The ethical implications of the Human Genome Project for the workplace

Patient-provider communication in nephrology care for adolescents and young adults.

Patient education and counseling·2017

Towards coronary plaque imaging using simultaneous PET-MR: a simulation study.

Physics in medicine and biology·2014

Benefits of a self-management program in low-income African-American women with systemic lupus erythematosus: results of a pilot test.

Lupus·2012

The prognostic value of C-reactive protein in long-term care patients requiring prolonged mechanical ventilation.

Chronic respiratory disease·2009

Hepatitis C virus (HCV) prevalence, and injecting risk behaviour in multiple sites in England in 2004.

Journal of viral hepatitis·2007

Malignant lymphoepithelial lesion of the parotid gland: a case report and review of the literature.

Ear, nose, & throat journal·2002

A Philosophical Concept of Deprivation and Its Use in the Attachment-Focused Treatment of Violence.

The International journal of applied philosophy·2015

The research misconception.

The International journal of applied philosophy·2006

Biocentric ethics and animal prosperity.

The International journal of applied philosophy·2005

Facing immortality.

The International journal of applied philosophy·2005

Earning points for moral behavior: organ allocation based on reciprocity.

The International journal of applied philosophy·2005

Lower income Hindu women's attitude towards abortion: a case study in urban India.

The International journal of applied philosophy·2004

[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

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Benefits of a self-management program in low-income African-American women with systemic lupus erythematosus: results of a pilot test.

The prognostic value of C-reactive protein in long-term care patients requiring prolonged mechanical ventilation.

Hepatitis C virus (HCV) prevalence, and injecting risk behaviour in multiple sites in England in 2004.

Malignant lymphoepithelial lesion of the parotid gland: a case report and review of the literature.

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Lower income Hindu women's attitude towards abortion: a case study in urban India.

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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.

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