-
1
-
-
0022457243
-
Subacute combined degeneration of the cord due to folate deficiency: Response to methyl folate treatment
-
Lever EG, Elwes Rdc, Williams A., Reynolds EH Subacute combined degeneration of the cord due to folate deficiency: Response to methyl folate treatment. J Neurol Neurosurg Psychiatry. 1986;49:1203-1207.
-
(1986)
J Neurol Neurosurg Psychiatry
, vol.49
, pp. 1203-1207
-
-
Lever, E.G.1
Elwes, Rdc.2
Williams, A.3
Reynolds, E.H.4
-
2
-
-
0003908489
-
Teratology, drugs and other medications
-
In: Cunningham FG, Leveno KJ, Bloom SL, et al, eds. 22nd ed. New York, NY: McGraw-Hill
-
Cunningham FG, Hauth JC, Kenneth JL, Gilstrap L., Bloom SL, Wenstrom KD Teratology, drugs and other medications. In: Cunningham FG, Leveno KJ, Bloom SL, et al, eds. Williams Obstetrics. 22 nd ed. New York, NY: McGraw-Hill; 2005:345.
-
(2005)
Williams Obstetrics
, pp. 345
-
-
Cunningham, F.G.1
Hauth, J.C.2
Kenneth, J.L.3
Gilstrap, L.4
Bloom, S.L.5
Wenstrom, K.D.6
-
3
-
-
1642558200
-
New inborn error of metabolism: Folic acid responsive megaloblastic anemia, ataxia, mental retardation, and convulsions (Abstract)
-
Luhby AL, Cooperman JM, Pesci-Bourel AA New inborn error of metabolism: folic acid responsive megaloblastic anemia, ataxia, mental retardation, and convulsions (Abstract). J Pediatr. 1965;6:1052.
-
(1965)
J Pediatr
, vol.67
, pp. 1052
-
-
Luhby, A.L.1
Cooperman, J.M.2
Pesci-Bourel, A.A.3
-
4
-
-
0032732594
-
Isolated congenital malabsorption of folic acid in a male infant: Insights into treatment and mechanism of defect
-
Malatack JJ, Moran MM, Moughan B. Isolated congenital malabsorption of folic acid in a male infant: Insights into treatment and mechanism of defect. Pediatrics. 1999;104:1133-1137.
-
(1999)
Pediatrics
, vol.104
, pp. 1133-1137
-
-
Malatack, J.J.1
Moran, M.M.2
Moughan, B.3
-
5
-
-
0032941095
-
Cobalamin and folate deficiency: Acquired and hereditary disorders in children
-
Rosenblatt DS, Whitehead VM Cobalamin and folate deficiency: Acquired and hereditary disorders in children. Semin Hematol. 1999;36:19-34.
-
(1999)
Semin Hematol
, vol.36
, pp. 19-34
-
-
Rosenblatt, D.S.1
Whitehead, V.M.2
-
6
-
-
0036143484
-
Hereditary folate malabsorption: Family report and review of the literature
-
Geller J., Kronn D., Jayabose S., Sandoval C. Hereditary folate malabsorption: Family report and review of the literature. Medicine. 2002;8:51-68.
-
(2002)
Medicine
, vol.81
, pp. 51-68
-
-
Geller, J.1
Kronn, D.2
Jayabose, S.3
Sandoval, C.4
-
7
-
-
0037708873
-
Raby BA The molecular basis of glutamate formiminotransferase deficiency
-
Hilton JF, Christensen KE, Watkins D., Raby BA The molecular basis of glutamate formiminotransferase deficiency. Hum Mutat. 2003;22:67-73.
-
(2003)
Hum Mutat
, vol.22
, pp. 67-73
-
-
Hilton, J.F.1
Christensen, K.E.2
Watkins, D.3
-
8
-
-
18344395924
-
Autoantibodies to folate receptors in the cerebral folate deficiency syndrome
-
Ramaekers V., Rothenberg SP, Sequeira JM, et al. Autoantibodies to folate receptors in the cerebral folate deficiency syndrome. NEJM. 2005;352:1985-1991.
-
(2005)
NEJM
, vol.352
, pp. 1985-1991
-
-
Ramaekers, V.1
Rothenberg, S.P.2
Sequeira, J.M.3
-
9
-
-
0036990821
-
Psychomotor retardation, spastic paraplegia, cerebellar ataxia and dyskinesia associated with low 5-methyltetrahydrofolate in cerebrospinal fluid: A novel neurometabolic condition responding to folinic acid substitution
-
Ramaekers V., Hausler M., Opladen T., et al. Psychomotor retardation, spastic paraplegia, cerebellar ataxia and dyskinesia associated with low 5-methyltetrahydrofolate in cerebrospinal fluid: A novel neurometabolic condition responding to folinic acid substitution. Neuropediatrics. 2002;33:301-308.
-
(2002)
Neuropediatrics
, vol.33
, pp. 301-308
-
-
Ramaekers, V.1
Hausler, M.2
Opladen, T.3
-
10
-
-
0014591579
-
Isolated defect of folic acid absorption associated with mental retardation and cerebral calcification
-
Lanzkowsky P., Erlandson ME, Bezan AI Isolated defect of folic acid absorption associated with mental retardation and cerebral calcification. Blood. 1969;34:452-465.
-
(1969)
Blood
, vol.34
, pp. 452-465
-
-
Lanzkowsky, P.1
Erlandson, M.E.2
Bezan, A.I.3
-
11
-
-
0027260486
-
Biochemical pathogenesis of subacute combined degeneration of the spinal cord and brain
-
Surtees R., Heales S., Bowron A. Biochemical pathogenesis of subacute combined degeneration of the spinal cord and brain. J Inherit Metab Dis. 1993;16:762-770.
-
(1993)
J Inherit Metab Dis
, vol.16
, pp. 762-770
-
-
Surtees, R.1
Heales, S.2
Bowron, A.3
-
12
-
-
0007759545
-
Relapsing megaloblastic anemia in an infant due to a specific defect in gastrointestinal absorption of folic acid
-
Lubhy AL, Eagle FJ, Roth E., Cooperman JM Relapsing megaloblastic anemia in an infant due to a specific defect in gastrointestinal absorption of folic acid. Am J Dis Child. 1961;102:482-483.
-
(1961)
Am J Dis Child
, vol.102
, pp. 482-483
-
-
Lubhy, A.L.1
Eagle, F.J.2
Roth, E.3
Cooperman, J.M.4
-
13
-
-
0014855687
-
Lymphocyte transformation in megaloblastic anemia: Morphology and DNA synthesis
-
Das KC, Hoffbrand AV Lymphocyte transformation in megaloblastic anemia: morphology and DNA synthesis. Br J Haematol. 1970;19:459-468.
-
(1970)
Br J Haematol
, vol.19
, pp. 459-468
-
-
Das, K.C.1
Hoffbrand, A.V.2
-
14
-
-
0014677844
-
Logarithmic-normal distribution of cerebrospinal fluid folate concentrations
-
Weckman N., Lehtovora R. Logarithmic-normal distribution of cerebrospinal fluid folate concentrations. Expericutia (Basel). 1969;25:585.
-
(1969)
Expericutia (Basel)
, vol.25
, pp. 585
-
-
Weckman, N.1
Lehtovora, R.2
-
15
-
-
85040025271
-
Transport characteristics of folates in cerebrospinal fluid: A study utilizing doubly labeled 5-methyltetrahydrofolate and 5-formyltetrahydrofolate
-
Levitt M., Nixon PF, Pincus JH, Bertino JR Transport characteristics of folates in cerebrospinal fluid: A study utilizing doubly labeled 5-methyltetrahydrofolate and 5-formyltetrahydrofolate. J Clin Invest. 1971;50:8-13
-
(1971)
J Clin Invest
, vol.50
, pp. 8-13
-
-
Levitt, M.1
Nixon, P.F.2
Pincus, J.H.3
Bertino, J.R.4
-
16
-
-
0032813393
-
Expression patterns of folate binding proteins one and two in the developing embryo
-
Barber RC, Bennett GD, Greer KA, et al. Expression patterns of folate binding proteins one and two in the developing embryo. Mol Genet Metab. 1999;66:31-39.
-
(1999)
Mol Genet Metab
, vol.66
, pp. 31-39
-
-
Barber, R.C.1
Bennett, G.D.2
Greer, K.A.3
-
17
-
-
0028029029
-
Folate deficiency in cerebrospinal fluid associated with a defect in folate binding protein in the central nervous system
-
Wevers RA, Hansen SI, van Hellenberg Hubar Jlm, Holm J. Folate deficiency in cerebrospinal fluid associated with a defect in folate binding protein in the central nervous system. J Neurol Neurosurg Psychiatr. 1994;57:223-226.
-
(1994)
J Neurol Neurosurg Psychiatr
, vol.57
, pp. 223-226
-
-
Wevers, R.A.1
Hansen, S.I.2
van Hellenberg Hubar, Jlm.3
Holm, J.4
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