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Results: 1-9 |
Results: 9
RELATION OF HFE GENE-MUTATIONS, HIGH IRON STORES AND EARLY-ONSET CORONARY-ARTERY DISEASE
Authors: NASSAR BA ZAYED EM TITLE LM ONEILL BJ BATA IR KIRKLAND SA DUNN J DEMPSEY GI TAN MH JOHNSTONE DE
Citation: Ba. Nassar et al., RELATION OF HFE GENE-MUTATIONS, HIGH IRON STORES AND EARLY-ONSET CORONARY-ARTERY DISEASE, Canadian journal of cardiology, 14(2), 1998, pp. 215-220
MORE ON BREAST-CANCER GUIDELINES
Authors: NASSAR BA LUDMAN MD COSTA MT WELCH JP BUTTS CA LOVE JR HOGG H BEIS MJ
Citation: Ba. Nassar et al., MORE ON BREAST-CANCER GUIDELINES, CMAJ. Canadian Medical Association journal, 158(11), 1998, pp. 1429-1429
A NOVEL MUTATION IN EXON-4 OF THE LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE RESULTING IN HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA ASSOCIATED WITH DECREASED LIGAND-BINDING
Authors: MORASH BA TAN MH NASSAR BA TOO CKL GUERNSEY DL
Citation: Ba. Morash et al., A NOVEL MUTATION IN EXON-4 OF THE LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE RESULTING IN HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA ASSOCIATED WITH DECREASED LIGAND-BINDING, Atherosclerosis, 136(1), 1998, pp. 9-16
RELATION OF A COMMON MUTATION IN METHYLENETETRAHYDROFOLATE REDUCTASE TO PLASMA HOMOCYSTEINE AND EARLY-ONSET CORONARY-ARTERY DISEASE
Authors: DUNN J TITLE LM BATA I JOHNSTONE DE KIRKLAND SA ONEILL BJ ZAYED E MACDONALD MC DEMPSEY GI NASSAR BA
Citation: J. Dunn et al., RELATION OF A COMMON MUTATION IN METHYLENETETRAHYDROFOLATE REDUCTASE TO PLASMA HOMOCYSTEINE AND EARLY-ONSET CORONARY-ARTERY DISEASE, Clinical biochemistry, 31(2), 1998, pp. 95-100
RELATION BETWEEN HOMOCYSTEINE, A MUTATION IN METHYLENETETRAHYDROFOLATE REDUCTASE AND EXTENT OF CORONARY-ARTERY DISEASE
Authors: TITLE LM DUNN J CUMMINGS P ZAYED E DEMPSEY GI ONEILL BJ JOHNSTONE DE BATA IR NASSAR BA
Citation: Lm. Title et al., RELATION BETWEEN HOMOCYSTEINE, A MUTATION IN METHYLENETETRAHYDROFOLATE REDUCTASE AND EXTENT OF CORONARY-ARTERY DISEASE, Circulation, 98(17), 1998, pp. 2312-2312
DETECTION OF A R173W MUTATION IN THE PORPHOBILINOGEN DEAMINASE GENE IN THE NOVA-SCOTIAN FOREIGN PROTESTANT POPULATION WITH ACUTE INTERMITTENT PORPHYRIA - A FOUNDER EFFECT
Authors: GREENEDAVIS ST NEUMANN PE MANN OE MOSS MA SCHREIBER WE WELCH JP LANGLEY GR SANGALANG VE DEMPSEY GI NASSAR BA
Citation: St. Greenedavis et al., DETECTION OF A R173W MUTATION IN THE PORPHOBILINOGEN DEAMINASE GENE IN THE NOVA-SCOTIAN FOREIGN PROTESTANT POPULATION WITH ACUTE INTERMITTENT PORPHYRIA - A FOUNDER EFFECT, Clinical biochemistry, 30(8), 1997, pp. 607-612
HETERODUPLEX ANALYSIS DETECTS FRAMESHIFT AND POINT MUTATIONS IN PATIENTS WITH ACUTE INTERMITTENT PORPHYRIA
Authors: SCHREIBER WE FONG FT NASSAR BA JAMANI A
Citation: We. Schreiber et al., HETERODUPLEX ANALYSIS DETECTS FRAMESHIFT AND POINT MUTATIONS IN PATIENTS WITH ACUTE INTERMITTENT PORPHYRIA, Human genetics, 96(2), 1995, pp. 161-166
EFFECTS OF ACUTELY RAISING INTRACRANIAL-PRESSURE ON CARDIAC SYMPATHETIC EFFERENT NEURON FUNCTION
Authors: MURPHY DA OBLENES S NASSAR BA ARMOUR JA
Citation: Da. Murphy et al., EFFECTS OF ACUTELY RAISING INTRACRANIAL-PRESSURE ON CARDIAC SYMPATHETIC EFFERENT NEURON FUNCTION, Cardiovascular Research, 30(5), 1995, pp. 716-724
DETECTION OF FAMILIAL DEFECTIVE APOLIPOPROTEIN B-100 AMONG PATIENTS CLINICALLY DIAGNOSED WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA INMARITIME CANADA
Authors: MORASH B GUERNSEY DL TAN MH DEMPSEY G NASSAR BA
Citation: B. Morash et al., DETECTION OF FAMILIAL DEFECTIVE APOLIPOPROTEIN B-100 AMONG PATIENTS CLINICALLY DIAGNOSED WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA INMARITIME CANADA, Clinical biochemistry, 27(4), 1994, pp. 265-272
Risultati: 1-9 |