Latest papers

Ardalan-Shoja-Kiuru syndrome--hereditary gelsolin amyloidosis plus retinitis pigmentosa.

Ardalan-Shoja-Kiuru syndrome--hereditary gelsolin amyloidosis plus retinitis pigmentosa.

[Pseudoxanthoma elasticum with cutis laxa and multiple coagulation factor deficiency: a single genetic entity].

Multiple myeloma-associated amyloidosis and acral localized acquired cutis laxa.

Elastic tissue damage in cephalic acquired cutis laxa.

Gerodermia osteodysplastica/wrinkly skin syndrome: report of three patients and brief review of the literature.

Diagnostic dilemma's: the congenital disorders of glycosylation are clinical chameleons.

Defining the phenotype in an autosomal recessive cutis laxa syndrome with a combined congenital defect of glycosylation.

Periorbital changes associated with topical bimatoprost.

Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2.

Pregnancy in a gerodermia osteodysplastica patient: A case report

Localized cutis laxa and blepharoplasty.

Compound heterozygous mutations in fibulin-4 causing neonatal lethal pulmonary artery occlusion, aortic aneurysm, arachnodactyly, and mild cutis laxa.

Association of cutis laxa and genital prolapse: a case report.

Functional rescue of elastin insufficiency in mice by the human elastin gene: implications for mouse models of human disease.

Nonsurgical tightening of skin laxity: a new radiofrequency approach.

[Body contouring surgery after massive weight loss. Part I: abdomen and extremities]

Pseudoxanthoma elasticum-like phenotype with cutis laxa and multiple coagulation factor deficiency represents a separate genetic entity.

Radiosurgery versus carbon dioxide laser for dermatochalasis correction in Asians.

[Acquired cutis laxa and myeloma: large vacuolated cells in the dermis].