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 *

53 related articles for article (PubMed ID: 757840)

  • 1. Familial corpus callosum agenesis.
    Ozdirim E; Renda Y
    Turk J Pediatr; 1978; 20(3-4):76-84. PubMed ID: 757840
    [No Abstract]   [Full Text] [Related]  

  • 2. Agenesis of the corpus callosum in a mother and son.
    Inbar D; Halpern GJ; Weitz R; Sadeh M; Shohat M
    Am J Med Genet; 1997 Mar; 69(2):152-4. PubMed ID: 9056551
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Spectrum of corpus callosum agenesis.
    Sztriha L
    Pediatr Neurol; 2005 Feb; 32(2):94-101. PubMed ID: 15664768
    [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. [Agenesis of the corpus callosum].
    Antonenko VG; Robak OP
    Zh Vopr Neirokhir Im N N Burdenko; 1980; (4):59-60. PubMed ID: 7424326
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, and sensorineural deafness: a newly recognized autosomal recessive disorder?
    Donnai D; Barrow M
    Am J Med Genet; 1993 Oct; 47(5):679-82. PubMed ID: 8266995
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Clinical and EEG findings in agenesis of the corpus callosum.
    Guizzaro A; Vizioli R; Paolozzi C
    Acta Neurol (Napoli); 1985; 7(3-4):252-69. PubMed ID: 4061139
    [No Abstract]   [Full Text] [Related]  

  • 9. Agenesis of the corpus callosum. Its associated anomalies and syndromes with special reference to the Apert syndrome.
    Cohen MM; Kreiborg S
    Neurosurg Clin N Am; 1991 Jul; 2(3):565-8. PubMed ID: 1821304
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Agenesis of the corpus callosum].
    Nielsen LH
    Ugeskr Laeger; 1995 Feb; 157(6):737-9. PubMed ID: 7701633
    [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. Agenesis of the corpus callosum: clinical and genetic study in 63 young patients.
    Bedeschi MF; Bonaglia MC; Grasso R; Pellegri A; Garghentino RR; Battaglia MA; Panarisi AM; Di Rocco M; Balottin U; Bresolin N; Bassi MT; Borgatti R
    Pediatr Neurol; 2006 Mar; 34(3):186-93. PubMed ID: 16504787
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Familial agenesis of the corpus callosum with hypothermia and apneic spells.
    Pineda M; Gonzalez A; Fàbregues I; Fernández-Alvarez E; Ferrer I
    Neuropediatrics; 1984 May; 15(2):63-7. PubMed ID: 6738818
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Prognosis of isolated agenesis of the corpus callosum].
    Moutard ML; Lewin F; Baron JM; Kieffer V; Descamps P
    Neurochirurgie; 1998 May; 44(1 Suppl):96-8. PubMed ID: 9757329
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Agenesis of the corpus callosum and chorioretinal lacunae. Aicardi's syndrome.
    Stănescu-Segall B; Stănescu D
    Oftalmologia; 1997; 41(4):323-5. PubMed ID: 9361492
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Bilateral sensorineural deafness, partial agenesis of the corpus callosum, and arachnoid cysts in two sisters.
    Hendriks YM; Laan LA; Vielvoye GJ; van Haeringen A
    Am J Med Genet; 1999 Sep; 86(2):183-6. PubMed ID: 10449658
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Possible new autosomal recessive syndrome of partial agenesis of the corpus callosum, pontine hypoplasia, focal white matter changes, hypotonia, mental retardation, and minor anomalies.
    Jonas RE; Kimonis VE; Morales A
    Am J Med Genet; 1997 Dec; 73(2):184-8. PubMed ID: 9409870
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Isolated familial corpus callosum agenesis prognosis].
    Nizard S; Barthez-Carpentier MA; Gelot A; Hebert C; Abimelech M; Esperandieu O
    Arch Pediatr; 2004 May; 11(5):429-31. PubMed ID: 15135425
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical, neuroimaging and cytogenetic findings in 20 patients with corpus callosum dysgenesis.
    dos Santos AC; Midleton SR; Fonseca RL; dos Santos SR; Llerena JC; Vargas FR
    Arq Neuropsiquiatr; 2002 Jun; 60(2-B):382-5. PubMed ID: 12131936
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Three familial midline malformtion syndromes of the central nervous system: agenesis of the corpus callosum and anterior horn-cell disease; agenesis of cerebellar vermis; and atrophy of the cerebellar vermis.
    Andermann E; Andermann F; Joubert M; Melançon D; Karpati G; Carpenter S
    Birth Defects Orig Artic Ser; 1975; 11(2):269-93. PubMed ID: 1227532
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 3.