Calcifying epithelioma of Malherbe. Association with myotonic muscular dystrophy

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Psychological Model for Presymptomatic Test Interviews: Lessons Learned from Huntington Disease.

Journal of genetic counseling·2015

Germinal mosaicism in facioscapulohumeral muscular dystrophy (FSHD).

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Phenotypic-genotypic correlation will assist genetic counseling in 4q35-facioscapulohumeral muscular dystrophy.

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A case of multiple cutaneous schwannomas; schwannomatosis or neurofibromatosis type 2?

Journal of neurology, neurosurgery, and psychiatry·2006

Population based study of late onset cerebellar ataxia in south east Wales.

Journal of neurology, neurosurgery, and psychiatry·2004

Comparison of Early and Late Latent Syphilis- Colorado, 1991.

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Case of Rhinoscleroma.

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An Ulcerated Plaque in a Gay Man.

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Solitary Violaceous Nodule on the Face.

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Erythematous Plaques on the Eyelids.

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The Meibomian Gland Composite Score (MGCS): A Novel Grading System Integrating Existing Scales for Meibomian Gland Dysfunction.

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M2 macrophage-derived exosomes and miR-132-3p promote gastric cancer cell aggressiveness and attenuate ferroptosis-related changes.

Frontiers in oncology·2026

Coarse grained molecular dynamics analysis of menthol interactions with ergosterol in a fungal mimetic membrane.

Journal of biomolecular structure & dynamics·2026

FAP adipogenesis drives early spinal muscle loss in dysferlinopathy and reveals a therapeutic target.

EMBO molecular medicine·2026

Supportive Care in Multiple Myeloma: Evidence-Based Recommendations From the Intergroupe Francophone du Myélome (IFM).

Clinical lymphoma, myeloma & leukemia·2026

Diagnostic Utility of Full-Length BP180 and Native BP180-α6β4 Integrin Complex ELISAs in Serologically Inconclusive Mucous Membrane Pemphigoid.

The Journal of dermatology·2026

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Calcifying epithelioma of Malherbe. Association with myotonic muscular dystrophy

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Conversations with French medical geneticists. A personal perspective on the origins and early years of medical genetics in France.

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