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

Juvenile xanthogranuloma, neurofibromatosis 1, and juvenile chronic myeloid leukemia

1 Nov 1996

Abstract excerpt

Neurofibromatosis 1 (NF1) is a common autosomal dominant disorder in which affected children have an approximate 200-fold greater risk of developing juvenile chronic myeloid leukemia (JCML) compared with children without NF1.1,2A recent article in theArchives3presented the results of a statistical analysis from a compilation of case reports suggesting that children with NF1 have an even higher risk of JCML...

Read the complete abstract on PubMed

Topics

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

Share to Neurofibromatosis and Schwannoma Cases
Share to Sarcoma Diagnosis and Treatment
Share to Soft tissue tumor case studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 8915325
DOI: 10.1001/archderm.132.11.1390

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Juvenile xanthogranuloma, neurofibromatosis 1, and juvenile chronic myeloid leukemiaPMID 8915325Read ↗

Juvenile Xanthogranuloma, Neurofibromatosis, and Juvenile Chronic Myelogenous LeukemiaSemantic proximity Read ↗

Juvenile Xanthogranuloma, Neurofibromatosis, and Juvenile Chronic Myelogenous LeukemiaSemantic proximity Read ↗

Association Between Juvenile Myelomonocytic Leukemia, Juvenile Xanthogranulomas and Neurofibromatosis Type 1: Case Report and Review of the LiteratureSemantic proximity Read ↗

Neurofibromatosis type 1 diagnosed in a child based on multiple juvenile xanthogranulomas and juvenile myelomonocytic leukemia.Semantic proximity Read ↗

Juvenile Myelomonocytic Leukemia Presenting With Features of Hemophagocytic Lymphohistiocytosis in Association With Neurofibromatosis and Juvenile XanthogranulomasSemantic proximity Read ↗

Juvenile xanthogranuloma in a child with previously unsuspected neurofibromatosis type 1 and juvenile myelomonocytic leukemia.Semantic proximity Read ↗

A child with juvenile myelomonocytic leukemia possessing a concurrent germline CBL mutation and a NF1 variant of uncertain significance: A rare case with a common problem in the era of high-throughput sequencing.Semantic proximity Read ↗

Germline Neurofibromin 1 mutation enhances the anti-tumour immune response and decreases juvenile myelomonocytic leukaemia tumourigenicity.Semantic proximity Read ↗

Juvenile xanthogranuloma in Noonan syndrome.Semantic proximity Read ↗

Patterns of hematopoietic lineage involvement in children with neurofibromatosis type 1 and malignant myeloid disorders.Semantic proximity Read ↗

Uncommon histiocytic disorders: Rosai-Dorfman, juvenile xanthogranuloma, and Erdheim-Chester disease.Semantic proximity Read ↗

Juvenile xanthogranuloma: A possible diagnostic criterion for Neurofibromatosis type 1 in young children.Semantic proximity Read ↗

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