85 related articles for article (PubMed ID: 8292134)
21. A new patient with Andermann syndrome: an underdiagnosed clinical genetics entity?
Degerliyurt A; Akgumus G; Caglar C; Bilguvar K; Caglayan AO
Genet Couns; 2013; 24(3):283-9. PubMed ID: 24341143
[TBL] [Abstract][Full Text] [Related]
22. Ullrich-Turner syndrome with agenesis of the corpus callosum.
Kimura M; Nakajima M; Yoshino K
Am J Med Genet; 1990 Oct; 37(2):227-8. PubMed ID: 2248289
[TBL] [Abstract][Full Text] [Related]
23. The Andermann syndrome: agenesis of the corpus callosum associated with mental retardation and progressive sensorimotor neuronopathy.
Larbrisseau A; Vanasse M; Brochu P; Jasmin G
Can J Neurol Sci; 1984 May; 11(2):257-61. PubMed ID: 6329500
[TBL] [Abstract][Full Text] [Related]
24. Mid-portion agenesis of corpus callosum in a presumed Baller-Gerold syndrome.
Dunac A; Van Bogaert P; David P; Avni EF; Paduart O; Szliwowski HB; Van Regemorter N
Neuropediatrics; 1995 Oct; 26(5):273-5. PubMed ID: 8552221
[TBL] [Abstract][Full Text] [Related]
25. Acrocallosal syndrome: association with cystic malformation of the brain and neurodevelopmental aspects.
Thyen U; Aksu F; Bartsch O; Herb E
Neuropediatrics; 1992 Dec; 23(6):292-6. PubMed ID: 1491747
[TBL] [Abstract][Full Text] [Related]
26. Unusual neurophysiological features in Cockayne's syndrome: a report of two cases as a contribution to diagnosis and classification.
Scaioli V; D'Arrigo S; Pantaleoni C
Brain Dev; 2004 Jun; 26(4):273-80. PubMed ID: 15130695
[TBL] [Abstract][Full Text] [Related]
27. Thrombocytopenia-absent radius (tar) syndrome: a case with agenesis of corpus callosum, hypoplasia of cerebellar vermis and horseshoe kidney.
Skórka A; Bielicka-Cymermann J; Gieruszczak-Białek D; Korniszewski L
Genet Couns; 2005; 16(4):377-82. PubMed ID: 16440880
[TBL] [Abstract][Full Text] [Related]
28. Mosaic tetrasomy 8p.
Newton D; Hammond L; Wiley J; Kushnick T
Am J Med Genet; 1993 Jun; 46(5):513-6. PubMed ID: 8322811
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. Complicated hereditary spastic paraplegia with peripheral neuropathy, optic atrophy and mental retardation.
Miyama S; Arimoto K; Kimiya S; Tomi H
Neuropediatrics; 2000 Aug; 31(4):214-7. PubMed ID: 11071149
[TBL] [Abstract][Full Text] [Related]
31. [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]
32. Expanding the differential diagnosis of inherited neuropathies with non-uniform conduction: Andermann syndrome.
Lourenço CM; Dupré N; Rivière JB; Rouleau GA; Marques VD; Genari AB; Santos AC; Barreira AA; Marques W
J Peripher Nerv Syst; 2012 Mar; 17(1):123-7. PubMed ID: 22462673
[TBL] [Abstract][Full Text] [Related]
33. [A case of spastic paraparesis with mental deterioration and markedly thin corpus callosum--callosal dysfunction demonstrated by magnetic stimulation].
Katayama T; Sakamoto N; Kuroda K; Yahara O; Ugawa Y
Rinsho Shinkeigaku; 1998 May; 38(5):418-22. PubMed ID: 9805987
[TBL] [Abstract][Full Text] [Related]
34. [Joubert's syndrome: report of 12 cases].
Barreirinho MS; Teixeira J; Moreira NC; Bastos S; Gonçalvez S; Barbot MC
Rev Neurol; 2001 May 1-15; 32(9):812-7. PubMed ID: 11424029
[TBL] [Abstract][Full Text] [Related]
35. Delayed myelination in a patient with 18q- syndrome.
Ono J; Harada K; Yamamoto T; Onoe S; Okada S
Pediatr Neurol; 1994 Jul; 11(1):64-7. PubMed ID: 7527214
[TBL] [Abstract][Full Text] [Related]
36. Myelination disturbance in a patient with hyperuricemia and hyperserotoninemia combined with 18q deletion syndrome.
László A; Vörös E; Buga K; Horváth K; Mayer P; Osztovics M; Pávics L; Svekus A; Patterson MC
Ideggyogy Sz; 2009 Nov; 62(11-12):413-7. PubMed ID: 20025132
[TBL] [Abstract][Full Text] [Related]
37. Subtotal corpus callosum agenesis with recurrent hyperhidrosis-hypothermia (Shapiro syndrome).
Tambasco N; Corea F; Bocola V
Neurology; 2005 Jul; 65(1):124. PubMed ID: 16009897
[No Abstract] [Full Text] [Related]
38. The acrocallosal syndrome.
Nelson MM; Thomson AJ
Am J Med Genet; 1982 Jun; 12(2):195-9. PubMed ID: 7102724
[TBL] [Abstract][Full Text] [Related]
39. [Motor and sensory neuropathies with or without agenesis of the corpus callosum: a radiological study of 64 cases].
Mathieu J; Bédard F; Prévost C; Langevin P
Can J Neurol Sci; 1990 May; 17(2):103-8. PubMed ID: 2357646
[TBL] [Abstract][Full Text] [Related]
40. A case of Høyeraal-Hreidarsson syndrome: delayed myelination and hypoplasia of corpus callosum are other important signs.
Akaboshi S; Yoshimura M; Hara T; Kageyama H; Nishikwa K; Kawakami T; Ieshima A; Takeshita K
Neuropediatrics; 2000 Jun; 31(3):141-4. PubMed ID: 10963101
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
