[DNA diagnosis of muscular dystrophies]

Novel splice site CACNA1A mutation causing episodic ataxia type 2.

Neurogenetics·2003

A distinct phenotype of distal myopathy in a large Finnish family.

Neurology·2003

Pure quadriceps myopathy in two sisters.

European journal of neurology·2003

Axial myopathy--an unrecognised entity.

Journal of neurology·2002

LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development.

Cell·2001

Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria.

Nature genetics·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

A CCNA1 Missense Variant Associated With Chromatid Non-Disjunction in Abnormal-Headed Sperm and Male Infertility.

Andrology·2026

Genomic characterization and phylogenetic placement of Matryoshka RNA virus 1 associated with Plasmodium vivax malaria in Africa.

Access microbiology·2026

Venous Plexus of Batson and Its Important Role in the Development of Cryptococcal Meningitis.

Cureus·2026

The affective impact of mixed reality on medical students' learning outcomes in clinical skills: A preliminary study.

Tzu chi medical journal·2026

Reverse vaccinology and immunoinformatics identify multi-epitope vaccine candidates against molluscum contagiosum virus.

Biology methods & protocols·2026

Assessing Demographic Characteristics, Microbiology, and Mortality Outcomes Associated With Vertebral Osteomyelitis: A National Single-Center Cohort Study in Malta.

Cureus·2026

Related Experiment Videos

[DNA diagnosis of muscular dystrophies]

Related Concept Videos

Novel splice site CACNA1A mutation causing episodic ataxia type 2.

A distinct phenotype of distal myopathy in a large Finnish family.

Pure quadriceps myopathy in two sisters.

Axial myopathy--an unrecognised entity.

LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development.

Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria.

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

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

Discussing a serious illness with a patient and family.

Invasive treatment of superficial veins of the lower extremities.

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

Diagnostics and current care of myasthenia gravis.

A CCNA1 Missense Variant Associated With Chromatid Non-Disjunction in Abnormal-Headed Sperm and Male Infertility.

Genomic characterization and phylogenetic placement of Matryoshka RNA virus 1 associated with Plasmodium vivax malaria in Africa.

Venous Plexus of Batson and Its Important Role in the Development of Cryptococcal Meningitis.

The affective impact of mixed reality on medical students' learning outcomes in clinical skills: A preliminary study.

Reverse vaccinology and immunoinformatics identify multi-epitope vaccine candidates against molluscum contagiosum virus.

Assessing Demographic Characteristics, Microbiology, and Mortality Outcomes Associated With Vertebral Osteomyelitis: A National Single-Center Cohort Study in Malta.

Related Experiment Videos

[DNA diagnosis of muscular dystrophies]

Related Concept Videos

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