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Results: 1-25 | 26-42
Results: 1-25/42
PULMONARY-EMBOLISM DEVELOPING IN PATIENTS WITH SICKLE-CELL DISEASE ONHYPERTRANSFUSION AND IV DEFEROXAMINE CHELATION-THERAPY
Authors: SHETH S RUZALSHAPIRO C HURLETJENSEN A PIOMELLI S BERDON WE
Citation: S. Sheth et al., PULMONARY-EMBOLISM DEVELOPING IN PATIENTS WITH SICKLE-CELL DISEASE ONHYPERTRANSFUSION AND IV DEFEROXAMINE CHELATION-THERAPY, Pediatric radiology, 27(12), 1997, pp. 926-928
ERYTHROPOIETIC PROTOPORPHYRIA - 4 NOVEL FRAMESHIFT MUTATIONS IN THE FERROCHELATASE GENE
Authors: WANG XH PIOMELLI S PEACOCKE M CHRISTIANO AM POHFITZPATRICK MB
Citation: Xh. Wang et al., ERYTHROPOIETIC PROTOPORPHYRIA - 4 NOVEL FRAMESHIFT MUTATIONS IN THE FERROCHELATASE GENE, Journal of investigative dermatology, 109(5), 1997, pp. 688-691
ERYTHROPOIETIC PROTOPORPHYRIA - A TRIALLELIC INHERITANCE MODEL
Authors: POHFITZPATRICK MB PIOMELLI S DEYBACH JC GOUYA L WANG XH
Citation: Mb. Pohfitzpatrick et al., ERYTHROPOIETIC PROTOPORPHYRIA - A TRIALLELIC INHERITANCE MODEL, Journal of investigative dermatology, 108(4), 1997, pp. 362-362
ERYTHROPOIETIC-PROTOPORPHYRIA - 4 NOVEL FRAMESHIFT MUTATIONS IN THE FERROCHELATASE GENE
Authors: WANG XH PIOMELLI S PEACOCKE M CHRISTIANO AM POHFITZPATRICK MB
Citation: Xh. Wang et al., ERYTHROPOIETIC-PROTOPORPHYRIA - 4 NOVEL FRAMESHIFT MUTATIONS IN THE FERROCHELATASE GENE, Journal of investigative dermatology, 108(4), 1997, pp. 657-657
CIRCULATING TRANSFERRIN RECEPTOR (TFR) LEVELS IN PATIENTS WITH SICKLE-CELL DISEASE AND THALASSEMIA ON CHRONIC TRANSFUSION
Authors: TANCABELIC J PAIK M PIOMELLI S
Citation: J. Tancabelic et al., CIRCULATING TRANSFERRIN RECEPTOR (TFR) LEVELS IN PATIENTS WITH SICKLE-CELL DISEASE AND THALASSEMIA ON CHRONIC TRANSFUSION, Blood, 90(10), 1997, pp. 2827-2827
THE ERYTHROCYTE-SPECIFIC HEXOKINASE ISOZYME (HKR) AND THE COMMON HEXOKINASE ISOZYME (HKI) ARE PRODUCED FROM A SINGLE-GENE BY ALTERNATE PROMOTERS
Authors: MURAKAMI K PIOMELLI S
Citation: K. Murakami et S. Piomelli, THE ERYTHROCYTE-SPECIFIC HEXOKINASE ISOZYME (HKR) AND THE COMMON HEXOKINASE ISOZYME (HKI) ARE PRODUCED FROM A SINGLE-GENE BY ALTERNATE PROMOTERS, Blood, 90(10), 1997, pp. 1198-1198
ACUTE CHEST SYNDROME IN SICKLE-CELL DISEASE - CLINICAL PRESENTATION AND COURSE
Authors: VICHINSKY EP STYLES LA COLANGELO LH WRIGHT EC CASTRO O NICKERSON B JOHNSON R MCMAHON L PLATT O GILL F FREMPONG KO LEIKIN S VICHINSKY E LUBIN B BANK A PIOMELLI S ROSSE W FALLETTA J KINNEY T LESSIN L SMITH J KHAKOO Y SCOTT RB REINDORF C DOSIK H DIAMOND S BELLEVUE R WANG W WILIMAS J MILNER P BROWN A MILLER S RIEDER R GILLETTE P LANDE W EMBURY S MENTZER W WETHERS D GROVER R KOSHY M TALISHY N PEGELOW C KLUG P STEINBERG M KRAUS A ZARKOWSKY H DAMPIER C PEARSON H RITCHEY AK LEVY P GALLAGHER D KORANDA A FLOURNOYGILL Z JONES E MCKINLAY S THORINGTON B BRAMBILLA D GASTON M REID C BONDS D VERTER J
Citation: Ep. Vichinsky et al., ACUTE CHEST SYNDROME IN SICKLE-CELL DISEASE - CLINICAL PRESENTATION AND COURSE, Blood, 89(5), 1997, pp. 1787-1792
IDENTIFICATION OF THE CDNA FOR HUMAN RED BLOOD CELL-SPECIFIC HEXOKINASE ISOZYME
Authors: MURAKAMI K PIOMELLI S
Citation: K. Murakami et S. Piomelli, IDENTIFICATION OF THE CDNA FOR HUMAN RED BLOOD CELL-SPECIFIC HEXOKINASE ISOZYME, Blood, 89(3), 1997, pp. 762-766
NEUROPSYCHOLOGICAL CONSEQUENCES OF SICKLE-CELL DISEASE
Authors: SANO M HAGGERTY R KUGLER S MARTIN B PROHOVNIK I HURLETJENSEN A PIOMELLI S DEVIVO D
Citation: M. Sano et al., NEUROPSYCHOLOGICAL CONSEQUENCES OF SICKLE-CELL DISEASE, Neuropsychiatry, neuropsychology, and behavioral neurology, 9(4), 1996, pp. 242-247
CONGENITAL ERYTHROPOIETIC PORPHYRIA - BIOCHEMICAL, ENZYMATIC, AND MOLECULAR-GENETIC CHARACTERISTICS OF A SEVERE PHENOTYPE
Authors: POHFITZPATRICK M HUANG J ZAIDER E WANG X ROTH P GARCIA O POLLACK S PIOMELLI S
Citation: M. Pohfitzpatrick et al., CONGENITAL ERYTHROPOIETIC PORPHYRIA - BIOCHEMICAL, ENZYMATIC, AND MOLECULAR-GENETIC CHARACTERISTICS OF A SEVERE PHENOTYPE, Hepatology, 23(1), 1996, pp. 306-306
FACTORS PREDICTIVE OF AN ABNORMAL MRI IN CHILDREN WITH SICKLE-CELL DISEASE
Authors: HURLET A RHO TH SANO M SHETH S MARTIN B DEVIVO D PIOMELLI S
Citation: A. Hurlet et al., FACTORS PREDICTIVE OF AN ABNORMAL MRI IN CHILDREN WITH SICKLE-CELL DISEASE, Blood, 88(10), 1996, pp. 40-40
HGB-F GREATER-THAN-OR-EQUAL-TO-4-PERCENT AND ALPHA-THALASSEMIA PROTECT FROM STROKE - A LARGE PROPORTION OF PATIENTS WITH SICKLE-CELL DISEASE ARE AT LOW-RISK
Authors: PIOMELLI S SHETH S HURLET A PAIK M
Citation: S. Piomelli et al., HGB-F GREATER-THAN-OR-EQUAL-TO-4-PERCENT AND ALPHA-THALASSEMIA PROTECT FROM STROKE - A LARGE PROPORTION OF PATIENTS WITH SICKLE-CELL DISEASE ARE AT LOW-RISK, Blood, 88(10), 1996, pp. 44-44
SYSTEMATIC SCREENING FOR RNA WITH SKIPPED EXONS - SPLICING MUTATIONS OF THE FERROCHELATASE GENE
Authors: WANG XH POHFITZPATRICK M CHEN T MALAVADE K CARRIERO D PIOMELLI S
Citation: Xh. Wang et al., SYSTEMATIC SCREENING FOR RNA WITH SKIPPED EXONS - SPLICING MUTATIONS OF THE FERROCHELATASE GENE, Biochimica et biophysica acta. Molecular basis of disease, 1271(2-3), 1995, pp. 358-362
HUMAN PROTOPORPHYRIA - GENETIC-HETEROGENEITY AT THE FERROCHELATASE LOCUS
Authors: OSTASIEWICZ LT HUANG JL WANG X PIOMELLI S POHFITZPATRICK MB
Citation: Lt. Ostasiewicz et al., HUMAN PROTOPORPHYRIA - GENETIC-HETEROGENEITY AT THE FERROCHELATASE LOCUS, Photodermatology, photoimmunology & photomedicine, 11(1), 1995, pp. 18-21
HAPLOTYPES OF THE HUMAN BETA-LIKE GLOBIN GENE-CLUSTER - ANALYZING THE3'-HPA-I POLYMORPHIC SITE BY LONG-DISTANCE PCR
Authors: SHETH S PIOMELLI S WANG XH
Citation: S. Sheth et al., HAPLOTYPES OF THE HUMAN BETA-LIKE GLOBIN GENE-CLUSTER - ANALYZING THE3'-HPA-I POLYMORPHIC SITE BY LONG-DISTANCE PCR, American journal of hematology, 50(1), 1995, pp. 57-59
MRI MARROW OBSERVATIONS IN THALASSEMIA - THE EFFECTS OF THE PRIMARY DISEASE, TRANSFUSIONAL THERAPY, AND CHELATION
Authors: LEVIN TL SHETH SS RUZALSHAPIRO C ABRAMSON S PIOMELLI S BERDON WE
Citation: Tl. Levin et al., MRI MARROW OBSERVATIONS IN THALASSEMIA - THE EFFECTS OF THE PRIMARY DISEASE, TRANSFUSIONAL THERAPY, AND CHELATION, Pediatric radiology, 25(8), 1995, pp. 607-613
MR MARROW SIGNS OF IRON OVERLOAD IN TRANSFUSION-DEPENDENT PATIENTS WITH SICKLE-CELL DISEASE
Authors: LEVIN TL SHETH SS HURLET A COMERCI SC RUZALSHAPIRO C PIOMELLI S BERDON WE
Citation: Tl. Levin et al., MR MARROW SIGNS OF IRON OVERLOAD IN TRANSFUSION-DEPENDENT PATIENTS WITH SICKLE-CELL DISEASE, Pediatric radiology, 25(8), 1995, pp. 614-618
DEFEROXAMINE-INDNCED PLATYSPONDYLY IN HYPERTRANSFUSED THALASSEMIC PATIENTS
Authors: LEVIN TL SHETH S BERDON WE RUZALSHAPIRO C PIOMELLI S
Citation: Tl. Levin et al., DEFEROXAMINE-INDNCED PLATYSPONDYLY IN HYPERTRANSFUSED THALASSEMIC PATIENTS, Pediatric radiology, 25, 1995, pp. 122-124
THE MANAGEMENT OF PATIENTS WITH COOLEYS-ANEMIA - TRANSFUSIONS AND SPLENECTOMY
Authors: PIOMELLI S
Citation: S. Piomelli, THE MANAGEMENT OF PATIENTS WITH COOLEYS-ANEMIA - TRANSFUSIONS AND SPLENECTOMY, Seminars in hematology, 32(4), 1995, pp. 262-268
A COMPARISON OF CONSERVATIVE AND AGGRESSIVE TRANSFUSION REGIMENS IN THE PERIOPERATIVE MANAGEMENT OF SICKLE-CELL DISEASE
Authors: VICHINSKY EP HABERKERN CH NEUMAYR L EARLES AN BLACK D KOSHY M PEGELOW C ABBOUD M OHENEFREMPONG K IYER RV NAGEL R JOHNSON R SEARS D WONG M PARKE J BRAY G HURST D KOBLENZ L VICHINSKY E DEALARCON P GROSSI M WALDRON P WALTERS M RUSSO C MURPHY S SMITH H WOODS G GUARINI L HURLET A PIOMELLI S KINNEY T PHILLIPS G DAESCHNER C HOLBROOK T BUCHANAN I ECKMAN J CLASTER S HUME H OLIVERI N BELLEVUE R MANKAD V WANG W MILNER P JACKSON S BENJAMIN L BESTAK M RADEL E BARUCHEL S ESSENTINE D BLEI F EMBURY S MENTZER W GILLETTE P MILLER S RAO S GROVER R RAMIREZ G WETHERS D GLADER B JENNINGS W RUCKNAGEL D KALINYAK K LANE P TALISCHY N IYER R STEINBERG M COOPER H ORRINGER E MANKAD V YANG Y JOHNSON C POWARS D
Citation: Ep. Vichinsky et al., A COMPARISON OF CONSERVATIVE AND AGGRESSIVE TRANSFUSION REGIMENS IN THE PERIOPERATIVE MANAGEMENT OF SICKLE-CELL DISEASE, The New England journal of medicine, 333(4), 1995, pp. 206-213
CONGENITAL ERYTHROPOIETIC PORPHYRIA - BIOCHEMICAL, ENZYMATIC, AND MOLECULAR-GENETIC CHARACTERISTICS OF A SEVERE PHENOTYPE
Authors: POHFITZPATRICK M HUANG J ZAIDER E WANG X ROTH P GARCIA O POLLACK S PIOMELLI S
Citation: M. Pohfitzpatrick et al., CONGENITAL ERYTHROPOIETIC PORPHYRIA - BIOCHEMICAL, ENZYMATIC, AND MOLECULAR-GENETIC CHARACTERISTICS OF A SEVERE PHENOTYPE, Journal of investigative dermatology, 104(4), 1995, pp. 602-602
PROTEIN-C (PC), PROTEIN-S (PS), PROTHROMBIN FRAGMENT-1- EFFECT OF TRANSFUSION THERAPY AND HEMOGLOBIN CONCENTRATION(2 (F1.2) IN PATIENTS WITH SICKLE DISEASE (SCD) )
Authors: HURLETJENSEN A MORRIS V SEAMAN C MARTIN B PIOMELLI S
Citation: A. Hurletjensen et al., PROTEIN-C (PC), PROTEIN-S (PS), PROTHROMBIN FRAGMENT-1- EFFECT OF TRANSFUSION THERAPY AND HEMOGLOBIN CONCENTRATION(2 (F1.2) IN PATIENTS WITH SICKLE DISEASE (SCD) ), Blood, 86(10), 1995, pp. 1178-1178
THE FIRST DE-NOVO MUTATION OF FERROCHELATASE IN ERYTHROPOIETIC PROTOPORPHYRIA (EPP)
Authors: WANG X POHFITZPATRICK M PIOMELLI S
Citation: X. Wang et al., THE FIRST DE-NOVO MUTATION OF FERROCHELATASE IN ERYTHROPOIETIC PROTOPORPHYRIA (EPP), Blood, 86(10), 1995, pp. 1872-1872
A NOVEL SPLICING MUTATION IN THE FERROCHELATASE GENE RESPONSIBLE FOR ERYTHROPOIETIC PROTOPORPHYRIA
Authors: WANG XH POHFITZPATRICK M PIOMELLI S
Citation: Xh. Wang et al., A NOVEL SPLICING MUTATION IN THE FERROCHELATASE GENE RESPONSIBLE FOR ERYTHROPOIETIC PROTOPORPHYRIA, Biochimica et biophysica acta. Molecular basis of disease, 1227(1-2), 1994, pp. 25-27
SCREENING FOR FERROCHELATASE MUTATIONS - MOLECULAR HETEROGENEITY OF ERYTHROPOIETIC PROTOPORPHYRIA
Authors: WANG XH POHFITZPATRICK M TAKETANI S CHEN T PIOMELLI S
Citation: Xh. Wang et al., SCREENING FOR FERROCHELATASE MUTATIONS - MOLECULAR HETEROGENEITY OF ERYTHROPOIETIC PROTOPORPHYRIA, Biochimica et biophysica acta. Molecular basis of disease, 1225(2), 1994, pp. 187-190
Risultati: 1-25 | 26-42