Inflammatory familial palmoplantar keratoderma: Greither's disease?

Palmoplantar keratoderma with dental abnormalities.

[Palmoplantar keratoderma syndromes: new findings].

Autosomal recessive epidermolytic palmoplantar keratoderma.

Xanthogranulomatous pyelonephritis presenting as palmoplantar keratoderma.

PIGO deficiency: palmoplantar keratoderma and novel mutations.

[Palmoplantar keratoderma: a rare manifestation of myxoedema].

Aquagenic palmoplantar keratoderma associated with acrokeratoelastoidosis.

Palmoplantar keratoderma with sclerodactyly (Huriez syndrome).

Two Japanese familial cases of punctate palmoplantar keratoderma caused by a novel AAGAB mutation, c.191_194delCAAA.

Possible anticipation in familial epidermolytic palmoplantar keratoderma with the p.R163W mutation of Keratin 9.

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

Desmoplakin mutations with palmoplantar keratoderma, woolly hair and cardiomyopathy.

New and recurrent AAGAB mutations in punctate palmoplantar keratoderma.

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

[Aquagenic palmoplantar keratoderma in children with cystic fibrosis].

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

Slurp2 double-knockout mice.

Sporadic and familial cases of aquagenic keratoderma.

Small Cell Variant of T-Cell Prolymphocytic Leukemia with Acquired Palmoplantar Keratoderma and Cutaneous Infiltration.

Autosomal dominant diffuse nonepidermolytic palmoplantar keratoderma due to a recurrent mutation in aquaporin-5.

Palmoplantar keratoderma along with neuromuscular and metabolic phenotypes in Slurp1-deficient mice.

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

A gain-of-function mutation in TRPV3 causes focal palmoplantar keratoderma in a Chinese family.

Aquagenic palmoplantar keratoderma with dorsal hand involvement in an adolescent female.

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Palmoplantar keratoderma with dental abnormalities.

[Palmoplantar keratoderma syndromes: new findings].

Autosomal recessive epidermolytic palmoplantar keratoderma.

Xanthogranulomatous pyelonephritis presenting as palmoplantar keratoderma.

PIGO deficiency: palmoplantar keratoderma and novel mutations.

[Palmoplantar keratoderma: a rare manifestation of myxoedema].

Aquagenic palmoplantar keratoderma associated with acrokeratoelastoidosis.

Palmoplantar keratoderma with sclerodactyly (Huriez syndrome).

Two Japanese familial cases of punctate palmoplantar keratoderma caused by a novel AAGAB mutation, c.191_194delCAAA.

Possible anticipation in familial epidermolytic palmoplantar keratoderma with the p.R163W mutation of Keratin 9.

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

Desmoplakin mutations with palmoplantar keratoderma, woolly hair and cardiomyopathy.

New and recurrent AAGAB mutations in punctate palmoplantar keratoderma.

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

[Aquagenic palmoplantar keratoderma in children with cystic fibrosis].

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

Slurp2 double-knockout mice.

Sporadic and familial cases of aquagenic keratoderma.

Small Cell Variant of T-Cell Prolymphocytic Leukemia with Acquired Palmoplantar Keratoderma and Cutaneous Infiltration.

Autosomal dominant diffuse nonepidermolytic palmoplantar keratoderma due to a recurrent mutation in aquaporin-5.

Palmoplantar keratoderma along with neuromuscular and metabolic phenotypes in Slurp1-deficient mice.

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

A gain-of-function mutation in TRPV3 causes focal palmoplantar keratoderma in a Chinese family.

Aquagenic palmoplantar keratoderma with dorsal hand involvement in an adolescent female.

Inflammatory familial palmoplantar keratoderma: Greither's disease?

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