Latest papers

Camurati-Engelmann disease (progressive diaphyseal dysplasia) in a Moroccan family.

[Ghosal haematodiaphyseal dysplasia: a new case].

Camurati-Engelmann disease: failure of response to bisphosphonates: report of two cases.

Camurati-Engelmann disease--a case report and literature review.

Imaging of the temporal bone in Camurati-Engelmann dysplasia with an 11-year follow-up.

Aggressive cranial vault decompression for cranial hyperostosis: technical case report of two cases.

Juvenile vertebrobasilar ischaemic stroke in a patient with Camurati-Engelmann disease.

Rare osteodysplasia of the temporal bone.

Camurati-Engelmann disease in conjunction with hypogonadism.

Mesenteric fibromatosis in a patient with Camurati-Engelmann disease. A case report and literature review.

Internal auditory canal decompression and cochlear implantation in Camurati-Engelmann disease.

GDD1 Is Identical to TMEM16E, a Member of the TMEM16 Family

Marked phenotypic variability in progressive diaphyseal dysplasia (Camurati-Engelmann disease): report of a four-generation pedigree, identification of a mutation in TGFB1, and review.

Situs inversus totalis with accompanying craniodiaphysial dysplasia: a new syndrome?

Radionuclide bone scintigraphy in Engelmann-Camurati disease.

The Novel Gene Encoding a Putative Transmembrane Protein Is Mutated in Gnathodiaphyseal Dysplasia (GDD)

About hemato-diaphyseal dysplegia.

TGFB1 mutations in four new families with Camurati-Engelmann disease: confirmation of independently arising LAP-domain-specific mutations.

MR imaging features of craniodiaphyseal dysplasia.

Van Buchem disease: lifetime evolution of radioclinical features.