Genetic diagnosis and treatment. Ethical considerations

Monitoring a clinical trial conducted under the Food and Drug Administration regulations allowing a waiver of prospective informed consent: the diaspirin cross-linked hemoglobin traumatic hemorrhagic shock efficacy trial.

Annals of emergency medicine·2001

Education about genetic testing for breast cancer susceptibility: patient preferences for a computer program or genetic counselor.

American journal of medical genetics·2001

An interactive computer program can effectively educate patients about genetic testing for breast cancer susceptibility.

American journal of medical genetics·2001

Ethical issues in research and innovative therapy in children with mood disorders.

Biological psychiatry·2001

Cystic fibrosis newborn screening: impact on reproductive behavior and implications for genetic counseling.

Pediatrics·1998

Ethical dilemmas in medical innovation and research: distinguishing experimentation from practice.

Seminars in perinatology·1998

Applicability of the Greulich and Pyle skeletal age standards to black and white children of today.

American journal of diseases of children (1960)·1993

Maltreatment of children born to cocaine-dependent mothers.

American journal of diseases of children (1960)·1993

Adrenal tumor complicating untreated 21-hydroxylase deficiency in a 5 1/2-year-old boy.

American journal of diseases of children (1960)·1993

Passive-active immunization in infants of hepatitis Be antigen-positive mothers. Comparison of the efficacy of early and delayed active immunization.

American journal of diseases of children (1960)·1993

Effects of methylphenidate on sleep in children with attention-deficient hyperactivity disorder. An activity monitor study.

American journal of diseases of children (1960)·1993

Autosomal recessive microcephaly, microcornea, congenital cataract, mental retardation, optic atrophy, and hypogenitalism. Micro syndrome.

American journal of diseases of children (1960)·1993

Genome sequencing reveals high diagnostic yield in children with severe sporadic developmental language disorder.

European journal of human genetics : EJHG·2026

Genetic Etiology and Neurodevelopmental Outcomes in Children With Craniosynostosis: A 15-Year Single-Center Retrospective Study.

The Journal of craniofacial surgery·2026

Population-Level Nucleotide Diversity and Genetic Differentiation at SOD1 Across Global Human Populations.

Annals of human genetics·2026

Gerstmann-Straussler-Scheinker Disease With F198S Mutation Diagnosis on Repeat Genetic Testing: A Case Report.

Cureus·2026

Update and recommendations on genetic testing for amyotrophic lateral sclerosis in clinical practice: a Brazilian expert view.

Frontiers in neurology·2026

Characterisation of the Novel HLA-DRB1*10:52 Allele by Next-Generation Sequencing and Oxford Nanopore Sequencing.

HLA·2026

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Genetic diagnosis and treatment. Ethical considerations

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Monitoring a clinical trial conducted under the Food and Drug Administration regulations allowing a waiver of prospective informed consent: the diaspirin cross-linked hemoglobin traumatic hemorrhagic shock efficacy trial.

Education about genetic testing for breast cancer susceptibility: patient preferences for a computer program or genetic counselor.

An interactive computer program can effectively educate patients about genetic testing for breast cancer susceptibility.

Ethical issues in research and innovative therapy in children with mood disorders.

Cystic fibrosis newborn screening: impact on reproductive behavior and implications for genetic counseling.

Ethical dilemmas in medical innovation and research: distinguishing experimentation from practice.

Applicability of the Greulich and Pyle skeletal age standards to black and white children of today.

Maltreatment of children born to cocaine-dependent mothers.

Adrenal tumor complicating untreated 21-hydroxylase deficiency in a 5 1/2-year-old boy.

Passive-active immunization in infants of hepatitis Be antigen-positive mothers. Comparison of the efficacy of early and delayed active immunization.

Effects of methylphenidate on sleep in children with attention-deficient hyperactivity disorder. An activity monitor study.

Autosomal recessive microcephaly, microcornea, congenital cataract, mental retardation, optic atrophy, and hypogenitalism. Micro syndrome.

Genome sequencing reveals high diagnostic yield in children with severe sporadic developmental language disorder.

Genetic Etiology and Neurodevelopmental Outcomes in Children With Craniosynostosis: A 15-Year Single-Center Retrospective Study.

Population-Level Nucleotide Diversity and Genetic Differentiation at SOD1 Across Global Human Populations.

Gerstmann-Straussler-Scheinker Disease With F198S Mutation Diagnosis on Repeat Genetic Testing: A Case Report.

Update and recommendations on genetic testing for amyotrophic lateral sclerosis in clinical practice: a Brazilian expert view.

Characterisation of the Novel HLA-DRB1*10:52 Allele by Next-Generation Sequencing and Oxford Nanopore Sequencing.

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Genetic diagnosis and treatment. Ethical considerations

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