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Results by year

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

Year Number of Results
1955 1
1960 1
1969 1
1970 3
1971 1
1974 2
1975 3
1976 3
1977 1
1978 3
1979 2
1980 4
1981 4
1982 4
1983 8
1984 8
1985 8
1986 5
1987 4
1988 5
1989 11
1990 8
1991 10
1992 7
1993 13
1994 14
1995 14
1996 16
1997 12
1998 12
1999 13
2000 13
2001 15
2002 11
2003 19
2004 18
2005 29
2006 29
2007 30
2008 23
2009 39
2010 29
2011 28
2012 30
2013 28
2014 35
2015 43
2016 37
2017 36
2018 34
2019 34
2020 51
2021 44
2022 42
2023 32
2024 12

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Search Results

844 results

Results by year

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Page 1
Blood-based biomarkers for Alzheimer's disease: towards clinical implementation.
Teunissen CE, Verberk IMW, Thijssen EH, Vermunt L, Hansson O, Zetterberg H, van der Flier WM, Mielke MM, Del Campo M. Teunissen CE, et al. Among authors: del campo m. Lancet Neurol. 2022 Jan;21(1):66-77. doi: 10.1016/S1474-4422(21)00361-6. Epub 2021 Nov 24. Lancet Neurol. 2022. PMID: 34838239 Review.
Walking improvement in chronic incomplete spinal cord injury with exoskeleton robotic training (WISE): a randomized controlled trial.
Edwards DJ, Forrest G, Cortes M, Weightman MM, Sadowsky C, Chang SH, Furman K, Bialek A, Prokup S, Carlow J, VanHiel L, Kemp L, Musick D, Campo M, Jayaraman A. Edwards DJ, et al. Among authors: campo m. Spinal Cord. 2022 Jun;60(6):522-532. doi: 10.1038/s41393-022-00751-8. Epub 2022 Jan 29. Spinal Cord. 2022. PMID: 35094007 Free PMC article. Clinical Trial.
CSF proteome profiling reveals biomarkers to discriminate dementia with Lewy bodies from Alzheimer´s disease.
Del Campo M, Vermunt L, Peeters CFW, Sieben A, Hok-A-Hin YS, Lleó A, Alcolea D, van Nee M, Engelborghs S, van Alphen JL, Arezoumandan S, Chen-Plotkin A, Irwin DJ, van der Flier WM, Lemstra AW, Teunissen CE. Del Campo M, et al. Nat Commun. 2023 Sep 13;14(1):5635. doi: 10.1038/s41467-023-41122-y. Nat Commun. 2023. PMID: 37704597 Free PMC article.
Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann-Steiner syndrome.
Sheppard SE, Campbell IM, Harr MH, Gold N, Li D, Bjornsson HT, Cohen JS, Fahrner JA, Fatemi A, Harris JR, Nowak C, Stevens CA, Grand K, Au M, Graham JM Jr, Sanchez-Lara PA, Campo MD, Jones MC, Abdul-Rahman O, Alkuraya FS, Bassetti JA, Bergstrom K, Bhoj E, Dugan S, Kaplan JD, Derar N, Gripp KW, Hauser N, Innes AM, Keena B, Kodra N, Miller R, Nelson B, Nowaczyk MJ, Rahbeeni Z, Ben-Shachar S, Shieh JT, Slavotinek A, Sobering AK, Abbott MA, Allain DC, Amlie-Wolf L, Au PYB, Bedoukian E, Beek G, Barry J, Berg J, Bernstein JA, Cytrynbaum C, Chung BH, Donoghue S, Dorrani N, Eaton A, Flores-Daboub JA, Dubbs H, Felix CA, Fong CT, Fung JLF, Gangaram B, Goldstein A, Greenberg R, Ha TK, Hersh J, Izumi K, Kallish S, Kravets E, Kwok PY, Jobling RK, Knight Johnson AE, Kushner J, Lee BH, Levin B, Lindstrom K, Manickam K, Mardach R, McCormick E, McLeod DR, Mentch FD, Minks K, Muraresku C, Nelson SF, Porazzi P, Pichurin PN, Powell-Hamilton NN, Powis Z, Ritter A, Rogers C, Rohena L, Ronspies C, Schroeder A, Stark Z, Starr L, Stoler J, Suwannarat P, Velinov M, Weksberg R, Wilnai Y, Zadeh N, Zand DJ, Falk MJ, Hakonarson H, Zackai EH, Quintero-Rivera F. Sheppard SE, et al. Among authors: campo md. Am J Med Genet A. 2021 Jun;185(6):1649-1665. doi: 10.1002/ajmg.a.62124. Epub 2021 Mar 30. Am J Med Genet A. 2021. PMID: 33783954 Free PMC article.
Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signaling.
Holtz AM, VanCoillie R, Vansickle EA, Carere DA, Withrow K, Torti E, Juusola J, Millan F, Person R, Guillen Sacoto MJ, Si Y, Wentzensen IM, Pugh J, Vasileiou G, Rieger M, Reis A, Argilli E, Sherr EH, Aldinger KA, Dobyns WB, Brunet T, Hoefele J, Wagner M, Haber B, Kotzaeridou U, Keren B, Heron D, Mignot C, Heide S, Courtin T, Buratti J, Murugasen S, Donald KA, O'Heir E, Moody S, Kim KH, Burton BK, Yoon G, Campo MD, Masser-Frye D, Kozenko M, Parkinson C, Sell SL, Gordon PL, Prokop JW, Karaa A, Bupp C, Raby BA. Holtz AM, et al. Among authors: campo md. Genet Med. 2022 Oct;24(10):2065-2078. doi: 10.1016/j.gim.2022.07.005. Epub 2022 Aug 18. Genet Med. 2022. PMID: 35980381 Free PMC article.
Editorial: Performance enhancement in rugby.
Carson F, Scott T, Campo M, Hamlin MJ. Carson F, et al. Among authors: campo m. Front Sports Act Living. 2023 May 9;5:1212390. doi: 10.3389/fspor.2023.1212390. eCollection 2023. Front Sports Act Living. 2023. PMID: 37229361 Free PMC article. No abstract available.
CSF proteomics in autosomal dominant Alzheimer's disease highlights parallels with sporadic disease.
van der Ende EL, In 't Veld SGJG, Hanskamp I, van der Lee S, Dijkstra JIR, Hok-A-Hin YS, Blujdea ER, van Swieten JC, Irwin DJ, Chen-Plotkin A, Hu WT, Lemstra AW, Pijnenburg YAL, van der Flier WM, Del Campo M, Teunissen CE, Vermunt L. van der Ende EL, et al. Among authors: del campo m. Brain. 2023 Nov 2;146(11):4495-4507. doi: 10.1093/brain/awad213. Brain. 2023. PMID: 37348871 Free PMC article.
Hemophagocytic Lymphohistiocytosis in Adults.
Campo M, Berliner N. Campo M, et al. Hematol Oncol Clin North Am. 2015 Oct;29(5):915-25. doi: 10.1016/j.hoc.2015.06.009. Epub 2015 Aug 14. Hematol Oncol Clin North Am. 2015. PMID: 26461151 Review.
CSF proteome profiling across the Alzheimer's disease spectrum reflects the multifactorial nature of the disease and identifies specific biomarker panels.
Del Campo M, Peeters CFW, Johnson ECB, Vermunt L, Hok-A-Hin YS, van Nee M, Chen-Plotkin A, Irwin DJ, Hu WT, Lah JJ, Seyfried NT, Dammer EB, Herradon G, Meeter LH, van Swieten J, Alcolea D, Lleó A, Levey AI, Lemstra AW, Pijnenburg YAL, Visser PJ, Tijms BM, van der Flier WM, Teunissen CE. Del Campo M, et al. Nat Aging. 2022 Nov;2(11):1040-1053. doi: 10.1038/s43587-022-00300-1. Epub 2022 Nov 10. Nat Aging. 2022. PMID: 37118088 Free PMC article.
844 results