Filters

Term Search
You can select from the dropdown list OR enter your own terms to refine the search.

Last Updated: 02/24/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 3348 publications

De Novo Germline L858R EGFR Variants and Generalized Acanthosis Nigricans.

De Novo Germline L858R EGFR Variants and Generalized Acanthosis Nigricans.

Journal: JAMA dermatology
Published: January 14, 2026

Skin Fragility-Woolly Hair Syndrome (SFWHS): A Case Report.

Skin Fragility-Woolly Hair Syndrome (SFWHS): A Case Report.

Journal: Cureus
Published: January 05, 2026

Establishment of Basic Compatibility Through Pathogen Sulfur Scavenging Is Essential for Laurel Wilt Disease Development.

Establishment of Basic Compatibility Through Pathogen Sulfur Scavenging Is Essential for Laurel Wilt Disease Development.

Journal: Molecular plant-microbe interactions : MPMI
Published: December 09, 2025

Paraneoplastic palmoplantar keratoderma secondary to multiple myeloma.

Paraneoplastic palmoplantar keratoderma secondary to multiple myeloma.

Journal: Polish archives of internal medicine
Published: November 17, 2025

Case Report: Severe palmoplantar hyperkeratosis and pain four months post-tepotinib initiation: A hand-foot skin reaction.

Case Report: Severe palmoplantar hyperkeratosis and pain four months post-tepotinib initiation: A hand-foot skin reaction.

Journal: JAAD case reports
Published: November 14, 2025

Severe Dilated Cardiomyopathy with PLACK Syndrome Caused by a Novel Truncating Variant in the CAST Gene.

Severe Dilated Cardiomyopathy with PLACK Syndrome Caused by a Novel Truncating Variant in the CAST Gene.

Journal: Genes
Published: October 14, 2025

Under Pressure: A unique mechanoresponsive mechanism of body site-specific keratin regulation in palmoplantar epidermis.

Under Pressure: A unique mechanoresponsive mechanism of body site-specific keratin regulation in palmoplantar epidermis.

Journal: bioRxiv : the preprint server for biology
Published: September 26, 2025

A rare case of LORICRIN gene c.684dup mutation associated with Vohwinkel syndrome in a Turkish patient, in silico analysis and literature review.

A rare case of LORICRIN gene c.684dup mutation associated with Vohwinkel syndrome in a Turkish patient, in silico analysis and literature review.

Journal: Molecular biology reports
Published: September 23, 2025

Atypical Presentation of Papillon-Lefèvre Syndrome: A Case of Isolated Cutaneous Manifestations Without Dental Involvement.

Atypical Presentation of Papillon-Lefèvre Syndrome: A Case of Isolated Cutaneous Manifestations Without Dental Involvement.

Journal: Reports (MDPI)
Published: August 27, 2025

Case Report: Autosomal recessive palmoplantar keratoderma with additional bilateral hearing loss due to a pathogenic frameshift deletion in FAM83G.

Case Report: Autosomal recessive palmoplantar keratoderma with additional bilateral hearing loss due to a pathogenic frameshift deletion in FAM83G.

Journal: Frontiers in medicine
Published: August 18, 2025

A case report of palmoplantar keratoderma in a 3-year-old girl: A structured approach in primary care settings.

A case report of palmoplantar keratoderma in a 3-year-old girl: A structured approach in primary care settings.

Journal: Malaysian family physician : the official journal of the Academy of Family Physicians of Malaysia
Published: August 11, 2025

Microbial Dysbiosis and Foot Odor in Nagashima-Type Palmoplantar Keratosis: Improvement with Topical Benzoyl Peroxide.

Microbial Dysbiosis and Foot Odor in Nagashima-Type Palmoplantar Keratosis: Improvement with Topical Benzoyl Peroxide.

Journal: The Journal of investigative dermatology
Published: August 06, 2025
Showing 1-12 of 3,348

Last Updated: 02/24/2026