This chapter advances SDGs 3 and 10 by proposing that patient confrontation of physician bias may serve as a self-advocacy tool that reduces physician bias and improves quality of patient care.
Tay–Sachs disease is an inherited lysosomal storage disease resulting from mutations in the lysosomal enzyme, β-hexosaminidase A, and leads to excessive accumulation of GM2 ganglioside.
Elsevier,

Free Radical Biology and Medicine, Volume 133, March 2019

The heme biosynthetic pathway in erythroid cells.
Sideroblastic anemia (SA) is characterized by bone marrow ring sideoblasts (RSs). RS reflect abnormal iron accumulation in the mitochondria of erythroblasts. Congenital SA is caused by the mutation of genes involved in iron-heme metabolism. The most frequent form of congenital SA is X-linked SA due to ALAS2 gene mutation.
Illustration of process for haplotype-specific reporter construct derivation.
This Article supports SDG 3 by analysing data from four international cohorts of patients with pulmonary arterial hypertension, a disease caused by rare genetic variants.
Elsevier,

Global Mental Health and Psychotherapy, Adapting Psychotherapy for Low- and Middle-Income Countries, Global Mental Health in Practice, 2019, Pages 87-126

This chapter addresses Goal 3 by exploring the use of cognitive behavioral therapy to treat mental health needs in low and middle income countries.
It has been estimated that European customers visit community pharmacies to access essential primary healthcare around 46 million times every day.

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