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Items: 18

1.
3.

Bilateral periventricular nodular heterotopia with mental retardation and syndactyly in boys: a new X-linked mental retardation syndrome.

Dobyns WB, Guerrini R, Czapansky-Beilman DK, Pierpont ME, Breningstall G, Yock DH Jr, Bonanni P, Truwit CL.

Neurology. 1997 Oct;49(4):1042-7. Review.

PMID:
9339687
4.

New syndrome with the Sakoda complex, bilateral anophthalmia, and cortical dysgenesis.

Ehara H, Kurimasa A, Ohno K, Takeshita K.

Pediatr Neurol. 1998 May;18(5):445-51. Review.

PMID:
9650690
5.

Familial MCA/MR syndrome due to inherited submicroscopic translocation t(18;21)(q22.1q21.3) with breakpoint at the Down syndrome critical region.

Horn D, Neitzel H, Tönnies H, Kalscheuer V, Kunze J, Hinkel GK, Bartsch O.

Am J Med Genet A. 2003 Mar 15;117A(3):236-44. Review.

PMID:
12599186
6.

Genetic malformations of the cerebral cortex and epilepsy.

Guerrini R.

Epilepsia. 2005;46 Suppl 1:32-7. Review.

7.

A case in the spectrum of the oculo-encephalo-hepato-renal syndrome.

Ehara H, Tamaoki Y, Eda I.

Pediatr Neurol. 1999 Oct;21(4):757-62. Review.

PMID:
10580893
8.

Fetal alcohol syndrome and the developing socio-emotional brain.

Niccols A.

Brain Cogn. 2007 Oct;65(1):135-42. Epub 2007 Jul 31. Review.

PMID:
17669569
9.

Ophthalmic involvement in the fetal alcohol syndrome: clinical and animal model studies.

Strömland K, Pinazo-Durán MD.

Alcohol Alcohol. 2002 Jan-Feb;37(1):2-8. Review.

PMID:
11825849
10.
11.

[Familial cases of spastic paraparesis, mental disturbance and thinning of the corpus callosum].

Honda Y, Sugihara E, Hino H, Shoji H, Oizumi K.

Rinsho Shinkeigaku. 1993 May;33(5):507-13. Review. Japanese.

PMID:
8365056
12.

Oligophrenin 1 (OPHN1) gene mutation causes syndromic X-linked mental retardation with epilepsy, rostral ventricular enlargement and cerebellar hypoplasia.

Bergmann C, Zerres K, Senderek J, Rudnik-Schoneborn S, Eggermann T, Häusler M, Mull M, Ramaekers VT.

Brain. 2003 Jul;126(Pt 7):1537-44. Epub 2003 May 21. Review.

PMID:
12805098
13.

Identification and evaluation of mental retardation.

Daily DK, Ardinger HH, Holmes GE.

Am Fam Physician. 2000 Feb 15;61(4):1059-67, 1070. Review. Erratum in: Am Fam Physician 2000 Sep 1;62(5):961-3.

14.

[Syndromes 19. Fetal alcohol syndrome].

Vissink A, Hoff M, Stremmelaar EF.

Ned Tijdschr Tandheelkd. 2000 Mar;107(3):97-9. Review. Dutch.

PMID:
11385771
15.

[Börjeson-Forssman-Lehmann syndrome].

Fujieda K.

Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):147-9. Review. Japanese. No abstract available.

PMID:
11057174
16.

Cerebral dysgenesis. An overview.

Schaefer GB, Sheth RD, Bodensteiner JB.

Neurol Clin. 1994 Nov;12(4):773-88. Review.

PMID:
7845342
17.

Case study. A child with Lennox-Gastaut syndrome.

Kongelbeck SR.

Clin Nurs Pract Epilepsy. 1996 Apr;3(2):8-10. Review. No abstract available.

PMID:
8788700
18.

[Overgrowth, macrocephaly-hemangioma, Riley-Smith type].

Narahara K.

Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):453-5. Review. Japanese. No abstract available.

PMID:
11528833

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