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Results by year

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

Year Number of Results
1948 1
1955 1
1961 1
1964 3
1966 1
1967 3
1968 1
1969 6
1970 4
1971 9
1972 15
1973 10
1974 4
1975 12
1976 9
1977 14
1978 9
1979 5
1980 11
1981 2
1982 3
1983 5
1984 6
1985 4
1986 2
1987 1
1988 1
1990 2
1991 2
1992 3
1993 15
1994 18
1995 11
1996 8
1997 7
1998 12
1999 3
2000 6
2001 6
2002 4
2003 11
2004 5
2005 5
2006 9
2007 7
2008 12
2009 16
2010 17
2011 16
2012 12
2013 11
2014 6
2015 9
2016 12
2017 13
2018 11
2019 14
2020 5
2021 14
2022 11
2023 14
2024 7

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450 results

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Page 1
Mutational spectrum of DMD mutations in dystrophinopathy patients: application of modern diagnostic techniques to a large cohort.
Flanigan KM, Dunn DM, von Niederhausern A, Soltanzadeh P, Gappmaier E, Howard MT, Sampson JB, Mendell JR, Wall C, King WM, Pestronk A, Florence JM, Connolly AM, Mathews KD, Stephan CM, Laubenthal KS, Wong BL, Morehart PJ, Meyer A, Finkel RS, Bonnemann CG, Medne L, Day JW, Dalton JC, Margolis MK, Hinton VJ; United Dystrophinopathy Project Consortium; Weiss RB. Flanigan KM, et al. Among authors: margolis mk. Hum Mutat. 2009 Dec;30(12):1657-66. doi: 10.1002/humu.21114. Hum Mutat. 2009. PMID: 19937601 Free PMC article.
Reply.
Alfawaz AM, Holland GN, Yu F, Margolis MS, Giaconi JA, Aldave AJ. Alfawaz AM, et al. Among authors: margolis ms. Ophthalmology. 2017 Apr;124(4):e44. doi: 10.1016/j.ophtha.2016.08.010. Ophthalmology. 2017. PMID: 28335959 No abstract available.
Radiology rounds. Osteochondroma.
Margolis M, McLennan MK. Margolis M, et al. Can Fam Physician. 1995 Feb;41:216, 220-2. Can Fam Physician. 1995. PMID: 7734994 Free PMC article. Review. No abstract available.
Postpneumonectomy and postlobectomy empyema.
Gharagozloo F, Margolis M, Facktor M, Tempesta B, Najam F. Gharagozloo F, et al. Among authors: margolis m. Thorac Surg Clin. 2006 Aug;16(3):215-22. doi: 10.1016/j.thorsurg.2006.05.012. Thorac Surg Clin. 2006. PMID: 17004549 Review.
Genotypic and phenotypic spectrum of infantile liver failure due to pathogenic TRMU variants.
Vogel GF, Mozer-Glassberg Y, Landau YE, Schlieben LD, Prokisch H, Feichtinger RG, Mayr JA, Brennenstuhl H, Schröter J, Pechlaner A, Alkuraya FS, Baker JJ, Barcia G, Baric I, Braverman N, Burnyte B, Christodoulou J, Ciara E, Coman D, Das AM, Darin N, Della Marina A, Distelmaier F, Eklund EA, Ersoy M, Fang W, Gaignard P, Ganetzky RD, Gonzales E, Howard C, Hughes J, Konstantopoulou V, Kose M, Kerr M, Khan A, Lenz D, McFarland R, Margolis MG, Morrison K, Müller T, Murayama K, Nicastro E, Pennisi A, Peters H, Piekutowska-Abramczuk D, Rötig A, Santer R, Scaglia F, Schiff M, Shagrani M, Sharrard M, Soler-Alfonso C, Staufner C, Storey I, Stormon M, Taylor RW, Thorburn DR, Teles EL, Wang JS, Weghuber D, Wortmann S. Vogel GF, et al. Among authors: margolis mg. Genet Med. 2023 Jun;25(6):100314. doi: 10.1016/j.gim.2022.09.015. Epub 2022 Oct 29. Genet Med. 2023. PMID: 36305855 Free article.
Genotypic and phenotypic spectrum of infantile liver failure due to pathogenic TRMU variants.
Vogel GF, Mozer-Glassberg Y, Landau YE, Schlieben LD, Prokisch H, Feichtinger RG, Mayr JA, Brennenstuhl H, Schröter J, Pechlaner A, Alkuraya FS, Baker JJ, Barcia G, Baric I, Braverman N, Burnyte B, Christodoulou J, Ciara E, Coman D, Das AM, Darin N, Della Marina A, Distelmaier F, Eklund EA, Ersoy M, Fang W, Gaignard P, Ganetzky RD, Gonzales E, Howard C, Hughes J, Konstantopoulou V, Kose M, Kerr M, Khan A, Lenz D, McFarland R, Margolis MG, Morrison K, Müller T, Murayama K, Nicastro E, Pennisi A, Peters H, Piekutowska-Abramczuk D, Rötig A, Santer R, Scaglia F, Schiff M, Shagrani M, Sharrard M, Soler-Alfonso C, Staufner C, Storey I, Stormon M, Taylor RW, Thorburn DR, Teles EL, Wang JS, Weghuber D, Wortmannd S. Vogel GF, et al. Among authors: margolis mg. Genet Med. 2023 Jun;25(6):100828. doi: 10.1016/j.gim.2023.100828. Epub 2023 Apr 13. Genet Med. 2023. PMID: 37272928 Free article. No abstract available.
450 results