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Journal Abstract Search

149 related items for PubMed ID: 8227394

  • 21. Rhombencephalosynapsis: Fused cerebellum, confused geneticists.
    Aldinger KA, Dempsey JC, Tully HM, Grout ME, Mehaffey MG, Dobyns WB, Doherty D.
    Am J Med Genet C Semin Med Genet; 2018 Dec; 178(4):432-439. PubMed ID: 30580482
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  • 22. [Rhombencephalosynapsis : a rare cerebellar malformation not to miss].
    Maquet J, Vanlinthout C, Desprechins B, Vandenbossche G.
    Rev Med Liege; 2023 Jul; 78(7-8):407-410. PubMed ID: 37560950
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  • 23. Neuro-ophthalmologic findings in patients with rhombencephalosynapsis.
    Phillips PH, Glasier CM, Brodsky MC.
    J AAPOS; 2008 Feb; 12(1):97-9. PubMed ID: 18155944
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  • 24. Cerebellar vermian defects: antenatal sonographic appearance and clinical significance.
    Keogan MT, DeAtkine AB, Hertzberg BS.
    J Ultrasound Med; 1994 Aug; 13(8):607-11. PubMed ID: 7933028
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  • 25. Partial rhombencephalosynapsis.
    Demaerel P, Morel C, Lagae L, Wilms G.
    AJNR Am J Neuroradiol; 2004 Jan; 25(1):29-31. PubMed ID: 14729524
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  • 26. [Rhombencephalosynapsis as a rare anomaly of the posterior skull base].
    Caffier S, Kittner T, Laniado M.
    Rofo; 2001 Sep; 173(9):850-1. PubMed ID: 11582567
    [No Abstract] [Full Text] [Related]

  • 27. Rhombencephalosynapsis associated with cutaneous pretibial hemangioma in an infant.
    Odemis E, Cakir M, Aynaci FM.
    J Child Neurol; 2003 Mar; 18(3):225-8. PubMed ID: 12731648
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  • 30. A rare cerebellar malformation: rhombencephalosynapsis.
    Silit E, Mutlu H, Ozturk T.
    J Neuroradiol; 2002 Sep; 29(3):208-10. PubMed ID: 12447147
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  • 33. Rhombencephalosynapsis with facial anomalies and probable autosomal recessive inheritance: a case report.
    Romanengo M, Tortori-Donati P, Di Rocco M.
    Clin Genet; 1997 Sep; 52(3):184-6. PubMed ID: 9377810
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  • 35. Fusion of the cerebellar hemispheres ventral to the brainstem: a rare hindbrain-related malformation.
    Sandalcioglu IE, Gasser T, van de Nes JA, Menken U, Stolke D, Wiedemayer H.
    Childs Nerv Syst; 2006 Jan; 22(1):73-7. PubMed ID: 15616855
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  • 37. Prenatal diagnosis of hemifacial microsomia and ipsilateral cerebellar hypoplasia in a fetus with oculoauriculovertebral spectrum.
    Martinelli P, Maruotti GM, Agangi A, Mazzarelli LL, Bifulco G, Paladini D.
    Ultrasound Obstet Gynecol; 2004 Aug; 24(2):199-201. PubMed ID: 15287060
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  • 38. Sonographic detection of inferior vermian agenesis in Dandy-Walker malformations: prognostic implications.
    Chang MC, Russell SA, Callen PW, Filly RA, Goldstein RB.
    Radiology; 1994 Dec; 193(3):765-70. PubMed ID: 7972821
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