-
1
-
-
69449103947
-
Inherited disorders in the conversion of methionine to homocysteine
-
Barić I. Inherited disorders in the conversion of methionine to homocysteine. J. Inherit. Metab. Dis. 2009, 32:459-471.
-
(2009)
J. Inherit. Metab. Dis.
, vol.32
, pp. 459-471
-
-
Barić, I.1
-
2
-
-
0027302694
-
Characterization of a full-length cDNA encoding human liver S-adenosylmethionine synthetase: tissue-specific gene expression and mRNA levels in hepatopathies
-
Alvarez L., Corrales F., Martín-Duce A., Mato J.M. Characterization of a full-length cDNA encoding human liver S-adenosylmethionine synthetase: tissue-specific gene expression and mRNA levels in hepatopathies. Biochem. J. 1993, 293:481-486.
-
(1993)
Biochem. J.
, vol.293
, pp. 481-486
-
-
Alvarez, L.1
Corrales, F.2
Martín-Duce, A.3
Mato, J.M.4
-
3
-
-
0033925776
-
Methionine adenosyltransferase I/III deficiency: novel mutations and clinical variations
-
Chamberlin M.E., Ubagai T., Mudd S.H., Thomas J., Pao V.Y., Nguyen T.K., Levy H.L., Greene C., Freehauf C., Chou J.Y. Methionine adenosyltransferase I/III deficiency: novel mutations and clinical variations. Am. J. Hum. Genet. 2000, 66:347-355.
-
(2000)
Am. J. Hum. Genet.
, vol.66
, pp. 347-355
-
-
Chamberlin, M.E.1
Ubagai, T.2
Mudd, S.H.3
Thomas, J.4
Pao, V.Y.5
Nguyen, T.K.6
Levy, H.L.7
Greene, C.8
Freehauf, C.9
Chou, J.Y.10
-
4
-
-
84867901719
-
Methionine S-adenosyltransferase deficiency
-
Springer, Heidelberg, J. Fernandes, J.-M. Saudubray, G. van den Berghe, J.H. Walter (Eds.)
-
Andria G., Fowler B., Sebastio G. Methionine S-adenosyltransferase deficiency. Inborn Metabolic Diseases: Diagnosis and Treatment 2006, 278-282. Springer, Heidelberg. J. Fernandes, J.-M. Saudubray, G. van den Berghe, J.H. Walter (Eds.).
-
(2006)
Inborn Metabolic Diseases: Diagnosis and Treatment
, pp. 278-282
-
-
Andria, G.1
Fowler, B.2
Sebastio, G.3
-
5
-
-
0029788238
-
Demyelination of the brain is associated with methionine adenosyltransferase I/III deficiency
-
Chamberlin M.E., Ubagai T., Mudd S.H., Wilson W.G., Leonard J.V., Chou J.Y. Demyelination of the brain is associated with methionine adenosyltransferase I/III deficiency. J. Clin. Invest. 1996, 98:1021-1027.
-
(1996)
J. Clin. Invest.
, vol.98
, pp. 1021-1027
-
-
Chamberlin, M.E.1
Ubagai, T.2
Mudd, S.H.3
Wilson, W.G.4
Leonard, J.V.5
Chou, J.Y.6
-
6
-
-
0032477711
-
Normal brain myelination in a patient homozygous for a mutation that encodes a severely truncated methionine adenosyltransferase I/III
-
Hazelwood S., Bernardini I., Shotelersuk V., Tangerman A., Guo J., Mudd H., Gahl W.A. Normal brain myelination in a patient homozygous for a mutation that encodes a severely truncated methionine adenosyltransferase I/III. Am. J. Med. Genet. 1998, 75:395-400.
-
(1998)
Am. J. Med. Genet.
, vol.75
, pp. 395-400
-
-
Hazelwood, S.1
Bernardini, I.2
Shotelersuk, V.3
Tangerman, A.4
Guo, J.5
Mudd, H.6
Gahl, W.A.7
-
7
-
-
79951701209
-
Hypermethioninemias of genetic and non-genetic origin: a review
-
Mudd S.H. Hypermethioninemias of genetic and non-genetic origin: a review. Am. J. Med. Genet. C Semin. Med. Genet. 2011, 157:3-32.
-
(2011)
Am. J. Med. Genet. C Semin. Med. Genet.
, vol.157
, pp. 3-32
-
-
Mudd, S.H.1
-
8
-
-
16644376107
-
Reversible white matter lesion in methionine adenosyltransferase I/III deficiency
-
Tada H., Takanashi J., Barkovich A.J., Yamamoto S., Kohno Y. Reversible white matter lesion in methionine adenosyltransferase I/III deficiency. Am. J. Neuroradiol. 2004, 25:1843-1845.
-
(2004)
Am. J. Neuroradiol.
, vol.25
, pp. 1843-1845
-
-
Tada, H.1
Takanashi, J.2
Barkovich, A.J.3
Yamamoto, S.4
Kohno, Y.5
-
9
-
-
77957234550
-
A methionine adenosyltransferase (MAT) deficiency patient treated with diet therapy
-
Ito M., Kotani Y., Matsuda J., Yokota I., Naito E., Mori K., Kuroda Y. A methionine adenosyltransferase (MAT) deficiency patient treated with diet therapy. J. Inherit. Metab. Dis. 2003, 26(Suppl. 2):76.
-
(2003)
J. Inherit. Metab. Dis.
, vol.26
, Issue.SUPPL. 2
, pp. 76
-
-
Ito, M.1
Kotani, Y.2
Matsuda, J.3
Yokota, I.4
Naito, E.5
Mori, K.6
Kuroda, Y.7
-
10
-
-
84858278325
-
S-adenosylmethionine treatment in methionine adenosyltransferase deficiency, a case report
-
Furujo M., Kinoshita M., Nagao M., Kubo T. S-adenosylmethionine treatment in methionine adenosyltransferase deficiency, a case report. Mol. Genet. Metab. 2012, 105:516-518.
-
(2012)
Mol. Genet. Metab.
, vol.105
, pp. 516-518
-
-
Furujo, M.1
Kinoshita, M.2
Nagao, M.3
Kubo, T.4
-
11
-
-
84867894221
-
Cerebral hypomyelination and maternal uniparental disomy 10 in a patient with MAT I/III deficiency
-
Faghfoury H., Shroff M., Blaser S., Mudd S.H., Wagner C., Corrales F.J., Stockley T., Schulze A.J. Cerebral hypomyelination and maternal uniparental disomy 10 in a patient with MAT I/III deficiency. Mol. Genet. Metab. 2009, 98:21-22.
-
(2009)
Mol. Genet. Metab.
, vol.98
, pp. 21-22
-
-
Faghfoury, H.1
Shroff, M.2
Blaser, S.3
Mudd, S.H.4
Wagner, C.5
Corrales, F.J.6
Stockley, T.7
Schulze, A.J.8
-
12
-
-
0031020197
-
Dominant inheritance of isolated hypermethioninemia is associated with a mutation in the human methionine adenosyltransferase 1A gene
-
Chamberlin M.E., Ubagai T., Mudd S.H., Levy H.L., Chou J.Y. Dominant inheritance of isolated hypermethioninemia is associated with a mutation in the human methionine adenosyltransferase 1A gene. Am. J. Hum. Genet. 1997, 60:540-546.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 540-546
-
-
Chamberlin, M.E.1
Ubagai, T.2
Mudd, S.H.3
Levy, H.L.4
Chou, J.Y.5
-
13
-
-
0030870869
-
Genetic analysis of isolated persistent hypermethioninemia with dominant inheritance
-
Nagao M., Oyanagi K. Genetic analysis of isolated persistent hypermethioninemia with dominant inheritance. Acta Paediatr. Jpn. 1997, 39:601-606.
-
(1997)
Acta Paediatr. Jpn.
, vol.39
, pp. 601-606
-
-
Nagao, M.1
Oyanagi, K.2
-
14
-
-
0026334413
-
Association of demyelination with deficiency of cerebrospinal-fluid S-adenosylmethionine in inborn errors of methyl-transfer pathway
-
Surtees R., Leonard J., Austin S. Association of demyelination with deficiency of cerebrospinal-fluid S-adenosylmethionine in inborn errors of methyl-transfer pathway. Lancet 1991, 338:1550-1554.
-
(1991)
Lancet
, vol.338
, pp. 1550-1554
-
-
Surtees, R.1
Leonard, J.2
Austin, S.3
-
15
-
-
0036344537
-
Elevated plasma total homocysteine in severe methionine adenosyltransferase I/III deficiency
-
Stabler S.P., Steegborn C., Wahl M.C., Oliveriusova J., Kraus J.P., Allen R.H., Wagner C., Mudd S.H. Elevated plasma total homocysteine in severe methionine adenosyltransferase I/III deficiency. Metabolism 2002, 51:981-988.
-
(2002)
Metabolism
, vol.51
, pp. 981-988
-
-
Stabler, S.P.1
Steegborn, C.2
Wahl, M.C.3
Oliveriusova, J.4
Kraus, J.P.5
Allen, R.H.6
Wagner, C.7
Mudd, S.H.8
-
16
-
-
0036975282
-
Methionine adenosyltransferase I/III deficiency: two Korean compound heterozygous siblings with a novel mutation
-
Kim S.Z., Santamaria E., Jeong T.E., Levy H.L., Mato J.M., Corrales F.J., Mudd S.H. Methionine adenosyltransferase I/III deficiency: two Korean compound heterozygous siblings with a novel mutation. J. Inherit. Metab. Dis. 2002, 25:661-671.
-
(2002)
J. Inherit. Metab. Dis.
, vol.25
, pp. 661-671
-
-
Kim, S.Z.1
Santamaria, E.2
Jeong, T.E.3
Levy, H.L.4
Mato, J.M.5
Corrales, F.J.6
Mudd, S.H.7
-
17
-
-
84855579234
-
Hypermethioninaemia due to methionine adenosyltransferase I/III (MAT I/III) deficiency: diagnosis in an expanded neonatal screening programme
-
Couce M.L., Bóveda M.D., Castiñeiras D.E., Corrales F.J., Mora M.I., Fraga J.M., Mudd S.H. Hypermethioninaemia due to methionine adenosyltransferase I/III (MAT I/III) deficiency: diagnosis in an expanded neonatal screening programme. J. Inherit. Metab. Dis. 2008, 31:S233-S239.
-
(2008)
J. Inherit. Metab. Dis.
, vol.31
-
-
Couce, M.L.1
Bóveda, M.D.2
Castiñeiras, D.E.3
Corrales, F.J.4
Mora, M.I.5
Fraga, J.M.6
Mudd, S.H.7
-
18
-
-
0009968702
-
Hypermethioninemia and hyperhomocysteinemia in methionine adenosyltransferase I/III deficiency
-
Lagler F., Muntau A.C., Beblo S., Röschinger W., Linnebank M., Fowler B., Koch H.G., Roscher A.A. Hypermethioninemia and hyperhomocysteinemia in methionine adenosyltransferase I/III deficiency. J. Inherit. Metab. Dis. 2000, 23:68.
-
(2000)
J. Inherit. Metab. Dis.
, vol.23
, pp. 68
-
-
Lagler, F.1
Muntau, A.C.2
Beblo, S.3
Röschinger, W.4
Linnebank, M.5
Fowler, B.6
Koch, H.G.7
Roscher, A.A.8
-
19
-
-
84856097359
-
Two patients with hepatic mtDNA depletion syndromes and marked elevations of S-adenosylmethionine and methionine
-
Mudd S.H., Wagner C., Luka Z., Stabler S.P., Allen R.H., Schroer R., Wood T., Wang J., Wong L.J. Two patients with hepatic mtDNA depletion syndromes and marked elevations of S-adenosylmethionine and methionine. Mol. Genet. Metab. 2012, 105:228-236.
-
(2012)
Mol. Genet. Metab.
, vol.105
, pp. 228-236
-
-
Mudd, S.H.1
Wagner, C.2
Luka, Z.3
Stabler, S.P.4
Allen, R.H.5
Schroer, R.6
Wood, T.7
Wang, J.8
Wong, L.J.9
-
20
-
-
0016199102
-
Methionine adenosyltransferase deficiency: new enzymatic defect associated with hypermethioninemia
-
Gaull G.E., Tallan H.H. Methionine adenosyltransferase deficiency: new enzymatic defect associated with hypermethioninemia. Science 1974, 186:59-60.
-
(1974)
Science
, vol.186
, pp. 59-60
-
-
Gaull, G.E.1
Tallan, H.H.2
-
21
-
-
0024434640
-
Isolation of a cDNA encoding the rat liver S-adenosylmethionine synthetase
-
Horikawa S., Ishikawa M., Ozasa H., Tsukada K. Isolation of a cDNA encoding the rat liver S-adenosylmethionine synthetase. Eur. J. Biochem. 1989, 184:497-501.
-
(1989)
Eur. J. Biochem.
, vol.184
, pp. 497-501
-
-
Horikawa, S.1
Ishikawa, M.2
Ozasa, H.3
Tsukada, K.4
-
22
-
-
0027210883
-
Cloning and expression of murine S-adenosylmethionine synthetase
-
Sakata S.F., Shelly L.L., Ruppert S., Schutz G., Chou J.Y. Cloning and expression of murine S-adenosylmethionine synthetase. J. Biol. Chem. 1993, 268:13978-13986.
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 13978-13986
-
-
Sakata, S.F.1
Shelly, L.L.2
Ruppert, S.3
Schutz, G.4
Chou, J.Y.5
-
23
-
-
0028810994
-
Molecular mechanisms of an inborn error of methionine pathway: methionine adenosyltransferase deficiency
-
Ubagai T., Lei K.-J., Huang S., Mudd S.H., Levy H.L., Chou J.Y. Molecular mechanisms of an inborn error of methionine pathway: methionine adenosyltransferase deficiency. J. Clin. Invest. 1995, 96:1943-1947.
-
(1995)
J. Clin. Invest.
, vol.96
, pp. 1943-1947
-
-
Ubagai, T.1
Lei, K.-J.2
Huang, S.3
Mudd, S.H.4
Levy, H.L.5
Chou, J.Y.6
-
24
-
-
0344464877
-
Atypical BECTS and homocystinuria
-
Buoni S., Di Bartolo R.M., Molinelli M., Palmeri S., Zannolli R. Atypical BECTS and homocystinuria. Neurology 2003, 61:1129-1131.
-
(2003)
Neurology
, vol.61
, pp. 1129-1131
-
-
Buoni, S.1
Di Bartolo, R.M.2
Molinelli, M.3
Palmeri, S.4
Zannolli, R.5
-
25
-
-
0028873416
-
Isolated persistent hypermethioninemia
-
Mudd S.H., Levy H.L., Tangerman A., Boujet C., Buist N., Davidson-Mundt A., Hudgins L., Oyanagi K., Nagao M., Wilson W.G. Isolated persistent hypermethioninemia. Am. J. Hum. Genet. 1995, 57:882-892.
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 882-892
-
-
Mudd, S.H.1
Levy, H.L.2
Tangerman, A.3
Boujet, C.4
Buist, N.5
Davidson-Mundt, A.6
Hudgins, L.7
Oyanagi, K.8
Nagao, M.9
Wilson, W.G.10
-
26
-
-
0034875592
-
Effect of vitamin B6 deficiency on the synthesis and accumulation of S-adenosylhomocysteine and S-adenosylmethionine in rat tissues
-
Nguyen T.T., Hayakawa T., Tsuge H. Effect of vitamin B6 deficiency on the synthesis and accumulation of S-adenosylhomocysteine and S-adenosylmethionine in rat tissues. J. Nutr. Sci. Vitaminol. (Tokyo) 2001, 47:188-194.
-
(2001)
J. Nutr. Sci. Vitaminol. (Tokyo)
, vol.47
, pp. 188-194
-
-
Nguyen, T.T.1
Hayakawa, T.2
Tsuge, H.3
-
27
-
-
0036828353
-
S-adenosyl-l-methionine (SAMe): from the bench to the bedside - molecular basis of a pleiotrophic molecule
-
(Suppl.)
-
Bottiglieri T. S-adenosyl-l-methionine (SAMe): from the bench to the bedside - molecular basis of a pleiotrophic molecule. Am. J. Clin. Nutr. 2002, 76:1151S-1157S. (Suppl.).
-
(2002)
Am. J. Clin. Nutr.
, vol.76
-
-
Bottiglieri, T.1
-
28
-
-
0036829068
-
Role of S-adenosyl-l-methionine in the treatment of depression: a review of the evidence
-
(Suppl.)
-
Mischoulon D., Fava M. Role of S-adenosyl-l-methionine in the treatment of depression: a review of the evidence. Am. J. Clin. Nutr. 2002, 76:1158S-1161S. (Suppl.).
-
(2002)
Am. J. Clin. Nutr.
, vol.76
-
-
Mischoulon, D.1
Fava, M.2
-
29
-
-
0025606597
-
Cerebrospinal fluid S-adenosylmethionine-in depression and dementia: effects of treatment with parenteral and oral S-adenosylmethionine
-
Bottiglieri T., Godfrey P., Flynn T., Carney M.W.P., Toone B.K., Reynolds E.H. Cerebrospinal fluid S-adenosylmethionine-in depression and dementia: effects of treatment with parenteral and oral S-adenosylmethionine. J. Neurol. Neurosurg. Psychiatry 1990, 53:1096-1098.
-
(1990)
J. Neurol. Neurosurg. Psychiatry
, vol.53
, pp. 1096-1098
-
-
Bottiglieri, T.1
Godfrey, P.2
Flynn, T.3
Carney, M.W.P.4
Toone, B.K.5
Reynolds, E.H.6
-
30
-
-
66849127876
-
Polyunsaturated fatty acid and S-adenosylmethionine supplementation in predementia syndromes and Alzheimer's disease: a review
-
Panza F., Frisardi V., Capurso C., D'Introno A., Colacicco A.M., Di Palo A., Imbimbo B.P., Vendemiale G., Capurso A., Solfrizzi V. Polyunsaturated fatty acid and S-adenosylmethionine supplementation in predementia syndromes and Alzheimer's disease: a review. ScientificWorldJournal 2009, 9:373-389.
-
(2009)
ScientificWorldJournal
, vol.9
, pp. 373-389
-
-
Panza, F.1
Frisardi, V.2
Capurso, C.3
D'Introno, A.4
Colacicco, A.M.5
Di Palo, A.6
Imbimbo, B.P.7
Vendemiale, G.8
Capurso, A.9
Solfrizzi, V.10
-
31
-
-
65549120331
-
Possible role of s-adenosylmethionine, s-adenosylhomocysteine, and polyunsaturated fatty acids in predementia syndromes and Alzheimer's disease
-
Panza F., Frisardi V., Capurso C., D'Introno A., Colacicco A.M., Vendemiale G., Capurso A., Solfrizzi V. Possible role of s-adenosylmethionine, s-adenosylhomocysteine, and polyunsaturated fatty acids in predementia syndromes and Alzheimer's disease. J. Alzheimers Dis. 2009, 16:467-470.
-
(2009)
J. Alzheimers Dis.
, vol.16
, pp. 467-470
-
-
Panza, F.1
Frisardi, V.2
Capurso, C.3
D'Introno, A.4
Colacicco, A.M.5
Vendemiale, G.6
Capurso, A.7
Solfrizzi, V.8
-
32
-
-
58149191631
-
Efficacy of a vitamin/nutriceutical formulation for early-stage Alzheimer's disease: a 1-year, open-label pilot study with a 16-month caregiver extension
-
Chan A., Paskavitz J., Remington R., Rasmussen S., Shea T.B. Efficacy of a vitamin/nutriceutical formulation for early-stage Alzheimer's disease: a 1-year, open-label pilot study with a 16-month caregiver extension. Am. J. Alzheimers Dis. Other Demen. 2008-2009, 23:571-585.
-
(2008)
Am. J. Alzheimers Dis. Other Demen.
, vol.23
, pp. 571-585
-
-
Chan, A.1
Paskavitz, J.2
Remington, R.3
Rasmussen, S.4
Shea, T.B.5
-
33
-
-
63349096757
-
Efficacy of a vitamin/nutriceutical formulation for moderate-stage to later-stage Alzheimer's disease: a placebo-controlled pilot study
-
Remington R., Chan A., Paskavitz J., Shea T.B. Efficacy of a vitamin/nutriceutical formulation for moderate-stage to later-stage Alzheimer's disease: a placebo-controlled pilot study. Am. J. Alzheimers Dis. Other Demen. 2009, 24:27-33.
-
(2009)
Am. J. Alzheimers Dis. Other Demen.
, vol.24
, pp. 27-33
-
-
Remington, R.1
Chan, A.2
Paskavitz, J.3
Shea, T.B.4
|