176 related articles for article (PubMed ID: 15679191)
1. Brief report: acrocallosal syndrome and autism.
Steiner CE; Guerreiro MM; Marques-de-Faria AP
J Autism Dev Disord; 2004 Dec; 34(6):723-6. PubMed ID: 15679191
[TBL] [Abstract][Full Text] [Related]
2. Spectrum of the acrocallosal syndrome.
Koenig R; Bach A; Woelki U; Grzeschik KH; Fuchs S
Am J Med Genet; 2002 Feb; 108(1):7-11. PubMed ID: 11857542
[TBL] [Abstract][Full Text] [Related]
3. Neurologic abnormalities in infantile autism.
Haas RH; Townsend J; Courchesne E; Lincoln AJ; Schreibman L; Yeung-Courchesne R
J Child Neurol; 1996 Mar; 11(2):84-92. PubMed ID: 8881982
[TBL] [Abstract][Full Text] [Related]
4. The cognitive neuroscience of autism.
Baron-Cohen S
J Neurol Neurosurg Psychiatry; 2004 Jul; 75(7):945-8. PubMed ID: 15201345
[No Abstract] [Full Text] [Related]
5. Acrocallosal syndrome: report of five Turkish patients.
Gül D; Ulucan H; Ünay B; Akın R; Gökçay E
Clin Dysmorphol; 2004 Oct; 13(4):241-246. PubMed ID: 15365461
[TBL] [Abstract][Full Text] [Related]
6. Acrocallosal syndrome.
Shilpa BJ; Ashok L; Sattur PA
J Indian Soc Pedod Prev Dent; 2006 Mar; 24(1):45-9. PubMed ID: 16582532
[TBL] [Abstract][Full Text] [Related]
7. Case report: autistic disorder in Kabuki syndrome.
Akin Sari B; Karaer K; Bodur S; Soysal AS
J Autism Dev Disord; 2008 Jan; 38(1):198-201. PubMed ID: 17721696
[No Abstract] [Full Text] [Related]
8. Schinzel acrocallosal syndrome.
Gulati S; Menon S; Kabra M; Kalra V
Indian J Pediatr; 2003 Feb; 70(2):173-6. PubMed ID: 12661815
[TBL] [Abstract][Full Text] [Related]
9. An additional manifestation in acrocallosal syndrome: temporal lobe hypoplasia.
Aykut A; Cogulu O; Ekmekci AY; Ozkinay F
Genet Couns; 2008; 19(2):237-40. PubMed ID: 18618999
[TBL] [Abstract][Full Text] [Related]
10. Acrocallosal syndrome in a young hypertensive male.
Ramteke VV; Darole PA; Shaikh ZF; Padwal NJ; Agrawal B; Shrivastava MS; Kamath S
BMJ Case Rep; 2011 May; 2011():. PubMed ID: 22696705
[TBL] [Abstract][Full Text] [Related]
11. Novel KIF7 mutations extend the phenotypic spectrum of acrocallosal syndrome.
Putoux A; Nampoothiri S; Laurent N; Cormier-Daire V; Beales PL; Schinzel A; Bartholdi D; Alby C; Thomas S; Elkhartoufi N; Ichkou A; Litzler J; Munnich A; Encha-Razavi F; Kannan R; Faivre L; Boddaert N; Rauch A; Vekemans M; Attié-Bitach T
J Med Genet; 2012 Nov; 49(11):713-20. PubMed ID: 23125460
[TBL] [Abstract][Full Text] [Related]
12. Autistic features in Joubert syndrome: a genetic disorder with agenesis of the cerebellar vermis.
Holroyd S; Reiss AL; Bryan RN
Biol Psychiatry; 1991 Feb; 29(3):287-94. PubMed ID: 2015333
[TBL] [Abstract][Full Text] [Related]
13. Brief report: the association between autism and fragile X syndrome: a case report.
Lenti C; Peruzzi C; Bianchini E
J Autism Dev Disord; 1995 Dec; 25(6):655-62. PubMed ID: 8720033
[No Abstract] [Full Text] [Related]
14. Partial Agenesis and Hypoplasia of the Corpus Callosum in Idiopathic Autism.
Wegiel J; Flory M; Kaczmarski W; Brown WT; Chadman K; Wisniewski T; Nowicki K; Kuchna I; Ma SY; Wegiel J
J Neuropathol Exp Neurol; 2017 Mar; 76(3):225-237. PubMed ID: 28395085
[TBL] [Abstract][Full Text] [Related]
15. The acrocallosal syndrome in a Turkish boy.
Yüksel M; Caliskan M; Oğur G; Ozmen M; Dolunay G; Apak S
J Med Genet; 1990 Jan; 27(1):48-9. PubMed ID: 2308155
[TBL] [Abstract][Full Text] [Related]
16. Acrocallosal syndrome: a new case.
Lungarotti MS; Marinelli D; Mezzetti D; Caputo N; Calabro A
Am J Med Genet; 1991 Jul; 40(1):94-6. PubMed ID: 1887856
[TBL] [Abstract][Full Text] [Related]
17. Sibs with anencephaly, anophthalmia, clefts, omphalocele, and polydactyly: hydrolethalus or acrocallosal syndrome?
Christensen B; Blaas HG; Isaksen CV; Roald B; Orstavik KH
Am J Med Genet; 2000 Mar; 91(3):231-4. PubMed ID: 10756349
[TBL] [Abstract][Full Text] [Related]
18. Agenesis of corpus callosum: clinical description and etiology.
Marszał E; Jamroz E; Pilch J; Kluczewska E; Jabłecka-Deja H; Krawczyk R
J Child Neurol; 2000 Jun; 15(6):401-5. PubMed ID: 10868784
[TBL] [Abstract][Full Text] [Related]
19. Autistic features in young children with significant cognitive impairment: autism or mental retardation?
Vig S; Jedrysek E
J Autism Dev Disord; 1999 Jun; 29(3):235-48. PubMed ID: 10425586
[TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis of ring chromosome 6 in a fetus with cerebellar hypoplasia and partial agenesis of corpus callosum: case report and review of the literature.
Andrieux J; Devisme L; Valat AS; Robert Y; Frnka C; Savary JB
Eur J Med Genet; 2005; 48(2):199-206. PubMed ID: 16053913
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
