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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2020 | 1 |
2021 | 4 |
2022 | 2 |
2023 | 1 |
2024 | 0 |
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Page 1
Re-emerging concepts of immune dysregulation in autism spectrum disorders.
Front Psychiatry. 2022 Oct 19;13:1006612. doi: 10.3389/fpsyt.2022.1006612. eCollection 2022.
Front Psychiatry. 2022.
PMID: 36339838
Free PMC article.
Review.
Autistic Behavior as Novel Clinical Finding in OFD1 Syndrome.
Papuc SM, Erbescu A, Glangher A, Streata I, Riza AL, Budisteanu M, Arghir A.
Papuc SM, et al. Among authors: erbescu a.
Genes (Basel). 2023 Jan 27;14(2):327. doi: 10.3390/genes14020327.
Genes (Basel). 2023.
PMID: 36833254
Free PMC article.
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The Phenotypic Spectrum of 15q13.3 Region Duplications: Report of 5 Patients.
Budisteanu M, Papuc SM, Streata I, Cucu M, Pirvu A, Serban-Sosoi S, Erbescu A, Andrei E, Iliescu C, Ioana D, Severin E, Ioana M, Arghir A.
Budisteanu M, et al. Among authors: erbescu a.
Genes (Basel). 2021 Jul 1;12(7):1025. doi: 10.3390/genes12071025.
Genes (Basel). 2021.
PMID: 34356041
Free PMC article.
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Clinical and genomic findings in brain heterotopia: Report of a pediatric patient cohort from Romania.
Budisteanu M, Papuc SM, Erbescu A, Iliescu C, Dobre M, Barca D, Tarta-Arsene O, Motoescu C, Dica A, Sandu C, Anghelescu C, Craiu D, Arghir A.
Budisteanu M, et al. Among authors: erbescu a.
Exp Ther Med. 2022 Jan;23(1):101. doi: 10.3892/etm.2021.11024. Epub 2021 Dec 1.
Exp Ther Med. 2022.
PMID: 34976143
Free PMC article.
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Delineation of Molecular Lesions in Acute Myeloid Leukemia Patients at Diagnosis: Integrated Next Generation Sequencing and Cytogenomic Studies.
Papuc SM, Erbescu A, Cisleanu D, Ozunu D, Enache C, Dumitru I, Lupoaia Andrus E, Gaman M, Popov VM, Dobre M, Stanca O, Angelescu S, Berbec N, Colita A, Vladareanu AM, Bumbea H, Arghir A.
Papuc SM, et al. Among authors: erbescu a.
Genes (Basel). 2021 May 30;12(6):846. doi: 10.3390/genes12060846.
Genes (Basel). 2021.
PMID: 34070898
Free PMC article.
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Autism and severe clinical phenotype in a patient with 8p21.2p11.21 deletion: Case report and literature review.
Arghir A, Papuc SM, Tutulan-Cunita AC, Erbescu A, Loddo S, Genovese S, Ciocca L, Goldoni M, Piscopo C, Bernardini L, Novelli A, Budisteanu M.
Arghir A, et al. Among authors: erbescu a.
Clin Case Rep. 2020 Nov 12;9(1):314-321. doi: 10.1002/ccr3.3523. eCollection 2021 Jan.
Clin Case Rep. 2020.
PMID: 33505690
Free PMC article.
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