Lipid Metabolism, Inborn Errors
This graph shows the total number of publications written about "Lipid Metabolism, Inborn Errors" by people in the URMC Research Network by year, and whether "Lipid Metabolism, Inborn Errors" was a major or minor topic of these publication.
Below are the most recent publications written about "Lipid Metabolism, Inborn Errors" by people in Profiles.
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McClaskey JH, Leman AR, Rothberg PG. Homogeneous amplification nucleobase quenching assay to detect the E474Q LCHAD deficiency mutation. Genet Test. 2005; 9(1):1-5.
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Hostetler MA, Arnold GL, Mooney R, Bennett MJ, Rinaldo P, Roe CR. Hypoketotic hypoglycemic coma in a 21-month-old child. Ann Emerg Med. 1999 Sep; 34(3):394-8.
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Siafakas CG, Brown MR, Miller TL. Neonatal pancreatitis associated with familial lipoprotein lipase deficiency. J Pediatr Gastroenterol Nutr. 1999 Jul; 29(1):95-8.
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Eviatar L, Sklower SL, Wisniewski K, Feldman RS, Gochoco A. Farber lipogranulomatosis: an unusual presentation in a black child. Pediatr Neurol. 1986 Nov-Dec; 2(6):371-4.
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Howard CP, Go VL, Infante AJ, Perrault J, Gerich JE, Haymond MW. Long-term survival in a case of functional pancreatic agenesis. J Pediatr. 1980 Nov; 97(5):786-9.
