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

Absence of TGFBR2 mutations in patients with spontaneous spinal CSF leaks and intracranial hypotension.

The journal of headache and pain - 1 Apr 2008

Schievink Wouter I, Gordon Ora K, Hyland James C, Ala-Kokko Leena

Abstract excerpt

A heritable connective-tissue-disorder often is suspected in patients with spontaneous spinal CSF leaks and intracranial hypotension, but the nature of the disorder remains unknown in most patients. The aim of this study was to assess the gene encoding TGF-beta receptor-2 (TGFBR2) as a candidate...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Aortic Aneurysm, Thoracic
Share to Arteries

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Bone Diseases

Share to Polymerase Chain Reaction

Share to Protein Serine-Threonine Kinases

Share to Receptor, Transforming Growth Factor-beta Type II

Share to Receptors, Transforming Growth Factor beta

Source

Open in PubMed Open full text

Identifiers

PMID: 18264665
DOI: 10.1007/s10194-008-0017-y
PMCID: PMC3476180

Genes

TGFBR2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18264665-2026-09-02.2. 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 · 11 closest

Absence of TGFBR2 mutations in patients with spontaneous spinal CSF leaks and intracranial hypotension.PMID 18264665Read ↗

Dural ectasia in individuals with Marfan-like features but exclusion of mutations in the genes FBN1, TGFBR1 and TGFBR2.Semantic proximity Read ↗

A new sporadic case of early-onset Loeys-Dietz syndrome due to the recurrent mutation p.R528C in the TGFBR2 gene substantiates interindividual clinical variability.Semantic proximity Read ↗

Spontaneous spinal CSF leaks: a rare variant exome sequencing study and functional analysis.Semantic proximity Read ↗

Dural ectasia in Loeys-Dietz syndrome: comprehensive study of 30 patients with a TGFBR1 or TGFBR2 mutation.Semantic proximity Read ↗

Identification of a novel TGFBR2 gene mutation in a Korean patient with Loeys-Dietz aortic aneurysm syndrome; no mutation in TGFBR2 gene in 30 patients with classic Marfan's syndrome.Semantic proximity Read ↗

Familial Occurrence and Heritable Connective Tissue Disorders in Spontaneous Intracranial Hypotension.Semantic proximity Read ↗

Absence of TGFBR1 and TGFBR2 mutations in patients with bicuspid aortic valve and aortic dilation.Semantic proximity Read ↗

CSF-Venous Fistulas Occurring in First-Degree Relatives: A Multicenter Case Series.Semantic proximity Read ↗

Mutations in TGFBR2 gene cause spontaneous cervical artery dissection.Semantic proximity Read ↗

Treatment of a patient with vertebral and subclavian aneurysms in the setting of a TGFBR2 mutation.Semantic proximity Read ↗

Importance of dural ectasia in phenotypic assessment of Marfan's syndrome.Semantic proximity Read ↗

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