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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1953 1
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1960 2
1962 2
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1964 2
1965 2
1966 3
1967 3
1969 8
1970 6
1971 2
1972 4
1973 5
1974 4
1975 10
1976 6
1977 2
1978 5
1979 8
1980 4
1981 2
1982 5
1983 6
1984 2
1985 4
1986 2
1987 7
1988 6
1989 6
1990 10
1991 7
1992 7
1993 13
1994 5
1995 6
1996 5
1997 6
1998 11
1999 8
2000 21
2001 12
2002 18
2003 15
2004 13
2005 22
2006 13
2007 20
2008 20
2009 24
2010 23
2011 36
2012 25
2013 40
2014 39
2015 47
2016 33
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2018 33
2019 37
2020 66
2021 65
2022 71
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2024 59
2025 58
2026 25

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1,049 results

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The following term was not found in PubMed: Milyana
Page 1
Pathology in Practice.
Andrada Borzollino M, María Rambaldi A, Stefanova EP, Paz-Sánchez Y, Acosta B, Díaz-Delgado J, Quesada-Canales O. Andrada Borzollino M, et al. J Am Vet Med Assoc. 2022 May 15;259(S2):1-4. doi: 10.2460/javma.21.02.0098. J Am Vet Med Assoc. 2022. PMID: 35560123 Free article.
Preface.
Stefanova N, Kordower JH, Wenning GK. Stefanova N, et al. Mov Disord. 2016 Feb;31(2):151. doi: 10.1002/mds.26554. Mov Disord. 2016. PMID: 26853078 No abstract available.
Microglia in Parkinson's Disease.
Stefanova N. Stefanova N. J Parkinsons Dis. 2022;12(s1):S105-S112. doi: 10.3233/JPD-223237. J Parkinsons Dis. 2022. PMID: 35754289 Free PMC article. Review.
Upper Lip Reconstruction.
Shipkov H, Stefanova P, Djambazov K, Uchikov A. Shipkov H, et al. Plast Reconstr Surg. 2018 Jul;142(1):102e-103e. doi: 10.1097/PRS.0000000000004510. Plast Reconstr Surg. 2018. PMID: 29952918 No abstract available.
A Boy with Sandestig-Stefanova Syndrome and Genital Abnormalities.
Korulmaz A, Başer B, Alakaya M, Arslanköylü AE. Korulmaz A, et al. Mol Syndromol. 2022 Jul;13(4):343-349. doi: 10.1159/000521331. Epub 2022 Mar 2. Mol Syndromol. 2022. PMID: 36158057 Free PMC article.
INTRODUCTION: Sandestig-Stefanova syndrome is an autosomal recessive developmental syndrome characterized by microcephaly, trigonocephaly, congenital cataracts, microphthalmia, facial findings, camptodactyly, periventricular white matter loss, thin corpus callosum, delayed …
INTRODUCTION: Sandestig-Stefanova syndrome is an autosomal recessive developmental syndrome characterized by microcephaly, trigonocep …
[Autohemotransfusion].
Stefanova A. Stefanova A. Akush Ginekol (Sofiia). 2003;42(4):21-7. Akush Ginekol (Sofiia). 2003. PMID: 14577364 Review. Bulgarian.
Rapid iPSC inclusionopathy models shed light on formation, consequence, and molecular subtype of α-synuclein inclusions.
Lam I, Ndayisaba A, Lewis AJ, Fu Y, Sagredo GT, Kuzkina A, Zaccagnini L, Celikag M, Sandoe J, Sanz RL, Vahdatshoar A, Martin TD, Morshed N, Ichihashi T, Tripathi A, Ramalingam N, Oettgen-Suazo C, Bartels T, Boussouf M, Schäbinger M, Hallacli E, Jiang X, Verma A, Tea C, Wang Z, Hakozaki H, Yu X, Hyles K, Park C, Wang X, Theunissen TW, Wang H, Jaenisch R, Lindquist S, Stevens B, Stefanova N, Wenning G, van de Berg WDJ, Luk KC, Sanchez-Pernaute R, Gómez-Esteban JC, Felsky D, Kiyota Y, Sahni N, Yi SS, Chung CY, Stahlberg H, Ferrer I, Schöneberg J, Elledge SJ, Dettmer U, Halliday GM, Bartels T, Khurana V. Lam I, et al. Neuron. 2025 Feb 19;113(4):637. doi: 10.1016/j.neuron.2025.01.018. Epub 2025 Feb 1. Neuron. 2025. PMID: 39894019 Free PMC article. No abstract available.
[Transfusion management].
Stefanova A. Stefanova A. Akush Ginekol (Sofiia). 2005;44(3):31-5. Akush Ginekol (Sofiia). 2005. PMID: 16028389 Review. Bulgarian.
Reply.
Dimitrova-Mladenova M, Stefanova E. Dimitrova-Mladenova M, et al. J Pediatr. 2017 Apr;183:203. doi: 10.1016/j.jpeds.2016.12.024. Epub 2016 Dec 30. J Pediatr. 2017. PMID: 28043683 No abstract available.
1,049 results