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

[Simultaneous occurrence of neurofibromatosis and tuberous sclerosis, acquired as neo-mutations].

Revista de neurologia - 1 Jan 2000

Janeiro P C, Cunha M S, Cordeiro I, Santos H G, Antunes N L

Abstract excerpt

INTRODUCTION: Neurofibromatosis type 1 and tuberous sclerosis are two distinct neurocutaneous syndromes that result of a mutation of tumoral suppressor genes, increasing the risk of tumorigenesis. They both have dominant autosomal hereditariness with half of the cases corresponding to new mutatio...

Read the complete abstract on PubMed

Topics

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

Share to Infant, Newborn
Share to Mutation
Share to Neurofibromatoses

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Tuberous Sclerosis

Source

Identifiers

PMID: 18368679

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18368679-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Simultaneous occurrence of neurofibromatosis and tuberous sclerosis, acquired as neo-mutations].PMID 18368679Read ↗

[Advances in the research on neurocutaneous syndromes: neurofibromatosis type 1 and tuberous sclerosis complex].Semantic proximity Read ↗

Tuberous sclerosis complex and neurofibromatosis type 1: the two most common neurocutaneous diseasesSemantic proximity Read ↗

[Diagnosis of tuberous sclerosis complex].Semantic proximity Read ↗

[Neurofibromatosis type 2].Semantic proximity Read ↗

[Unusual clinical manifestations of type 1 neurofibromatosis].Semantic proximity Read ↗

Angiofibromas with multiple epidermoid cysts in tuberous sclerosis: new mutation or post-traumatic?Semantic proximity Read ↗

[Molecular genetic diagnosis of neurofibromatosis type I].Semantic proximity Read ↗

Molecular genetic aspects of the phakomatoses: tuberous sclerosis complex and neurofibromatosis 1.Semantic proximity Read ↗

[Familial clinical manifestation in patients with neuromesoectodermic defect].Semantic proximity Read ↗

A dermatological assessment of pediatric patients with tuberous sclerosis complex (TSC).Semantic proximity Read ↗

[From gene to disease; TSC1 and TSC2 genes and tuberous sclerosis complex].Semantic proximity Read ↗

[Novel TSC1 mutation associated with variable phenotypes in tuberous sclerosis].Semantic proximity Read ↗

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