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Results: 1-8 |
Results: 8
DEFECTIVE GALACTOSYLATION OF SERUM TRANSFERRIN IN GALACTOSEMIA
Authors: CHARLWOOD J CLAYTON P KEIR G MIAN N WINCHESTER B
Citation: J. Charlwood et al., DEFECTIVE GALACTOSYLATION OF SERUM TRANSFERRIN IN GALACTOSEMIA, Glycobiology, 8(4), 1998, pp. 351-357
PRENATAL-DIAGNOSIS OF THE CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE 1A (CDG1A) BY A COMBINATION OF ENZYMOLOGY AND GENETIC-LINKAGE ANALYSIS AFTER AMNIOCENTESIS OR CHORIONIC VILLUS SAMPLING
Authors: CHARLWOOD J CLAYTON P KEIR G MIAN N YOUNG E WINCHESTER B
Citation: J. Charlwood et al., PRENATAL-DIAGNOSIS OF THE CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE 1A (CDG1A) BY A COMBINATION OF ENZYMOLOGY AND GENETIC-LINKAGE ANALYSIS AFTER AMNIOCENTESIS OR CHORIONIC VILLUS SAMPLING, Prenatal diagnosis, 18(7), 1998, pp. 693-699
EFFECT OF ACADEMIC DETAILING UPON PROVIDER PRESCRIPTION PATTERNS OF BLOOD-GLUCOSE MONITORING (BGM) SUPPLIES IN PERSONS WITH TYPE-2 DIABETES
Authors: LIEBERMAN B MYERS VS XENACHIS C MIAN N POGACH L
Citation: B. Lieberman et al., EFFECT OF ACADEMIC DETAILING UPON PROVIDER PRESCRIPTION PATTERNS OF BLOOD-GLUCOSE MONITORING (BGM) SUPPLIES IN PERSONS WITH TYPE-2 DIABETES, Diabetes, 47, 1998, pp. 715-715
A CASE OF THE CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE-1 (CDGS TYPE-1) WITH NORMAL PHOSPHOMANNOMUTASE ACTIVITY
Authors: CHARLWOOD J CLAYTON P JOHNSON A KEIR G MIAN N WINCHESTER B
Citation: J. Charlwood et al., A CASE OF THE CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE-1 (CDGS TYPE-1) WITH NORMAL PHOSPHOMANNOMUTASE ACTIVITY, Journal of inherited metabolic disease, 20(6), 1997, pp. 817-827
THE IDENTIFICATION OF ABNORMAL GLYCOFORMS OF SERUM TRANSFERRIN IN CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE-I BY CAPILLARY ZONE ELECTROPHORESIS
Authors: IOURIN O MATTU TS MIAN N KEIR G WINCHESTER B DWEK RA RUDD PM
Citation: O. Iourin et al., THE IDENTIFICATION OF ABNORMAL GLYCOFORMS OF SERUM TRANSFERRIN IN CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE-I BY CAPILLARY ZONE ELECTROPHORESIS, Glycoconjugate journal, 13(6), 1996, pp. 1031-1042
RESONANT PHOTOEMISSION FROM COMPLEX CUPRATES AND NICKELATES
Authors: FLAVELL WR HOLLINGWORTH J HOWLETT JF THOMAS AG SARKER MM SQUIRE S HASHIM Z MIAN N WINCOTT PL TEEHAN D DOWNES S
Citation: Wr. Flavell et al., RESONANT PHOTOEMISSION FROM COMPLEX CUPRATES AND NICKELATES, Journal of synchrotron radiation, 2, 1995, pp. 264-271
THE CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME - AN EXPERIMENT OF NATURE IN GLYCOSYLATION
Authors: WINCHESTER B CLAYTON P MIAN N DITOMASO E DELL A REASON A KEIR G
Citation: B. Winchester et al., THE CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME - AN EXPERIMENT OF NATURE IN GLYCOSYLATION, Biochemical Society transactions, 23(1), 1995, pp. 185-188
CONCERNING AGAMANOLIS DISEASE
Authors: CLAYTON PT MIAN N
Citation: Pt. Clayton et N. Mian, CONCERNING AGAMANOLIS DISEASE, American journal of medical genetics, 56(3), 1995, pp. 289-289
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