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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

236 related items for PubMed ID: 10029348

  • 21. A two base pair deletion in the PQBP1 gene is associated with microphthalmia, microcephaly, and mental retardation.
    Martínez-Garay I, Tomás M, Oltra S, Ramser J, Moltó MD, Prieto F, Meindl A, Kutsche K, Martínez F.
    Eur J Hum Genet; 2007 Jan; 15(1):29-34. PubMed ID: 17033686
    [Abstract] [Full Text] [Related]

  • 22. Delineation of the da-Silva syndrome.
    Naritomi K, Tohma T, Goya Y, Shiroma N, Hirayama K.
    Am J Med Genet; 1994 Feb 01; 49(3):313-6. PubMed ID: 8209892
    [Abstract] [Full Text] [Related]

  • 23. Spectrum of corpus callosum agenesis.
    Sztriha L.
    Pediatr Neurol; 2005 Feb 01; 32(2):94-101. PubMed ID: 15664768
    [Abstract] [Full Text] [Related]

  • 24. Deletions in the VPS13B (COH1) gene as a cause of Cohen syndrome.
    Balikova I, Lehesjoki AE, de Ravel TJ, Thienpont B, Chandler KE, Clayton-Smith J, Träskelin AL, Fryns JP, Vermeesch JR.
    Hum Mutat; 2009 Sep 01; 30(9):E845-54. PubMed ID: 19533689
    [Abstract] [Full Text] [Related]

  • 25. MRI evidence of white matter damage in a mouse model of Nijmegen breakage syndrome.
    Assaf Y, Galron R, Shapira I, Nitzan A, Blumenfeld-Katzir T, Solomon AS, Holdengreber V, Wang ZQ, Shiloh Y, Barzilai A.
    Exp Neurol; 2008 Jan 01; 209(1):181-91. PubMed ID: 17976584
    [Abstract] [Full Text] [Related]

  • 26. Reduced area of the corpus callosum in posttraumatic stress disorder.
    Villarreal G, Hamilton DA, Graham DP, Driscoll I, Qualls C, Petropoulos H, Brooks WM.
    Psychiatry Res; 2004 Sep 15; 131(3):227-35. PubMed ID: 15465292
    [Abstract] [Full Text] [Related]

  • 27. Multiple congenital anomalies syndrome with myopathy in chromosome 16 abnormality.
    Ionasescu V, Patil S, Hart M, Rhead W, Smith W.
    Am J Med Genet; 1987 Jan 15; 26(1):189-94. PubMed ID: 3812561
    [Abstract] [Full Text] [Related]

  • 28. Microcephaly with simplified gyral pattern: MRI classification.
    Vermeulen RJ, Wilke M, Horber V, Krägeloh-Mann I.
    Neurology; 2010 Feb 02; 74(5):386-91. PubMed ID: 20124203
    [Abstract] [Full Text] [Related]

  • 29. New radiological finding by magnetic resonance imaging examination of the brain in Coffin-Lowry syndrome.
    Kondoh T, Matsumoto T, Ochi M, Sukegawa K, Tsuji Y.
    J Hum Genet; 1998 Feb 02; 43(1):59-61. PubMed ID: 9610000
    [Abstract] [Full Text] [Related]

  • 30. Prospective neuroimaging study in hereditary spastic paraplegia with thin corpus callosum.
    França MC, D'Abreu A, Maurer-Morelli CV, Seccolin R, Appenzeller S, Alessio A, Damasceno BP, Nucci A, Cendes F, Lopes-Cendes I.
    Mov Disord; 2007 Aug 15; 22(11):1556-62. PubMed ID: 17516453
    [Abstract] [Full Text] [Related]

  • 31. Frameshift mutation of the zinc finger homeo box 1 B gene in syndromic corpus callosum agenesis (Mowat-Wilson syndrome).
    Sztriha L, Espinosa-Parrilla Y, Gururaj A, Amiel J, Lyonnet S, Gerami S, Johansen JG.
    Neuropediatrics; 2003 Dec 15; 34(6):322-5. PubMed ID: 14681759
    [Abstract] [Full Text] [Related]

  • 32. X-linked mental retardation and neurological symptoms: a nosological approach.
    Schrander-Stumpel CT, Höweler CJ, Fryns JP.
    Genet Couns; 1995 Dec 15; 6(1):21-32. PubMed ID: 7794558
    [Abstract] [Full Text] [Related]

  • 33. New POMT2 mutations causing congenital muscular dystrophy: identification of a founder mutation.
    Yanagisawa A, Bouchet C, Van den Bergh PY, Cuisset JM, Viollet L, Leturcq F, Romero NB, Quijano-Roy S, Fardeau M, Seta N, Guicheney P.
    Neurology; 2007 Sep 18; 69(12):1254-60. PubMed ID: 17634419
    [Abstract] [Full Text] [Related]

  • 34. Seckel syndrome with asymptomatic tonsillar herniation and congenital mirror movements.
    Thapa R, Mukherjee K.
    J Child Neurol; 2010 Feb 18; 25(2):231-3. PubMed ID: 19372093
    [Abstract] [Full Text] [Related]

  • 35. 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; 18(4):414-9. PubMed ID: 14508777
    [Abstract] [Full Text] [Related]

  • 36. Microlissencephaly in microcephalic osteodysplastic primordial dwarfism: a case report and review of the literature.
    Klinge L, Schaper J, Wieczorek D, Voit T.
    Neuropediatrics; 2002 Dec 18; 33(6):309-13. PubMed ID: 12571786
    [Abstract] [Full Text] [Related]

  • 37. Nail aplasia, microcephaly, severe mental retardation and MRI abnormalities: report of two unrelated cases.
    Musumeci SA, Elia M, Fichera M, Amato C, Ferri R, Romano C, Federico A.
    Neurol Sci; 2006 Dec 18; 27(6):425-31. PubMed ID: 17205229
    [Abstract] [Full Text] [Related]

  • 38. Anatomical MRI study of corpus callosum in unipolar depression.
    Lacerda AL, Brambilla P, Sassi RB, Nicoletti MA, Mallinger AG, Frank E, Kupfer DJ, Keshavan MS, Soares JC.
    J Psychiatr Res; 2005 Jul 18; 39(4):347-54. PubMed ID: 15804385
    [Abstract] [Full Text] [Related]

  • 39. Abnormalities of the corpus callosum in nonpsychotic children with chromosome 22q11 deletion syndrome.
    Shashi V, Muddasani S, Santos CC, Berry MN, Kwapil TR, Lewandowski E, Keshavan MS.
    Neuroimage; 2004 Apr 18; 21(4):1399-406. PubMed ID: 15050565
    [Abstract] [Full Text] [Related]

  • 40. Agenesis of the corpus callosum: clinical and genetic study in 63 young patients.
    Bedeschi MF, Bonaglia MC, Grasso R, Pellegri A, Garghentino RR, Battaglia MA, Panarisi AM, Di Rocco M, Balottin U, Bresolin N, Bassi MT, Borgatti R.
    Pediatr Neurol; 2006 Mar 18; 34(3):186-93. PubMed ID: 16504787
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 12.