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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

104 related articles for article (PubMed ID: 6642619)

  • 21. Symptomatic tethering of the cerebellar vermis: case report.
    Comey CH; Albright AL
    Neurosurgery; 1994 Jan; 34(1):177-80. PubMed ID: 8121557
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Craniofacial correction of occipital encephalocele.
    Habal MB
    J Craniofac Surg; 1993 Oct; 4(4):215-22. PubMed ID: 8110902
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Cranium bifidum with abnormal foetal attachment of placenta.
    Purohit M; Purohit NN; Garg OP; Gupta CB
    Indian Pediatr; 1977 Aug; 14(8):665-6. PubMed ID: 563375
    [No Abstract]   [Full Text] [Related]  

  • 24. [Occipital encephaloceles; embryological considerations and neurosurgical treatment].
    Alliez B; Sow M; Tranier J; Gueye M; Sainte-Rose C
    Bull Soc Med Afr Noire Lang Fr; 1977; 22(1):96-9. PubMed ID: 328183
    [No Abstract]   [Full Text] [Related]  

  • 25. Supra- and infra-torcular double occipital encephalocele.
    Canaz H; Ayçiçek E; Akçetin MA; Akdemir O; Alataş I; Özdemir B
    Neurocirugia (Astur); 2015; 26(1):43-7. PubMed ID: 25307275
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Morphometric measurements of the cranium in patients with Chiari type I malformation and comparison with the normal population.
    Karagöz F; Izgi N; Kapíjcíjoğlu Sencer S
    Acta Neurochir (Wien); 2002 Feb; 144(2):165-71; discussion 171. PubMed ID: 11862517
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Hereditary cranium bifidum persisting as enlarged parietal foramina (Catlin marks) on cephalometric radiographs.
    Mupparapu M; Binder RE; Duarte F
    Am J Orthod Dentofacial Orthop; 2006 Jun; 129(6):825-8. PubMed ID: 16769502
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A boy with a sac-like protrusion at the occipital region.
    Zhou YH; Zheng MH
    BMJ; 2016 Apr; 353():i2073. PubMed ID: 27079497
    [No Abstract]   [Full Text] [Related]  

  • 29. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Congenital hereditary cranium bifidum occultum frontalis with a review of anatomical variations in lower medsagittal region of frontal bones.
    TERRAFRANCA RJ; ZELLIS A
    Radiology; 1953 Jul; 61(1):60-6. PubMed ID: 13064405
    [No Abstract]   [Full Text] [Related]  

  • 31. [Occipital encephalocele with cerebellar dysontogenesis (at birth and 10 years later)].
    Bignardi C; Zini GC; Provvisionato G
    Chir Organi Mov; 1978; 64(5):509-22. PubMed ID: 754913
    [No Abstract]   [Full Text] [Related]  

  • 32. Imaging Assessment of Re-Exploratory Repair of an Occipital Bone Defect-Associated Tectocerebellar Dysraphism via Hybrid Cranioplasty.
    Ginat DT; Reid R; Frim DM
    Pediatr Neurosurg; 2016; 51(3):164-6. PubMed ID: 26978789
    [No Abstract]   [Full Text] [Related]  

  • 33. Spectrum of anomalies in the Meckel syndrome, or: "Maybe there is a malformation syndrome with at least one constant anomaly".
    Fraser FC; Lytwyn A
    Am J Med Genet; 1981; 9(1):67-73. PubMed ID: 7246621
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Intracranial occipital hyperostosis with cerebellar syndrome].
    POGGIALI A
    Riv Sper Freniatr Med Leg Alien Ment; 1951 Dec; 75(4):507-31. PubMed ID: 14930679
    [No Abstract]   [Full Text] [Related]  

  • 35. Four cases with hypoplastic thumbs and encephaloceles.
    Huang T; Korson MS; Krauss C; Holmes LB
    Am J Med Genet; 2002 Aug; 111(2):178-81. PubMed ID: 12210346
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Polydactyly in a carrier of the gene for the Meckel syndrome.
    Nelson J; Nevin NC; Hanna EJ
    Am J Med Genet; 1994 Nov; 53(3):207-9. PubMed ID: 7856653
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Institutional experience with cranial vault encephaloceles.
    Bui CJ; Tubbs RS; Shannon CN; Acakpo-Satchivi L; Wellons JC; Blount JP; Oakes WJ
    J Neurosurg; 2007 Jul; 107(1 Suppl):22-5. PubMed ID: 17644916
    [TBL] [Abstract][Full Text] [Related]  

  • 38. von Voss-Cherstvoy syndrome: a variable perinatally lethal syndrome of multiple congenital anomalies.
    Lubinsky MS; Kahler SG; Speer IE; Hoyme HE; Kirillova IA; Lurie IW
    Am J Med Genet; 1994 Sep; 52(3):272-8. PubMed ID: 7810558
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Autosomal recessive congenital cerebellar hypoplasia and short stature in a large inbred family.
    Mégarbané A; Delague V; Salem N; Loiselet J
    Am J Med Genet; 1999 Nov; 87(1):88-90. PubMed ID: 10528257
    [No Abstract]   [Full Text] [Related]  

  • 40. [Congenital dermal sinus].
    Arseni C; Horvath L; Carp N; Ciurea V
    Rev Pediatr Obstet Ginecol Pediatr; 1976; 25(4):309-16. PubMed ID: 828761
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.