HYPER-METHIONINEMIA ASSOCIATED WITH METHIONINE ADENOSYLTRANSFERASE DEFICIENCY - CLINICAL, MORPHOLOGIC, AND BIOCHEMICAL OBSERVATIONS ON FOUR PATIENTS

被引：52

作者：

GAULL, GE

TALLAN, HH

LONSDALE, D

PRZYREMBEL, H

SCHAFFNER, F

VONBASSEWITZ, DB

机构：

[1] CUNY MT SINAI SCH MED, DEPT MED, DIV LIVER DIS, NEW YORK, NY 10029 USA

[2] CUNY MT SINAI SCH MED, DEPT PEDIAT, DIV HUMAN GENET, NEW YORK, NY 10029 USA

[3] UNIV MUNSTER, INST PATHOL, D-4400 MUNSTER, FED REP GER

[4] CUNY MT SINAI SCH MED, CLIN RES CTR, NEW YORK, NY 10029 USA

[5] CLEVELAND CLIN, DEPT PEDIAT, CLEVELAND, OH 44106 USA

[6] UNIV DUSSELDORF, DEPT PEDIAT, D-4000 DUSSELDORF 1, FED REP GER

来源：

JOURNAL OF PEDIATRICS | 1981年 / 98卷 / 05期

关键词：

D O I：

10.1016/S0022-3476(81)80833-5

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：734 / 741

页数：8

共 34 条

[1] S-ADENOSYLMETHIONINE IN BRAIN AND OTHER TISSUES [J].

BALDESSARINI, RJ ;

KOPIN, IJ .

JOURNAL OF NEUROCHEMISTRY, 1966, 13 (08) :769-+

[2]

BERATIS NG, 1973, MAMMALIAN CHROMOSOME, V14, P114

[3]

BROWN GW, 1959, J BIOL CHEM, V234, P1769

[4] HOMOCYSTINURIA - A NEW INBORN ERROR OF METABOLISM ASSOCIATED WITH MENTAL DEFICIENCY [J].

CARSON, NAJ ;

DENT, CE ;

FIELD, CMB ;

NEILL, DW ;

WESTALL, RG ;

CUSWORTH, DC .

ARCHIVES OF DISEASE IN CHILDHOOD, 1963, 38 (201) :425-+

[5] ABNORMAL METHIONINE ADENOSYLTRANSFERASE IN HYPERMETHIONINEMIA [J].

FINKELSTEIN, JD ;

KYLE, WE ;

MARTIN, JJ .

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1975, 66 (04) :1491-1497

[6] CYSTATHIONINE SYNTHASE DEFICIENCY - HETEROZYGOTE DETECTION USING CULTURED SKIN FIBROBLASTS [J].

FLEISHER, LD ;

TALLAN, HH ;

BERATIS, NG ;

HIRSCHHORN, K ;

GAULL, GE .

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1973, 55 (01) :38-44

[7] METHIONINE METABOLISM IN MAN - DEVELOPMENT AND DEFICIENCIES [J].

FLEISHER, LD ;

GAULL, GE .

CLINICS IN ENDOCRINOLOGY AND METABOLISM, 1974, 3 (01) :37-55

[8] DEVELOPMENT OF MAMMALIAN SULFUR METABOLISM - ABSENCE OF CYSTATHIONASE IN HUMAN FETAL TISSUES [J].

GAULL, G ;

STURMAN, JA ;

RAIHA, NCR .

PEDIATRIC RESEARCH, 1972, 6 (06) :538-&

[9]

GAULL G E, 1969, Neuropaediatrie, V1, P199, DOI 10.1055/s-0028-1091874

[10] BIOCHEMICAL OBSERVATIONS ON SO-CALLED HEREDITARY TYROSINEMIA [J].

GAULL, GE ;

RASSIN, DK ;

SOLOMON, GE ;

HARRIS, RC ;

STURMAN, JA .

PEDIATRIC RESEARCH, 1970, 4 (04) :337-&

← 1 2 3 4 →