carcel S, Carrera P, Casari G, Chaïbi K, Colobran R, Condino-Neto A, Covill LE, Delmonte OM, Zein LE, Flores C, Gregersen PK, Gut M, Haerynck F, Halwani R, Hancerli S, Hammarström L, Hatipoğlu N, Karbuz A, Keles S, Kyheng C, Leon-Lopez R, Franco JL, Mansouri D, Martinez-Picado J, Akcan OM, Migeotte I, Morange PE, Morelle G, Martin-Nalda A, Novelli G, Novelli A, Ozcelik T, Palabiyik F, Pan-Hammarström Q, de Diego RP, Planas-Serra L, Pleguezuelo DE, Prando C, Pujol A, Reyes LF, Rivière JG, Rodriguez-Gallego C, Rojas J, Rovere-Querini P, Schlüter A, Shahrooei M, Sobh A, Soler-Palacin P, Tandjaoui-Lambiotte Y, Tipu I, Tresoldi C, Troya J, van de Beek D, Zatz M, Zawadzki P, Al-Muhsen SZ, Alosaimi MF, Alsohime FM, Baris-Feldman H, Butte MJ, Constantinescu SN, Cooper MA, Dalgard CL, Fellay J, Heath JR, Lau YL, Lifton RP, Maniatis T, Mogensen TH, von Bernuth H, Le…
Genome Med. 2024 Jan 6;16(1):6. doi: 10.1186/s13073-023-01278-0.
PMID:38184654
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