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

Journal Abstract Search


119 related items for PubMed ID: 8053769

  • 1. [Lethal osteogenesis imperfecta in a Congolese newborn infant].
    Moyen G, Nkoua JL, Pongui M, Mafouta AM, Nzingoula S.
    Arch Fr Pediatr; 1993 Dec; 50(10):891-3. PubMed ID: 8053769
    [Abstract] [Full Text] [Related]

  • 2. Bone dysplasia in a child born to parents with osteogenesis imperfecta and pseudoachondroplasia.
    Kitoh H, Oki T, Arao K, Nogami H.
    Am J Med Genet; 1994 Jul 01; 51(3):187-90. PubMed ID: 8074142
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. [Shaken baby syndrome and osteogenesis imperfecta].
    Cabrerizo de Diago R, Ureña-Hornos T, Conde-Barreiro S, Labarta-Aizpun J, Peña-Segura JL, López-Pisón J.
    Rev Neurol; 1994 Jul 01; 40(10):598-600. PubMed ID: 15926132
    [Abstract] [Full Text] [Related]

  • 5. Prenatal diagnosis of perinatally lethal osteogenesis imperfecta.
    Elejalde BR, de Elejalde MM.
    Am J Med Genet; 1983 Feb 01; 14(2):353-9. PubMed ID: 6837630
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. The prenatal ultrasonographic diagnosis of osteogenesis imperfecta lethalis.
    Brown BS.
    J Can Assoc Radiol; 1984 Mar 01; 35(1):63-6. PubMed ID: 6725374
    [Abstract] [Full Text] [Related]

  • 8. Osteogenesis imperfecta type II delineation of the phenotype with reference to genetic heterogeneity.
    Sillence DO, Barlow KK, Garber AP, Hall JG, Rimoin DL.
    Am J Med Genet; 1984 Feb 01; 17(2):407-23. PubMed ID: 6702894
    [Abstract] [Full Text] [Related]

  • 9. Perinatal lethal osteogenesis imperfecta in a Thai newborn: the autopsy and histopathogical findings.
    Himakhun W, Rojnueangnit K, Prachukthum S.
    J Med Assoc Thai; 2012 Jan 01; 95 Suppl 1():S190-4. PubMed ID: 23964465
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Osteogenesis imperfecta due to compound heterozygosity for the LEPRE1 gene.
    Moul A, Alladin A, Navarrete C, Abdenour G, Rodriguez MM.
    Fetal Pediatr Pathol; 2013 Oct 01; 32(5):319-25. PubMed ID: 23301918
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Radiological "metamorphosis" in a patient with severe congenital osteogenesis imperfecta.
    Pendola F, Borrone C, Filocamo M, Lituania M, Steinmann B, Superti-Furga A.
    Eur J Pediatr; 1990 Mar 01; 149(6):403-5. PubMed ID: 2332008
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 6.