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2. 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]
3. Congenital muscular dystrophy: a review of the literature. Leyten QH; Gabreëls FJ; Renier WO; ter Laak HJ Clin Neurol Neurosurg; 1996 Nov; 98(4):267-80. PubMed ID: 8930416 [TBL] [Abstract][Full Text] [Related]
4. [Western type cerebro-muscular dystrophy and congenital merosin deficiency muscular dystrophy: two terms for the same disorder]. Castro-Gago M; Novo-Rodríguez MI; Pintos-Martínez E; Alonso-Martín A; Morales-Redondo R; Eirís-Puñal J Rev Neurol; 1998 Sep; 27(157):459-62. PubMed ID: 9774819 [TBL] [Abstract][Full Text] [Related]
5. New FKRP mutations causing congenital muscular dystrophy associated with mental retardation and central nervous system abnormalities. Identification of a founder mutation in Tunisian families. Louhichi N; Triki C; Quijano-Roy S; Richard P; Makri S; Méziou M; Estournet B; Mrad S; Romero NB; Ayadi H; Guicheney P; Fakhfakh F Neurogenetics; 2004 Feb; 5(1):27-34. PubMed ID: 14652796 [TBL] [Abstract][Full Text] [Related]
6. Neuroimaging manifestations and classification of congenital muscular dystrophies. Barkovich AJ AJNR Am J Neuroradiol; 1998 Sep; 19(8):1389-96. PubMed ID: 9763366 [TBL] [Abstract][Full Text] [Related]
8. Merosin-positive congenital muscular dystrophy: a large inbred family. Mahjneh I; Bushby K; Anderson L; Muntoni F; Tolvanen-Mahjneh H; Bashir R; Pizzi A; Brockington M; Marconi G Neuropediatrics; 1999 Feb; 30(1):22-8. PubMed ID: 10222457 [TBL] [Abstract][Full Text] [Related]
9. Congenital muscular dystrophy with cerebral white matter hypodensity. Correlation of clinical features and merosin deficiency. Reed UC; Marie SK; Vainzof M; Salum PB; Levy JA; Zatz M; Diament A Brain Dev; 1996; 18(1):53-8. PubMed ID: 8907344 [TBL] [Abstract][Full Text] [Related]
10. Congenital muscular dystrophy with complete laminin-alpha2-deficiency, cortical dysplasia, and cerebral white-matter changes in children. Tsao CY; Mendell JR; Rusin J; Luquette M J Child Neurol; 1998 Jun; 13(6):253-6. PubMed ID: 9660506 [TBL] [Abstract][Full Text] [Related]
11. Magnetic resonance imaging in classification of congenital muscular dystrophies with brain abnormalities. van der Knaap MS; Smit LM; Barth PG; Catsman-Berrevoets CE; Brouwer OF; Begeer JH; de Coo IF; Valk J Ann Neurol; 1997 Jul; 42(1):50-9. PubMed ID: 9225685 [TBL] [Abstract][Full Text] [Related]
12. Congenital muscular dystrophy. Huang FL; Mak SC; Chi CS Zhonghua Yi Xue Za Zhi (Taipei); 2000 Feb; 63(2):165-9. PubMed ID: 10677931 [TBL] [Abstract][Full Text] [Related]
13. Cobblestone lissencephaly with normal eyes and muscle. Dobyns WB; Patton MA; Stratton RF; Mastrobattista JM; Blanton SH; Northrup H Neuropediatrics; 1996 Apr; 27(2):70-5. PubMed ID: 8737821 [TBL] [Abstract][Full Text] [Related]
15. Involvement of the central nervous system in congenital muscular dystrophies. Egger J; Kendall BE; Erdohazi M; Lake BD; Wilson J; Brett EM Dev Med Child Neurol; 1983 Feb; 25(1):32-42. PubMed ID: 6832496 [TBL] [Abstract][Full Text] [Related]
16. Congenital muscular dystrophy of non-Fukuyama type with characteristic CT images. Yoshioka M; Kuroki S; Mizue H Brain Dev; 1987; 9(3):316-8. PubMed ID: 3661912 [TBL] [Abstract][Full Text] [Related]
17. Congenital muscular dystrophy associated with calf hypertrophy, microcephaly and severe mental retardation in three Italian families: evidence for a novel CMD syndrome. Villanova M; Mercuri E; Bertini E; Sabatelli P; Morandi L; Mora M; Sewry C; Brockington M; Brown SC; Ferreiro A; Maraldi NM; Toda T; Guicheney P; Merlini L; Muntoni F Neuromuscul Disord; 2000 Dec; 10(8):541-7. PubMed ID: 11053679 [TBL] [Abstract][Full Text] [Related]
18. Dropped head congenital muscular dystrophy caused by de novo mutations in LMNA. Karaoglu P; Quizon N; Pergande M; Wang H; Polat AI; Ersen A; Özer E; Willkomm L; Hiz Kurul S; Heredia R; Yis U; Selcen D; Çirak S Brain Dev; 2017 Apr; 39(4):361-364. PubMed ID: 27876398 [TBL] [Abstract][Full Text] [Related]
19. Clinical variation within sibships in Fukuyama-type congenital muscular dystrophy. Yoshioka M; Kuroki S; Nigami H; Kawai T; Nakamura H Brain Dev; 1992 Sep; 14(5):334-7. PubMed ID: 1456390 [TBL] [Abstract][Full Text] [Related]
20. Occidental type cerebromuscular dystrophy: a report of eleven cases. Topaloğlu H; Yalaz K; Renda Y; Cağlar M; Göğüs S; Kale G; Gücüyener K; Nurlu G J Neurol Neurosurg Psychiatry; 1991 Mar; 54(3):226-9. PubMed ID: 2030350 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]