A Guiochon-Mantel
Overview
Explore the profile of A Guiochon-Mantel including associated specialties, affiliations and a list of published articles.
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46
Citations
586
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Recent Articles
1.
Adams D, Cintas P, Sole G, Tard C, Labeyrie C, Echaniz-Laguna A, et al.
Rev Neurol (Paris)
. 2024 Apr;
180(7):661-672.
PMID: 38643028
Objective: We aimed to describe characteristics of patients with ATTR variant polyneuropathy (ATTRv-PN) and ATTRv-mixed and assess the real-world use and safety profile of tafamidis meglumine 20mg. Methods: Thirty-eight French...
2.
Theaudin M, Lozeron P, Algalarrondo V, Lacroix C, Cauquil C, Labeyrie C, et al.
Eur J Neurol
. 2018 Oct;
26(3):497-e36.
PMID: 30350904
Background And Purpose: The aim is to describe an uncommon phenotype of hereditary ATTR neuropathy with upper limb onset. Methods: The French TTR Familial Amyloid Polyneuropathy database was used for...
3.
Anghelescu C, Francou B, Cardas R, Guiochon-Mantel A, Aubourg P, Servais L, et al.
Eur J Neurol
. 2017 Feb;
24(3):e15-e16.
PMID: 28211244
No abstract available.
4.
Bouali N, Francou B, Bouligand J, Lakhal B, Malek I, Kammoun M, et al.
Clin Genet
. 2016 Feb;
89(5):608-13.
PMID: 26848058
Premature ovarian insufficiency (POI) affects approximately 1% of women before the age of 40. Genetic contribution is a significant component of POI. In this context, heterozygous mutations in NOBOX, BMP15...
5.
Briand-Suleau A, Martinovic J, Tosca L, Tou B, Brisset S, Bouligand J, et al.
Eur J Med Genet
. 2014 Feb;
57(4):174-80.
PMID: 24486774
Interstitial duplication within the long arm of chromosome 20 is an uncommon chromosome structural abnormality. We report here the clinical and molecular characterization associated with pure 20q13.2 duplication in three...
6.
Guediche N, Tosca L, Kara Terki A, Bas C, Lecerf L, Young J, et al.
Reprod Biomed Online
. 2011 Nov;
24(1):72-82.
PMID: 22116069
Small supernumerary marker chromosomes (sSMC) are structurally abnormal chromosomes that cannot be unambiguously identified by conventional banding cytogenetics. This study describes four patients with sSMC in relation with infertility. Patient...
7.
Bouligand J, Cabaret O, Canonico M, Verstuyft C, Dubert L, Becquemont L, et al.
Clin Pharmacol Ther
. 2010 Nov;
89(1):60-4.
PMID: 21107315
Oral, but not transdermal, estrogen therapy increases the risk of venous thromboembolism (VTE) in women who are past menopause. Data from the Estrogen and Thromboembolism Risk (ESTHER) study were used...
8.
Bry-Gauillard H, Trabado S, Bouligand J, Sarfati J, Francou B, Salenave S, et al.
Ann Endocrinol (Paris)
. 2010 Apr;
71(3):158-62.
PMID: 20363464
Congenital hypogonadotropic hypogonadisms (CHH) are a well-known cause of pubertal development failure in women. In a majority of patients, the clinical spectrum results from an insufficient and concomitant secretion of...
9.
Verstuyft C, Canonico M, Bouaziz E, Guiochon-Mantel A, Scarabin P
J Thromb Haemost
. 2009 Mar;
7(6):1034-6.
PMID: 19320825
No abstract available.
10.
Slama A, Lacroix C, Plante-Bordeneuve V, Lombes A, Conti M, Reimund J, et al.
Mol Genet Metab
. 2005 Mar;
84(4):326-31.
PMID: 15781193
The mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) syndrome is characterized by the association of gastrointestinal and neurological symptoms. It is a rare autosomal recessive mitochondrial disorder with multiple mitochondrial DNA deletions and/or...