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6 in total

1. Gcn5 loss-of-function accelerates cerebellar and retinal degeneration in a SCA7 mouse model.

Authors: Yi Chun Chen; Jennifer R Gatchel; Rebecca W Lewis; Chai-An Mao; Patrick A Grant; Huda Y Zoghbi; Sharon Y R Dent
Journal: Hum Mol Genet Date: 2011-10-14 Impact factor: 6.150

2. Hereditary spastic ataxia with congenital miosis: four cases in one family.

Authors: D J Dick; P K Newman; P G Cleland
Journal: Br J Ophthalmol Date: 1983-02 Impact factor: 4.638

3. Genetic aspects of autosomal dominant late onset cerebellar ataxia.

Authors: A E Harding
Journal: J Med Genet Date: 1981-12 Impact factor: 6.318

4. Hereditary cerebellar atrophy (Holmes type) with optic atrophy: a clinico-pathological study of four generations in a family.

Authors: H Budka; D Seemann; W Danielczyk
Journal: Arch Psychiatr Nervenkr (1970) Date: 1979-04-12

5. A syndrome of congenital retinal dystrophy and saccade palsy--a subset of Leber's amaurosis.

Authors: A T Moore; D S Taylor
Journal: Br J Ophthalmol Date: 1984-06 Impact factor: 4.638

6. Familial olivopontocerebellar atrophy with neonatal onset: a recessively inherited syndrome with systemic and biochemical abnormalities.

Authors: B N Harding; D B Dunger; D B Grant; M Erdohazi
Journal: J Neurol Neurosurg Psychiatry Date: 1988-03 Impact factor: 10.154

6 in total