[Genetic diagnosis and insurance law--4 theses]

A template for broad consent in biobank research. Results and explanation of an evidence and consensus-based development process.

European journal of medical genetics·2016

The necessity of broad consent and complementary regulations for the protection of personal data in biobanks: what can we learn from the German case?

Public health genomics·2012

[Ethical and legal aspects of including patients unable to consent in acute therapy studies. Example of a medication study for the treatment of intracerebral hemorrhage--the Heidelberg procedure].

Deutsche medizinische Wochenschrift (1946)·2008

[The right not to know, in the German legislation (Part I)].

Revista de derecho y genoma humano = Law and the human genome review·2005

The conflict of understanding the genetic make-up of man and his knowledge of it.

Forensic science international·2000

[What do company health insurance plans provide?]

Versicherungsmedizin·2017

[Assessment of prescriptive therapies and remedies - Experience and results].

Versicherungsmedizin·2017

[The importance of biosimilars medicines for private and statutory health insurance].

Versicherungsmedizin·2017

[Can we transfer the mechanisms of the generics market to biosimilars?]

Versicherungsmedizin·2017

[Potential for intervention of private health insurers in discharge management using the example of stroke patients].

Versicherungsmedizin·2016

[Quantified self movement--the new mantra of life insurance companies].

Versicherungsmedizin·2016

[Autism - Phenotypic variability].

Medicina·2026

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

Neurogenetics·2026

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Neural plasticity·2026

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

Frontiers in genetics·2026

Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss.

International journal of general medicine·2026

Biallelic VPS41 Variants in Autosomal Recessive Spinocerebellar Ataxia 29 Resolved by Long-Read Sequencing and RNA Analysis.

Molecular genetics & genomic medicine·2026

Related Experiment Videos

[Genetic diagnosis and insurance law--4 theses]

Related Concept Videos

A template for broad consent in biobank research. Results and explanation of an evidence and consensus-based development process.

The necessity of broad consent and complementary regulations for the protection of personal data in biobanks: what can we learn from the German case?

[Ethical and legal aspects of including patients unable to consent in acute therapy studies. Example of a medication study for the treatment of intracerebral hemorrhage--the Heidelberg procedure].

[The right not to know, in the German legislation (Part I)].

The conflict of understanding the genetic make-up of man and his knowledge of it.

[What do company health insurance plans provide?]

[Assessment of prescriptive therapies and remedies - Experience and results].

[The importance of biosimilars medicines for private and statutory health insurance].

[Can we transfer the mechanisms of the generics market to biosimilars?]

[Potential for intervention of private health insurers in discharge management using the example of stroke patients].

[Quantified self movement--the new mantra of life insurance companies].

[Autism - Phenotypic variability].

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss.

Biallelic VPS41 Variants in Autosomal Recessive Spinocerebellar Ataxia 29 Resolved by Long-Read Sequencing and RNA Analysis.

Related Experiment Videos

[Genetic diagnosis and insurance law--4 theses]

Related Concept Videos

Related Articles