[Editorial: Prenatal diagnosis of hereditary diseases]

5-Aminolevulinic acid-based photodynamic therapy. Clinical research and future challenges.

Cancer·1997

Use of 5-aminolevulinic acid esters to improve photodynamic therapy on cells in culture.

Cancer research·1997

Effects of MnDPDP, DPDP--, and MnCl2 on cardiac energy metabolism and manganese accumulation. An experimental study in the isolated perfused rat heart.

Investigative radiology·1997

Increased levels of intercellular adhesion molecules and vascular cell adhesion molecules in pre-eclampsia.

British journal of obstetrics and gynaecology·1997

Molecular genetics of familial hypercholesterolaemia in Norway.

Journal of internal medicine·1997

[Craniosynostosis operations in childhood].

Anasthesiologie, Intensivmedizin, Notfallmedizin, Schmerztherapie : AINS·1997

Perspectives on the use of coercion in highly specialised rehabilitation: a focus group study.

Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke·2026

Occupational injuries treated at Oslo A&E - a prospective study.

Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke·2026

Cross-reactivity in cashew nut allergy.

Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke·2026

AGG repeat expansion and aggregation of BIN1 in multiple system atrophy.

Brain : a journal of neurology·2026

[Optical genome mapping analysis of a Chinese pedigree with a complex balanced translocation involving four chromosomes].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics·2026

[Pathogenicity analysis and prenatal genetic counseling for five Chinese pedigrees harboring a hemizygous c.-32C>G variant of FGF13 gene].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics·2026

Interim analysis of an international multi-site prospective natural history study evaluating the clinical presentation and progression of Leigh syndrome spectrum disorders.

Therapeutic advances in rare disease·2026

Systematic genotype-phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22-q23 deletions.

Journal of human genetics·2026

Autism mutations rewire protein interaction networks to drive neurodevelopmental pathology.

Science (New York, N.Y.)·2026

Related Experiment Videos

[Editorial: Prenatal diagnosis of hereditary diseases]

Related Concept Videos

5-Aminolevulinic acid-based photodynamic therapy. Clinical research and future challenges.

Use of 5-aminolevulinic acid esters to improve photodynamic therapy on cells in culture.

Effects of MnDPDP, DPDP--, and MnCl2 on cardiac energy metabolism and manganese accumulation. An experimental study in the isolated perfused rat heart.

Increased levels of intercellular adhesion molecules and vascular cell adhesion molecules in pre-eclampsia.

Molecular genetics of familial hypercholesterolaemia in Norway.

[Craniosynostosis operations in childhood].

Perspectives on the use of coercion in highly specialised rehabilitation: a focus group study.

Occupational injuries treated at Oslo A&E - a prospective study.

Cross-reactivity in cashew nut allergy.

AGG repeat expansion and aggregation of BIN1 in multiple system atrophy.

[Optical genome mapping analysis of a Chinese pedigree with a complex balanced translocation involving four chromosomes].

[Pathogenicity analysis and prenatal genetic counseling for five Chinese pedigrees harboring a hemizygous c.-32C>G variant of FGF13 gene].

Interim analysis of an international multi-site prospective natural history study evaluating the clinical presentation and progression of Leigh syndrome spectrum disorders.

Systematic genotype-phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22-q23 deletions.

Autism mutations rewire protein interaction networks to drive neurodevelopmental pathology.

Related Experiment Videos

[Editorial: Prenatal diagnosis of hereditary diseases]

Related Concept Videos

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