Publications by authors named "M Pholsena"

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A recurrent familial partial lipodystrophy due to a monoallelic or biallelic LMNA founder variant highlights the multifaceted cardiac manifestations of metabolic laminopathies.
Guillaume Treiber, Ania Flaus Furmaniuk, Alice Guilleux, Samir Medjane, Oriane Bonfanti, Maryse Pholsena

Eur J Endocrinol· August 2021

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Hyperandrogenism revealing an unexpected granulosa cell tumor.
Jean-Christophe Maiza, Maryse Pholsena, Sebastien Duquenne

J Gynecol Obstet Hum Reprod· April 2020

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[High prevalence of proteinuric nephropathy screened in patients with type 2 diabetes consulting community-based general practitioners in French overseas departments and territories. ALBUM study].
Xavier Debussche, Maryse Pholsena, Alain Fournier, Pauline Kangambega, Jean-Marc Gabriel

Rev Prat· June 2014

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Primary adrenal and thyroid insufficiencies associated with hypopituitarism: a diagnostic challenge.
M Pholsena, J Young, B Couzinet, G Schaison

Clin Endocrinol (Oxf)· May 1994

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Plasma 3 beta-hydroxy-delta 5-steroids in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
J Young, B Couzinet, M Pholsena, K Nahoul, F Labrie

J Clin Endocrinol Metab· February 1994

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