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Journal Abstract Search

221 related items for PubMed ID: 8363156

  • 1. [Seckel syndrome: study of 2 new cases].
    Martínez Algora MA, Ruiz Lázaro PJ, Olivares López JL, Garagorri Otero JM.
    An Esp Pediatr; 1993 Jul; 39(1):65-8. PubMed ID: 8363156
    [No Abstract] [Full Text] [Related]

  • 2. [Congenital dwarfisms with dysmorphism. 2. Bird-head congenital dwarfism (Virchow-Seckel type)].
    Anoussakis C, Liakakos D, Zervos N, Karpathios T.
    Pediatrie; 1974 Jul; 29(3):261-7. PubMed ID: 4438033
    [No Abstract] [Full Text] [Related]

  • 3. [Congenital dwarfisms with dysmorphism. 1. Congenital dwarfism with craniofacial dysmorphism and body asymmetry (Silver-Russel type)].
    Anoussakis C, Karpathios T, Zervos N, Liakakos D.
    Pediatrie; 1974 Jul; 29(3):249-59. PubMed ID: 4438032
    [No Abstract] [Full Text] [Related]

  • 4. [Dwarfism with high and narrow vertebrae. 2 new cases].
    Rochiccioli P, Malpuech G.
    Ann Pediatr (Paris); 1983 Nov; 30(9):709-12. PubMed ID: 6660804
    [No Abstract] [Full Text] [Related]

  • 5. Anesthesia for cleft lip surgery in a child with Seckel syndrome--a case report.
    Rajamani A, Kamat V, Murthy J, Hussain SA.
    Paediatr Anaesth; 2005 Apr; 15(4):338-41. PubMed ID: 15787928
    [Abstract] [Full Text] [Related]

  • 6. [Clinical study of a case of micromelic dwarfism with congenital bowing of the bones and facial dysmorphism].
    Brackman B, Blanc A, Busuttil R, Poissonnier M, Maroteaux P.
    Ann Pediatr (Paris); 1983 Nov; 30(9):705-7. PubMed ID: 6660803
    [No Abstract] [Full Text] [Related]

  • 7. [Seckel syndrome (the bird-headed dwarf)].
    Fehlow P.
    Z Arztl Fortbild (Jena); 1986 Nov; 80(19):821-2. PubMed ID: 3811419
    [No Abstract] [Full Text] [Related]

  • 8. Costello syndrome: the natural history of a true postnatal growth retardation syndrome.
    Umans S, Decock P, Fryns JP.
    Genet Couns; 1995 Nov; 6(2):121-5. PubMed ID: 7546454
    [Abstract] [Full Text] [Related]

  • 9. Orofacial manifestations of the Seckel syndrome.
    Chilvarquer LW, dos Santos VI, Silva MG, Young RS, Jorgenson RJ, Arena JF.
    ASDC J Dent Child; 1987 Nov; 54(2):129-31. PubMed ID: 3470330
    [No Abstract] [Full Text] [Related]

  • 10. Costello syndrome: a postnatal growth retardation syndrome with distinct phenotype.
    Fryns JP, Vogels A, Haegeman J, Eggermont E, van den Berghe H.
    Genet Couns; 1994 Nov; 5(4):337-43. PubMed ID: 7888135
    [Abstract] [Full Text] [Related]

  • 11. Picture of the month. Campomelic syndrome.
    Polidori G.
    Am J Dis Child; 1975 May; 129(5):615-6. PubMed ID: 1136950
    [No Abstract] [Full Text] [Related]

  • 12. Four siblings with malformations due to maternal epilepsy and anticonvulsants.
    Lau K, Lee A, Ch'ien L.
    J Tenn Med Assoc; 1994 May; 87(5):193-4. PubMed ID: 8041159
    [No Abstract] [Full Text] [Related]

  • 13. Cardio-facio-cutaneous (CFC) syndrome: report of two patients without hyperkeratotic skin lesions.
    Matsuda Y, Murano I, Kondoh O, Matsuo K, Kajii T.
    Am J Med Genet; 1991 May 01; 39(2):144-7. PubMed ID: 1842204
    [Abstract] [Full Text] [Related]

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  • 16. [Seckel syndrome (bird-head dwarf)].
    Fehlow P.
    Padiatr Grenzgeb; 1985 May 01; 24(5):371-4. PubMed ID: 4069712
    [No Abstract] [Full Text] [Related]

  • 17. [Cerebro-hepato-renal syndrome. Apropos of a new case].
    García Burriel JI, Carbajosa Herrero MT, Pedraz García C, Santos Borbujos J, Mateos Cañizal M, García González P.
    An Esp Pediatr; 1986 Jul 01; 25(1):67-9. PubMed ID: 3752742
    [No Abstract] [Full Text] [Related]

  • 18. [Heterogeneity of Seckel syndrome? Apropos of a case].
    Toudic L, Maroteaux P, Castel Y, Gouedard H, Parent P.
    Ann Pediatr (Paris); 1983 Nov 01; 30(9):700-4. PubMed ID: 6660802
    [No Abstract] [Full Text] [Related]

  • 19. [The value of microcomputers in the diagnosis of craniofacial dysmorphism with multiple congenital abnormalities in children].
    Bijaoui G, Billette de Villemeur T.
    Arch Fr Pediatr; 1990 Nov 01; 47(6):468. PubMed ID: 2206109
    [No Abstract] [Full Text] [Related]

  • 20. Coffin-Lowry syndrome: clinical aspects at different ages and symptoms in female carriers.
    Plomp AS, De Die-Smulders CE, Meinecke P, Ypma-Verhulst JM, Lissone DA, Fryns JP.
    Genet Couns; 1995 Nov 01; 6(3):259-68. PubMed ID: 8588856
    [Abstract] [Full Text] [Related]

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