Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2007 | 1 |
2018 | 1 |
2019 | 2 |
2021 | 1 |
2022 | 1 |
2023 | 2 |
2024 | 0 |
Search Results
6 results
Results by year
Filters applied: . Clear all
It looks like you are searching for an author.
Results are currently sorted by Best Match. To see the newest results first,
change the sort order to Most Recent.
Page 1
Group A streptococcal disease in paediatric inpatients: a European perspective.
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.
Congenital Diarrhea and Cholestatic Liver Disease: Phenotypic Spectrum Associated with MYO5B Mutations.
Aldrian D, Vogel GF, Frey TK, Ayyıldız Civan H, Aksu AÜ, Avitzur Y, Ramos Boluda E, Çakır M, Demir AM, Deppisch C, Duba HC, Düker G, Gerner P, Hertecant J, Hornová J, Kathemann S, Koeglmeier J, Koutroumpa A, Lanzersdorfer R, Lev-Tzion R, Lima R, Mansour S, Meissl M, Melek J, Miqdady M, Montoya JH, Posovszky C, Rachman Y, Siahanidou T, Tabbers M, Uhlig HH, Ünal S, Wirth S, Ruemmele FM, Hess MW, Huber LA, Müller T, Sturm E, Janecke AR.
Aldrian D, et al. Among authors: meissl m.
J Clin Med. 2021 Jan 28;10(3):481. doi: 10.3390/jcm10030481.
J Clin Med. 2021.
PMID: 33525641
Free PMC article.
Item in Clipboard
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.
Item in Clipboard
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.
Item in Clipboard
Somatic mosaic monosomy 7 and UPD7q in a child with MIRAGE syndrome caused by a novel SAMD9 mutation.
Csillag B, Ilencikova D, Meissl M, Webersinke G, Laccone F, Narumi S, Haas O, Duba HC.
Csillag B, et al. Among authors: meissl m.
Pediatr Blood Cancer. 2019 Apr;66(4):e27589. doi: 10.1002/pbc.27589. Epub 2018 Dec 19.
Pediatr Blood Cancer. 2019.
PMID: 30565860
Item in Clipboard
Protein C promoter polymorphisms associate with sepsis in children with systemic meningococcemia.
Binder A, Endler G, Rieger S, Geishofer G, Resch B, Mannhalter C, Zenz W; Central European Meningococcal Genetic Study Group.
Binder A, et al.
Hum Genet. 2007 Sep;122(2):183-90. doi: 10.1007/s00439-007-0392-5. Epub 2007 Jun 14.
Hum Genet. 2007.
PMID: 17569089
Item in Clipboard
Cite
Cite