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Genome-wide association study across pediatric central nervous system tumors implicates shared predisposition and points to 1q25.2 (PAPPA2) and 11p12 (LRRC4C) as novel candidate susceptibility loci.
Foss-Skiftesvik J, Hagen CM, Mathiasen R, Adamsen D, Bækvad-Hansen M, Børglum AD, Nordentoft M, Werge T, Christiansen M, Schmiegelow K, Juhler M, Mortensen PB, Hougaard DM, Bybjerg-Grauholm J. Foss-Skiftesvik J, et al. Among authors: schmiegelow k. Childs Nerv Syst. 2021 Mar;37(3):819-830. doi: 10.1007/s00381-020-04946-3. Epub 2020 Nov 23. Childs Nerv Syst. 2021. PMID: 33226468
Cerebellar mutism: review of the literature.
Gudrunardottir T, Sehested A, Juhler M, Schmiegelow K. Gudrunardottir T, et al. Among authors: schmiegelow k. Childs Nerv Syst. 2011 Mar;27(3):355-63. doi: 10.1007/s00381-010-1328-2. Childs Nerv Syst. 2011. PMID: 21061011 Review.
Cerebellar mutism: incidence, risk factors and prognosis.
Gudrunardottir T, Sehested A, Juhler M, Schmiegelow K. Gudrunardottir T, et al. Among authors: schmiegelow k. Childs Nerv Syst. 2011 Apr;27(4):513-4; author reply 515. doi: 10.1007/s00381-010-1383-8. Epub 2011 Feb 12. Childs Nerv Syst. 2011. PMID: 21318616 No abstract available.
Cerebellar mutism: definitions, classification and grading of symptoms.
Gudrunardottir T, Sehested A, Juhler M, Grill J, Schmiegelow K. Gudrunardottir T, et al. Among authors: schmiegelow k. Childs Nerv Syst. 2011 Sep;27(9):1361-3. doi: 10.1007/s00381-011-1509-7. Epub 2011 Jul 6. Childs Nerv Syst. 2011. PMID: 21732118 No abstract available.
Cerebellar mutism syndrome in children with brain tumours of the posterior fossa.
Wibroe M, Cappelen J, Castor C, Clausen N, Grillner P, Gudrunardottir T, Gupta R, Gustavsson B, Heyman M, Holm S, Karppinen A, Klausen C, Lönnqvist T, Mathiasen R, Nilsson P, Nysom K, Persson K, Rask O, Schmiegelow K, Sehested A, Thomassen H, Tonning-Olsson I, Zetterqvist B, Juhler M. Wibroe M, et al. Among authors: schmiegelow k. BMC Cancer. 2017 Jun 21;17(1):439. doi: 10.1186/s12885-017-3416-0. BMC Cancer. 2017. PMID: 28637445 Free PMC article. Clinical Trial.
Nationwide germline whole genome sequencing of 198 consecutive pediatric cancer patients reveals a high incidence of cancer prone syndromes.
Byrjalsen A, Hansen TVO, Stoltze UK, Mehrjouy MM, Barnkob NM, Hjalgrim LL, Mathiasen R, Lautrup CK, Gregersen PA, Hasle H, Wehner PS, Tuckuviene R, Sackett PW, Laspiur AO, Rossing M, Marvig RL, Tommerup N, Olsen TE, Scheie D, Gupta R, Gerdes AM, Schmiegelow K, Wadt K. Byrjalsen A, et al. Among authors: schmiegelow k. PLoS Genet. 2020 Dec 17;16(12):e1009231. doi: 10.1371/journal.pgen.1009231. eCollection 2020 Dec. PLoS Genet. 2020. PMID: 33332384 Free PMC article.
604 results