Publications by authors named "P Chedin"

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Immunocytochemistry with cytokeratin 19 and anti-human mesothelial cell antibody (HBME1) increases the diagnostic accuracy of thyroid fine-needle aspirations: preliminary report of 150 liquid-based fine-needle aspirations with histological control.
Beatrix Cochand-Priollet, Henri Dahan, Marie Laloi-Michelin, Marc Polivka, Michele Saada, Pierre Chedin

Thyroid· October 2011

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The clinical variability of maternally inherited diabetes and deafness is associated with the degree of heteroplasmy in blood leukocytes.
M Laloi-Michelin, T Meas, C Ambonville, C Bellanné-Chantelot, S Beaufils, P Chedin

J Clin Endocrinol Metab· August 2009

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Retinal and renal complications in patients with a mutation of mitochondrial DNA at position 3,243 (maternally inherited diabetes and deafness). A case-control study.
P Massin, D Dubois-Laforgue, T Meas, M Laloi-Michelin, H Gin, P Chedin

Diabetologia· September 2008

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Heterogeneity of diabetes phenotype in patients with 3243 bp mutation of mitochondrial DNA (Maternally Inherited Diabetes and Deafness or MIDD).
P J Guillausseau, D Dubois-Laforgue, P Massin, M Laloi-Michelin, C Bellanné-Chantelot, P Chedin

Diabetes Metab· April 2004

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Maternally inherited diabetes and deafness: a multicenter study.
P J Guillausseau, P Massin, D Dubois-LaForgue, J Timsit, M Virally, P Chedin

Ann Intern Med· May 2001

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