手紙: スパイナ・ビフィダのスクリーニング

Same author

Eicosanoid involvement in the regulation of behavioral fever in the desert locust, Schistocerca gregaria.

Archives of insect biochemistry and physiology·2003

Same author

Rufous albinism.

Journal of pediatric ophthalmology and strabismus·2001

Same author

A mutation (2314delG) in the Usher syndrome type IIA gene: high prevalence and phenotypic variation.

American journal of human genetics·1999

Same author

A gene for autosomal recessive symmetrical spastic cerebral palsy maps to chromosome 2q24-25.

American journal of human genetics·1999

Same author

Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndrome.

American journal of human genetics·1998

Same author

A comparison of disease and gene frequencies of inborn errors of metabolism among different ethnic groups in the West Midlands, UK.

Journal of medical genetics·1998

Same journal

Rethinking anticoagulation intensity during extracorporeal membrane oxygenation.

Lancet (London, England)·2026

Same journal

Standard-dose unfractionated heparin versus low-dose unfractionated heparin and low-molecular-weight heparin in extracorporeal life support (RATE): an open-label, randomised, non-inferiority trial.

Lancet (London, England)·2026

Same journal

Inherited retinal degenerations: clinical phenotypes and emerging therapies.

Lancet (London, England)·2026

Same journal

Documenting hospice care.

Lancet (London, England)·2026

Same journal

After the wood chipper.

Lancet (London, England)·2026

Same journal

Assisted dying and the silencing of medicine's next generation.

Lancet (London, England)·2026

関連する実験動画

手紙: スパイナ・ビフィダのスクリーニング

関連する概念動画

Eicosanoid involvement in the regulation of behavioral fever in the desert locust, Schistocerca gregaria.

Rufous albinism.

A mutation (2314delG) in the Usher syndrome type IIA gene: high prevalence and phenotypic variation.

A gene for autosomal recessive symmetrical spastic cerebral palsy maps to chromosome 2q24-25.

Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndrome.

A comparison of disease and gene frequencies of inborn errors of metabolism among different ethnic groups in the West Midlands, UK.

Rethinking anticoagulation intensity during extracorporeal membrane oxygenation.

Standard-dose unfractionated heparin versus low-dose unfractionated heparin and low-molecular-weight heparin in extracorporeal life support (RATE): an open-label, randomised, non-inferiority trial.

Inherited retinal degenerations: clinical phenotypes and emerging therapies.

Documenting hospice care.

After the wood chipper.

Assisted dying and the silencing of medicine's next generation.

関連する実験動画

手紙: スパイナ・ビフィダのスクリーニング

関連する概念動画

関連記事

Eicosanoid involvement in the regulation of behavioral fever in the desert locust, Schistocerca gregaria.

Rufous albinism.

A mutation (2314delG) in the Usher syndrome type IIA gene: high prevalence and phenotypic variation.

A gene for autosomal recessive symmetrical spastic cerebral palsy maps to chromosome 2q24-25.

Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndrome.

A comparison of disease and gene frequencies of inborn errors of metabolism among different ethnic groups in the West Midlands, UK.

Rethinking anticoagulation intensity during extracorporeal membrane oxygenation.

Standard-dose unfractionated heparin versus low-dose unfractionated heparin and low-molecular-weight heparin in extracorporeal life support (RATE): an open-label, randomised, non-inferiority trial.

Inherited retinal degenerations: clinical phenotypes and emerging therapies.

Documenting hospice care.

After the wood chipper.

Assisted dying and the silencing of medicine's next generation.