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Literature DB >> 2030350

Occidental type cerebromuscular dystrophy: a report of eleven cases.

H Topaloğlu¹, K Yalaz, Y Renda, M Cağlar, S Göğüs, G Kale, K Gücüyener, G Nurlu.

Abstract

Occidental type cerebromuscular dystrophy (OCMD) forms a substantial distinct group within congenital muscular dystrophy (CMD). These patients invariably present with amyotrophy, multiple joint contractures, facial muscle involvement, normal or nearly normal intelligence, leukodystrophic appearance on CT scan, and dystrophic changes in muscle.

Entities: Disease Species

Mesh：

Year: 1991 PMID： 2030350 PMCID： PMC1014390 DOI： 10.1136/jnnp.54.3.226

Source DB: PubMed Journal: J Neurol Neurosurg Psychiatry ISSN： 0022-3050 Impact factor: 10.154

19 in total

1. Congenital muscular dystrophy as a disease of the central nervous system.

Authors: S Kamoshita; Y Konishi; M Segawa; Y Fukuyama
Journal: Arch Neurol Date: 1976-07

2. Congenital muscular dystrophy of a non-Fukuyama type.

Authors: B Echenne
Journal: Brain Dev Date: 1988 Impact factor: 1.961

3. Fukuyama-type congenital muscular dystrophy.

Authors: J B McMenamin; L E Becker; E G Murphy
Journal: J Pediatr Date: 1982-10 Impact factor: 4.406

4. Congenital muscle disease and abnormal findings on computerized tomography.

Authors: A G Nogen
Journal: Dev Med Child Neurol Date: 1980-10 Impact factor: 5.449

5. Changes in cerebral white matter in a case of congenital muscular dystrophy.

Authors: J M Gobernado; A Gimeno
Journal: Pediatr Radiol Date: 1982

6. Congenital muscular dystrophy: a clinico-pathological and follow-up study of 15 patients.

Authors: M Donner; J Rapola; H Somer
Journal: Neuropadiatrie Date: 1975-08

7. Congenital progressive muscular dystrophy of the Fukuyama type - clinical, genetic and pathological considerations.

Authors: Y Fukuyama; M Osawa; H Suzuki
Journal: Brain Dev Date: 1981 Impact factor: 1.961

8. Congenital muscular dystrophy: a clinicopathologic report of 24 cases.

Authors: J B McMenamin; L E Becker; E G Murphy
Journal: J Pediatr Date: 1982-05 Impact factor: 4.406

9. Involvement of the central nervous system in congenital muscular dystrophies.

Authors: J Egger; B E Kendall; M Erdohazi; B D Lake; J Wilson; E M Brett
Journal: Dev Med Child Neurol Date: 1983-02 Impact factor: 5.449

10. Congenital muscular dystrophy and cerebral dysgenesis in a Dutch family.

Authors: J B Krijgsman; P G Barth; F C Stam; J L Slooff; H H Jaspar
Journal: Neuropadiatrie Date: 1980-05

5 in total

1. Medical education and the challenge of neurological disability.

Authors: C D Ward
Journal: J Neurol Neurosurg Psychiatry Date: 1992-03 Impact factor: 10.154

2. Neurology in the United Kingdom. I: Historical development.

Authors: R Langton Hewer; V A Wood
Journal: J Neurol Neurosurg Psychiatry Date: 1992-03 Impact factor: 10.154

3. Refinement of the laminin alpha2 chain locus to human chromosome 6q2 in severe and mild merosin deficient congenital muscular dystrophy.

Authors: I S Naom; M D'Alessandro; H Topaloglu; C Sewry; A Ferlini; A Helbling-Leclerc; P Guicheney; J Weissenbach; K Schwartz; K Bushby; J Philpot; V Dubowitz; F Muntoni
Journal: J Med Genet Date: 1997-02 Impact factor: 6.318

4. Congenital muscular dystrophy. A study on the variability of morphological changes and dystrophin distribution in muscle biopsies.

Authors: Q H Leyten; H J ter Laak; F J Gabreëls; W O Renier; K Renkawek; R C Sengers
Journal: Acta Neuropathol Date: 1993 Impact factor: 17.088

5. Congenital muscular dystrophy and severe central nervous system atrophy in two siblings.

Authors: Q H Leyten; P G Barth; F J Gabreëls; K Renkawek; W O Renier; A A Gabreëls-Festen; H J ter Laak; M G Smits
Journal: Acta Neuropathol Date: 1995 Impact factor: 17.088

5 in total