Subacute Necrotising Encephalomyelopathy in Three Siblings

Author:

Gordon Neil,Marsden H.B.,Lewis D.M.

Publisher

Wiley

Subject

Clinical Neurology,Developmental Neuroscience,Pediatrics, Perinatology, and Child Health

Reference17 articles.

1. A defect in pyruvate decarboxylase in a child with an intermittent movement disorder.‘;Blass;Journal of Clinical Investigation,1970

2. ‘Clinical studies of a patient with pyruvate decarboxylase deficiency’.;Blass;Archives of Neurology.,1971

3. Thiamine responsive lactic acidosis in a patient with low-KM pyruvate carboxylase activity in liver.‘;Brunette;Pediatrics,1972

4. ‘Leigh's subacute necroiizing encephalopathy: clinical and biochemical study with special reference to therapy with lipoate.’;Clayton;Archives of Disease in Childhood.,1967

5. ‘Thiamine triphosphate deficiency in subacute necrotizing encephalomyelopathy.’;Cooper;Science,1969

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1. Leigh Syndrome in a Filipino Child: A Case Report;Journal of Medicine, University of Santo Tomas;2022-10-31

2. Characterization of 16 novel human genes showing high similarity to yeast sequences;Yeast;2000

3. Degenerative cerebral diseases;Neurological Problems in Childhood;1993

4. Leigh syndrome, a mitochondrial encephalo(myo)pathy;Clinical Neurology and Neurosurgery;1987-01

5. Clinical Chemistry of Thiamin;Advances in Clinical Chemistry;1983

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