Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Multiple linear spiradenomas and ALPK1 mutation: A case report and literature review.

The Australasian journal of dermatology - 1 Feb 2024

Furukawa Yukiko, Koga Monji, Oyama Takuto, Koga Kaori, Takagi Satoshi, Imafuku Shinichi

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Mutation
Share to Skin

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 37877435
DOI: 10.1111/ajd.14181

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Multiple linear spiradenomas and ALPK1 mutation: A case report and literature review.PMID 37877435Read ↗

ALPK1 hotspot mutation as a driver of human spiradenoma and spiradenocarcinomaSemantic proximity Read ↗

Syndromes Aassociated with Lipomatous Tumors (SALT): A comprehensive review.Semantic proximity Read ↗

Expanding Phenotype of De Novo Mutations in GNAO1: Four New Cases and Review of Literature.Semantic proximity Read ↗

Malignant fibroadenoma with CHEK2 mutation: a novel case.Semantic proximity Read ↗

A Rare Case of Metastatic Spiradenocarcinoma With CDKN2A Mutation.Semantic proximity Read ↗

Exploring the genetic driver events of eccrine poromas and porocarcinomas: a retrospective, cross-institutional study of 54 casesSemantic proximity Read ↗

NTHL1-associate polyposis: first Australian case reportSemantic proximity Read ↗

Novel Report of Ophthalmoparesis Associated With CMT Type 2P Secondary to LRSAM1 Mutation.Semantic proximity Read ↗

Lymphangioma of the fetal neck within the PIK3CA-Related-Overgrowth Spectrum (PROS): A case report.Semantic proximity Read ↗

A Distinctive Adnexal (Usually Paratubal) Neoplasm Often Associated With Peutz-Jeghers Syndrome and Characterized by STK11 Alterations (STK11 Adnexal Tumor): A Report of 22 Cases.Semantic proximity Read ↗

Novel mutation of OCRL1 in Lowe syndrome with multiple epidermal cysts.Semantic proximity Read ↗

Retroperitoneal Cystic Adenopecoma with Genetic Analysis: A Rare Neoplasm.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.