Infantile Type of So-called Neuronal Ceroid-lipofuscinosis
Author:
Publisher
Wiley
Subject
Neurology (clinical),Developmental Neuroscience,Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-8749.1974.tb04183.x/fullpdf
Reference25 articles.
1. Brett , E. M. 1973 ‘Gangliosidosis of late onset.’
2. ‘Late onset GM2-gangliosidosis. Clinical, pathological and biochemical studies on eight patients.’;Brett;Archives of Disease in Childhood,1973
3. ‘Late infantile systemic lipidosis. Major monosialogangliosidosis. Delineation of two types.’;Derry;Neurology,1968
4. ‘Late infantile progressive encephalopathy with disturbed polyunsaturated fat metabolism.’;Hagberg;Acta Paediatrica Scandinavica,1968
5. ‘Polyunsaturated fatty acid lipidosis-infantile form of so-called neuronal ceroid-lipofuscinosis. I. Clinical and morphological aspects.’;Hagberg;Acta Paediatrica Scandinavica,1974
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