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Results by year

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

Year Number of Results
1950 1
1963 1
1965 2
1967 2
1970 2
1971 2
1972 3
1973 1
1974 1
1975 8
1976 2
1977 2
1978 5
1979 6
1980 6
1981 2
1982 4
1983 3
1984 8
1985 7
1986 4
1987 1
1988 4
1989 3
1990 4
1992 2
1993 3
1994 2
1995 1
1996 2
1997 1
1998 3
1999 4
2000 13
2001 7
2002 5
2003 3
2004 6
2005 9
2006 7
2007 14
2008 28
2009 28
2010 19
2011 22
2012 21
2013 25
2014 17
2015 24
2016 27
2017 25
2018 23
2019 48
2020 40
2021 40
2022 51
2023 44
2024 20

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Search Results

614 results

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Page 1
Widespread alterations in systemic immune profile are linked to lung function heterogeneity and airway microbes in cystic fibrosis.
Rossi E, Lausen M, Øbro NF, Colque A, Nielsen BU, Møller R, de Gier C, Hald A, Skov M, Pressler T, Molin S, Ostrowski SR, Marquart HV, Johansen HK. Rossi E, et al. Among authors: moller r. J Cyst Fibros. 2024 May 2:S1569-1993(24)00059-6. doi: 10.1016/j.jcf.2024.04.015. Online ahead of print. J Cyst Fibros. 2024. PMID: 38702223 Free article.
Mono and biallelic variants in HCN2 cause severe neurodevelopmental disorders.
Houdayer C, Phillips AM, Chabbert M, Bourreau J, Maroofian R, Houlden H, Richards K, Saadi NW, Dad'ová E, Van Bogaert P, Rupin M, Keren B, Charles P, Smol T, Riquet A, Pais L, O'Donnell-Luria A, VanNoy GE, Bayat A, Møller RS, Olofsson K, Abou Jamra R, Syrbe S, Dasouki M, Seaver LH, Sullivan JA, Shashi V, Alkuraya FS, Poss AF, Spence JE, Schnur RE, Forster IC, Mckenzie CE, Simons C, Wang M, Snell P, Kothur K, Buckley M, Roscioli T, Elserafy N, Dauriat B, Procaccio V, Henrion D, Lenaers G, Colin E, Verbeek NE, Van Gassen KL, Legendre C, Bonneau D, Reid CA, Howell KB, Ziegler A, Legros C. Houdayer C, et al. Among authors: moller rs. medRxiv [Preprint]. 2024 Mar 22:2024.03.19.24303984. doi: 10.1101/2024.03.19.24303984. medRxiv. 2024. PMID: 38562733 Free PMC article. Preprint.
Clinical and molecular characterization of patients with YWHAG-related epilepsy.
Cetica V, Pisano T, Lesca G, Marafi D, Licchetta L, Riccardi F, Mei D, Chung HB, Bayat A, Balasubramanian M, Lowenstein DH, Endzinienė M, Alotaibi M, Villeneuve N, Jacobs J, Isidor B, Solazzi R, den Hollander NS, Marjanovic D, Rougeot-Jung C, Jung J, Lesieur-Sebellin M, Accogli A, Salpietro V, Saadi NW, Panagiotakaki E, Foiadelli T, Redon S, Tsai MH, Bisulli F, Hammer TB, Lupski JR, Parrini E, Guerrini R; YWHAG Study Group. Cetica V, et al. Epilepsia. 2024 May;65(5):1439-1450. doi: 10.1111/epi.17939. Epub 2024 Mar 16. Epilepsia. 2024. PMID: 38491959
Providing quality care for people with CDKL5 deficiency disorder: A European expert panel opinion on the patient journey.
Amin S, Møller RS, Aledo-Serrano A, Arzimanoglou A, Bager P, Jóźwiak S, Kluger GJ, López-Cabeza S, Nabbout R, Partridge CA, Schubert-Bast S, Specchio N, Kälviäinen R. Amin S, et al. Among authors: moller rs. Epilepsia Open. 2024 Mar 7. doi: 10.1002/epi4.12914. Online ahead of print. Epilepsia Open. 2024. PMID: 38450883 Free article. Review.
Genotype-phenotype associations in 1018 individuals with SCN1A-related epilepsies.
Gallagher D, Pérez-Palma E, Bruenger T, Ghanty I, Brilstra E, Ceulemans B, Chemaly N, de Lange I, Depienne C, Guerrini R, Mei D, Møller RS, Nabbout R, Regan BM, Schneider AL, Scheffer IE, Schoonjans AS, Symonds JD, Weckhuysen S, Zuberi SM, Lal D, Brunklaus A. Gallagher D, et al. Among authors: moller rs. Epilepsia. 2024 Apr;65(4):1046-1059. doi: 10.1111/epi.17882. Epub 2024 Feb 27. Epilepsia. 2024. PMID: 38410936
614 results