Philippe Touraine
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Explore the profile of Philippe Touraine including associated specialties, affiliations and a list of published articles.
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167
Citations
2481
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Recent Articles
1.
Touraine P, Chabbert-Buffet N, Plu-Bureau G, Duranteau L, Sinclair A, Tucker E
Nat Rev Dis Primers
. 2024 Sep;
10(1):63.
PMID: 39266563
Premature ovarian insufficiency (POI) is a cause of infertility and endocrine dysfunction in women, defined by loss of normal, predictable ovarian activity before the age of 40 years. POI is...
2.
Krysiak R, Claahsen-van der Grinten H, Reisch N, Touraine P, Falhammar H
Endocr Rev
. 2024 Sep;
46(1):80-148.
PMID: 39240753
Treatment of classic congenital adrenal hyperplasia (CAH) is directed at replacing deficient hormones and reducing androgen excess. However, even in the era of early diagnosis and lifelong hormonal substitution, the...
3.
Jordan P, Verebi C, Herve B, Perol S, Bernard V, Karila D, et al.
Gene
. 2024 Jun;
927:148734.
PMID: 38942181
Background: Primary ovarian insufficiency (POI) affects around 2-4% of women before the age of 40. Genetic factors play an important role in POI. The GDF9 gene has been identified as...
4.
Tucker E, Sharp M, Lokchine A, Bell K, Palmer C, Kline B, et al.
Clin Genet
. 2024 May;
106(3):321-335.
PMID: 38779778
Premature ovarian insufficiency is a common form of female infertility affecting up to 4% of women and characterised by amenorrhea with elevated gonadotropin before the age of 40. Oocytes require...
5.
Humbert L, Proust-Lemoine E, Dubucquoi S, Kemp E, Saugier-Veber P, Fabien N, et al.
J Clin Endocrinol Metab
. 2024 Apr;
110(3):e757-e773.
PMID: 38605470
Background: Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome is a rare disease caused by biallelic mutations of the AIRE gene, usually presenting with the triad hypoparathyroidism-adrenal failure-chronic mucocutaneous candidiasis (CMC) and nonendocrine manifestations....
6.
Jordan P, Verebi C, Herve B, Perol S, Chakhtoura Z, Courtillot C, et al.
Clin Genet
. 2024 Apr;
106(1):102-108.
PMID: 38558253
Pathogenic germline variants in the FOXL2 gene are associated with Blepharophimosis, Ptosis, and Epicanthus Inversus syndrome (BPES) in humans, an autosomal dominant condition. Two forms of BPES have emerged: (i)...
7.
Bakhshalizadeh S, Bird A, Sreenivasan R, Bell K, Robevska G, van den Bergen J, et al.
Genes (Basel)
. 2024 Mar;
15(3).
PMID: 38540391
Disruption of meiosis and DNA repair genes is associated with female fertility disorders like premature ovarian insufficiency (POI). In this study, we identified a homozygous missense variant in the gene...
8.
Morin A, Allodji R, Kariyawasam D, Touraine P, Puget S, Beccaria K, et al.
Neuro Oncol
. 2024 Mar;
26(7):1310-1324.
PMID: 38465768
Background: Optic pathway gliomas (OPGs) represent 5% of childhood brain tumors. Successive relapses lead to multiple treatments exposing to late complications. Methods: We included patients treated at Gustave Roussy (GR)...
9.
Castets S, Albarel F, Bachelot A, Brun G, Bouligand J, Briet C, et al.
Ann Endocrinol (Paris)
. 2024 Mar;
85(4):327-339.
PMID: 38452869
Pituitary deficiency, or hypopituitarism, is a rare chronic disease. It is defined by insufficient synthesis of one or more pituitary hormones (growth hormone, TSH, ACTH, LH-FSH, prolactin), whether or not...
10.
Gatta-Cherifi B, Mohammedi K, Cariou T, Poitou C, Touraine P, Raverot G, et al.
Eur J Endocrinol
. 2024 Mar;
190(4):257-265.
PMID: 38450721
Importance: A major issue in the management of craniopharyngioma-related obesity (CRO) is the ineffectiveness of the current therapeutic approaches. Objective: To study the efficacy of glucagon-like peptide-1 analogs compared with...