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Results: 1-9 |
Results: 9
MYOINOSITOL LEVELS IN TRISOMY-21 CELLS
Authors: MALLEE JJ WANG Y PARRELLA T WEHRLI S STATES B REYNOLDS RA BERRY GT
Citation: Jj. Mallee et al., MYOINOSITOL LEVELS IN TRISOMY-21 CELLS, Pediatric research, 39(4), 1996, pp. 865-865
RECOMBINANT INTERFERON-ALPHA(2A) HASTENS THE RATE OF HBEAG CLEARANCE IN CHILDREN WITH CHRONIC HEPATITIS-B
Authors: BARBERA C BORTOLOTTI F CRIVELLARO C COSCIA A ZANCAN L CADROBBI P NEBBIA G PILLAN MN LEPORE L PARRELLA T DASTOLI G BRUNETTO MR BONINO F
Citation: C. Barbera et al., RECOMBINANT INTERFERON-ALPHA(2A) HASTENS THE RATE OF HBEAG CLEARANCE IN CHILDREN WITH CHRONIC HEPATITIS-B, Hepatology, 20(2), 1994, pp. 287-290
MAPLE-SYRUP-URINE-DISEASE (MSUD) - SCREENING FOR KNOWN MUTATIONS IN ITALIAN PATIENTS
Authors: PARRELLA T SURREY S IOLASCON A SARTORE M HEIDENREICH R DIAMOND G PONZONE A GUARDAMAGNA O BURLINA AB CERONE R PARINI R DIONISIVICI C RAPPAPORT E FORTINA P
Citation: T. Parrella et al., MAPLE-SYRUP-URINE-DISEASE (MSUD) - SCREENING FOR KNOWN MUTATIONS IN ITALIAN PATIENTS, Journal of inherited metabolic disease, 17(6), 1994, pp. 652-660
RAPID DETECTION OF MEDIUM-CHAIN ACYL-COA DEHYDROGENASE GENE-MUTATIONSBY NONRADIOACTIVE, SINGLE-STRAND CONFORMATION POLYMORPHISM MINIGELS
Authors: IOLASCON A PARRELLA T PERROTTA S GUARDAMAGNA O COATES PM SARTORE M SURREY S FORTINA P
Citation: A. Iolascon et al., RAPID DETECTION OF MEDIUM-CHAIN ACYL-COA DEHYDROGENASE GENE-MUTATIONSBY NONRADIOACTIVE, SINGLE-STRAND CONFORMATION POLYMORPHISM MINIGELS, Journal of Medical Genetics, 31(7), 1994, pp. 551-554
GLANZMANN THROMBASTHENIA SECONDARY TO A GLY273-]ASP MUTATION ADJACENTTO THE FIRST CALCIUM-BINDING DOMAIN OF PLATELET GLYCOPROTEIN IIB
Authors: PONCZ M RIFAT S COLLER BS NEWMAN PJ SHATTIL SJ PARRELLA T FORTINA P BENNETT JS
Citation: M. Poncz et al., GLANZMANN THROMBASTHENIA SECONDARY TO A GLY273-]ASP MUTATION ADJACENTTO THE FIRST CALCIUM-BINDING DOMAIN OF PLATELET GLYCOPROTEIN IIB, The Journal of clinical investigation, 93(1), 1994, pp. 172-179
INTERACTION OF A RARE ILLEGITIMATE RECOMBINATION EVENT AND A POLY-A ADDITION SITE MUTATION RESULTING IN A SEVERE FORM OF ALPHA-THALASSEMIA
Authors: FORTINA P PARRELLA T SARTORE M GOTTARDI E GABUTTI V DELGROSSO K MANSFIELD E RAPPAPORT E SCHWARTZ E CAMASCHELLA C SURREY S
Citation: P. Fortina et al., INTERACTION OF A RARE ILLEGITIMATE RECOMBINATION EVENT AND A POLY-A ADDITION SITE MUTATION RESULTING IN A SEVERE FORM OF ALPHA-THALASSEMIA, Blood, 83(11), 1994, pp. 3356-3362
FLUORESCENT APPROACHES TO DIAGNOSIS OF LESCH-NYHAN SYNDROME AND QUANTITATIVE-ANALYSIS OF CARRIER STATUS
Authors: MANSFIELD ES BLASBAND A KRONICK MN WRABETZ L KAPLAN P RAPPAPORT E SARTORE M PARRELLA T SURREY S FORTINA P
Citation: Es. Mansfield et al., FLUORESCENT APPROACHES TO DIAGNOSIS OF LESCH-NYHAN SYNDROME AND QUANTITATIVE-ANALYSIS OF CARRIER STATUS, Molecular and cellular probes, 7(4), 1993, pp. 311-324
DUCHENNE-BECKER MUSCULAR-DYSTROPHY CARRIER DETECTION USING QUANTITATIVE PCR AND FLUORESCENCE-BASED STRATEGIES
Authors: MANSFIELD ES ROBERTSON JM LEBO RV LUCERO MY MAYRAND PE RAPPAPORT E PARRELLA T SARTORE M SURREY S FORTINA P
Citation: Es. Mansfield et al., DUCHENNE-BECKER MUSCULAR-DYSTROPHY CARRIER DETECTION USING QUANTITATIVE PCR AND FLUORESCENCE-BASED STRATEGIES, American journal of medical genetics, 48(4), 1993, pp. 200-208
INTERACTION OF A RARE ILLEGITIMATE RECOMBINATION EVENT AND A POLY-A ADDITION SITE MUTATION RESULTING IN A SEVERE FORM OF ALPHA-THALASSEMIA
Authors: FORTINA P PARRELLA T SARTORE M GOTTARDI E GABUTTI V DELGROSSO K MANSFIELD E RAPPAPORT E SCHWARTZ E CAMASCHELLA C SURREY S
Citation: P. Fortina et al., INTERACTION OF A RARE ILLEGITIMATE RECOMBINATION EVENT AND A POLY-A ADDITION SITE MUTATION RESULTING IN A SEVERE FORM OF ALPHA-THALASSEMIA, Blood, 82(10), 1993, pp. 10000362-10000362
Risultati: 1-9 |