BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

431 related articles for article (PubMed ID: 11822087)

  • 1. Association of severe autosomal recessive osteopetrosis and Dandy-Walker syndrome with agenesis of the corpus callosum.
    Ben Hamouda H; Sfar MN; Braham R; Ben Salah M; Ayadi A; Soua H; Hamza H; Sfar MT
    Acta Orthop Belg; 2001 Dec; 67(5):528-32. PubMed ID: 11822087
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Asphyxiating thoracic dysplasia associated with hepatic ductal hypoplasia, agenesis of the corpus callosum and Dandy-Walker syndrome].
    Trabelsi M; Hammou-Jeddi A; Kammoun A; Bennaceur B; Gharbi HA
    Pediatrie; 1990; 45(1):35-8. PubMed ID: 2158046
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Agenesis of the corpus callosum and Dandy-Walker malformation associated with hemimegalencephaly in the sebaceous nevus syndrome.
    Dodge NN; Dobyns WB
    Am J Med Genet; 1995 Mar; 56(2):147-50. PubMed ID: 7625436
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Familial agenesis of the corpus callosum: a new form].
    Castro-Gago M; Rodriguez-Nuñez A; Eiris J; Peña J; Tojo R; Novo-Rodriguez I
    Arch Fr Pediatr; 1993 Apr; 50(4):327-30. PubMed ID: 8379821
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Dandy-Walker syndrome and corpus callosum agenesis in 5p deletion.
    Vialard F; Robyr R; Hillion Y; Molina Gomes D; Selva J; Ville Y
    Prenat Diagn; 2005 Apr; 25(4):311-3. PubMed ID: 15849798
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. [Agenesis of the vermis cerebelli in the developmental age].
    Mercuri S; Curatolo P; Giuffrè R
    Minerva Pediatr; 1980 Jan; 32(1):53-60. PubMed ID: 6789049
    [No Abstract]   [Full Text] [Related]  

  • 8. Acrocallosal syndrome: new findings.
    Moeschler JB; Pober BR; Holmes LB; Graham JM
    Am J Med Genet; 1989 Mar; 32(3):306-10. PubMed ID: 2729349
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Association of infantile neuroaxonal dystrophy and osteopetrosis: a rare autosomal recessive disorder.
    Rees H; Ang LC; Casey R; George DH
    Pediatr Neurosurg; 1995; 22(6):321-7. PubMed ID: 7577667
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Agenesis of the corpus callosum: real-time ultrasonographic diagnosis and autopsy findings.
    Fawer CL; Calame A; Anderegg A; Deonna T; Perentes E
    Helv Paediatr Acta; 1985 Dec; 40(5):371-80. PubMed ID: 4086310
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Peters'-Plus syndrome with agenesis of the corpus callosum: report of a case and confirmation of autosomal recessive inheritance.
    Camera G; Centa A; Pozzolo S; Camera A
    Clin Dysmorphol; 1993 Oct; 2(4):317-21. PubMed ID: 8305962
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Dysgenesis of the corpus callosum].
    Kurokawa K; Sunada Y
    Ryoikibetsu Shokogun Shirizu; 2000; (32):332-4. PubMed ID: 11212735
    [No Abstract]   [Full Text] [Related]  

  • 13. Dandy-Walker malformation: a rare association with hypoparathyroidism.
    Coban D; Akin MA; Kurtoglu S; Oktem S; Yikilmaz A
    Pediatr Neurol; 2010 Dec; 43(6):439-41. PubMed ID: 21093738
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [A variant of Dandy-Walker malformation associated with agenesis of the corpus callosum].
    Trabelsi M; Boudhina T; Beyram R; Khaldi F; Bennaceur B; Hamza M; Hamza B
    Tunis Med; 1986 Oct; 64(10):861-5. PubMed ID: 3824544
    [No Abstract]   [Full Text] [Related]  

  • 15. Familial occurrence of isolated Dandy-Walker variant in two consecutive male fetuses.
    Lin YH; Chen CP; Chen TC; Liang SJ; Hsu CS
    Genet Couns; 2006; 17(4):461-3. PubMed ID: 17375534
    [No Abstract]   [Full Text] [Related]  

  • 16. Dandy-Walker(like) malformation, atrio-ventricular septal defect and a similar pattern of minor anomalies in 2 sisters: a new syndrome?
    Ritscher D; Schinzel A; Boltshauser E; Briner J; Arbenz U; Sigg P
    Am J Med Genet; 1987 Feb; 26(2):481-91. PubMed ID: 3812597
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Recessive osteopetrosis. Identification of a form of medium severity].
    Bejaoui M; Baraket M; Lakhoua R; Mezni F; Hammou Jeddi A; Kamoun A; Kharrat H; Essoussi S; Harbi A; Ben Dridi MF
    Arch Fr Pediatr; 1992; 49(7):627-31. PubMed ID: 1476480
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Aicardi syndrome with Dandy-Walker malformation.
    Jageerhussain M; Dhinagar S; Nadaradjan S; Bhat BV
    Indian Pediatr; 2000 Jun; 37(6):673-6. PubMed ID: 10869154
    [No Abstract]   [Full Text] [Related]  

  • 19. The Dandy-Walker variant: a case series of 24 pediatric patients and evaluation of associated anomalies, incidence of hydrocephalus, and developmental outcomes.
    Sasaki-Adams D; Elbabaa SK; Jewells V; Carter L; Campbell JW; Ritter AM
    J Neurosurg Pediatr; 2008 Sep; 2(3):194-9. PubMed ID: 18759601
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Corpus callosum agenesis, facial anomalies, Robin sequence, and other anomalies: a new autosomal recessive syndrome?
    Toriello HV; Carey JC
    Am J Med Genet; 1988 Sep; 31(1):17-23. PubMed ID: 3223497
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 22.