Familial cavernous angioma: an unknown, known disease

ERBIN deficiency links STAT3 and TGF-β pathway defects with atopy in humans.

The Journal of experimental medicine·2017

Generalised peliosis hepatis mimicking metastases after long-term use of oral contraceptives.

The Netherlands journal of medicine·2015

Inherited cavernous malformations of the central nervous system: clinical and genetic features in 19 Swiss families.

Neurosurgical review·2009

Psychiatric co-morbidity in 75 patients undergoing epilepsy surgery: lack of correlation with pathological findings.

Epilepsy research·2008

Using dynamic low-coherence interferometry to image Brownian motion within highly scattering media.

Optics letters·2007

Large germline deletions and duplication in isolated cerebral cavernous malformation patients.

Neurogenetics·2007

Advances in sudden unexpected death in epilepsy.

Acta neurologica Scandinavica·2022

Non-convulsive seizures and non-convulsive status epilepticus in neuro-intensive care unit.

Acta neurologica Scandinavica·2022

Positron emission tomography in autoimmune encephalitis: Clinical implications and future directions.

Acta neurologica Scandinavica·2022

Seizure detection based on wearable devices: A review of device, mechanism, and algorithm.

Acta neurologica Scandinavica·2022

Walking confidence and perceived locomotion ability explain participation after stroke: A cross-sectional experimental study.

Acta neurologica Scandinavica·2022

Clinical features of Guillain-Barré syndrome with anti-neurofascin 155 antibody.

Acta neurologica Scandinavica·2022

Abdominal aortic aneurysm in a patient with situs ambiguous and polyspleny (heterotaxy syndrome): a very rare occurrence in vascular surgery! Short literature review.

Surgical and radiologic anatomy : SRA·2026

Congenital anosmia.

Danish medical journal·2026

Retraction notice to "Chemical composition and antimicrobial study of Crossobamon orientalis body oil" [Heliyon 10 (2024) e28225].

Heliyon·2026

Divergent total synthesis and reactivity of 2,3-dihydroxypropylphosphonic acid dipeptides.

Organic & biomolecular chemistry·2026

Bulbar "Red Flag" Symptoms and a 21-Year Diagnostic Delay in Adult Arnold-Chiari Type II Malformation With Tracheoesophageal Fistula and Syringomyelia: A Case Report.

Clinical case reports·2026

Erratum.

European addiction research·2026

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Familial cavernous angioma: an unknown, known disease

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ERBIN deficiency links STAT3 and TGF-β pathway defects with atopy in humans.

Generalised peliosis hepatis mimicking metastases after long-term use of oral contraceptives.

Inherited cavernous malformations of the central nervous system: clinical and genetic features in 19 Swiss families.

Psychiatric co-morbidity in 75 patients undergoing epilepsy surgery: lack of correlation with pathological findings.

Using dynamic low-coherence interferometry to image Brownian motion within highly scattering media.

Large germline deletions and duplication in isolated cerebral cavernous malformation patients.

Advances in sudden unexpected death in epilepsy.

Non-convulsive seizures and non-convulsive status epilepticus in neuro-intensive care unit.

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Walking confidence and perceived locomotion ability explain participation after stroke: A cross-sectional experimental study.

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Retraction notice to "Chemical composition and antimicrobial study of Crossobamon orientalis body oil" [Heliyon 10 (2024) e28225].

Divergent total synthesis and reactivity of 2,3-dihydroxypropylphosphonic acid dipeptides.

Bulbar "Red Flag" Symptoms and a 21-Year Diagnostic Delay in Adult Arnold-Chiari Type II Malformation With Tracheoesophageal Fistula and Syringomyelia: A Case Report.

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Familial cavernous angioma: an unknown, known disease

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