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Journal Abstract Search


152 related items for PubMed ID: 1848742

  • 1. [Apert's syndrome with polymetatarsia].
    Nivelon A, Nivelon JL, Matthieu M, Piussan C, Maroteaux P.
    Ann Pediatr (Paris); 1991 Jan; 38(1):9-13. PubMed ID: 1848742
    [Abstract] [Full Text] [Related]

  • 2. Acrocephalosyndactyly--type I (Apert's syndrome).
    Singh SK, Chaturvedi R, Pal SK, Singh KK, Sinha SK, Singh SK, Agrawal JK.
    J Assoc Physicians India; 1999 Aug; 47(8):842-3. PubMed ID: 10778643
    [No Abstract] [Full Text] [Related]

  • 3. [Syndrome of craniosynostosis with syn- or polydactylia].
    Lorenz P, Hinkel GK, Rupprecht E.
    Kinderarztl Prax; 1991 Aug; 59(7-8):195-9. PubMed ID: 1656132
    [Abstract] [Full Text] [Related]

  • 4. Apert's syndrome--a report of five cases.
    Yonenobu K, Tada K, Tsuyuguchi Y.
    Hand; 1982 Oct; 14(3):317-25. PubMed ID: 7152383
    [Abstract] [Full Text] [Related]

  • 5. [A case of Apert's syndrome].
    Spada A, Pejrone F.
    Arch Sci Med (Torino); 1969 Apr; 126(4):201-5. PubMed ID: 17342891
    [Abstract] [Full Text] [Related]

  • 6. Phenotypic variation in acrocephalosyndactyly syndromes: unusual findings in patient with features of Apert and Saethre-Chotzen syndromes.
    Cantrell SB, Moore MH, Trott JA, Morris RJ, David DJ.
    Cleft Palate Craniofac J; 1994 Nov; 31(6):487-93. PubMed ID: 7833342
    [Abstract] [Full Text] [Related]

  • 7. [Surgical treatment of hand syndactyly in Apert syndrome].
    Guzanin S, Zábavníková M, Kacmár P, Sabovcík R, Kluka T.
    Acta Chir Orthop Traumatol Cech; 2001 Nov; 68(4):249-55. PubMed ID: 11706550
    [Abstract] [Full Text] [Related]

  • 8. ["Apert's foot" (in acrocephalo-syndactyly) (author's transl)].
    Blauth W, von Törne O.
    Z Orthop Ihre Grenzgeb; 1978 Feb; 116(1):1-6. PubMed ID: 654428
    [Abstract] [Full Text] [Related]

  • 9. Asymmetrical coronal synostosis, cutaneous syndactyly of the fingers and toes, and jejunal atresia in a male infant.
    Pfeiffer RA, Rinnert S, Popp R, Röckelein G.
    Am J Med Genet; 1996 May 03; 63(1):175-6. PubMed ID: 8723105
    [Abstract] [Full Text] [Related]

  • 10. Apert syndrome with partial polysyndactyly: a proposal on the classification of acrocephalosyndactyly.
    Izumikawa Y, Naritomi K, Ikema S, Goya Y, Shiroma N, Yoshida K, Yara A, Hirayama K.
    Jinrui Idengaku Zasshi; 1988 Dec 03; 33(4):487-92. PubMed ID: 3251081
    [No Abstract] [Full Text] [Related]

  • 11. Autosomal dominant inheritance of hypothalamic hamartoma associated with polysyndactyly: heterogeneity or variable expressivity?
    Grebe TA, Clericuzio C.
    Am J Med Genet; 1996 Dec 11; 66(2):129-37. PubMed ID: 8958318
    [Abstract] [Full Text] [Related]

  • 12. Craniosynostosis, Philadelphia type: a new autosomal dominant syndrome with sagittal craniosynostosis and syndactyly of the fingers and toes.
    Robin NH, Segel B, Carpenter G, Muenke M.
    Am J Med Genet; 1996 Mar 15; 62(2):184-91. PubMed ID: 8882401
    [Abstract] [Full Text] [Related]

  • 13. Apert's syndrome (acrocephalosyndactyly) in a patient with hyperhidrosis.
    Cohn MS, Mahon MJ.
    Cutis; 1993 Oct 15; 52(4):205-8. PubMed ID: 8261804
    [Abstract] [Full Text] [Related]

  • 14. Apert syndrome with partial preaxial polydactyly.
    Lefort G, Sarda P, Humeau C, Rieu D.
    Genet Couns; 1992 Oct 15; 3(2):107-9. PubMed ID: 1642807
    [Abstract] [Full Text] [Related]

  • 15. Apert's syndrome: (acrocephalosyndactylism).
    Meyer JL.
    J Foot Surg; 1981 Oct 15; 20(4):210-13. PubMed ID: 6274945
    [Abstract] [Full Text] [Related]

  • 16. A newborn infant with craniofacial dysmorphism and polysyndactyly (Greig's syndrome).
    Merlob P, Grünebaum M, Reisner SH.
    Acta Paediatr Scand; 1981 Mar 15; 70(2):275-7. PubMed ID: 6263040
    [Abstract] [Full Text] [Related]

  • 17. [Acrocephalosyndactyly (ACS) (author's transl)].
    Fajardo Carmona AV, Pascual Castroviejo I.
    An Esp Pediatr; 1975 Mar 15; 8(6):639-50. PubMed ID: 174468
    [Abstract] [Full Text] [Related]

  • 18. Pfeiffer syndrome.
    Vogels A, Fryns JP.
    Orphanet J Rare Dis; 2006 Jun 01; 1():19. PubMed ID: 16740155
    [Abstract] [Full Text] [Related]

  • 19. Apert's syndrome--a type of acrocephalosyndactyly (a case report).
    Punwani DV, Purohit V, Irani SF, Kumta NB.
    J Postgrad Med; 1979 Apr 01; 25(2):109-11. PubMed ID: 501671
    [No Abstract] [Full Text] [Related]

  • 20. Is the Apert foot an overlooked aspect of this rare genetic disease? Clinical findings and treatment options for foot deformities in Apert syndrome.
    Stauffer A, Farr S.
    BMC Musculoskelet Disord; 2020 Nov 28; 21(1):788. PubMed ID: 33248465
    [Abstract] [Full Text] [Related]


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