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Mara Toderici
Observed names:
M. Toderici,
Toderici, Mara
Institutions:
Centro Regional de Hemodonación,
Universidad de Murcia
Observed institutions:
Hospital General Universitario Morales Meseguer,
Centro Regional de Hemodonación,
Instituto Murciano de Investigación Biosanitaria,
Universidad de Murcia
OpenAlex ID:
A5058013191
Hypoglycosylation is a common finding in antithrombin deficiency in the absence of a SERPINC1 gene defect
2016
·
M.E. de la Morena‐Barrio
, I. Martínez‐Martínez
, et al.
·
Journal of Thrombosis and Haemostasis
·
59
High levels of latent antithrombin in plasma from patients with antithrombin deficiency
2017
·
María de la Morena-Barrio
, Edna Sandoval
, et al.
·
Thrombosis and Haemostasis
·
27
Identification of Regulatory Mutations in SERPINC1 Affecting Vitamin D Response Elements Associated with Antithrombin Deficiency
2016
·
Mara Toderici
, María Eugenia de la Morena-Barrio
, et al.
·
PLoS ONE
·
21
PDF
ALG12‐CDG: An unusual patient without intellectual disability and facial dysmorphism, and with a novel variant
2020
·
María Eugenia de la Morena‐Barrio
, María Sabater
, et al.
·
Molecular Genetics & Genomic Medicine
·
13
PDF
Full-length antithrombin frameshift variant with aberrant C-terminus causes endoplasmic reticulum retention with a dominant-negative effect
2022
·
Carlos Bravo-Pérez
, Mara Toderici
, et al.
·
JCI Insight
·
12
PDF
Recurrent mutations in aSERPINC1hotspot associate with venous thrombosis without apparent antithrombin deficiency
2017
·
Wei Zeng
, Bei Hu
, et al.
·
Oncotarget
·
11
PDF
Transient desialylation in combination with a novel antithrombin deficiency causing a severe and recurrent thrombosis despite anticoagulation therapy
2017
·
Nuria Revilla
, María Eugenia de la Morena-Barrio
, et al.
·
Scientific Reports
·
8
PDF
Correction: Identification of Regulatory Mutations in SERPINC1 Affecting Vitamin D Response Elements Associated with Antithrombin Deficiency
2016
·
Mara Toderici
, María Eugenia de la Morena-Barrio
, et al.
·
PLoS ONE
·
8
PDF
Biochemical and cellular consequences of the antithrombin p.Met1? mutation identified in a severe thrombophilic family
2018
·
José Navarro-Fernández
, María Eugenia de la Morena-Barrio
, et al.
·
Oncotarget
·
4
PDF
Correction: Recurrent mutations in a SERPINC1 hotspot associate with venous thrombosis without apparent antithrombin deficiency
2018
·
Wei Zeng
, Bei Hu
, et al.
·
Oncotarget
PDF
Predominant mutations in a hotspot of SERPINC1 associated with venous thromboembolism in the Chinese population: a case-control study
2016
·
Liang Tang
, Wei Zeng
, et al.
·
The Lancet
Deubiquitnase BAP1 Downregulation in Myeloid Malignances: A New Pathogenic Mechanism, Dominant in Chronic Myelomonocytic Leukemia
2014
·
Ana Maria Hurtado
, Eva Caparrós
, et al.
·
Blood
C0260: Identification of RXRA/VDR Elements Involved in the Regulation of Antithrombin Levels. Relevance in Antithrombin Deficiency
2014
·
M.E. de la Morena-Barrio
, M. Toderici
, et al.
·
Thrombosis Research
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Works count:
14
Citation count:
163
H-index:
8
I10-index:
6
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