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Journal Abstract Search

144 related items for PubMed ID: 8830611

  • 61. Adams Oliver Syndrome.
    Madan A, Sardana K, Garg VK.
    Indian Pediatr; 2015 Jul; 52(7):633-4. PubMed ID: 26244971
    [No Abstract] [Full Text] [Related]

  • 62. Townes-Brocks syndrome associated with mental retardation.
    Ishikiriyama S, Kudoh F, Shimojo N, Iwai J, Inoue T.
    Am J Med Genet; 1996 Jan 11; 61(2):191-2. PubMed ID: 8669452
    [No Abstract] [Full Text] [Related]

  • 63. Atypical aplasia cutis in association with Xia Gibbs syndrome.
    Ellis C, Pai GS, Wine Lee L.
    Pediatr Dermatol; 2021 Mar 11; 38(2):533-535. PubMed ID: 33464633
    [Abstract] [Full Text] [Related]

  • 64. Levetiracetam in the treatment of Lennox-Gastaut syndrome.
    De Los Reyes EC, Sharp GB, Williams JP, Hale SE.
    Pediatr Neurol; 2004 Apr 11; 30(4):254-6. PubMed ID: 15087103
    [Abstract] [Full Text] [Related]

  • 65. Identical twins with mental retardation, dysarthria, progressive spastic paraplegia, and brachydactyly type E: a new syndrome or variant of Fitzsimmons-Guilbert syndrome?
    Lacassie Y, Arriaza MI, Duncan MC, Dijamco C, McElveen C, Stahls PF.
    Am J Med Genet; 1999 May 21; 84(2):90-3. PubMed ID: 10323731
    [Abstract] [Full Text] [Related]

  • 66. [Angelman syndrome].
    Eber SW, Joost S, Gabriel M.
    Monatsschr Kinderheilkd; 1986 Mar 21; 134(3):158-60. PubMed ID: 3084953
    [Abstract] [Full Text] [Related]

  • 67. Ectodermal dysplasia, osteosclerosis, atrial septal defect, malabsorption, neutropenia, growth, and mental retardation: the Côté-Katsantoni syndrome?
    Blau EB.
    Am J Med Genet; 1987 Mar 21; 26(3):729-32. PubMed ID: 3565486
    [No Abstract] [Full Text] [Related]

  • 68. Autosomal dominant inheritance of aplasia cutis congenita and congenital heart defect: a possible link to the Adams-Oliver syndrome.
    Digilio MC, Marino B, Dallapiccola B.
    Am J Med Genet A; 2008 Nov 01; 146A(21):2842-4. PubMed ID: 18924173
    [No Abstract] [Full Text] [Related]

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  • 71. [Unmanageable hair syndrome associated with epilepsy, deafness and phalangeal aplasia].
    Plantin P, Le Berre A, Guillet G, Parent P.
    Arch Fr Pediatr; 1987 Nov 01; 44(9):822, 824. PubMed ID: 3446077
    [No Abstract] [Full Text] [Related]

  • 72. Bart syndrome associated with skeletal deformities: An uncommon case report.
    Shahidi-Dadras M, Niknezhad N, Asadi-Kani Z, Zaresharifi S, Hamedani B, Abdollahimajd F.
    Dermatol Ther; 2019 Nov 01; 32(6):e13131. PubMed ID: 31631476
    [Abstract] [Full Text] [Related]

  • 73. Vascular abnormalities in Adams-Oliver syndrome: cause or effect?
    Swartz EN, Sanatani S, Sandor GG, Schreiber RA.
    Am J Med Genet; 1999 Jan 01; 82(1):49-52. PubMed ID: 9916843
    [Abstract] [Full Text] [Related]

  • 74. [Ito syndrome from the orthopedic viewpoint].
    Stein V, Weickert H, Braun HS.
    Beitr Orthop Traumatol; 1983 Oct 01; 30(10):546-9. PubMed ID: 6318722
    [No Abstract] [Full Text] [Related]

  • 75. Manifestations in four males with and an obligate carrier of the Lenz microphthalmia syndrome.
    Forrester S, Kovach MJ, Reynolds NM, Urban R, Kimonis V.
    Am J Med Genet; 2001 Jan 01; 98(1):92-100. PubMed ID: 11426460
    [Abstract] [Full Text] [Related]

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  • 78. MRI and neurological findings in macrocephaly-cutis marmorata telangiectatica congenita syndrome: report of ten cases and review of the literature.
    Garavelli L, Leask K, Zanacca C, Pedori S, Albertini G, Della Giustina E, Croci GF, Magnani C, Banchini G, Clayton-Smith J, Bocian M, Firth H, Gold JA, Hurst J.
    Genet Couns; 2005 Jan 01; 16(2):117-28. PubMed ID: 16080291
    [Abstract] [Full Text] [Related]

  • 79. Kabuki syndrome and diaphragmatic defect.
    Sethi SK, Faridi MM.
    Indian Pediatr; 2006 Jun 01; 43(6):552-3. PubMed ID: 16820668
    [No Abstract] [Full Text] [Related]

  • 80. The ectrodactyly-ectodermal dysplasia-clefting syndrome: a literature review and case report.
    King NM, Tong MC, Ling JY.
    Quintessence Int; 1994 Oct 01; 25(10):731-6. PubMed ID: 9161252
    [Abstract] [Full Text] [Related]

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