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

Year Number of Results
1990 1
1991 1
1992 1
1993 3
1994 2
1997 1
1999 1
2000 1
2001 2
2002 3
2003 1
2006 1
2007 2
2013 1
2019 1
2022 1
2023 2
2024 0

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24 results

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Page 1
Group A streptococcal disease in paediatric inpatients: a European perspective.
Boeddha NP, Atkins L, de Groot R, Driessen G, Hazelzet J, Zenz W, Carrol ED, Anderson ST, Martinon-Torres F, Agyeman PKA, Galassini R, Herberg J, Levin M, Schlapbach LJ, Emonts M; EUCLIDS consortium. Boeddha NP, et al. Eur J Pediatr. 2023 Feb;182(2):697-706. doi: 10.1007/s00431-022-04718-y. Epub 2022 Nov 30. Eur J Pediatr. 2023. PMID: 36449079 Free PMC article.
Correction to: Group A streptococcal disease in paediatric inpatients: a European perspective.
Boeddha NP, Atkins L, de Groot R, Driessen G, Hazelzet J, Zenz W, Carrol ED, Anderson ST, Martinon-Torres F, Agyeman PKA, Galassini R, Herberg J, Levin M, Schlapbach LJ, Emonts M; EUCLIDS consortium. Boeddha NP, et al. Eur J Pediatr. 2023 Feb;182(2):707. doi: 10.1007/s00431-022-04787-z. Eur J Pediatr. 2023. PMID: 36689004 Free PMC article. No abstract available.
Does migraine-related stroke occur in childhood?
Rossi LN, Penzien JM, Deonna T, Goutières F, Vassella F. Rossi LN, et al. Among authors: penzien jm. Dev Med Child Neurol. 1990 Nov;32(11):1016-21. doi: 10.1111/j.1469-8749.1990.tb08126.x. Dev Med Child Neurol. 1990. PMID: 1702743
Identification of regulatory variants associated with genetic susceptibility to meningococcal disease.
Borghini L, Png E, Binder A, Wright VJ, Pinnock E, de Groot R, Hazelzet J, Emonts M, Van der Flier M, Schlapbach LJ, Anderson S, Secka F, Salas A, Fink C, Carrol ED, Pollard AJ, Coin LJ, Kuijpers TW, Martinon-Torres F, Zenz W, Levin M, Hibberd ML, Davila S; EUCLIDS consortium. Borghini L, et al. Sci Rep. 2019 May 6;9(1):6966. doi: 10.1038/s41598-019-43292-6. Sci Rep. 2019. PMID: 31061469 Free PMC article.
MRI in Smith-Lemli-Opitz syndrome type 1.
Penzien JM, Hoffmann GF. Penzien JM, et al. Childs Nerv Syst. 1997 Oct;13(10):505-6. doi: 10.1007/s003810050125. Childs Nerv Syst. 1997. PMID: 9403196 No abstract available.
Opsoclonus polymyoclonia syndrome.
Penzien JM, Speck S, Vassella F. Penzien JM, et al. Acta Paediatr. 1993 Mar;82(3):319-20. doi: 10.1111/j.1651-2227.1993.tb12672.x. Acta Paediatr. 1993. PMID: 8495095 No abstract available.
The diagnosis of mitochondrial HMG-CoA synthase deficiency.
Zschocke J, Penzien JM, Bielen R, Casals N, Aledo R, Pié J, Hoffmann GF, Hegardt FG, Mayatepek E. Zschocke J, et al. Among authors: penzien jm. J Pediatr. 2002 Jun;140(6):778-80. doi: 10.1067/mpd.2002.123854. J Pediatr. 2002. PMID: 12072887
Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders.
Travaglini L, Brancati F, Silhavy J, Iannicelli M, Nickerson E, Elkhartoufi N, Scott E, Spencer E, Gabriel S, Thomas S, Ben-Zeev B, Bertini E, Boltshauser E, Chaouch M, Cilio MR, de Jong MM, Kayserili H, Ogur G, Poretti A, Signorini S, Uziel G, Zaki MS; International JSRD Study Group; Johnson C, Attié-Bitach T, Gleeson JG, Valente EM. Travaglini L, et al. Eur J Hum Genet. 2013 Oct;21(10):1074-8. doi: 10.1038/ejhg.2012.305. Epub 2013 Feb 6. Eur J Hum Genet. 2013. PMID: 23386033 Free PMC article.
24 results