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Clustering of mutations in the 5 tertile of the NF1 gene in Slovakia patients with optic pathway glioma.

  1. TitleClustering of mutations in the 5 tertile of the NF1 gene in Slovakia patients with optic pathway glioma.
    Author Bolčeková Anna
    Co-authors Némethová Martina 1986- SAVMOFYZ - Ústav molekulárnej fyziológie a genetiky SAV

    Another authors Zaťková Andrea 1971- (Author) SAVMOFYZ - Ústav molekulárnej fyziológie a genetiky SAV    SCOPUS    RID    ORCID

    Hlinková K. (Author)

    Pozgayová S. (Author)

    Hlavatá A. (Author)

    Kádaši Ľudevít 1952- (Author) SAVMOFYZ - Ústav molekulárnej fyziológie a genetiky SAV    ORCID

    Ďurovčíková Darina (Author)

    Gerinec A (Author)

    Husáková K (Author)

    Pavlovičová Z. (Author)

    Holobrada M. (Author)

    Kovács László (Author)

    Ilenčíková Denisa (Author)

    Source document Neoplasma. Vol. 60, no.6 (2013), p. 655-665
    Languageeng - English
    NoteITMS 26240220058, ITMS 26240220071, VEGA 2/0104/10, KEGA 003UK-4/2012
    Document kindrozpis článkov z periodík (rbx)
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    HUTTER, Sonja - PIRO, Rosario M. - WASZAK, Sebastian M. - KEHRER-SAWATZKI, Hildegard - FRIEDRICH, Reinhard E. - LASSALETTA, Alvaro - WITT, Olaf - KORBEL, Jan O. - LICHTER, Peter - SCHUHMANN, Martin U. - PFISTER, Stefan M. - TABORI, Uri - MAUTNER, Victor F. - JONES, David T. W. No correlation between NF1 mutation position and risk of optic pathway glioma in 77 unrelated NF1 patients. In HUMAN GENETICS. ISSN 0340-6717, 2016, vol. 135, no. 5, pp. 469-475.
    JOHNSON, Kimberly J. - ZOELLNER, Nancy L. - GUTMANN, David H. Peri-gestational risk factors for pediatric brain tumors in Neurofibromatosis Type 1. In CANCER EPIDEMIOLOGY. ISSN 1877-7821, 2016, vol. 42, no., pp. 53-59.
    PORCELLI, Bree - ZOELLNER, Nancy L. - ABADIN, Salmafatima S. - GUTMANN, David H. - JOHNSON, Kimberly J. Associations between allergic conditions and pediatric brain tumors in Neurofibromatosis type 1. In FAMILIAL CANCER. ISSN 1389-9600, 2016, vol. 15, no. 2, pp. 301-308.
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    ANASTASAKI, Corina - MORRIS, Stephanie M. - GAO, Feng - GUTMANN, David H. Children with 5 '-end &ITNF1&IT gene mutations are more likely to have glioma. In NEUROLOGY-GENETICS. ISSN 2376-7839, 2017, vol. 3, no. 5, pp.
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    XU, Min - XIONG, Hui - HAN, Yanfang - LI, Chijun - MAI, Shaozhen - HUANG, Zhongzhou - AI, Xuechen - GUO, Zhixuan - ZENG, Fanqin - GUO, Qing. Identification of Mutation Regions on NF1 Responsible for High- and Low-Risk Development of Optic Pathway Glioma in Neurofibromatosis Type I. In FRONTIERS IN GENETICS. ISSN 1664-8021, 2018, vol. 9, no., pp.
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    CASSINA, Matteo - FRIZZIERO, Luisa - OPOCHER, Enrico - PARROZZANI, Raffaele - SORRENTINO, Ugo - VISCARDI, Elisabetta - MIGLIONICO, Giacomo - MIDENA, Edoardo - CLEMENTI, Maurizio - TREVISSON, Eva. Optic Pathway Glioma in Type 1 Neurofibromatosis: Review of Its Pathogenesis, Diagnostic Assessment, and Treatment Recommendations. In CANCERS, 2019, vol. 11, no. 11, pp.
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    CategoryADDA - Scientific papers in domestic journals registered in Current Contents Connect with IF (impacted)
    Category of document (from 2022)V3 - Vedecký výstup publikačnej činnosti z časopisu
    Type of documentčlánok
    Year2013
    Registered inWOS
    Registered inSCOPUS
    Registered inCCC
    DOI 10.4149/neo_2013_084
    article

    article

    rokCCIFIF Q (best)JCR Av Jour IF PercSJRSJR Q (best)CiteScore
    A
    rok vydaniarok metrikyIFIF Q (best)SJRSJR Q (best)
    201320121.574Q40.762Q3
Number of the records: 1  

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