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Results of search for 'au:"Ware, R E"', page 4 of 6
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Authors
Adams, D M
Ball, D L
Binns, D S
Filston, H C
Hall, S E
Hatcher, C R
Haynes, B F
Hicks, R J
Hogg, A
Howard, T A
Kalff, V
Kinney, T R
MacManus, M P
McKenzie, A F
Rosse, W F
Schultz, W H
Symbas, P N
Ware, R E
Winter, S S
Zimmerman, S A
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Topics
Adolescent
Adult
Anemia, Sickle Cell
Child
Child, Preschool
Female
Glycosylphosphatidylinositols
Hemoglobinuria, Paroxysmal
Humans
Infant
Male
Mutation
Retrospective Studies
analysis
blood
complications
etiology
genetics
immunology
metabolism
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English
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61.
An operation for relief of severe left ventricular outflow tract obstruction.
[electronic resource]
by
Symbas, P N
Ware, R E
Hatcher, C R
Temesy-Armos, P N
Producer:
19760324
In:
The Journal of thoracic and cardiovascular surgery
vol. 71
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62.
Hepatosplenic T-cell lymphoma: an unusual case of a gamma delta T-cell lymphoma with a blast-like terminal transformation.
[electronic resource]
by
Mastovich, S
Ratech, H
Ware, R E
Moore, J O
Borowitz, M J
Producer:
19940321
In:
Human pathology
vol. 25
Online resources:
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63.
Coronary arterial injection of radioactive albumin microspheres in diagnosis of experimental myocardial contusion.
[electronic resource]
by
Ware, R E
Martin, L G
Tyras, D H
Kourias, E
Symbas, P N
Producer:
19740905
In:
Surgical forum
vol. 23
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64.
Paroxysmal nocturnal hemoglobinuria: molecular pathogenesis and molecular therapeutic approaches.
[electronic resource]
by
Nishimura, J
Smith, C A
Phillips, K L
Ware, R E
Rosse, W F
Producer:
19990310
In:
Hematopathology and molecular hematology
vol. 11
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65.
Novel mechanisms of brequinar sodium immunosuppression on T cell activation.
[electronic resource]
by
Forrest, T L
Ware, R E
Howard, T
Jaffee, B D
Denning, S M
Producer:
19941117
In:
Transplantation
vol. 58
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66.
Delayed development of sensorineural hearing loss after neonatal hyperbilirubinemia: a case report with brain magnetic resonance imaging.
[electronic resource]
by
Worley, G
Erwin, C W
Goldstein, R F
Provenzale, J M
Ware, R E
Producer:
19960703
In:
Developmental medicine and child neurology
vol. 38
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67.
Identification and characterization of an inherited mutation of PIG-A in a patient with paroxysmal nocturnal haemoglobinuria.
[electronic resource]
by
Endo, M
Ware, R E
Vreeke, T M
Howard, T A
Parker, C J
Producer:
19960729
In:
British journal of haematology
vol. 93
Online resources:
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68.
Quantitative analysis of erythrocytes containing fetal hemoglobin (F cells) in children with sickle cell disease.
[electronic resource]
by
Marcus, S J
Kinney, T R
Schultz, W H
O'Branski, E E
Ware, R E
Producer:
19970130
In:
American journal of hematology
vol. 54
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69.
Laparoscopic cholecystectomy in young patients with sickle hemoglobinopathies.
[electronic resource]
by
Ware, R E
Kinney, T R
Casey, J R
Pappas, T N
Meyers, W C
Producer:
19920219
In:
The Journal of pediatrics
vol. 120
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70.
Elevated levels of tumor necrosis factor-beta, gamma-interferon, and IL-6 mRNA in Castleman's disease.
[electronic resource]
by
Winter, S S
Howard, T A
Ritchey, A K
Keller, F G
Ware, R E
Producer:
19960111
In:
Medical and pediatric oncology
vol. 26
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71.
Influence of bilirubin uridine diphosphate-glucuronosyltransferase 1A promoter polymorphisms on serum bilirubin levels and cholelithiasis in children with sickle cell anemia.
[electronic resource]
by
Passon, R G
Howard, T A
Zimmerman, S A
Schultz, W H
Ware, R E
Producer:
20020321
In:
Journal of pediatric hematology/oncology
vol. 23
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72.
Genetic instability and the etiology of somatic PIG-A mutations in paroxysmal nocturnal hemoglobinuria.
[electronic resource]
by
Purow, D B
Howard, T A
Marcus, S J
Rosse, W F
Ware, R E
Producer:
19990818
In:
Blood cells, molecules & diseases
vol. 25
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73.
Resolution of Budd-Chiari syndrome following bone marrow transplantation for paroxysmal nocturnal haemoglobinuria.
[electronic resource]
by
Graham, M L
Rosse, W F
Halperin, E C
Miller, C R
Ware, R E
Producer:
19960610
In:
British journal of haematology
vol. 92
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74.
Erythrocyte autoantibodies in paediatric patients with sickle cell disease receiving transfusion therapy: frequency, characteristics and significance.
[electronic resource]
by
Castellino, S M
Combs, M R
Zimmerman, S A
Issitt, P D
Ware, R E
Producer:
19990322
In:
British journal of haematology
vol. 104
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75.
Penetrating cardiac wounds. Significant residual and delayed sequelae.
[electronic resource]
by
Symbas, P N
DiOrio, D A
Tyras, D H
Ware, R E
Hatcher, C R
Producer:
19740119
In:
The Journal of thoracic and cardiovascular surgery
vol. 66
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76.
Prevalence and clinical correlates of glomerulopathy in children with sickle cell disease.
[electronic resource]
by
Wigfall, D R
Ware, R E
Burchinal, M R
Kinney, T R
Foreman, J W
Producer:
20000718
In:
The Journal of pediatrics
vol. 136
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77.
Research directions in paroxysmal nocturnal hemoglobinuria.
[electronic resource]
by
Dunn, D E
Ware, R E
Parker, C J
Mishoe, H O
Young, N S
Producer:
20000914
In:
Immunology today
vol. 20
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78.
The PIG-A mutation and absence of glycosylphosphatidylinositol-linked proteins do not confer resistance to apoptosis in paroxysmal nocturnal hemoglobinuria.
[electronic resource]
by
Ware, R E
Nishimura, J
Moody, M A
Smith, C
Rosse, W F
Howard, T A
Producer:
19981019
In:
Blood
vol. 92
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79.
Identification of mutations and polymorphisms in the factor XI genes of an African American family by dideoxyfingerprinting.
[electronic resource]
by
Martincic, D
Zimmerman, S A
Ware, R E
Sun, M F
Whitlock, J A
Gailani, D
Producer:
19981130
In:
Blood
vol. 92
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80.
Effects of inherited thrombophilic mutations in an adolescent with antiphospholipid syndrome and systemic lupus erythematosus.
[electronic resource]
by
Higginbotham, E A
Zimmerman, S A
Howard, T A
Schanberg, L
Kredich, D
Ware, R E
Producer:
20010614
In:
The Journal of rheumatology
vol. 28
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