-
1
-
-
33750614247
-
12, serum folate and red cell folate
-
Rowan R.M., van Assendelft O.W., and Preston F.E. (Eds), Arnold, London
-
12, serum folate and red cell folate. In: Rowan R.M., van Assendelft O.W., and Preston F.E. (Eds). Advanced Laboratory Methods in Haematology (2002), Arnold, London 264-289
-
(2002)
Advanced Laboratory Methods in Haematology
, pp. 264-289
-
-
Wickramasinghe, S.N.1
Rezvani, K.2
-
2
-
-
0025335524
-
Diagnosis of cobalamin deficiency: II. Relative sensitivities of serum cobalamin, methylmalonic acid, and total homocysteine concentrations
-
Lindenbaum J., Savage D.G., Stabler S.P., and Allen R.H. Diagnosis of cobalamin deficiency: II. Relative sensitivities of serum cobalamin, methylmalonic acid, and total homocysteine concentrations. Am J Hematol 34 (1990) 99-107
-
(1990)
Am J Hematol
, vol.34
, pp. 99-107
-
-
Lindenbaum, J.1
Savage, D.G.2
Stabler, S.P.3
Allen, R.H.4
-
3
-
-
0032740452
-
Serum cobalamin, homocysteine, and methylmalonic acid concentrations in a multiethnic elderly population: Ethnic and sex differences in cobalamin and metabolite abnormalities
-
Carmel R., Green R., Jacobsen D.W., Rasmussen K., Florea M., and Azen C. Serum cobalamin, homocysteine, and methylmalonic acid concentrations in a multiethnic elderly population: Ethnic and sex differences in cobalamin and metabolite abnormalities. Am J Clin Nutr 70 (1999) 904-910
-
(1999)
Am J Clin Nutr
, vol.70
, pp. 904-910
-
-
Carmel, R.1
Green, R.2
Jacobsen, D.W.3
Rasmussen, K.4
Florea, M.5
Azen, C.6
-
4
-
-
2942545500
-
Update on cobalamin, folate, and homocysteine
-
Carmel R., Green R., Rosenblatt D.S., and Watkins D. Update on cobalamin, folate, and homocysteine. Hematology (Am Soc Hematol Educ Program) (2003) 62-81
-
(2003)
Hematology (Am Soc Hematol Educ Program)
, pp. 62-81
-
-
Carmel, R.1
Green, R.2
Rosenblatt, D.S.3
Watkins, D.4
-
5
-
-
0042367727
-
Mild transcobalamin I (haptocorrin) deficiency and low serum cobalamin concentrations
-
Carmel R. Mild transcobalamin I (haptocorrin) deficiency and low serum cobalamin concentrations. Clin Chem 49 (2003) 1367-1374
-
(2003)
Clin Chem
, vol.49
, pp. 1367-1374
-
-
Carmel, R.1
-
6
-
-
0028223165
-
Sensitivity of serum methylmalonic acid and total homocysteine determinations for diagnosing cobalamin and folate deficiencies
-
Savage D.G., Lindenbaum J., Stabler S.P., and Allen R.H. Sensitivity of serum methylmalonic acid and total homocysteine determinations for diagnosing cobalamin and folate deficiencies. Am J Med 96 (1994) 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
-
7
-
-
0025331267
-
Diagnosis of cobalamin deficiency I: Usefulness of serum methylmalonic acid and total homocysteine concentrations
-
Allen R.H., Stabler S.P., Savage D.G., and Lindenbaum J. Diagnosis of cobalamin deficiency I: Usefulness of serum methylmalonic acid and total homocysteine concentrations. Amer J Hematol 4 (1990) 90-98
-
(1990)
Amer J Hematol
, vol.4
, pp. 90-98
-
-
Allen, R.H.1
Stabler, S.P.2
Savage, D.G.3
Lindenbaum, J.4
-
8
-
-
0029840824
-
Limited value of serum holo-transcobalamin II measurements in the differential diagnosis of macrocytosis
-
Wickramasinghe S.N., and Ratnayaka I.D. Limited value of serum holo-transcobalamin II measurements in the differential diagnosis of macrocytosis. J Clin Pathol 49 (1996) 755-758
-
(1996)
J Clin Pathol
, vol.49
, pp. 755-758
-
-
Wickramasinghe, S.N.1
Ratnayaka, I.D.2
-
9
-
-
31844440194
-
Measurement of total vitamin B12 and holotranscobalamin, singly and in combination, in screening for metabolic vitamin B12 deficiency
-
Dec 29; Epub ahead of print
-
Miller J.W., Garrod M.G., Rockwood A.L., Kushnir M.M., Allen L.H., Haan M.N., et al. Measurement of total vitamin B12 and holotranscobalamin, singly and in combination, in screening for metabolic vitamin B12 deficiency. Clin Chem (2005) Dec 29; Epub ahead of print
-
(2005)
Clin Chem
-
-
Miller, J.W.1
Garrod, M.G.2
Rockwood, A.L.3
Kushnir, M.M.4
Allen, L.H.5
Haan, M.N.6
-
10
-
-
0345169173
-
Holotranscobalamin as a predictor of vitamin B12 status
-
Hvas A.M., and Nexo E. Holotranscobalamin as a predictor of vitamin B12 status. Clin Chem Lab Med 41 (2003) 1489-1492
-
(2003)
Clin Chem Lab Med
, vol.41
, pp. 1489-1492
-
-
Hvas, A.M.1
Nexo, E.2
-
11
-
-
0344256728
-
Functional vitamin B12 deficiency and determination of holotranscobalamin in populations at risk
-
Herrmann W., Obeid R., Schorr H., and Geisel J. Functional vitamin B12 deficiency and determination of holotranscobalamin in populations at risk. Clin Chem Lab Med 41 (2003) 1478-1488
-
(2003)
Clin Chem Lab Med
, vol.41
, pp. 1478-1488
-
-
Herrmann, W.1
Obeid, R.2
Schorr, H.3
Geisel, J.4
-
12
-
-
3242744561
-
Clinical utility of serum holotranscobalamin as a marker of cobalamin status in elderly patients with neuropsychiatric symptoms
-
Nilsson K., Isaksson A., Gustafson L., and Hultberg B. Clinical utility of serum holotranscobalamin as a marker of cobalamin status in elderly patients with neuropsychiatric symptoms. Clin Chem Lab Med 42 (2004) 637-643
-
(2004)
Clin Chem Lab Med
, vol.42
, pp. 637-643
-
-
Nilsson, K.1
Isaksson, A.2
Gustafson, L.3
Hultberg, B.4
-
13
-
-
14044269477
-
The usefulness of holotranscobalamin in predicting vitamin B12 status in different clinical settings
-
Herrmann W., Obeid R., Schorr H., and Geisel J. The usefulness of holotranscobalamin in predicting vitamin B12 status in different clinical settings. Curr Drug Metab 6 (2005) 47-53
-
(2005)
Curr Drug Metab
, vol.6
, pp. 47-53
-
-
Herrmann, W.1
Obeid, R.2
Schorr, H.3
Geisel, J.4
-
14
-
-
13744254651
-
Influence of cobalamin deficiency compared with that of cobalamin absorption on serum holo-transcobalamin II
-
Chen X., Remacha A.F., Sarda M.P., and Carmel R. Influence of cobalamin deficiency compared with that of cobalamin absorption on serum holo-transcobalamin II. Am J Clin Nutr 81 (2005) 110-114
-
(2005)
Am J Clin Nutr
, vol.81
, pp. 110-114
-
-
Chen, X.1
Remacha, A.F.2
Sarda, M.P.3
Carmel, R.4
-
15
-
-
0014301409
-
Deranged DNA synthesis by bone marrow from vitamin B-12-deficient humans
-
Metz J., Kelly A., Swett V.C., Waxman S., and Herbert V. Deranged DNA synthesis by bone marrow from vitamin B-12-deficient humans. Br J Haematol 14 (1968) 575-592
-
(1968)
Br J Haematol
, vol.14
, pp. 575-592
-
-
Metz, J.1
Kelly, A.2
Swett, V.C.3
Waxman, S.4
Herbert, V.5
-
16
-
-
0019411794
-
The deoxyuridine suppression test: a review of its clinical and research applications
-
Wickramasinghe S.N. The deoxyuridine suppression test: a review of its clinical and research applications. Clin Lab Haematol 3 (1981) 1-18
-
(1981)
Clin Lab Haematol
, vol.3
, pp. 1-18
-
-
Wickramasinghe, S.N.1
-
17
-
-
0023759683
-
Deoxyuridine suppression: biochemical basis and diagnostic applications
-
Wickramasinghe S.N., and Matthews J.H. Deoxyuridine suppression: biochemical basis and diagnostic applications. Blood Rev 2 (1988) 168-177
-
(1988)
Blood Rev
, vol.2
, pp. 168-177
-
-
Wickramasinghe, S.N.1
Matthews, J.H.2
-
18
-
-
0030010213
-
Comparison of the deoxyuridine suppression test with serum levels of methylmalonic acid and homocysteine in mild cobalamin deficiency
-
Carmel R., Rasmussen K., Jacobsen D.W., and Green R. Comparison of the deoxyuridine suppression test with serum levels of methylmalonic acid and homocysteine in mild cobalamin deficiency. Br J Haematol 93 (1996) 311-318
-
(1996)
Br J Haematol
, vol.93
, pp. 311-318
-
-
Carmel, R.1
Rasmussen, K.2
Jacobsen, D.W.3
Green, R.4
-
20
-
-
0018403763
-
Interpretation of serum and red cell folate results. A comparison of microbiological and radioisotopic methods
-
Jones P., Grace C.S., and Rozenberg M.C. Interpretation of serum and red cell folate results. A comparison of microbiological and radioisotopic methods. Pathology 11 (1979) 45-52
-
(1979)
Pathology
, vol.11
, pp. 45-52
-
-
Jones, P.1
Grace, C.S.2
Rozenberg, M.C.3
-
21
-
-
0026061262
-
Erythrocyte folate levels: a clinical study
-
Jaffe J.P., and Schilling R.F. Erythrocyte folate levels: a clinical study. Am J Hematol 36 (1991) 116-121
-
(1991)
Am J Hematol
, vol.36
, pp. 116-121
-
-
Jaffe, J.P.1
Schilling, R.F.2
-
22
-
-
0031132185
-
Folate assays: Serum or red cell?
-
Phekoo K., Williams Y., Schey S.A., Andrews V.E., Dudley J.M., and Hoffbrand A.V. Folate assays: Serum or red cell?. J R Coll Physicians Lond 31 (1997) 291-295
-
(1997)
J R Coll Physicians Lond
, vol.31
, pp. 291-295
-
-
Phekoo, K.1
Williams, Y.2
Schey, S.A.3
Andrews, V.E.4
Dudley, J.M.5
Hoffbrand, A.V.6
-
23
-
-
85047687509
-
Comparison of five automated serum and whole blood folate assays
-
Owen W.E., and Roberts W.L. Comparison of five automated serum and whole blood folate assays. Am J Clin Pathol 120 (2003) 121-126
-
(2003)
Am J Clin Pathol
, vol.120
, pp. 121-126
-
-
Owen, W.E.1
Roberts, W.L.2
-
24
-
-
11844276026
-
Erythrocyte folate and its response to folic acid supplementation is assay dependent in women
-
Clifford A.J., Noceti E.M., Block-Joy A., Block T., and Block G. Erythrocyte folate and its response to folic acid supplementation is assay dependent in women. J Nutr 135 (2005) 137-143
-
(2005)
J Nutr
, vol.135
, pp. 137-143
-
-
Clifford, A.J.1
Noceti, E.M.2
Block-Joy, A.3
Block, T.4
Block, G.5
-
25
-
-
0021267980
-
Assessment of the value of a competitive protein binding radioassay of folic acid in the detection of folic acid deficiency
-
Bain B.J., Wickramasinghe S.N., Broom G.N., Litwinczuk R.A., and Sims J. Assessment of the value of a competitive protein binding radioassay of folic acid in the detection of folic acid deficiency. J Clin Pathol 37 (1984) 888-894
-
(1984)
J Clin Pathol
, vol.37
, pp. 888-894
-
-
Bain, B.J.1
Wickramasinghe, S.N.2
Broom, G.N.3
Litwinczuk, R.A.4
Sims, J.5
-
26
-
-
0000726204
-
The long-term evaluation of folic acid in the treatment of pernicious anemia
-
Schwartz S.O., Kaplan S.R., and Armstrong B.E. The long-term evaluation of folic acid in the treatment of pernicious anemia. J Lab Clin Med 35 (1950) 894-898
-
(1950)
J Lab Clin Med
, vol.35
, pp. 894-898
-
-
Schwartz, S.O.1
Kaplan, S.R.2
Armstrong, B.E.3
-
27
-
-
85047694031
-
Pernicious anemia. The expected findings of very low serum cobalamin levels, anemia and macrocytosis are often lacking
-
Carmel R. Pernicious anemia. The expected findings of very low serum cobalamin levels, anemia and macrocytosis are often lacking. Arch Intern Med 148 (1988) 1712-1714
-
(1988)
Arch Intern Med
, vol.148
, pp. 1712-1714
-
-
Carmel, R.1
-
29
-
-
0024994773
-
Clinical spectrum and diagnosis of cobalamin deficiency
-
Stabler S.P., Allen R.H., Savage D.G., and Lindenbaum J. Clinical spectrum and diagnosis of cobalamin deficiency. Blood 76 (1990) 871-881
-
(1990)
Blood
, vol.76
, pp. 871-881
-
-
Stabler, S.P.1
Allen, R.H.2
Savage, D.G.3
Lindenbaum, J.4
-
30
-
-
0025939341
-
Neurologic aspects of cobalamin deficiency
-
Healton E.B., Savage D.G., Brust J.C.M., Garrett T.J., and Lindenbaum J. Neurologic aspects of cobalamin deficiency. Medicine 70 (1991) 229-245
-
(1991)
Medicine
, vol.70
, pp. 229-245
-
-
Healton, E.B.1
Savage, D.G.2
Brust, J.C.M.3
Garrett, T.J.4
Lindenbaum, J.5
-
31
-
-
0023946537
-
Neuropsychiatric disorders caused by cobalamin deficiency in the absence of anemia or macrocytosis
-
Lindenbaum J., Healton E.B., Savage D.G., et al. Neuropsychiatric disorders caused by cobalamin deficiency in the absence of anemia or macrocytosis. New Engl J Med 318 (1988) 1720-1728
-
(1988)
New Engl J Med
, vol.318
, pp. 1720-1728
-
-
Lindenbaum, J.1
Healton, E.B.2
Savage, D.G.3
-
32
-
-
0025041824
-
Subacute combined degeneration of the spinal cord due to folate deficiency in association with a psychotic illness
-
Donnelly S., and Callaghan N. Subacute combined degeneration of the spinal cord due to folate deficiency in association with a psychotic illness. Ir Med J 83 (1990) 73-74
-
(1990)
Ir Med J
, vol.83
, pp. 73-74
-
-
Donnelly, S.1
Callaghan, N.2
-
33
-
-
0027954514
-
Folate responsive neuropathy
-
Parry T.E. Folate responsive neuropathy. Presse Med 23 (1994) 131-137
-
(1994)
Presse Med
, vol.23
, pp. 131-137
-
-
Parry, T.E.1
-
34
-
-
0028837748
-
Case report: subacute combined degeneration of the spinal cord from folate deficiency
-
Ravakhah K., and West B.C. Case report: subacute combined degeneration of the spinal cord from folate deficiency. Am J Med Sci 310 (1995) 214-216
-
(1995)
Am J Med Sci
, vol.310
, pp. 214-216
-
-
Ravakhah, K.1
West, B.C.2
-
35
-
-
0030792224
-
Folic acid deficiency with leukoencephalopathy and chronic axonal neuropathy of sensory predominance
-
Guettat L., Gille M., Delbecq J., and Depre A. Folic acid deficiency with leukoencephalopathy and chronic axonal neuropathy of sensory predominance. Rev Neurol (Paris) 153 (1997) 351-353
-
(1997)
Rev Neurol (Paris)
, vol.153
, pp. 351-353
-
-
Guettat, L.1
Gille, M.2
Delbecq, J.3
Depre, A.4
-
36
-
-
0036209390
-
Optic neuropathy from folic acid deficiency without alcohol abuse
-
Hsu C.T., Miller N.R., and Wray M.L. Optic neuropathy from folic acid deficiency without alcohol abuse. Ophthalmologica 216 (2002) 65-67
-
(2002)
Ophthalmologica
, vol.216
, pp. 65-67
-
-
Hsu, C.T.1
Miller, N.R.2
Wray, M.L.3
-
37
-
-
0037217507
-
Depression and folate status in the US Population
-
Morris M.S., Fava M., Jacques P.F., Selhub J., and Rosenberg I.H. Depression and folate status in the US Population. Psychother Psychosom 72 (2003) 80-87
-
(2003)
Psychother Psychosom
, vol.72
, pp. 80-87
-
-
Morris, M.S.1
Fava, M.2
Jacques, P.F.3
Selhub, J.4
Rosenberg, I.H.5
-
39
-
-
10044253415
-
Long-term ovo-lacto vegetarian diet impairs vitamin B-12 status in pregnant women
-
Koebnick C., Hoffmann I., Dagnelie P.C., Heins U.A., Wickramasinghe S.N., Ratnayaka I.D., et al. Long-term ovo-lacto vegetarian diet impairs vitamin B-12 status in pregnant women. J Nutr 134 (2004) 3319-3326
-
(2004)
J Nutr
, vol.134
, pp. 3319-3326
-
-
Koebnick, C.1
Hoffmann, I.2
Dagnelie, P.C.3
Heins, U.A.4
Wickramasinghe, S.N.5
Ratnayaka, I.D.6
-
40
-
-
0023472737
-
The 1986 Herman Award Lecture. Nutrition science as a continually unfolding story: The folate and vitamin B-12 paradigm
-
Herbert V. The 1986 Herman Award Lecture. Nutrition science as a continually unfolding story: The folate and vitamin B-12 paradigm. Am J Clin Nutr 46 (1987) 387-402
-
(1987)
Am J Clin Nutr
, vol.46
, pp. 387-402
-
-
Herbert, V.1
-
41
-
-
0028265890
-
Staging vitamin B-12 (cobalamin) status in vegetarians
-
Herbert V. Staging vitamin B-12 (cobalamin) status in vegetarians. Am J Clin Nutr 59 Suppl (1994) 1213S-1222S
-
(1994)
Am J Clin Nutr
, vol.59
, Issue.SUPPL
-
-
Herbert, V.1
-
42
-
-
1842340426
-
Subtle cobalamin deficiency
-
Bhatt H.R., James V.H.T., Besser G.M., et al. (Eds), Journal of Endocrinology Ltd, Bristol
-
Carmel R. Subtle cobalamin deficiency. In: Bhatt H.R., James V.H.T., Besser G.M., et al. (Eds). Advances in Thomas Addison's Diseases vol 1 (1994), Journal of Endocrinology Ltd, Bristol 281-294
-
(1994)
Advances in Thomas Addison's Diseases
, vol.1
, pp. 281-294
-
-
Carmel, R.1
-
43
-
-
0038507376
-
Vitamin B-12 status, particularly holotranscobalamin II and methylmalonic acid concentrations, and hyperhomocysteinemia in vegetarians
-
Herrmann W., Schorr H., Obeid R., and Geisel J. Vitamin B-12 status, particularly holotranscobalamin II and methylmalonic acid concentrations, and hyperhomocysteinemia in vegetarians. Am J Clin Nutr 78 (2003) 131-136
-
(2003)
Am J Clin Nutr
, vol.78
, pp. 131-136
-
-
Herrmann, W.1
Schorr, H.2
Obeid, R.3
Geisel, J.4
-
44
-
-
2442668914
-
Severe encephalopathy with epilepsy in an infant caused by subclinical maternal pernicious anaemia: Case report and review of the literature
-
Korenke G.C., Hunneman D.H., Eber S., and Hanefeld F. Severe encephalopathy with epilepsy in an infant caused by subclinical maternal pernicious anaemia: Case report and review of the literature. Eur J Pediatr 163 (2004) 196-201
-
(2004)
Eur J Pediatr
, vol.163
, pp. 196-201
-
-
Korenke, G.C.1
Hunneman, D.H.2
Eber, S.3
Hanefeld, F.4
-
45
-
-
24644482103
-
Encephalopathy with methylmalonic aciduria and homocystinuria secondary to a deficient exogenous supply of vitamin B12
-
Gutierrez-Aguilar G., Abenia-Uson P., Garcia-Cazorla A., Vilaseca M.A., and Campistol J. Encephalopathy with methylmalonic aciduria and homocystinuria secondary to a deficient exogenous supply of vitamin B12. Rev Neurol 40 (2005) 605-608
-
(2005)
Rev Neurol
, vol.40
, pp. 605-608
-
-
Gutierrez-Aguilar, G.1
Abenia-Uson, P.2
Garcia-Cazorla, A.3
Vilaseca, M.A.4
Campistol, J.5
-
47
-
-
0023683909
-
Food cobalamin malabsorption occurs frequently in patients with unexplained low serum cobalamin levels
-
Carmel R., Sinow R.M., Siegel M.E., and Samloff I.M. Food cobalamin malabsorption occurs frequently in patients with unexplained low serum cobalamin levels. Arch Intern Med 148 (1988) 1715-1719
-
(1988)
Arch Intern Med
, vol.148
, pp. 1715-1719
-
-
Carmel, R.1
Sinow, R.M.2
Siegel, M.E.3
Samloff, I.M.4
-
49
-
-
0030771355
-
Cobalamin, the stomach, and aging
-
Carmel R. Cobalamin, the stomach, and aging. Am J Clin Nutr 66 (1997) 750-759
-
(1997)
Am J Clin Nutr
, vol.66
, pp. 750-759
-
-
Carmel, R.1
-
51
-
-
0023223851
-
Atypical cobalamin deficiency. Subtle biochemical evidence of deficiency is commonly demonstrable in patients without megaloblastic anemia and is often associated with protein-bound cobalamin malabsorption
-
Carmel R., Sinow R.M., and Karnaze D.S. Atypical cobalamin deficiency. Subtle biochemical evidence of deficiency is commonly demonstrable in patients without megaloblastic anemia and is often associated with protein-bound cobalamin malabsorption. J Lab Clin Med 109 (1987) 454-463
-
(1987)
J Lab Clin Med
, vol.109
, pp. 454-463
-
-
Carmel, R.1
Sinow, R.M.2
Karnaze, D.S.3
-
52
-
-
0023287007
-
Incidence and clinical significance of protein-bound vitamin B12 malabsorption
-
Jones B.P., Broomhead A.F., Kwan Y.L., and Grace C.S. Incidence and clinical significance of protein-bound vitamin B12 malabsorption. Eur J Haematol 38 (1987) 131-136
-
(1987)
Eur J Haematol
, vol.38
, pp. 131-136
-
-
Jones, B.P.1
Broomhead, A.F.2
Kwan, Y.L.3
Grace, C.S.4
-
53
-
-
0025030393
-
Neurologic and evoked potential abnormalities in subtle cobalamin deficiency states, including deficiency without anemia and with normal absorption of free cobalamin
-
Karnaze D.S., and Carmel R. Neurologic and evoked potential abnormalities in subtle cobalamin deficiency states, including deficiency without anemia and with normal absorption of free cobalamin. Arch Neurol 47 (1990) 1008-1012
-
(1990)
Arch Neurol
, vol.47
, pp. 1008-1012
-
-
Karnaze, D.S.1
Carmel, R.2
-
54
-
-
0029054411
-
The frequently low cobalamin levels in dementia usually signify treatable metabolic, neurologic and electrophysiologic abnormalities
-
Carmel R., Gott P.S., Waters C.H., Cairo K., Green R., Bondareff W., et al. The frequently low cobalamin levels in dementia usually signify treatable metabolic, neurologic and electrophysiologic abnormalities. Eur J Haematol 54 (1995) 245-253
-
(1995)
Eur J Haematol
, vol.54
, pp. 245-253
-
-
Carmel, R.1
Gott, P.S.2
Waters, C.H.3
Cairo, K.4
Green, R.5
Bondareff, W.6
-
55
-
-
0020858452
-
Evolution of protein-bound cobalamin malabsorption
-
King C.E., and Toskes P.P. Evolution of protein-bound cobalamin malabsorption. Arch Intern Med 143 (1983) 2219
-
(1983)
Arch Intern Med
, vol.143
, pp. 2219
-
-
King, C.E.1
Toskes, P.P.2
-
56
-
-
3042575809
-
Is there a link between the food-cobalamin malabsorption and the pernicious anemia?
-
Andres E., Noel E., Henoun Loukili N., Coca C., Vinzio S., and Blickle J.F. Is there a link between the food-cobalamin malabsorption and the pernicious anemia?. Ann Endocrinol (Paris) 65 (2004) 118-120
-
(2004)
Ann Endocrinol (Paris)
, vol.65
, pp. 118-120
-
-
Andres, E.1
Noel, E.2
Henoun Loukili, N.3
Coca, C.4
Vinzio, S.5
Blickle, J.F.6
-
57
-
-
25444504855
-
Food-cobalamin malabsorption in elderly patients: Clinical manifestations and treatment
-
Andres E., Affenberger S., Vinzio S., Kurtz J.E., Noel E., Kaltenbach G., et al. Food-cobalamin malabsorption in elderly patients: Clinical manifestations and treatment. Am J Med 118 (2005) 1154-1159
-
(2005)
Am J Med
, vol.118
, pp. 1154-1159
-
-
Andres, E.1
Affenberger, S.2
Vinzio, S.3
Kurtz, J.E.4
Noel, E.5
Kaltenbach, G.6
-
58
-
-
0034090534
-
Current concepts in cobalamin deficiency
-
Carmel R. Current concepts in cobalamin deficiency. Annu Rev Med 51 (2000) 357-375
-
(2000)
Annu Rev Med
, vol.51
, pp. 357-375
-
-
Carmel, R.1
-
59
-
-
0029891583
-
Prevalence of undiagnosed pernicious anemia in the elderly
-
Carmel R. Prevalence of undiagnosed pernicious anemia in the elderly. Arch Intern Med 156 (1996) 1097-1100
-
(1996)
Arch Intern Med
, vol.156
, pp. 1097-1100
-
-
Carmel, R.1
-
60
-
-
0023749222
-
Pepsinogens and other serum markers in pernicious anemia
-
Carmel R. Pepsinogens and other serum markers in pernicious anemia. Am J Clin Pathol 90 (1988) 442-445
-
(1988)
Am J Clin Pathol
, vol.90
, pp. 442-445
-
-
Carmel, R.1
-
61
-
-
0026285820
-
Serum pepsinogen I and serum gastrin in the screening of severe atrophic corpus gastritis
-
Kekki M., Samloff I.M., Varis K., and Ihamaki T. Serum pepsinogen I and serum gastrin in the screening of severe atrophic corpus gastritis. Scand J Gastroenterol Suppl 186 (1991) 109-116
-
(1991)
Scand J Gastroenterol Suppl
, vol.186
, pp. 109-116
-
-
Kekki, M.1
Samloff, I.M.2
Varis, K.3
Ihamaki, T.4
-
62
-
-
0026612934
-
Reassessment of the relative prevalences of antibodies to gastric parietal cell and to intrinsic factor in patients with pernicious anaemia: Influence of patient age and race
-
Carmel R. Reassessment of the relative prevalences of antibodies to gastric parietal cell and to intrinsic factor in patients with pernicious anaemia: Influence of patient age and race. Clin Exp Immunol 89 (1992) 74-77
-
(1992)
Clin Exp Immunol
, vol.89
, pp. 74-77
-
-
Carmel, R.1
-
63
-
-
0020687219
-
Gastric juice in congenital pernicious anemia contains no immunoreactive intrinsic factor molecule: Study of three kindreds with variable ages at presentation, including a patient first diagnosed in adulthood
-
Carmel R. Gastric juice in congenital pernicious anemia contains no immunoreactive intrinsic factor molecule: Study of three kindreds with variable ages at presentation, including a patient first diagnosed in adulthood. Am J Hum Genet 35 (1983) 67-77
-
(1983)
Am J Hum Genet
, vol.35
, pp. 67-77
-
-
Carmel, R.1
-
64
-
-
0001912321
-
Inherited disorders of folate and cobalamin transport and metabolism
-
Scriver C.R., Beaudet A.L., Sly W.S., Valle D., Childs B., Kinzler K.W., and Vogelstein B. (Eds), McGraw-Hill, New york
-
Rosenblatt D., and Fenton W.A. Inherited disorders of folate and cobalamin transport and metabolism. In: Scriver C.R., Beaudet A.L., Sly W.S., Valle D., Childs B., Kinzler K.W., and Vogelstein B. (Eds). The metabolic & molecular bases of inherited disease. Eighth ed. (2001), McGraw-Hill, New york 3897-3933
-
(2001)
The metabolic & molecular bases of inherited disease. Eighth ed.
, pp. 3897-3933
-
-
Rosenblatt, D.1
Fenton, W.A.2
-
65
-
-
9144238746
-
A genetic polymorphism in the coding region of the gastric intrinsic factor gene (GIF) is associated with congenital intrinsic factor deficiency
-
Gordon M.M., Brada N., Remacha A., Badell I., del Rio E., Baiget M., et al. A genetic polymorphism in the coding region of the gastric intrinsic factor gene (GIF) is associated with congenital intrinsic factor deficiency. Hum Mutat 23 (2004) 85-91
-
(2004)
Hum Mutat
, vol.23
, pp. 85-91
-
-
Gordon, M.M.1
Brada, N.2
Remacha, A.3
Badell, I.4
del Rio, E.5
Baiget, M.6
-
66
-
-
20144372885
-
Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene
-
Tanner S.M., Li Z., Perko J.D., Oner C., Cetin M., Altay C., et al. Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene. Proc Natl Acad Sci U S A 102 (2005) 4130-4133
-
(2005)
Proc Natl Acad Sci U S A
, vol.102
, pp. 4130-4133
-
-
Tanner, S.M.1
Li, Z.2
Perko, J.D.3
Oner, C.4
Cetin, M.5
Altay, C.6
-
67
-
-
0016158547
-
Isolation and characterization of an abnormal human intrinsic factor
-
Katz M., Mehlman C.S., and Allen R.H. Isolation and characterization of an abnormal human intrinsic factor. J Clin Invest 53 (1974) 1274-1283
-
(1974)
J Clin Invest
, vol.53
, pp. 1274-1283
-
-
Katz, M.1
Mehlman, C.S.2
Allen, R.H.3
-
68
-
-
0022369431
-
Cobalamin malabsorption in three siblings due to an abnormal intrinsic factor that is markedly susceptible to acid and proteolysis
-
Yang Y.M., Ducos R., Rosenberg A.J., Catrou P.G., Levine J.S., Podell E.R., et al. Cobalamin malabsorption in three siblings due to an abnormal intrinsic factor that is markedly susceptible to acid and proteolysis. J Clin Invest 76 (1985) 2057-2065
-
(1985)
J Clin Invest
, vol.76
, pp. 2057-2065
-
-
Yang, Y.M.1
Ducos, R.2
Rosenberg, A.J.3
Catrou, P.G.4
Levine, J.S.5
Podell, E.R.6
-
69
-
-
25644436276
-
Current situation of human diphyllobothriasis in Europe
-
Dupouy-Camet J., and Peduzzi R. Current situation of human diphyllobothriasis in Europe. Euro Surveill 9 (2004) 31-35
-
(2004)
Euro Surveill
, vol.9
, pp. 31-35
-
-
Dupouy-Camet, J.1
Peduzzi, R.2
-
70
-
-
1442357042
-
The functional cobalamin (vitamin B12)-intrinsic factor receptor is a novel complex of cubilin and amnionless
-
Fyfe J.C., Madsen M., Hojrup P., Christensen E.I., Tanner S.M., de la Chapelle A., et al. The functional cobalamin (vitamin B12)-intrinsic factor receptor is a novel complex of cubilin and amnionless. Blood 103 (2004) 1573-1579
-
(2004)
Blood
, vol.103
, pp. 1573-1579
-
-
Fyfe, J.C.1
Madsen, M.2
Hojrup, P.3
Christensen, E.I.4
Tanner, S.M.5
de la Chapelle, A.6
-
71
-
-
11144354849
-
Genetically heterogeneous selective intestinal malabsorption of vitamin B12: Founder effects, consanguinity, and high clinical awareness explain aggregations in Scandinavia and the Middle East
-
Tanner S.M., Li Z., Bisson R., Acar C., Oner C., Oner R., et al. Genetically heterogeneous selective intestinal malabsorption of vitamin B12: Founder effects, consanguinity, and high clinical awareness explain aggregations in Scandinavia and the Middle East. Hum Mutat 23 (2004) 327-333
-
(2004)
Hum Mutat
, vol.23
, pp. 327-333
-
-
Tanner, S.M.1
Li, Z.2
Bisson, R.3
Acar, C.4
Oner, C.5
Oner, R.6
-
72
-
-
0023282592
-
Low serum cobalamin levels occur frequently in the acquired immune deficiency syndrome and related disorders
-
Burkes R.L., Cohen H., Krailo M., Sinow R.M., and Carmel R. Low serum cobalamin levels occur frequently in the acquired immune deficiency syndrome and related disorders. Eur J Haematol 38 (1987) 141-147
-
(1987)
Eur J Haematol
, vol.38
, pp. 141-147
-
-
Burkes, R.L.1
Cohen, H.2
Krailo, M.3
Sinow, R.M.4
Carmel, R.5
-
74
-
-
0029085625
-
Clinical correlates of subnormal vitamin B12 levels in patients infected with the human immunodeficiency virus
-
Paltiel O., Falutz J., Veilleux M., Rosenblatt D.S., and Gordon K. Clinical correlates of subnormal vitamin B12 levels in patients infected with the human immunodeficiency virus. Am J Hematol 49 (1995) 318-322
-
(1995)
Am J Hematol
, vol.49
, pp. 318-322
-
-
Paltiel, O.1
Falutz, J.2
Veilleux, M.3
Rosenblatt, D.S.4
Gordon, K.5
-
75
-
-
0032941421
-
Cobalamin deficiency in patients infected with the human immunodeficiency virus
-
Remacha A.F., and Cadafalch J. Cobalamin deficiency in patients infected with the human immunodeficiency virus. Semin Hematol 36 (1999) 75-87
-
(1999)
Semin Hematol
, vol.36
, pp. 75-87
-
-
Remacha, A.F.1
Cadafalch, J.2
-
76
-
-
0026496784
-
Decreased intrinsic factor secretion in AIDS: Relation to parietal cell acid secretory capacity and vitamin B12 malabsorption
-
Herzlich B.C., Schiano T.D., Moussa Z., Zimbalist E., Panagopoulos G., Ast A., et al. Decreased intrinsic factor secretion in AIDS: Relation to parietal cell acid secretory capacity and vitamin B12 malabsorption. Am J Gastroenterol 87 (1992) 1781-1788
-
(1992)
Am J Gastroenterol
, vol.87
, pp. 1781-1788
-
-
Herzlich, B.C.1
Schiano, T.D.2
Moussa, Z.3
Zimbalist, E.4
Panagopoulos, G.5
Ast, A.6
-
77
-
-
0019304218
-
Cobalamins and nitrous oxide: A review
-
Chanarin I. Cobalamins and nitrous oxide: A review. J Clin Pathol 33 (1980) 909-916
-
(1980)
J Clin Pathol
, vol.33
, pp. 909-916
-
-
Chanarin, I.1
-
78
-
-
0018070010
-
Myeloneuropathy after prolonged exposure to nitrous oxide
-
Layzer R.B. Myeloneuropathy after prolonged exposure to nitrous oxide. Lancet ii (1978) 1227-1230
-
(1978)
Lancet
, vol.ii
, pp. 1227-1230
-
-
Layzer, R.B.1
-
79
-
-
0020064871
-
Megaloblastic haemopoiesis after multiple short-term exposure to nitrous oxide
-
Nunn J.F., Sharer N.M., Gorchein A., Jones J.A., and Wickramasinghe S.N. Megaloblastic haemopoiesis after multiple short-term exposure to nitrous oxide. Lancet i (1982) 1379-1381
-
(1982)
Lancet
, vol.i
, pp. 1379-1381
-
-
Nunn, J.F.1
Sharer, N.M.2
Gorchein, A.3
Jones, J.A.4
Wickramasinghe, S.N.5
-
80
-
-
2942687070
-
"Whippets"-induced cobalamin deficiency manifesting as cervical myelopathy
-
Diamond A.L., Diamond R., Freedman S.M., and Thomas F.P. "Whippets"-induced cobalamin deficiency manifesting as cervical myelopathy. J Neuroimaging 14 (2004) 277-280
-
(2004)
J Neuroimaging
, vol.14
, pp. 277-280
-
-
Diamond, A.L.1
Diamond, R.2
Freedman, S.M.3
Thomas, F.P.4
-
81
-
-
2942635796
-
Toxicity after intermittent inhalation of nitrous oxide for analgesia
-
Doran M., Rassam S.S., Jones L.M., and Underhill S. Toxicity after intermittent inhalation of nitrous oxide for analgesia. Br Med J 328 (2004) 1364-1365
-
(2004)
Br Med J
, vol.328
, pp. 1364-1365
-
-
Doran, M.1
Rassam, S.S.2
Jones, L.M.3
Underhill, S.4
-
82
-
-
0018581459
-
Inherited lack of transcobalamin II in serum and megaloblastic anaemia: A further patient
-
Burman J.F., Mollin D.L., Sourial N.A., and Sladden R.A. Inherited lack of transcobalamin II in serum and megaloblastic anaemia: A further patient. Br J Haematol 43 (1979) 27-38
-
(1979)
Br J Haematol
, vol.43
, pp. 27-38
-
-
Burman, J.F.1
Mollin, D.L.2
Sourial, N.A.3
Sladden, R.A.4
-
83
-
-
0026528815
-
The neurologic aspects of transcobalamin II deficiency
-
Hall C.A. The neurologic aspects of transcobalamin II deficiency. Br J Haematol 80 (1992) 117-120
-
(1992)
Br J Haematol
, vol.80
, pp. 117-120
-
-
Hall, C.A.1
-
84
-
-
0025945537
-
Transcobalamin II deficiency: Case report and review of the literature
-
Kaikov Y., Wadsworth L.D., Hall C.A., and Rogers P.C. Transcobalamin II deficiency: Case report and review of the literature. Eur J Pediatr 150 (1991) 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.4
-
85
-
-
0018547880
-
Megaloblastic anemia as a result of an abnormal transcobalamin II (Cardoza)
-
Haurani F.I., Hall C.A., and Rubin R. Megaloblastic anemia as a result of an abnormal transcobalamin II (Cardoza). J Clin Invest 64 (1979) 1253-1259
-
(1979)
J Clin Invest
, vol.64
, pp. 1253-1259
-
-
Haurani, F.I.1
Hall, C.A.2
Rubin, R.3
-
86
-
-
0019120131
-
Studies of a patient with megaloblastic anemia and an abnormal transcobalamin II
-
Seligman P.A., Steiner L.L., and Allen R.H. Studies of a patient with megaloblastic anemia and an abnormal transcobalamin II. N Engl J Med 303 (1980) 1209-1212
-
(1980)
N Engl J Med
, vol.303
, pp. 1209-1212
-
-
Seligman, P.A.1
Steiner, L.L.2
Allen, R.H.3
-
87
-
-
0036305322
-
Congenital transcobalamin II deficiency due to errors in RNA editing
-
discussion 143-5
-
Qian L., Quadros E.V., Regec A., Zittoun J., and Rothenberg S.P. Congenital transcobalamin II deficiency due to errors in RNA editing. Blood Cells Mol Dis 28 (2002) 134-142 discussion 143-5
-
(2002)
Blood Cells Mol Dis
, vol.28
, pp. 134-142
-
-
Qian, L.1
Quadros, E.V.2
Regec, A.3
Zittoun, J.4
Rothenberg, S.P.5
-
88
-
-
0347480355
-
Transcobalamin deficiency due to activation of an intra exonic cryptic splice site
-
Namour F., Helfer A.-C., Quadros E.V., Alberto J.-M., Bibi H.M., Orning L., et al. Transcobalamin deficiency due to activation of an intra exonic cryptic splice site. Br J Haematol 123 (2003) 915-920
-
(2003)
Br J Haematol
, vol.123
, pp. 915-920
-
-
Namour, F.1
Helfer, A.-C.2
Quadros, E.V.3
Alberto, J.-M.4
Bibi, H.M.5
Orning, L.6
-
89
-
-
0029132162
-
Inherited errors of cobalamin metabolism and their management
-
Linnell J.C., and Bhatt H.R. Inherited errors of cobalamin metabolism and their management. Bailliere's Clin Haematol 8/3 (1995) 567-601
-
(1995)
Bailliere's Clin Haematol
, vol.8-3
, pp. 567-601
-
-
Linnell, J.C.1
Bhatt, H.R.2
-
90
-
-
27744463119
-
Vitamin B12 deficiency is the dominant nutritional cause of hyperhomocysteinemia in a folic acid-fortified population
-
Green R., and Miller J.W. Vitamin B12 deficiency is the dominant nutritional cause of hyperhomocysteinemia in a folic acid-fortified population. Clin Chem Lab Med 43 (2005) 1048-1051
-
(2005)
Clin Chem Lab Med
, vol.43
, pp. 1048-1051
-
-
Green, R.1
Miller, J.W.2
-
91
-
-
0019075068
-
Drug-induced megaloblastic change
-
Scott J.M., and Weir D.G. Drug-induced megaloblastic change. Clin Haematol 9 (1980) 587-606
-
(1980)
Clin Haematol
, vol.9
, pp. 587-606
-
-
Scott, J.M.1
Weir, D.G.2
-
92
-
-
0018084517
-
Haematological effects of anticonvulsant treatment
-
Reynolds E.H., and Laundy M. Haematological effects of anticonvulsant treatment. Lancet ii (1978) 682
-
(1978)
Lancet
, vol.ii
, pp. 682
-
-
Reynolds, E.H.1
Laundy, M.2
-
93
-
-
0037467402
-
Serum folate and Vitamin B12 levels in women using modern oral contraceptives (OC) containing 20 microg ethinyl estradiol
-
Sutterlin M.W., Bussen S.S., Rieger L., Dietl J., and Steck T. Serum folate and Vitamin B12 levels in women using modern oral contraceptives (OC) containing 20 microg ethinyl estradiol. Eur J Obstet Gynecol Reprod Biol 107 (2003) 57-61
-
(2003)
Eur J Obstet Gynecol Reprod Biol
, vol.107
, pp. 57-61
-
-
Sutterlin, M.W.1
Bussen, S.S.2
Rieger, L.3
Dietl, J.4
Steck, T.5
-
94
-
-
0031983432
-
Oral contraceptives did not affect biochemical folate indexes and homocysteine concentrations in adolescent females
-
Green T.J., Houghton L.A., Donovan U., Gibson R.S., and O'Connor D.L. Oral contraceptives did not affect biochemical folate indexes and homocysteine concentrations in adolescent females. J Am Diet Assoc 98 (1998) 49-55
-
(1998)
J Am Diet Assoc
, vol.98
, pp. 49-55
-
-
Green, T.J.1
Houghton, L.A.2
Donovan, U.3
Gibson, R.S.4
O'Connor, D.L.5
-
95
-
-
0033667509
-
Oral contraceptives can cause falsely low vitamin B(12) levels
-
Gardyn J., Mittelman M., Zlotnik J., Sela B.A., and Cohen A.M. Oral contraceptives can cause falsely low vitamin B(12) levels. Acta Haematol 104 (2000) 22-24
-
(2000)
Acta Haematol
, vol.104
, pp. 22-24
-
-
Gardyn, J.1
Mittelman, M.2
Zlotnik, J.3
Sela, B.A.4
Cohen, A.M.5
-
96
-
-
0029165414
-
Congenital errors of folate metabolism
-
Zittoun J. Congenital errors of folate metabolism. Bailliere's Clin Haematol 8/3 (1995) 603-616
-
(1995)
Bailliere's Clin Haematol
, vol.8-3
, pp. 603-616
-
-
Zittoun, J.1
-
97
-
-
0037708873
-
The molecular basis of glutamate formiminotransferase deficiency
-
Hilton J.F., Christensen K.E., Watkins D., Raby B.A., Renaud Y., de la Luna S., et al. The molecular basis of glutamate formiminotransferase deficiency. Hum Mutat 22 (2003) 67-73
-
(2003)
Hum Mutat
, vol.22
, pp. 67-73
-
-
Hilton, J.F.1
Christensen, K.E.2
Watkins, D.3
Raby, B.A.4
Renaud, Y.5
de la Luna, S.6
-
98
-
-
0020657557
-
Cellular immune deficiency in two siblings with hereditary orotic aciduria
-
Girot R., Hamet M., Perignon J.-L., Guesnu M., Fox R.M., Cartier P., et al. Cellular immune deficiency in two siblings with hereditary orotic aciduria. N Engl J Med 308 (1983) 700-704
-
(1983)
N Engl J Med
, vol.308
, pp. 700-704
-
-
Girot, R.1
Hamet, M.2
Perignon, J.-L.3
Guesnu, M.4
Fox, R.M.5
Cartier, P.6
-
99
-
-
26444551223
-
Disorders of purine and pyrimidine metabolism
-
Nyhan W.L. Disorders of purine and pyrimidine metabolism. Mol Genet Metab 86 (2005) 25-33
-
(2005)
Mol Genet Metab
, vol.86
, pp. 25-33
-
-
Nyhan, W.L.1
-
100
-
-
0031028360
-
Molecular cloning of the human UMP synthase gene and characterization of point mutations in two hereditary orotic aciduria families
-
Suchi M., Mizuno H., Kawai Y., Tsuboi T., Sumi S., Okajima K., et al. Molecular cloning of the human UMP synthase gene and characterization of point mutations in two hereditary orotic aciduria families. Am J Hum Genet 60 (1997) 525-539
-
(1997)
Am J Hum Genet
, vol.60
, pp. 525-539
-
-
Suchi, M.1
Mizuno, H.2
Kawai, Y.3
Tsuboi, T.4
Sumi, S.5
Okajima, K.6
-
101
-
-
0037027859
-
Diagnostic value of urinary orotic acid levels: Applicable separation methods
-
Salerno C., and Crifo C. Diagnostic value of urinary orotic acid levels: Applicable separation methods. J Chromatogr B Analyt Technol Biomed Life Sci 781 (2002) 57-71
-
(2002)
J Chromatogr B Analyt Technol Biomed Life Sci
, vol.781
, pp. 57-71
-
-
Salerno, C.1
Crifo, C.2
-
102
-
-
0030917368
-
The recognition of Lesch-Nyhan syndrome as an inborn error of purine metabolism
-
Nyhan W.L. The recognition of Lesch-Nyhan syndrome as an inborn error of purine metabolism. J Inherit Metab Dis 20 (1997) 171-178
-
(1997)
J Inherit Metab Dis
, vol.20
, pp. 171-178
-
-
Nyhan, W.L.1
-
103
-
-
16444366230
-
Lesch-Nyhan Disease
-
Nyhan W.L. Lesch-Nyhan Disease. J Hist Neurosci 14 (2005) 1-10
-
(2005)
J Hist Neurosci
, vol.14
, pp. 1-10
-
-
Nyhan, W.L.1
-
105
-
-
29644444570
-
HPRT (Sardinia): A new point mutation causing HPRT deficiency without Lesch-Nyhan disease
-
Cossu A., Orru S., Jacomelli G., Carcassi C., Contu L., Sestini S., et al. HPRT (Sardinia): A new point mutation causing HPRT deficiency without Lesch-Nyhan disease. Biochim Biophys Acta 1762 (2005) 29-33
-
(2005)
Biochim Biophys Acta
, vol.1762
, pp. 29-33
-
-
Cossu, A.1
Orru, S.2
Jacomelli, G.3
Carcassi, C.4
Contu, L.5
Sestini, S.6
-
106
-
-
0027468639
-
Possible role of macrophages in the pathogenesis of ethanol-induced bone marrow damage
-
Wickramasinghe S.N., and Hasan R. Possible role of macrophages in the pathogenesis of ethanol-induced bone marrow damage. Br J Haematol 83 (1993) 574-579
-
(1993)
Br J Haematol
, vol.83
, pp. 574-579
-
-
Wickramasinghe, S.N.1
Hasan, R.2
-
107
-
-
0023220694
-
Role of macrophages in the pathogenesis of alcohol-induced tissue damage
-
Wickramasinghe S.N. Role of macrophages in the pathogenesis of alcohol-induced tissue damage. Br Med J 294 (1987) 1137-1139
-
(1987)
Br Med J
, vol.294
, pp. 1137-1139
-
-
Wickramasinghe, S.N.1
-
108
-
-
0023257361
-
Circulating cytotoxic protein generated after ethanol consumption: Identification and mechanism of reaction with cells
-
Wickramasinghe S.N., Gardner B., and Barden G. Circulating cytotoxic protein generated after ethanol consumption: Identification and mechanism of reaction with cells. Lancet ii (1987) 122-126
-
(1987)
Lancet
, vol.ii
, pp. 122-126
-
-
Wickramasinghe, S.N.1
Gardner, B.2
Barden, G.3
-
109
-
-
33644815241
-
Advances in the understanding of the congenital dyserythropoietic anaemias
-
Wickramasinghe S.N., and Wood W.G. Advances in the understanding of the congenital dyserythropoietic anaemias. Br J Haematol 131 (2005) 431-446
-
(2005)
Br J Haematol
, vol.131
, pp. 431-446
-
-
Wickramasinghe, S.N.1
Wood, W.G.2
-
111
-
-
0033064140
-
The gene mutated in thiamine-responsive anaemia with diabetes and deafness (TRMA) encodes a functional thiamine transporter
-
Fleming J.C., Tartaglini E., Steinkamp M.P., Schorderet D.F., Cohen N., and Neufeld E.J. The gene mutated in thiamine-responsive anaemia with diabetes and deafness (TRMA) encodes a functional thiamine transporter. Nat Genet 22 (1999) 305-308
-
(1999)
Nat Genet
, vol.22
, pp. 305-308
-
-
Fleming, J.C.1
Tartaglini, E.2
Steinkamp, M.P.3
Schorderet, D.F.4
Cohen, N.5
Neufeld, E.J.6
-
112
-
-
0033059196
-
Mutations in a new gene encoding a thiamine transporter cause thiamine-responsive megaloblastic anaemia syndrome
-
Diaz G.A., Banikazemi M., Oishi K., Desnick R.J., and Gelb B.D. Mutations in a new gene encoding a thiamine transporter cause thiamine-responsive megaloblastic anaemia syndrome. Nat Genet 22 (1999) 309-312
-
(1999)
Nat Genet
, vol.22
, pp. 309-312
-
-
Diaz, G.A.1
Banikazemi, M.2
Oishi, K.3
Desnick, R.J.4
Gelb, B.D.5
-
113
-
-
0032990411
-
Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness
-
Labay V., Raz T., Baron D., Mandel H., Williams H., Barrett T., et al. Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness. Nat Genet 22 (1999) 300-304
-
(1999)
Nat Genet
, vol.22
, pp. 300-304
-
-
Labay, V.1
Raz, T.2
Baron, D.3
Mandel, H.4
Williams, H.5
Barrett, T.6
|