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

Year Number of Results
1966 1
1967 1
1968 1
1971 2
1972 2
1973 1
1974 3
1975 5
1977 1
1979 3
1981 4
1982 2
1983 4
1985 1
1986 1
1987 2
1988 2
1991 2
1992 1
1993 1
1997 1
1998 1
1999 1
2000 3
2002 1
2007 1
2010 1
2011 1
2013 2
2014 2
2015 2
2018 1
2019 4
2020 1
2021 2
2023 1
2024 1

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62 results

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Page 1
Evidence-based medicine.
Procopis PG. Procopis PG. Dev Med Child Neurol. 2002 Jul;44(7):435. doi: 10.1017/s001216220100233x. Dev Med Child Neurol. 2002. PMID: 12162380 Free article. No abstract available.
DHDDS and NUS1: A Converging Pathway and Common Phenotype.
Williams LJ, Waller S, Qiu J, Innes E, Elserafy N, Procopis P, Sampaio H, Mahant N, Tchan MC, Mohammad SS, Morales-Briceño H, Fung VSC. Williams LJ, et al. Among authors: procopis p. Mov Disord Clin Pract. 2024 Jan;11(1):76-85. doi: 10.1002/mdc3.13920. Epub 2023 Nov 28. Mov Disord Clin Pract. 2024. PMID: 38291835 Review.
Complication of circumcision.
Procopis PG, Kewley GD. Procopis PG, et al. Med J Aust. 1982 Jan 9;1(1):15. doi: 10.5694/j.1326-5377.1982.tb132115.x. Med J Aust. 1982. PMID: 7038414 No abstract available.
The spectrum of intermediate SCN8A-related epilepsy.
Johannesen KM, Gardella E, Encinas AC, Lehesjoki AE, Linnankivi T, Petersen MB, Lund ICB, Blichfeldt S, Miranda MJ, Pal DK, Lascelles K, Procopis P, Orsini A, Bonuccelli A, Giacomini T, Helbig I, Fenger CD, Sisodiya SM, Hernandez-Hernandez L, Krithika S, Rumple M, Masnada S, Valente M, Cereda C, Giordano L, Accorsi P, Bürki SE, Mancardi M, Korff C, Guerrini R, von Spiczak S, Hoffman-Zacharska D, Mazurczak T, Coppola A, Buono S, Vecchi M, Hammer MF, Varesio C, Veggiotti P, Lal D, Brünger T, Zara F, Striano P, Rubboli G, Møller RS. Johannesen KM, et al. Among authors: procopis p. Epilepsia. 2019 May;60(5):830-844. doi: 10.1111/epi.14705. Epub 2019 Apr 10. Epilepsia. 2019. PMID: 30968951
NAD(P)HX dehydratase (NAXD) deficiency: a novel neurodegenerative disorder exacerbated by febrile illnesses.
Van Bergen NJ, Guo Y, Rankin J, Paczia N, Becker-Kettern J, Kremer LS, Pyle A, Conrotte JF, Ellaway C, Procopis P, Prelog K, Homfray T, Baptista J, Baple E, Wakeling M, Massey S, Kay DP, Shukla A, Girisha KM, Lewis LES, Santra S, Power R, Daubeney P, Montoya J, Ruiz-Pesini E, Kovacs-Nagy R, Pritsch M, Ahting U, Thorburn DR, Prokisch H, Taylor RW, Christodoulou J, Linster CL, Ellard S, Hakonarson H. Van Bergen NJ, et al. Among authors: procopis p. Brain. 2019 Jan 1;142(1):50-58. doi: 10.1093/brain/awy310. Brain. 2019. PMID: 30576410
Delayed motor development.
Procopis PG. Procopis PG. Med J Aust. 1977 Aug 20;2(8):251-3. doi: 10.5694/j.1326-5377.1977.tb117650.x. Med J Aust. 1977. PMID: 71651 No abstract available.
Benign acute childhood myositis.
Antony JH, Procopis PG, Ouvrier RA. Antony JH, et al. Among authors: procopis pg. Neurology. 1979 Jul;29(7):1068-71. doi: 10.1212/wnl.29.7.1068. Neurology. 1979. PMID: 572938
Clinical features of conversion disorder.
Grattan-Smith P, Fairley M, Procopis P. Grattan-Smith P, et al. Among authors: procopis p. Arch Dis Child. 1988 Apr;63(4):408-14. doi: 10.1136/adc.63.4.408. Arch Dis Child. 1988. PMID: 3365011 Free PMC article.
Febrile convulsions.
Procopis PG. Procopis PG. Aust Fam Physician. 1983 Sep;12(9):699-701. Aust Fam Physician. 1983. PMID: 6418124 No abstract available.
NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns.
Stamberger H, Hammer TB, Gardella E, Vlaskamp DRM, Bertelsen B, Mandelstam S, de Lange I, Zhang J, Myers CT, Fenger C, Afawi Z, Almanza Fuerte EP, Andrade DM, Balcik Y, Ben Zeev B, Bennett MF, Berkovic SF, Isidor B, Bouman A, Brilstra E, Busk ØL, Cairns A, Caumes R, Chatron N, Dale RC, de Geus C, Edery P, Gill D, Granild-Jensen JB, Gunderson L, Gunning B, Heimer G, Helle JR, Hildebrand MS, Hollingsworth G, Kharytonov V, Klee EW, Koeleman BPC, Koolen DA, Korff C, Küry S, Lesca G, Lev D, Leventer RJ, Mackay MT, Macke EL, McEntagart M, Mohammad SS, Monin P, Montomoli M, Morava E, Moutton S, Muir AM, Parrini E, Procopis P, Ranza E, Reed L, Reif PS, Rosenow F, Rossi M, Sadleir LG, Sadoway T, Schelhaas HJ, Schneider AL, Shah K, Shalev R, Sisodiya SM, Smol T, Stumpel CTRM, Stuurman K, Symonds JD, Mau-Them FT, Verbeek N, Verhoeven JS, Wallace G, Yosovich K, Zarate YA, Zerem A, Zuberi SM, Guerrini R, Mefford HC, Patel C, Zhang YH, Møller RS, Scheffer IE. Stamberger H, et al. Among authors: procopis p. Genet Med. 2021 Feb;23(2):363-373. doi: 10.1038/s41436-020-00988-9. Epub 2020 Nov 4. Genet Med. 2021. PMID: 33144681 Free article.
62 results