Patricia Aguilar-Martinez
Overview
Explore the profile of Patricia Aguilar-Martinez including associated specialties, affiliations and a list of published articles.
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Articles
43
Citations
314
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0
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Recent Articles
1.
Chiffre-Rakotoarivony D, Diaz-Cau I, Ranc A, Champiat M, Rousseau F, Gournay-Garcia C, et al.
Blood Coagul Fibrinolysis
. 2024 May;
35(5):232-237.
PMID: 38700721
Background: Predicting the bleeding risk in hemophilia A and B carriers (HAC, HBC) is challenging. Objective: The objectives of this study were to describe the bleeding phenotype in HAC and...
2.
Dupuy A, Cristol J, Bargnoux A, Plawecki M, Lotierzo M, Aguilar-Martinez P, et al.
Health Sci Rep
. 2023 Jul;
6(7):e1270.
PMID: 37465239
Background And Aims: Mobility and migration flows are growing from different countries of the world to European countries, including France and in particular the Mediterranean basin. This study aimed to...
3.
Szepetowski S, Berger C, Joly P, Baron-Joly S, Huguenin Y, Cantais A, et al.
Am J Hematol
. 2022 Sep;
97(11):E393-E395.
PMID: 36052950
No abstract available.
4.
Badiou S, Dupuy A, Cunat S, Delay A, Alcaraz S, Aguilar-Martinez P, et al.
Clin Chim Acta
. 2022 Aug;
535:27-29.
PMID: 35963305
Background And Objective: A clinician was intrigued about HbA1c upper 9% (75 mmol/mol) in a 76 year-old women with normal glycemia. Further explorations were performed in order to understand this...
5.
Dupuy A, Badiou S, Marrolley J, Plawecki M, Aguilar-Martinez P, Cristol J
Clin Chem Lab Med
. 2022 Jun;
60(9):e216-e220.
PMID: 35749133
No abstract available.
6.
Filser M, Gardie B, Wemeau M, Aguilar-Martinez P, Giansily-Blaizot M, Girodon F
Genes (Basel)
. 2022 Jan;
13(1).
PMID: 35052472
High oxygen affinity hemoglobin (HOAH) is the main cause of constitutional erythrocytosis. Mutations in the genes coding the alpha and beta globin chains (, and ) strengthen the binding of...
7.
Landemaine A, Hamdi-Roze H, Cunat S, Loustaud-Ratti V, Causse X, Si Ahmed S, et al.
J Hepatol
. 2021 Nov;
76(3):568-576.
PMID: 34748893
Background & Aims: Ferroportin disease is a rare genetic iron overload disorder which may be underdiagnosed, with recent data suggesting it occurs at a higher prevalence than suspected. Costs and...
8.
Filser M, Giansily-Blaizot M, Grenier M, Monedero Alonso D, Bouyer G, Peres L, et al.
Blood
. 2020 Nov;
137(13):1828-1832.
PMID: 33181827
No abstract available.
9.
Cilla N, Domitien L, Arrada N, Chiffre D, Mahe P, Vincent L, et al.
IDCases
. 2020 May;
21:e00802.
PMID: 32461906
Acute parvovirus B19 infection may lead to erythroblastopenia crisis in patients with underlying red blood cells disorders. We report herein an uncommon concomitant transient aplastic crisis in a mother and...
10.
Picard V, Guitton C, Thuret I, Rose C, Bendelac L, Ghazal K, et al.
Haematologica
. 2019 Jan;
104(8):1554-1564.
PMID: 30655378
We describe the clinical, hematologic and genetic characteristics of a retrospective series of 126 subjects from 64 families with hereditary xerocytosis. Twelve patients from six families carried a mutation, five...