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

139 related items for PubMed ID: 1933921

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Chronic tonsillar herniation in Crouzon's and Apert's syndromes: the role of premature synostosis of the lambdoid suture.
    Cinalli G, Renier D, Sebag G, Sainte-Rose C, Arnaud E, Pierre-Kahn A.
    J Neurosurg; 1995 Oct; 83(4):575-82. PubMed ID: 7674004
    [Abstract] [Full Text] [Related]

  • 3. Agenesis of the corpus callosum and limbic malformation in Apert's syndrome.
    Jeret JS, Serur D, Wisniewski K.
    Arch Neurol; 1989 Jan; 46(1):10. PubMed ID: 2910254
    [No Abstract] [Full Text] [Related]

  • 4. Cranial suture disease in the Apert's syndrome infant.
    Moore MH, Bourne AJ.
    J Craniofac Surg; 1996 Jul; 7(4):271-4. PubMed ID: 9133830
    [Abstract] [Full Text] [Related]

  • 5. Psychosis in Apert's syndrome with partial agenesis of the corpus callosum.
    Gupta S, Popli A.
    J Psychiatry Neurosci; 1995 Jul; 20(4):307-9. PubMed ID: 7647085
    [Abstract] [Full Text] [Related]

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

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Sphenopharyngeal encephalocele associated with agenesis of the corpus callosum.
    Mauersberger W, Diaz LA.
    Neurochirurgia (Stuttg); 1985 Nov; 28(6):238-42. PubMed ID: 4080059
    [Abstract] [Full Text] [Related]

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

  • 11. Dandy-Walker syndrome together with occipital encephalocele.
    Cakmak A, Zeyrek D, Cekin A, Karazeybek H.
    Minerva Pediatr; 2008 Aug; 60(4):465-8. PubMed ID: 18511899
    [Abstract] [Full Text] [Related]

  • 12. Posterior orbital encephalocele with anophthalmos and other brain malformations. Case report.
    Fargueta JS, Menezo JL, Bordes M.
    J Neurosurg; 1973 Feb; 38(2):215-7. PubMed ID: 4694220
    [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. Absence of the superior rectus muscle in Apert's syndrome.
    Cuttone JM, Brazis PT, Miller MT, Folk ER.
    J Pediatr Ophthalmol Strabismus; 1979 Feb; 16(6):349-54. PubMed ID: 521875
    [Abstract] [Full Text] [Related]

  • 18. Schizencephaly accompanied by occipital encephalocele and deletion of chromosome 22q13.32: a case report.
    Inan C, Sayin NC, Gurkan H, Atli E, Gursoy Erzincan S, Uzun I, Sutcu H, Dogan S, Ikbal Atli E, Varol F.
    Fetal Pediatr Pathol; 2019 Dec; 38(6):496-502. PubMed ID: 31130048
    [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 7.