Perspective from a Sudanese refugee camp.

Por Buist, N R
Publicado em 1985

Letter: Deliberate injury of children.

Por Buist, N R
Publicado em 1973

Letter: Ketotic hypoglycaemia.

Por Buist, N R
Publicado em 1974

Perspective from Khao-I-Dang refugee camp.

Por Buist, N R
Publicado em 1980

Set of simple side-room urine tests for detection of inborn errors of metabolism.

Por Buist, N. R.
Publicado em 1968

Familial haemophagocytic reticulosis in first cousins.

Por Buist, N R, Jones, R N, Cavens, T R
Publicado em 1971

Absence of -N-acetyl-D-hexosaminidase A activity in a healthy woman.

Por Vidgoff, J, Buist, N R, O'Brien, J S
Publicado em 1973

Gyrate atrophy of the choroid and retina with hyperornithinemia: biochemical and histologic studies and response to vitamin B6.

Por Kennaway, N G, Weleber, R G, Buist, N R
Publicado em 1980

Identification of a splice-site mutation in the aldolase B gene from an individual with hereditary fructose intolerance.

Por Brooks, C C, Buist, N, Tuerck, J, Tolan, D R
Publicado em 1991

Myotonic dystrophy and hyperparathyroidism: association with neurofibromatosis and multiple endocrine adenomatosis type 2A.

Por Rosenberg, N L, Diliberti, J H, Andrews, A M, Buist, N R
Publicado em 1988

Copper poppers: a benign cause of blue diapers.

Por Buist, N R, Ramberg, D A, Strandholm, J J, Ferry, P C
Publicado em 1971

Deficiency in ubiquinone cytochrome c reductase in a patient with mitochondrial myopathy and lactic acidosis.

Por Darley-Usmar, V M, Kennaway, N G, Buist, N R, Capaldi, R A
Publicado em 1983

Computerized surveillance of errors in newborn screening practice.

Por Tuerck, J M, Buist, N R, Skeels, M R, Miyahira, R S, Beach, P G
Publicado em 1987

Carbohydrate-deficient glycoprotein syndrome: not an N-linked oligosaccharide processing defect, but an abnormality in lipid-linked oligosaccharide biosynthesis?

Por Powell, L D, Paneerselvam, K, Vij, R, Diaz, S, Manzi, A, Buist, N, Freeze, H, Varki, A
Publicado em 1994

31P NMR study of improvement in oxidative phosphorylation by vitamins K3 and C in a patient with a defect in electron transport at complex III in skeletal muscle.

Por Eleff, S, Kennaway, N G, Buist, N R, Darley-Usmar, V M, Capaldi, R A, Bank, W J, Chance, B
Publicado em 1984

Localization of the gene for thiamine-responsive megaloblastic anemia syndrome, on the long arm of chromosome 1, by homozygosity mapping.

Por Neufeld, E J, Mandel, H, Raz, T, Szargel, R, Yandava, C N, Stagg, A, Fauré, S, Barrett, T, Buist, N, Cohen, N
Publicado em 1997

Isolated persistent hypermethioninemia.

Por Mudd, S H, Levy, H L, Tangerman, A, Boujet, C, Buist, N, Davidson-Mundt, A, Hudgins, L, Oyanagi, K, Nagao, M, Wilson, W G
Publicado em 1995

Mutations in the liver glycogen synthase gene in children with hypoglycemia due to glycogen storage disease type 0.

Por Orho, M, Bosshard, N U, Buist, N R, Gitzelmann, R, Aynsley-Green, A, Blümel, P, Gannon, M C, Nuttall, F Q, Groop, L C
Publicado em 1998

S-Adenosylhomocysteine hydrolase deficiency in a 26-year-old man

Por Buist, N. R. M., Glenn, B., Vugrek, O., Wagner, C., Stabler, S., Allen, R. H., Pogribny, I., Schulze, A., Zeisel, S. H., Barić, I., Mudd, S. H.
Publicado em 2006

Proficiency testing for biochemical genetics laboratories: the first 10 rounds of testing.

Por Hommes, F A, Brewster, M A, Burton, B K, Buist, N R, Elsas, L J, Goldsmith, B M, Hammond, J, Kruckeberg, W C, Leichtman, L G, Lin, K T
Publicado em 1990