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Cutis laxa in hereditary gelsolin amyloidosis.

The British journal of dermatology·2005

The normal population distribution of PRNP codon 129 polymorphism.

Acta neurologica Scandinavica·2003

Status epilepticus induces changes in the expression and localization of endogenous palmitoyl-protein thioesterase 1.

Neurobiology of disease·2002

Contribution of APOE promoter polymorphisms to Alzheimer's disease risk.

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Association of lipoprotein lipase Ser447Ter polymorphism with brain infarction: a population-based neuropathological study.

Annals of medicine·2001

Update on Current Care Guideline: Psoriasis (skin and joints).

Duodecim; laaketieteellinen aikakauskirja·2017

FOUR score in monitoring the level of consciousness of an intensive care patient: first experience of the use of the Finnish language version.

Duodecim; laaketieteellinen aikakauskirja·2017

Discussing a serious illness with a patient and family.

Duodecim; laaketieteellinen aikakauskirja·2017

Invasive treatment of superficial veins of the lower extremities.

Duodecim; laaketieteellinen aikakauskirja·2017

When should a drain be left in the abdominal cavity upon surgery?

Duodecim; laaketieteellinen aikakauskirja·2017

Diagnostics and current care of myasthenia gravis.

Duodecim; laaketieteellinen aikakauskirja·2017

Juanbi Tang Attenuates Intervertebral Disc Degeneration by Suppressing p38MAPK/NF-κB Signaling and Activating Atg5-Dependent Autophagy to Promote Macrophage M2 Polarization: In Vivo and In Vitro Evidence.

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An overview of the relation between tuberculosis and autoantibodies: a systematic review.

Reumatismo·2026

Progressive multifocal leukoencephalopathy during bispecific antibody therapy in multiple myeloma: from immune dysfunction to early recognition. Comment on: "Progressive multifocal leukoencephalopathy and BK virus-nephropathy with bispecific antibody therapy in multiple myeloma".

Haematologica·2026

Isolated atrial amyloidosis from atrial natriuretic peptide - a common but overlooked cardiac condition.

Upsala journal of medical sciences·2026

Epigenetic reprogramming in autoimmune and immune-mediated skin disease.

Frontiers in immunology·2026

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A prospective radiologic and neurologic follow-up study of 61 HIV-1 -infected subjects: early beginning and slow progression of brain atrophy.

Cutis laxa in hereditary gelsolin amyloidosis.

The normal population distribution of PRNP codon 129 polymorphism.

Status epilepticus induces changes in the expression and localization of endogenous palmitoyl-protein thioesterase 1.

Contribution of APOE promoter polymorphisms to Alzheimer's disease risk.

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