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Items: 1 to 20 of 61

  • The following term was not found in PubMed: Razvan-Mihail.
1.

Correction to: Early Detection, Diagnosis and Intervention Services for Young Children with Autism Spectrum Disorder in the European Union (ASDEU): Family and Professional Perspectives.

Bejarano-Martín Á, Canal-Bedia R, Magán-Maganto M, Fernández-Álvarez C, Martín-Cilleros MV, Sánchez-Gómez MC, García-Primo P, Rose-Sweeney M, Boilson A, Linertová R, Roeyers H, Van der Paelt S, Schendel D, Warberg C, Cramer S, Narzisi A, Muratori F, Scattoni ML, Moilanen I, Yliherva A, Saemundsen E, Loa Jónsdóttir S, Efrim-Budisteanu M, Arghir A, Papuc SM, Vicente A, Rasga C, Rogé B, Guillon Q, Baduel S, Kafka JX, Poustka L, Kothgassner OD, Kawa R, Pisula E, Sellers T, Posada de la Paz M.

J Autism Dev Disord. 2019 Nov 28. doi: 10.1007/s10803-019-04303-7. [Epub ahead of print]

PMID:
31782082
2.

Neurofibromatosis type 1 associated with moyamoya syndrome. Case report and review of the literature.

Budişteanu M, Burloiu CM, Papuc SM, Focşa IO, Riga D, Riga S, Arghir A.

Rom J Morphol Embryol. 2019;60(2):713-716. Review.

3.

Early Detection, Diagnosis and Intervention Services for Young Children with Autism Spectrum Disorder in the European Union (ASDEU): Family and Professional Perspectives.

Bejarano-Martín Á, Canal-Bedia R, Magán-Maganto M, Fernández-Álvarez C, Cilleros-Martín MV, Sánchez-Gómez MC, García-Primo P, Rose-Sweeney M, Boilson A, Linertová R, Roeyers H, Van der Paelt S, Schendel D, Warberg C, Cramer S, Narzisi A, Muratori F, Scattoni ML, Moilanen I, Yliherva A, Saemundsen E, Loa Jónsdóttir S, Efrim-Budisteanu M, Arghir A, Papuc SM, Vicente A, Rasga C, Rogé B, Guillon Q, Baduel S, Kafka JX, Poustka L, Kothgassner OD, Kawa R, Pisula E, Sellers T, Posada de la Paz M.

J Autism Dev Disord. 2019 Oct 12. doi: 10.1007/s10803-019-04253-0. [Epub ahead of print] Erratum in: J Autism Dev Disord. 2019 Nov 28;:.

PMID:
31606886
4.

Bone regeneration response in an experimental long bone defect orthotopically implanted with alginate-pullulan-glass-ceramic composite scaffolds.

Popescu RA, Tăbăran FA, Bogdan S, Fărcăṣanu A, Purdoiu R, Magyari K, Vulpoi A, Dreancă A, Sevastre B, Simon S, Papuc I, Baia L.

J Biomed Mater Res B Appl Biomater. 2020 Apr;108(3):1129-1140. doi: 10.1002/jbm.b.34464. Epub 2019 Aug 9.

PMID:
31397056
5.

Continuous subcutaneous apomorphine monotherapy in Parkinson's disease.

Papuć E, Trzciniecka O, Rejdak K.

Ann Agric Environ Med. 2019 Mar 22;26(1):133-137. doi: 10.26444/aaem/99699. Epub 2018 Dec 5.

6.

Spatially clustering de novo variants in CYFIP2, encoding the cytoplasmic FMRP interacting protein 2, cause intellectual disability and seizures.

Zweier M, Begemann A, McWalter K, Cho MT, Abela L, Banka S, Behring B, Berger A, Brown CW, Carneiro M, Chen J, Cooper GM; Deciphering Developmental Disorders (DDD) Study, Finnila CR, Guillen Sacoto MJ, Henderson A, Hüffmeier U, Joset P, Kerr B, Lesca G, Leszinski GS, McDermott JH, Meltzer MR, Monaghan KG, Mostafavi R, Õunap K, Plecko B, Powis Z, Purcarin G, Reimand T, Riedhammer KM, Schreiber JM, Sirsi D, Wierenga KJ, Wojcik MH, Papuc SM, Steindl K, Sticht H, Rauch A.

Eur J Hum Genet. 2019 May;27(5):747-759. doi: 10.1038/s41431-018-0331-z. Epub 2019 Jan 21.

PMID:
30664714
7.

Skin wound regeneration with bioactive glass-gold nanoparticles ointment.

Mârza SM, Magyari K, Bogdan S, Moldovan M, Peştean C, Nagy A, Tăbăran F, Licarete E, Suarasan S, Dreanca A, Baia L, Papuc I.

Biomed Mater. 2019 Feb 8;14(2):025011. doi: 10.1088/1748-605X/aafd7d.

PMID:
30630137
8.

The role of recessive inheritance in early-onset epileptic encephalopathies: a combined whole-exome sequencing and copy number study.

Papuc SM, Abela L, Steindl K, Begemann A, Simmons TL, Schmitt B, Zweier M, Oneda B, Socher E, Crowther LM, Wohlrab G, Gogoll L, Poms M, Seiler M, Papik M, Baldinger R, Baumer A, Asadollahi R, Kroell-Seger J, Schmid R, Iff T, Schmitt-Mechelke T, Otten K, Hackenberg A, Addor MC, Klein A, Azzarello-Burri S, Sticht H, Joset P, Plecko B, Rauch A.

Eur J Hum Genet. 2019 Mar;27(3):408-421. doi: 10.1038/s41431-018-0299-8. Epub 2018 Dec 14.

9.

[Review of diagnostic criteria for multiple sclerosis].

Pietruczuk A, Zsybska A, Rejdak K, Papuć E.

Wiad Lek. 2018;71(7):1365-1371. Review. Polish.

PMID:
30448812
10.

Floating-Harbor Syndrome: Presentation of the First Romanian Patient with a SRCAP Mutation and Review of the Literature.

Budisteanu M, Bögershausen N, Papuc SM, Moosa S, Thoenes M, Riga D, Arghir A, Wollnik B.

Balkan J Med Genet. 2018 Oct 29;21(1):83-86. doi: 10.2478/bjmg-2018-0005. eCollection 2018 Jun.

11.

[Stigmatisation of people with dementi].

Mazurek M, Papuć E.

Wiad Lek. 2018;71(6):1275-1278. Review. Polish.

PMID:
30267513
12.

[Dementia - diagnostic and therapeutic problems].

Mazurek M, Papuć E, Rejdak K.

Wiad Lek. 2018;71(6):1235-1238. Polish.

PMID:
30267506
13.

[Paroxysmal dyskinesias - disorder categories, their causes and treatment].

Gontarz M, Papuć E, Rejdak K.

Wiad Lek. 2018;71(5):1056-1060. Review. Polish.

PMID:
30176640
14.

The role of myelin damage in Alzheimer's disease pathology.

Papuć E, Rejdak K.

Arch Med Sci. 2018 Aug 28;16(2):345-351. doi: 10.5114/aoms.2018.76863. eCollection 2020.

16.

New alginate-pullulan-bioactive glass composites with copper oxide for bone tissue regeneration trials.

Popescu RA, Magyari K, Taulescu M, Vulpoi A, Berce C, Bogdan S, Lelescu C, Dreancă A, Tudoran O, Papuc I, Baia L.

J Tissue Eng Regen Med. 2018 Oct;12(10):2112-2121. doi: 10.1002/term.2746. Epub 2018 Aug 16.

PMID:
30070023
17.

[Brain microbleeds - definition, pathophysiology and the consequences].

Mazurek M, Papuć E, Rejdak K.

Wiad Lek. 2018;71(2 pt 2):408-412. Review. Polish.

PMID:
29786594
18.
19.

Novel bioactive glass-AuNP composites for biomedical applications.

Magyari K, Nagy-Simon T, Vulpoi A, Popescu RA, Licarete E, Stefan R, Hernádi K, Papuc I, Baia L.

Mater Sci Eng C Mater Biol Appl. 2017 Jul 1;76:752-759. doi: 10.1016/j.msec.2017.03.138. Epub 2017 Mar 18.

PMID:
28482587
20.

Plasma metabolomics reveals a diagnostic metabolic fingerprint for mitochondrial aconitase (ACO2) deficiency.

Abela L, Spiegel R, Crowther LM, Klein A, Steindl K, Papuc SM, Joset P, Zehavi Y, Rauch A, Plecko B, Simmons TL.

PLoS One. 2017 May 2;12(5):e0176363. doi: 10.1371/journal.pone.0176363. eCollection 2017.

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