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Results: 1-13 |
Results: 13
MOLECULAR CHARACTERIZATION OF A UNIQUE PATIENT WITH EPIMERASE-DEFICIENCY GALACTOSEMIA
Authors: ALANO A ALMASHANU S CHINSKY JM COSTEAS P BLITZER MG WULFSBERG EA COWAN TM
Citation: A. Alano et al., MOLECULAR CHARACTERIZATION OF A UNIQUE PATIENT WITH EPIMERASE-DEFICIENCY GALACTOSEMIA, Journal of inherited metabolic disease, 21(4), 1998, pp. 341-350
PATIENT-CENTERED CLINICAL DECISIONS AND THEIR IMPACT ON PHYSICIAN ADHERENCE TO CLINICAL GUIDELINES
Authors: JAMES PA COWAN TM GRAHAM RP
Citation: Pa. James et al., PATIENT-CENTERED CLINICAL DECISIONS AND THEIR IMPACT ON PHYSICIAN ADHERENCE TO CLINICAL GUIDELINES, Journal of family practice, 46(4), 1998, pp. 311-318
RETROSPECTIVE BIOCHEMICAL SCREENING OF FATTY-ACID OXIDATION DISORDERSIN POSTMORTEM LIVERS OF 418 CASES OF SUDDEN-DEATH IN THE FIRST-YEAR OF LIFE
Authors: BOLES RG BUCK EA BLITZER MG PLATT MS COWAN TM MARTIN SK YOON HR MADSEN JA REYESMUGICA M RINALDO P
Citation: Rg. Boles et al., RETROSPECTIVE BIOCHEMICAL SCREENING OF FATTY-ACID OXIDATION DISORDERSIN POSTMORTEM LIVERS OF 418 CASES OF SUDDEN-DEATH IN THE FIRST-YEAR OF LIFE, The Journal of pediatrics, 132(6), 1998, pp. 924-933
FAMILY PHYSICIANS ATTITUDES ABOUT AND USE OF CLINICAL-PRACTICE GUIDELINES
Authors: JAMES PA COWAN TM GRAHAM RP MAJERONI BA
Citation: Pa. James et al., FAMILY PHYSICIANS ATTITUDES ABOUT AND USE OF CLINICAL-PRACTICE GUIDELINES, Journal of family practice, 45(4), 1997, pp. 341-347
HETEROALLELISM FOR A NOVEL RECOMBINANT ALLELE AND A RARE SPLICE JUNCTION MUTATION IN THE GLUCOCEREBROSIDASE LOCUS PRESENTING WITH HYDROPS-FETALIS
Authors: REISSNER K TAYEBI N ALMASHANA S BLITZER M COWAN TM HASSAN M MADDALENA A SPENCE C SIDRANSKY E KARSON E
Citation: K. Reissner et al., HETEROALLELISM FOR A NOVEL RECOMBINANT ALLELE AND A RARE SPLICE JUNCTION MUTATION IN THE GLUCOCEREBROSIDASE LOCUS PRESENTING WITH HYDROPS-FETALIS, American journal of human genetics, 61(4), 1997, pp. 923-923
CHARACTERIZATION OF 2 MUTATIONS ASSOCIATED WITH EPIMERASE-DEFICIENCY GALACTOSEMIA, BY USE OF A YEAST EXPRESSION SYSTEM FOR HUMAN UDP-GALACTOSE-4-EPIMERASE
Authors: QUIMBY BB ALANO A ALMASHANU S DESANDRO AM COWAN TM FRIDOVICHKEIL JL
Citation: Bb. Quimby et al., CHARACTERIZATION OF 2 MUTATIONS ASSOCIATED WITH EPIMERASE-DEFICIENCY GALACTOSEMIA, BY USE OF A YEAST EXPRESSION SYSTEM FOR HUMAN UDP-GALACTOSE-4-EPIMERASE, American journal of human genetics, 61(3), 1997, pp. 590-598
REPLOTTING CORDA TYMPANI DATA AND ITS IMPLICATIONS FOR THEORIES OF TASTE
Authors: COWAN TM
Citation: Tm. Cowan, REPLOTTING CORDA TYMPANI DATA AND ITS IMPLICATIONS FOR THEORIES OF TASTE, Journal of mathematical psychology, 40(4), 1996, pp. 350-350
CORRELATES OF MAJOR AND MINOR OFFENDING AMONG YOUTH WITH SEVERE EMOTIONAL DISTURBANCE
Authors: BRYANT ES RIVARD JC ADDY CL HINKLE KT COWAN TM WRIGHT G
Citation: Es. Bryant et al., CORRELATES OF MAJOR AND MINOR OFFENDING AMONG YOUTH WITH SEVERE EMOTIONAL DISTURBANCE, Journal of emotional and behavioral disorders, 3(2), 1995, pp. 76-84
A SNAPSHOT OF AUTOBIOGRAPHICAL MEMORY RETRIEVAL CHARACTERISTICS
Authors: BURT CDB MITCHELL DA RAGGATT PTF JONES CA COWAN TM
Citation: Cdb. Burt et al., A SNAPSHOT OF AUTOBIOGRAPHICAL MEMORY RETRIEVAL CHARACTERISTICS, Applied cognitive psychology, 9(1), 1995, pp. 61-74
COMMON MUTATIONS IN THE PHOSPHOFRUCTOKINASE-M GENE IN ASHKENAZI JEWISH PATIENTS WITH GLYCOGENESIS-VII - AND THEIR POPULATION FREQUENCY
Authors: SHERMAN JB RABEN N NICASTRI C ARGOV Z NAKAJIMA H ADAMS EM ENG CM COWAN TM PLOTZ PH
Citation: Jb. Sherman et al., COMMON MUTATIONS IN THE PHOSPHOFRUCTOKINASE-M GENE IN ASHKENAZI JEWISH PATIENTS WITH GLYCOGENESIS-VII - AND THEIR POPULATION FREQUENCY, American journal of human genetics, 55(2), 1994, pp. 305-313
INTRAFAMILIAL VARIABILITY IN HURLER-SYNDROME AND SANFILIPPO SYNDROME TYPE-A - IMPLICATIONS FOR EVALUATION OF NEW THERAPIES
Authors: MCDOWELL GA COWAN TM BLITZER MG GREENE CL
Citation: Ga. Mcdowell et al., INTRAFAMILIAL VARIABILITY IN HURLER-SYNDROME AND SANFILIPPO SYNDROME TYPE-A - IMPLICATIONS FOR EVALUATION OF NEW THERAPIES, American journal of medical genetics, 47(7), 1993, pp. 1092-1095
TRANSIENT NEONATAL GALACTOSEMIA IDENTIFIED BY NEWBORN SCREENING
Authors: RAFFEL LJ COWAN TM BLITZER MG
Citation: Lj. Raffel et al., TRANSIENT NEONATAL GALACTOSEMIA IDENTIFIED BY NEWBORN SCREENING, Journal of inherited metabolic disease, 16(5), 1993, pp. 894-895
HPLC METHOD FOR QUANTITATIVE-ANALYSIS OF GALACTOSE-1-PHOSPHATE URIDYL-TRANSFERASE ACTIVITY
Authors: ANDREWS JM COWAN TM BLITZER MG
Citation: Jm. Andrews et al., HPLC METHOD FOR QUANTITATIVE-ANALYSIS OF GALACTOSE-1-PHOSPHATE URIDYL-TRANSFERASE ACTIVITY, American journal of human genetics, 53(3), 1993, pp. 885-885
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