Valerie Barbier
Overview
Explore the profile of Valerie Barbier including associated specialties, affiliations and a list of published articles.
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43
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1692
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Recent Articles
11.
Pontoizeau C, Roda C, Arnoux J, Vignolo-Diard P, Brassier A, Habarou F, et al.
Mol Genet Metab
. 2020 Apr;
130(2):110-117.
PMID: 32273051
Purpose: We aimed to identify prognostic factors for survival and long-term intellectual and developmental outcome in neonatal patients with early-onset urea cycle disorders (UCD) experiencing hyperammonaemic coma. Methods: We retrospectively...
12.
Bouchemal N, Ouss L, Brassier A, Barbier V, Gobin S, Hubert L, et al.
Orphanet J Rare Dis
. 2019 Sep;
14(1):222.
PMID: 31533761
Background: Trimethylaminuria (TMAU) is a metabolic disorder characterized by the excessive excretion of the malodorous compound trimethylamine (TMA). The diagnosis of TMAU is challenging because this disorder is situated at...
13.
Abi-Warde M, Roda C, Arnoux J, Servais A, Habarou F, Brassier A, et al.
J Inherit Metab Dis
. 2017 Sep;
40(6):783-792.
PMID: 28905140
Background: Maple syrup urine disease (MSUD) is a rare disease that requires a protein-restricted diet for successful management. Little is known, however, about the psychosocial outcome of MSUD patients. This...
14.
de la Batie C, Barbier V, Roda C, Brassier A, Arnoux J, Valayannopoulos V, et al.
J Inherit Metab Dis
. 2017 Sep;
41(4):623-629.
PMID: 28856627
Propionic acidemia is the result of a deficiency in propionyl-CoA carboxylase activity. Chronic neurologic and cognitive complications frequently occur, but the psychiatric evolution of the disorder is not well documented....
15.
Bouchereau J, Leduc-Leballeur J, Pichard S, Imbard A, Benoist J, Abi Warde M, et al.
J Inherit Metab Dis
. 2017 Mar;
40(3):377-383.
PMID: 28324240
Maple syrup urine disease (MSUD), an inborn error of amino acids catabolism is characterized by accumulation of branched chain amino acids (BCAAs) leucine, isoleucine, valine and their corresponding alpha-ketoacids. Impact...
16.
Winkler I, Wiercinska E, Barbier V, Nowlan B, Bonig H, Levesque J
Exp Hematol
. 2016 Feb;
44(4):303-14.e1.
PMID: 26827874
Harvest of granulocyte colony-stimulating factor (G-CSF)-mobilized hematopoietic stem cells (HSCs) begins at day 5 of G-CSF administration, when most donors have achieved maximal mobilization. This is based on surrogate markers...
17.
Jacobsen R, Nowlan B, Brunck M, Barbier V, Winkler I, Levesque J
Exp Hematol
. 2015 Nov;
44(3):207-12.e4.
PMID: 26607596
The cytokines granulocyte colony-stimulating factor (G-CSF) and Flt3 ligand (Flt3-L) mobilize hematopoietic stem and progenitor cells into the peripheral blood of primates, humans, and mice. We recently reported that G-CSF...
18.
Cook M, Doran M, Kollar K, Barbier V, Winkler I, Levesque J, et al.
J Clin Med
. 2015 Aug;
2(3):115-35.
PMID: 26237066
Haematopoietic stem cell (HSC) transplantation is an established cell-based therapy for a number of haematological diseases. To enhance this therapy, there is considerable interest in expanding HSCs in artificial niches...
19.
Holzapfel B, Hutmacher D, Nowlan B, Barbier V, Thibaudeau L, Theodoropoulos C, et al.
Biomaterials
. 2015 May;
61:103-14.
PMID: 26001075
Advances in tissue-engineering have resulted in a versatile tool-box to specifically design a tailored microenvironment for hematopoietic stem cells (HSCs) in order to study diseases that develop within this setting....
20.
Brassier A, Gobin S, Arnoux J, Valayannopoulos V, Habarou F, Kossorotoff M, et al.
Orphanet J Rare Dis
. 2015 May;
10:58.
PMID: 25958381
Background: The principal aim of this study was to investigate the long-term outcomes of a large cohort of patients with ornithine transcarbamylase deficiency (OTCD) who were followed up at a...