GLUCOSE-6-P-DEHYDROGENASE DEFECT IN GERMANY .2. PROPERTIES OF FREIBURG-TYPE ENZYME

被引：13

作者：

BUSCH, D

BOIE, K

机构：

来源：

KLINISCHE WOCHENSCHRIFT | 1970年 / 48卷 / 02期

关键词：

D O I：

10.1007/BF01484620

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：74 / &

共 27 条

[21] EVIDENCE FOR 4 TYPES OF ERYTHROCYTE GLUCOSE-6-PHOSPHATE DEHYDROGENASE FROM G-6-PD-DEFICIENT HUMAN SUBJECTS [J].

PINTO, PVC ;

NEWTON, WA ;

RICHARDSON, KE .

JOURNAL OF CLINICAL INVESTIGATION, 1966, 45 (06) :823-+

[22]

PORTER IH, 1964, LANCET, V1, P895

[23] ERYTHROCYTE GLUCOSE-6-PHOSPHATE DEHYDROGENASE IN CAUCASIANS - NEW INHERITED VARIANT [J].

SHOWS, TB ;

BREWER, GJ ;

TASHIAN, RE .

SCIENCE, 1964, 145 (363) :1056-&

[24] ATHENS VARIANT OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE [J].

STAMATOYANNOPOULOS, G ;

YOSHIDA, A ;

BACOPOULOS, C ;

MOTULKSY, AG .

SCIENCE, 1967, 157 (3790) :831-+

[25] HEREDITARE NICHTSPHAROCYTARE HAMOLYTISCHE ANAMIE DURCH GLUCOSE-6-PHOSPHATDEHYDROGENASE-MANGEL (BILDUNG EINES ENZYMPROTEINS MIT VERANDERTEN EIGENSCHAFTEN IN DEN BLUTZELLEN EINER DEUTSCHEN FAMILIE) [J].

WALLER, HD ;

LOHR, GW ;

GAYER, J .

KLINISCHE WOCHENSCHRIFT, 1966, 44 (03) :122-+

[26] 2 NEW CASES OF HEREDITARY NON-SPHEROCYTARY HEMOLYTIC ANEMIA IN PRESENCE OF GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFECT IN A NORTHERN GERMAN FAMILY .I. [J].

WEINREICH, J ;

BUSCH, D ;

GOTTSTEIN, U ;

SCHAEFER, J ;

ROHR, J .

KLINISCHE WOCHENSCHRIFT, 1968, 46 (03) :146-+

[27]

1967, WHO366 TECHN REP SER

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