These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

86 related articles for article (PubMed ID: 2210088)

  • 1. The brain in the 18q-syndrome.
    Vogel H; Urich H; Horoupian DS; Wertelecki W
    Dev Med Child Neurol; 1990 Aug; 32(8):732-7. PubMed ID: 2210088
    [TBL] [Abstract][Full Text] [Related]  

  • 2. White matter changes associated with deletions of the long arm of chromosome 18 (18q- syndrome): a dysmyelinating disorder?
    Loevner LA; Shapiro RM; Grossman RI; Overhauser J; Kamholz J
    AJNR Am J Neuroradiol; 1996; 17(10):1843-8. PubMed ID: 8933867
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Combined deletion 18q22.2 and duplication/triplication 18q22.1 causes microcephaly, mental retardation and leukencephalopathy.
    Nguyen-Minh S; Drossel K; Horn D; Rost I; Spors B; Kaindl AM
    Gene; 2013 Jul; 523(1):92-8. PubMed ID: 23566840
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 46,XY del(18)(q21.3q22.2) with mosaicism of r(18) and a milder form of the 18q- syndrome.
    Maaswinkel-Mooij PD; de Jong P; Beverstock GC
    Clin Genet; 1993 Feb; 43(2):76-8. PubMed ID: 8448905
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 18q-syndrome: brain MRI shows poor differentiation of gray and white matter on T2-weighted images.
    Linnankivi TT; Autti TH; Pihko SH; Somer MS; Tienari PJ; Wirtavuori KO; Valanne LK
    J Magn Reson Imaging; 2003 Oct; 18(4):414-9. PubMed ID: 14508777
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cerebral white matter abnormalities associated with chromosome 18q duplication.
    Huang J; Saint-Martin C; Tchakarska G; Lavoie J; Myers KA
    Brain Dev; 2022 Sep; 44(8):562-566. PubMed ID: 35469635
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular characterisation of a proximal chromosome 18q deletion.
    McEntagart M; Carey A; Breen C; McQuaid S; Stallings RL; Green AJ; King MD
    J Med Genet; 2001 Feb; 38(2):128-9. PubMed ID: 11288715
    [No Abstract]   [Full Text] [Related]  

  • 8. MR spectroscopy in 18q(-) syndrome suggesting other than hypomyelination.
    Tada H; Takanashi J
    Brain Dev; 2014 Jan; 36(1):57-60. PubMed ID: 23332863
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The brain in partial trisomy 18: a case report.
    Novotny EJ; Urich H
    J Child Neurol; 1987 Jul; 2(3):194-7. PubMed ID: 3611633
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Catathrenia in Pitt-Hopkins syndrome associated with 18q interstitial deletion.
    Motojima T; Fujii K; Ohashi H; Arakawa H
    Pediatr Int; 2018 May; 60(5):479-481. PubMed ID: 29633422
    [No Abstract]   [Full Text] [Related]  

  • 11. Triple structural mosaicism of chromosome 18 in a child with MR/MCA syndrome and abnormal skin pigmentation.
    Bocian E; Mazurczak T; Buława E; Stańczak H; Rowicka G
    J Med Genet; 1993 Jul; 30(7):614-5. PubMed ID: 8411041
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Intractable epilepsy (apneic seizure) in an infant with 18q deletion syndrome].
    Kumada T; Ito M; Miyajima T; Fujii T; Okuno T; Kumakura A
    No To Hattatsu; 2003 Nov; 35(6):521-6. PubMed ID: 14631750
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Abnormal brain MRI signal in 18q-syndrome not due to dysmyelination.
    Tanaka R; Iwasaki N; Hayashi M; Nakayama J; Ohto T; Takahashi M; Numano T; Homma K; Hamano K; Sumazaki R
    Brain Dev; 2012 Mar; 34(3):234-7. PubMed ID: 21669507
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Puppet-like syndrome of Angelman: a pathologic and neurochemical study.
    Jay V; Becker LE; Chan FW; Perry TL
    Neurology; 1991 Mar; 41(3):416-22. PubMed ID: 2006012
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Creutzfeldt-Jakob disease with congophilic kuru plaques: CT and pathological findings of the cerebral white matter.
    Kawata A; Suga M; Oda M; Hayashi H; Tanabe H
    J Neurol Neurosurg Psychiatry; 1992 Sep; 55(9):849-51. PubMed ID: 1402981
    [TBL] [Abstract][Full Text] [Related]  

  • 16. An 18q- syndrome breakpoint resides between the duplicated serpins SCCA1 and SCCA2 and arises via a cryptic rearrangement with satellite III DNA.
    Katz SG; Schneider SS; Bartuski A; Trask BJ; Massa H; Overhauser J; Lalande M; Lansdorp PM; Silverman GA
    Hum Mol Genet; 1999 Jan; 8(1):87-92. PubMed ID: 9887335
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Neurologic manifestations in 18q- syndrome.
    Miller G; Mowrey PN; Hopper KD; Frankel CA; Ladda RL
    Am J Med Genet; 1990 Sep; 37(1):128-32. PubMed ID: 1700607
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 18q- syndrome in mother and daughter.
    Fryns JP; Logghe N; van Eygen M; van den Berghe H
    Eur J Pediatr; 1979 Mar; 130(3):189-92. PubMed ID: 421697
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Patchy white matter hyperintensity in ring chromosome 18 syndrome.
    Anzai M; Arai-Ichinoi N; Takezawa Y; Endo W; Inui T; Sato R; Kikuchi A; Uematsu M; Kure S; Haginoya K
    Pediatr Int; 2016 Sep; 58(9):919-22. PubMed ID: 27577543
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Brain dysplasia associated with Larsen-like syndrome.
    Yamaguchi K; Ogawa Y; Handa T
    Pediatr Neurol; 1996 Jan; 14(1):75-9. PubMed ID: 8652025
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.