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Results by year

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

Year Number of Results
1973 1
1976 1
1977 2
1978 2
1980 2
1981 1
1982 3
1986 2
1987 1
1988 2
1989 1
1990 2
1991 2
1992 5
1993 4
1994 5
1995 7
1996 6
1997 7
1998 9
1999 7
2000 7
2001 5
2002 4
2003 5
2004 7
2005 5
2006 9
2007 8
2008 5
2009 3
2010 8
2011 6
2012 9
2013 13
2014 10
2015 3
2016 4
2017 9
2018 3
2019 4
2020 2
2021 4
2022 6
2023 3
2024 1

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Publication date

PubMed for id: 322038

197 results

Results by year

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Page 1
Transcriptional response of the heart to vagus nerve stimulation.
Kellett DO, Aziz Q, Humphries JD, Korsak A, Braga A, Gutierrez Del Arroyo A, Crescente M, Tinker A, Ackland GL, Gourine AV. Kellett DO, et al. Physiol Genomics. 2024 Feb 1;56(2):167-178. doi: 10.1152/physiolgenomics.00095.2023. Epub 2023 Dec 4. Physiol Genomics. 2024. PMID: 38047311 Free PMC article.
Ophthalmic Manifestations of ROSAH (Retinal Dystrophy, Optic Nerve Edema, Splenomegaly, Anhidrosis, and Headache) Syndrome, an Inherited NF κB-Mediated Autoinflammatory Disease with Retinal Dystrophy.
Huryn LA, Kozycki CT, Serpen JY, Zein WM, Ullah E, Iannaccone A, Williams LB, Sobrin L, Brooks BP, Sen HN, Hufnagel RB, Kastner DL, Kodati S. Huryn LA, et al. Ophthalmology. 2023 Apr;130(4):423-432. doi: 10.1016/j.ophtha.2022.10.026. Epub 2022 Nov 2. Ophthalmology. 2023. PMID: 36332842 Free PMC article.
A founder mutation in the GMPPB gene [c.1000G > A (p.Asp334Asn)] causes a mild form of limb-girdle muscular dystrophy/congenital myasthenic syndrome (LGMD/CMS) in South Indian patients.
Polavarapu K, Mathur A, Joshi A, Nashi S, Preethish-Kumar V, Bardhan M, Sharma P, Parveen S, Seth M, Vengalil S, Chawla T, Shingavi L, Shamim U, Nayak S, Vivekanand A, Töpf A, Roos A, Horvath R, Lochmüller H, Nandeesh B, Arunachal G, Nalini A, Faruq M. Polavarapu K, et al. Neurogenetics. 2021 Oct;22(4):271-285. doi: 10.1007/s10048-021-00658-1. Epub 2021 Aug 1. Neurogenetics. 2021. PMID: 34333724
197 results