PUBLICACIÓN

Congenital dyserythropoietic anemia associated to a GATA1 mutation aggravated by pyruvate kinase deficiency

ACCEDER A LA PUBLICACIÓN: Scopus

Pereira J., Bento C., Manco L., Gonzalez A., Vagace J., Ribeiro M.L.

2016 ANNALS OF HEMATOLOGY

Hematology (Q2), Medicine (miscellaneous) (Q1)

JCR: 3.083

SJR: 1.269

CITAS

13

DOI

10.1007/s00277-016-2720-0

EID

2-s2.0-84976273796

ISSN

0939-5555

EISSN

1432-0584

AUTORES DE LA UEX

José Manuel Vagace Valero

OTRAS PUBLICACIONES DE INTERÉS

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Association Between Adherence To Patient Blood Management Recommendations And Postoperative Complications In Hip And Knee Arthroplasty
Haploidentical Vs. Hla-Matched Donor Hematopoietic Stem-Cell Transplantation For Pediatric Patients With Acute Lymphoblastic Leukemia In Second Remission: A Collaborative Retrospective Study Of The Spanish Group For Bone Marrow Transplantation In Children (Getmon/geth) And The Spanish Childhood Relapsed All Board (Reallnet)
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Measurable Residual Disease Assessed By Flow-Cytometry Is A Stable Prognostic Factor For Pediatric T-Cell Acute Lymphoblastic Leukemia In Consecutive Sehop Protocols Whereas The Impact Of Oncogenetics Depends On Treatment
Phase 2 Clinical Trial Of Infusing Haploidentical K562-Mb15-41bbl–activated And Expanded Natural Killer Cells As Consolidation Therapy For Pediatric Acute Myeloblastic Leukemia
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Optimised Molecular Genetic Diagnostics Of Fanconi Anaemia By Whole Exome Sequencing And Functional Studies
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Optimised Molecular Genetic Diagnostics Of Fanconi Anaemia By Whole Exome Sequencing And Functional Studies
C>a Substitution In Nt 46 Of The 3' Utr Region (The Α Complex Protected Region) Of The Alpha-1 Globin Gene: A Non-Deletional Mutation Or Polymorphism?
Optimised Molecular Genetic Diagnostics Of Fanconi Anaemia By Whole Exome Sequencing And Functional Studies
C>a Substitution In Nt 46 Of The 3' Utr Region (The Α Complex Protected Region) Of The Alpha-1 Globin Gene: A Non-Deletional Mutation Or Polymorphism?
Expanding The Clinical And Genetic Spectra Of Primary Immunodeficiency-Related Disorders With Clinical Exome Sequencing: Expected And Unexpected Findings
C>a Substitution In Nt 46 Of The 3' Utr Region (The Α Complex Protected Region) Of The Alpha-1 Globin Gene: A Non-Deletional Mutation Or Polymorphism?
Expanding The Clinical And Genetic Spectra Of Primary Immunodeficiency-Related Disorders With Clinical Exome Sequencing: Expected And Unexpected Findings
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Impact Of Genetic Polymorphisms On Chemotherapy Toxicity In Childhood Acute Lymphoblastic Leukemia
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Retinal Toxic Reactions Following Photopheresis
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Aplastic Anemia During Treatment With Albendazole [8]
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Aplastic Anemia During Treatment With Albendazole [8]
Changes In Platelet Count: A Primary Or Secondary Effect Of Rhu-Epo Therapy?
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Prognostic Significance Of Mutation Type And Chromosome Fragility In Fanconi Anemia
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