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.
117 related articles for article (PubMed ID: 7608731)
1. White matter abnormalities in congenital muscular dystrophy. Leyten QH; Gabreëls FJ; Renier WO; van Engelen BG; ter Laak HJ; Sengers RC; Thijssen HO J Neurol Sci; 1995 Apr; 129(2):162-9. PubMed ID: 7608731 [TBL] [Abstract][Full Text] [Related]
2. Divergence of central nervous system involvement in 2 Italian sisters with congenital muscular dystrophy: a clinical and neuroradiological follow-up. Trevisan CP; Martinello F; Ferruzza E; Angelini C Eur Neurol; 1995; 35(4):230-5. PubMed ID: 7671985 [TBL] [Abstract][Full Text] [Related]
3. Congenital muscular dystrophy with cerebral involvement--report of a case of "occidental type cerebromuscular dystrophy"? Topaloglu H; Yalaz K; Kale G; Ergin M Neuropediatrics; 1990 Feb; 21(1):53-4. PubMed ID: 2314559 [TBL] [Abstract][Full Text] [Related]
4. Congenital muscular dystrophy of a non-Fukuyama type with white matter hyperlucency on CT scan. Kao KP; Lin KP Brain Dev; 1992 Nov; 14(6):420-2. PubMed ID: 1492657 [TBL] [Abstract][Full Text] [Related]
5. Central nervous system involvement in progressive muscular dystrophy. Yoshioka M; Okuno T; Honda Y; Nakano Y Arch Dis Child; 1980 Aug; 55(8):589-94. PubMed ID: 7436514 [TBL] [Abstract][Full Text] [Related]
6. Changes in cerebral white matter in a case of congenital muscular dystrophy (non-Fukuyama type). Tanaka J; Mimaki T; Okada S; Fujimura H Neuropediatrics; 1990 Nov; 21(4):183-6. PubMed ID: 2290477 [TBL] [Abstract][Full Text] [Related]
7. Long-term prognosis of epilepsies and related seizure disorders in Fukuyama-type congenital muscular dystrophy. Yoshioka M; Higuchi Y J Child Neurol; 2005 Apr; 20(4):385-91. PubMed ID: 15921243 [TBL] [Abstract][Full Text] [Related]
8. CNS in congenital muscular dystrophy without mental retardation. Pihko H; Louhimo T; Valanne L; Donner M Neuropediatrics; 1992 Jun; 23(3):116-22. PubMed ID: 1641078 [TBL] [Abstract][Full Text] [Related]
9. Merosin-negative congenital muscular dystrophy, occipital epilepsy with periodic spasms and focal cortical dysplasia. Report of three Italian cases in two families. Pini A; Merlini L; Tomé FM; Chevallay M; Gobbi G Brain Dev; 1996; 18(4):316-22. PubMed ID: 8879653 [TBL] [Abstract][Full Text] [Related]
16. Lissencephaly with congenital muscular dystrophy and ocular abnormalities: cerebro-oculo-muscular syndrome. Sasaki M; Yoshioka K; Yanagisawa T; Nemoto A; Takasago Y; Nagano T Childs Nerv Syst; 1989 Feb; 5(1):35-7. PubMed ID: 2495176 [TBL] [Abstract][Full Text] [Related]
17. A case of merosin-negative congenital muscular dystrophy with extensive white matter abnormalities and electroencephalographic changes in a Syrian boy. Al-Ajmi MO; Abdulla JK; Neubauer D J Med Liban; 2001; 49(3):173-8. PubMed ID: 12184464 [TBL] [Abstract][Full Text] [Related]
18. Fukuyama type congenital muscular dystrophy with central-temporal EEG foci (rolandic spikes). Wu L; Hirokazu O; Makiko O; Yukio F Chin Med Sci J; 1993 Sep; 8(3):162-6. PubMed ID: 8142632 [TBL] [Abstract][Full Text] [Related]