Nedra Whitehead

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DMD gene and dystrophinopathy phenotypes associated with mutations: A systematic review for clinicians

Sources of variation in estimates of Duchenne and Becker muscular dystrophy prevalence in the United States

Role attainment in emerging adulthood: Subjective evaluation by male adolescents and adults with Duchenne and Becker muscular dystrophy

Health profile of preterm males with duchenne muscular dystrophy

Association of genetic mutations and loss of ambulation in childhood-onset dystrophinopathy

Recurrent thrombosis in patients with antiphospholipid antibodies and an initial venous or arterial thromboembolic event: A systematic review and meta-analysis

From clinical phenotype to genotypic modelling: Incidence and prevalence of recessive dystrophic epidermolysis bullosa (RDEB)

Interventions to prevent iatrogenic anemia: A laboratory medicine best practices systematic review

From clinical to genotypic modeling: Recessive Dystrophic Epidermolysis Bullosa (RDEB)

The effect of laboratory test-based clinical decision support tools on medication errors and adverse drug events: A laboratory medicine best practices systematic review

Estimated prevalence of aromatic l-amino acid decarboxylase (AADC) deficiency in the United States, European Union, and Japan

The effect of steroid treatment on weight in nonambulatory males with Duchenne muscular dystrophy

Recurrent thrombosis in patients with antiphospholipid antibodies following an initial venous or arterial thromboembolic event

Interventions to improve follow-up of laboratory test results pending at discharge: A systematic review

Completeness of prenatal records in community hospital charts

A Framework for One Health Research

Genetic contributions to urgency urinary incontinence in women

Urgency Urinary Incontinence Genome Wide Association Study

Prenatal Counseling on Seat Belt Use and Crash-Related Medical Care

PhenX—Establishing a consensus process to select common measures for collaborative research