Mal de Meleda: recessive transgressive palmoplantar keratoderma with three unusual facultative features.

Autosomal recessive epidermolytic palmoplantar keratoderma.

A Japanese case of Mal de Meleda with SLURP1 mutation.

Palmoplantar keratoderma of the Gamborg-Nielsen type is caused by mutations in the SLURP1 gene and represents a variant of Mal de Meleda.

Acitretin in the treatment of mal de Meleda.

Palmoplantar keratoderma with dental abnormalities.

Aquagenic palmoplantar keratoderma associated with acrokeratoelastoidosis.

Palmoplantar keratoderma with sclerodactyly (Huriez syndrome).

[Palmoplantar keratoderma syndromes: new findings].

The first Mal de Meleda case in Libya: identification of a SLURP1 mutation.

Xanthogranulomatous pyelonephritis presenting as palmoplantar keratoderma.

PIGO deficiency: palmoplantar keratoderma and novel mutations.

Autosomal-recessive SASH1 variants associated with a new genodermatosis with pigmentation defects, palmoplantar keratoderma and skin carcinoma.

[Palmoplantar keratoderma: a rare manifestation of myxoedema].

Inflammatory familial palmoplantar keratoderma: Greither's disease?

Desmoplakin mutations with palmoplantar keratoderma, woolly hair and cardiomyopathy.

[Aquagenic palmoplantar keratoderma in children with cystic fibrosis].

R75Q de novo dominant mutation of GJB2 in a Chinese family with hearing loss and palmoplantar keratoderma.

Classification of autosomal dominant palmoplantar keratoderma: past-present-future.

urokinase receptor-related protein 1 (SLURP1) in Mal de Meleda.

New and recurrent AAGAB mutations in punctate palmoplantar keratoderma.

[Aquagenic palmoplantar keratoderma during treatment of Langerhans cell histiocytosis].

[Palmoplantar keratoderma: molecular identification of two new subtypes].

Slurp2 double-knockout mice.

Survey of mal de debarquement.

Suggest Documents

Autosomal recessive epidermolytic palmoplantar keratoderma.

A Japanese case of Mal de Meleda with SLURP1 mutation.

Palmoplantar keratoderma of the Gamborg-Nielsen type is caused by mutations in the SLURP1 gene and represents a variant of Mal de Meleda.

Acitretin in the treatment of mal de Meleda.

Palmoplantar keratoderma with dental abnormalities.

Aquagenic palmoplantar keratoderma associated with acrokeratoelastoidosis.

Palmoplantar keratoderma with sclerodactyly (Huriez syndrome).

[Palmoplantar keratoderma syndromes: new findings].

The first Mal de Meleda case in Libya: identification of a SLURP1 mutation.

Xanthogranulomatous pyelonephritis presenting as palmoplantar keratoderma.

PIGO deficiency: palmoplantar keratoderma and novel mutations.

Autosomal-recessive SASH1 variants associated with a new genodermatosis with pigmentation defects, palmoplantar keratoderma and skin carcinoma.

[Palmoplantar keratoderma: a rare manifestation of myxoedema].

Inflammatory familial palmoplantar keratoderma: Greither's disease?

Desmoplakin mutations with palmoplantar keratoderma, woolly hair and cardiomyopathy.

[Aquagenic palmoplantar keratoderma in children with cystic fibrosis].

R75Q de novo dominant mutation of GJB2 in a Chinese family with hearing loss and palmoplantar keratoderma.

Classification of autosomal dominant palmoplantar keratoderma: past-present-future.

urokinase receptor-related protein 1 (SLURP1) in Mal de Meleda.

New and recurrent AAGAB mutations in punctate palmoplantar keratoderma.

[Aquagenic palmoplantar keratoderma during treatment of Langerhans cell histiocytosis].

[Palmoplantar keratoderma: molecular identification of two new subtypes].

Slurp2 double-knockout mice.

Survey of mal de debarquement.

Mal de Meleda: recessive transgressive palmoplantar keratoderma with three unusual facultative features.

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