Pages that link to "Q42517399"

The following pages link to Cortical dysplasia in a 23-week fetus with Fukuyama congenital muscular dystrophy (FCMD). (Q42517399):

Displaying 19 items.

• Presenilin-1 deficiency leads to loss of Cajal-Retzius neurons and cortical dysplasia similar to human type 2 lissencephaly (Q28587858) (← links)
• Surgical pathology of epilepsy-associated non-neoplastic cerebral lesions: a brief introduction with special reference to hippocampal sclerosis and focal cortical dysplasia (Q33998374) (← links)
• A review of functional and structural components of the respiratory center involved in the arousal response (Q35573223) (← links)
• Prenatal diagnosis of congenital myopathies and muscular dystrophies. (Q38838661) (← links)
• Cortical dysplasia in Fukuyama congenital muscular dystrophy (FCMD): a Golgi and angioarchitectonic analysis (Q41253593) (← links)
• Congenital muscular dystrophies: 1997 update (Q41739772) (← links)
• Cerebellar micropolygyria in Fukuyama congenital muscular dystrophy: observations in fetal and pediatric cases. (Q41833665) (← links)
• Clinicopathological study on eyes from cases of Fukuyama type congenital muscular dystrophy (Q43542175) (← links)
• Oxidative stress in the brain of Fukuyama type congenital muscular dystrophy: immunohistochemical study on astrocytes (Q44314338) (← links)
• Aberrant neuronal migration in the brainstem of fukuyama-type congenital muscular dystrophy (Q44455402) (← links)
• Development of the cortical dysplasia of type II lissencephaly (Q48274378) (← links)
• Early ultrastructural changes in the central nervous system in Fukuyama congenital muscular dystrophy (Q48676665) (← links)
• Prenatal diagnosis of Fukuyama type congenital muscular dystrophy by polymorphism analysis (Q48830604) (← links)
• Neuropathological findings in muscle-eye-brain disease (MEB-D). Neuropathological delineation of MEB-D from congenital muscular dystrophy of the Fukuyama type (Q52053850) (← links)
• Developmental aspects of type II lissencephaly. Comparative study of dysplastic lesions in fetal and post-natal brains. (Q52211654) (← links)
• Cerebro-ocular dysplasia--muscular dystrophy (Walker Warburg) syndrome. Findings in 20-week-old fetus (Q68023956) (← links)
• Fetal type II lissencephaly: a case report (Q72769157) (← links)
• Pial-glial barrier abnormalities in fetuses with Fukuyama congenital muscular dystrophy (Q73157681) (← links)
• Experimental production of leptomeningeal heterotopias from dissociated fetal tissue (Q93533178) (← links)