Published in Ann Indian Acad Neurol on January 01, 2014
Malformation of the erythrocytes in a case of atypical retinitis pigmentosa. Blood (1950) 2.76
Absence of microsomal triglyceride transfer protein in individuals with abetalipoproteinemia. Science (1992) 2.24
Abetalipoproteinemia is caused by defects of the gene encoding the 97 kDa subunit of a microsomal triglyceride transfer protein. Hum Mol Genet (1993) 1.54
Long-term assessment of combined vitamin A and E treatment for the prevention of retinal degeneration in abetalipoproteinaemia and hypobetalipoproteinaemia patients. Eye (Lond) (2001) 1.33
Differential diagnosis of cerebellar atrophy in childhood. Eur J Paediatr Neurol (2007) 1.24
Abetalipoproteinemia: two case reports and literature review. Orphanet J Rare Dis (2008) 1.20
The Bassen-Kornzweig syndrome: 18 years in evolution. J Mt Sinai Hosp N Y (1968) 0.99
Spinal MRI in progressive myeloneuropathy associated with vitamin E deficiency. Neuroradiology (1996) 0.94
Hepatic peroxisomal abnormalities in abetalipoproteinemia. Gastroenterology (1989) 0.94
Neurologic findings in vitamin E deficiency. Am Fam Physician (1997) 0.93
Ataxia caused by mutations in the alpha-tocopherol transfer protein gene. J Neurol Neurosurg Psychiatry (2000) 0.92
Endocrine function in abetalipoproteinemia: a study of a female patient of Greek origin. Ann Ital Chir (2005) 0.89
Experimental vitamin E deficiency in rats. Morphological and functional evidence of abnormal axonal transport secondary to free radical damage. Brain (1991) 0.87
Mega-corpus callosum, polymicrogyria, and psychomotor retardation syndrome. Pediatr Neurol (2010) 0.85
Prevalence of fatigue in Guillain-Barre syndrome in neurological rehabilitation setting. Ann Indian Acad Neurol (2014) 0.81
The "double panda" sign in Leigh disease. J Child Neurol (2013) 0.77