-
1
-
-
0028171222
-
Vitamin B12 metabolism and status during pregnancy, lactation and infancy
-
Allen LH (1994) Vitamin B12 metabolism and status during pregnancy, lactation and infancy. Adv Exp Med Biol 352: 13-186
-
(1994)
Adv Exp Med Biol
, vol.352
, pp. 13-186
-
-
Allen, L.H.1
-
2
-
-
0030971748
-
Oral treatment in selective vitamine B12 malabsorption
-
Altay C, Cetin M (1997) Oral treatment in selective vitamine B12 malabsorption. Pediatr Hematol Oncol 3: 245-246
-
(1997)
Pediatr Hematol Oncol
, vol.3
, pp. 245-246
-
-
Altay, C.1
Cetin, M.2
-
3
-
-
0033051889
-
Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anaemia 1
-
Aminoff M, Carter JE, Chadwick RB, Johnson C, Gräsbeck R, Abdelaal MA, Brach H, Jenner LB, Verroust PJ, Moestrop SK, Chapelle A de la, Krahe R (1999) Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anaemia 1. Nat Genet 21: 309-313
-
(1999)
Nat Genet
, vol.21
, pp. 309-313
-
-
Aminoff, M.1
Carter, J.E.2
Chadwick, R.B.3
Johnson, C.4
Gräsbeck, R.5
Abdelaal, M.A.6
Brach, H.7
Jenner, L.B.8
Verroust, P.J.9
Moestrop, S.K.10
De La Chapelle, A.11
Krahe, R.12
-
4
-
-
0023879722
-
Plasma R binder deficiency
-
Carmel R (1988) Plasma R binder deficiency. N Engl J Med 318: 1401
-
(1988)
N Engl J Med
, vol.318
, pp. 1401
-
-
Carmel, R.1
-
5
-
-
0000099257
-
Megaloblastic anemia
-
Nathan DG, Oski FA (eds) Saunders, Philadelphia
-
Cooper BA, Rodenblatt DS, Whitehead VM (1998) Megaloblastic anemia. In: Nathan DG, Oski FA (eds) Hematology of infancy and childhood, 5th edn. Saunders, Philadelphia, pp 385-422
-
(1998)
Hematology of Infancy and Childhood, 5th Edn.
, pp. 385-422
-
-
Cooper, B.A.1
Rodenblatt, D.S.2
Whitehead, V.M.3
-
6
-
-
0000526332
-
Inherited disorders of cobalamin transport and metabolism
-
Scriver CR, Beaudet AL, Sly WS, Valle D (eds) McGraw-Hill, New York
-
Fenton WA, Rosenberg LE (1995) Inherited disorders of cobalamin transport and metabolism. In: Scriver CR, Beaudet AL, Sly WS, Valle D (eds) The metabolic and molecular bases of inherited disease, 7th edn. McGraw-Hill, New York, pp 3129-3150
-
(1995)
The Metabolic and Molecular Bases of Inherited Disease, 7th Edn.
, pp. 3129-3150
-
-
Fenton, W.A.1
Rosenberg, L.E.2
-
7
-
-
0031749452
-
Genetic defects of folate and cobalamin metabolism
-
Fowler B (1999) Genetic defects of folate and cobalamin metabolism. Eur J Pediatr 157: S60-S66
-
(1999)
Eur J Pediatr
, vol.157
-
-
Fowler, B.1
-
8
-
-
0003884146
-
-
de Gruyer, Berlin New York
-
Friedrich W (1988) Vitamins. de Gruyer, Berlin New York
-
(1988)
Vitamins
-
-
Friedrich, W.1
-
9
-
-
0026574886
-
Long-term neurologic consequences of nutritional vitamin B12 deficiency in infants
-
Graham SM, Arvela OM, Wise GA (1992) Long-term neurologic consequences of nutritional vitamin B12 deficiency in infants. J Pediatr 121: 710-714
-
(1992)
J Pediatr
, vol.121
, pp. 710-714
-
-
Graham, S.M.1
Arvela, O.M.2
Wise, G.A.3
-
10
-
-
0001601083
-
Selective vitamin B12 malabsorption and proteinuria in young people
-
Gräsbeck R, Gordin R, Kantero I, Kuhlback B (1960) Selective vitamin B12 malabsorption and proteinuria in young people. Acta Med Scand 167: 289-96
-
(1960)
Acta Med Scand
, vol.167
, pp. 289-296
-
-
Gräsbeck, R.1
Gordin, R.2
Kantero, I.3
Kuhlback, B.4
-
11
-
-
0006040365
-
Cobalamin-binding proteins in human blood
-
Guéant JL, Nicolas JP (eds) Elsevier, Amsterdam New York
-
Hansen M (1990) Cobalamin-binding proteins in human blood.In: Guéant JL, Nicolas JP (eds) Cobalamin and related binding proteins in clinical nutrition. Elsevier, Amsterdam New York, pp 69-79
-
(1990)
Cobalamin and Related Binding Proteins in Clinical Nutrition
, pp. 69-79
-
-
Hansen, M.1
-
12
-
-
0018087613
-
A syndrome of methylmalonic aciduria, homocystinuria, megaloblastic anemia and neurologic abnormalities in a vitamin B12-deficient breast-fed infant of a strict vegetarian
-
Higginbottom MC, Sweetman L, Nyhan WL (1978) A syndrome of methylmalonic aciduria, homocystinuria, megaloblastic anemia and neurologic abnormalities in a vitamin B12-deficient breast-fed infant of a strict vegetarian. N Engl J Med 299: 317-323
-
(1978)
N Engl J Med
, vol.299
, pp. 317-323
-
-
Higginbottom, M.C.1
Sweetman, L.2
Nyhan, W.L.3
-
13
-
-
72849184034
-
Idiopathic chronic megaloblastic anemia in children
-
Imerslund O (1960) Idiopathic chronic megaloblastic anemia in children. Acta Paediatr Scand [Suppl] 49: 119
-
(1960)
Acta Paediatr Scand [Suppl]
, vol.49
, pp. 119
-
-
Imerslund, O.1
-
14
-
-
0000131450
-
Vitamin B12 deficiency in Indian infants
-
Jadhav M, Webb JKG, Vaishnava S (1962) Vitamin B12 deficiency in Indian infants. Lancet 2: 903-907
-
(1962)
Lancet
, vol.2
, pp. 903-907
-
-
Jadhav, M.1
Webb, J.K.G.2
Vaishnava, S.3
-
15
-
-
0025945537
-
Transcobalamin-II deficiency -Case report and review of the literature
-
Kaikov Y, Wadsworth LD, Hall CA, Rogers PCJ (1991 ) Transcobalamin-II deficiency -Case report and review of the literature. Eur J Pediatr 150: 841-843
-
(1991)
Eur J Pediatr
, vol.150
, pp. 841-843
-
-
Kaikov, Y.1
Wadsworth, L.D.2
Hall, C.A.3
Rogers, P.C.J.4
-
16
-
-
0032525203
-
The human intrinsic factor-vitamin B12 receptor, cubilin: Molecular characterization and chromosomal mapping of the gene to 10p within the autosomal recessive megaloblastic anemia (MAG 1) region
-
Kozyraki R, Kristiansen M, Silahtaroglu A, Hansen C, Jacobsen C, Tommerup N, Verroust PJ, Moestrup SK (1998) The human intrinsic factor-vitamin B12 receptor, cubilin: molecular characterization and chromosomal mapping of the gene to 10p within the autosomal recessive megaloblastic anemia (MAG 1) region. Blood 10: 3593-3600
-
(1998)
Blood
, vol.10
, pp. 3593-3600
-
-
Kozyraki, R.1
Kristiansen, M.2
Silahtaroglu, A.3
Hansen, C.4
Jacobsen, C.5
Tommerup, N.6
Verroust, P.J.7
Moestrup, S.K.8
-
17
-
-
0026083850
-
Maternal vegan diet causing a serious infantile neurological disorder due to vitamin B12 deficiency
-
Kühne T, Baumgartner R (1991) Maternal vegan diet causing a serious infantile neurological disorder due to vitamin B12 deficiency. Eur J Pediatr 150: 205-208
-
(1991)
Eur J Pediatr
, vol.150
, pp. 205-208
-
-
Kühne, T.1
Baumgartner, R.2
-
19
-
-
0028223165
-
Sensitivity of serum methylmalonic acid and total homocysteine determinations for diagnosing cobalamin and folate deficiencies
-
Savage DG, Lindenbaum J, Stabler SP, Allen RH (1994) Sensitivity of serum methylmalonic acid and total homocysteine determinations for diagnosing cobalamin and folate deficiencies. Am J Med 96: 239-246
-
(1994)
Am J Med
, vol.96
, pp. 239-246
-
-
Savage, D.G.1
Lindenbaum, J.2
Stabler, S.P.3
Allen, R.H.4
-
20
-
-
0028357258
-
Methylmalonic acid and homocysteine in plasma as indicators of functional cobalamin deficiency in infants on macrobiotic diets
-
Schneede J, Dagnelie PC, Staveren WA van, Vollset SE, Refsum H, Ueland PM (1994) Methylmalonic acid and homocysteine in plasma as indicators of functional cobalamin deficiency in infants on macrobiotic diets. Pediatr Res 36: 194-201
-
(1994)
Pediatr Res
, vol.36
, pp. 194-201
-
-
Schneede, J.1
Dagnelie, P.C.2
Van Staveren, W.A.3
Vollset, S.E.4
Refsum, H.5
Ueland, P.M.6
-
21
-
-
0342985123
-
Vitamin B12 and brain development
-
Stollhoff SG, Reddy V (1967) Vitamin B12 and brain development. Eur J Pediatr 13: 949-953
-
(1967)
Eur J Pediatr
, vol.13
, pp. 949-953
-
-
Stollhoff, S.G.1
Reddy, V.2
-
22
-
-
0022369431
-
Cobalamin malabsorption in three siblings due to an abnormal intrinsic factor that is markedly susceptible to acid and proteolysis
-
Yang YM, Ducos R, Rosenberg AJ, Catrou PG, Levine JS, Podell ER, Allen RH (1985) Cobalamin malabsorption in three siblings due to an abnormal intrinsic factor that is markedly susceptible to acid and proteolysis. J Clin Invest 76: 1057-2065
-
(1985)
J Clin Invest
, vol.76
, pp. 1057-2065
-
-
Yang, Y.M.1
Ducos, R.2
Rosenberg, A.J.3
Catrou, P.G.4
Levine, J.S.5
Podell, E.R.6
Allen, R.H.7
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