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Comparative Biological and Clinical Outcomes after a Switch from a …
… patients in whom a first protease inhibitor–containing cART regimen failed to
control viral replication and whose treatment was switched to cART containing efavirenz,
nevirapine, or abacavir, we studied 1440 patients … 
Volume 43, number S4: Pharmacokinetic Interactions between Buprenorphine and Antiretroviral …
… patients and physicians from initiating potentially lifesaving therapy or lead to
complications among patients whose treatment is already under way. Complications
include nonadherence to antiretroviral therapy and the development of …
Volume 43, number S4: Overcoming Policy and Financing Barriers to …
… patients with opioid dependence …
Volume 43, number S4: Buprenorphine and HIV Primary Care: Report …
… patients; for improving programs and services, including integration of opioid
dependence and HIV infection into chronic disease models, providing flexible access to
core and support services, and monitoring and evaluation …
Volume 43, number S4: Opioid Dependence: Rationale for and Efficacy …
… patients with HIV infection …
Volume 43, number S4: A Trial of Integrated Buprenorphine/Naloxone and …
… patients. Buprenorphine, a partial opioid agonist, is available for maintenance
treatment of opioid dependence in HIV specialty settings. We investigated the feasibility
and efficacy of integrating buprenorphine, along with 2 …
Volume 43, number S4: Initial Strategies for Integrating Buprenorphine into …
… patients with both disorders. Buprenorphine, a recently approved medication for
the treatment of opioid dependence in physicians’ offices, provides the opportunity to
integrate the treatment of HIV infection and substance …
The Meckel-Gruber Syndrome Gene, MKS3, Is Mutated in Joubert Syndrome
… patients with a mild form of cerebellar and brainstem anomaly. Occipital
encephalocele and/or polydactyly have occasionally been reported in some patients
with JS, and these phenotypic features can also be …
Infantile Encephalopathy and Defective Mitochondrial DNA Translation in Patients with …
… patients with defective mitochondrial translation led us to the discovery of
novel mutations in the mitochondrial elongation factor G1 (EFG1) in one affected baby and,
for the first time, in …
Identification of a Novel BBS Gene (BBS12) Highlights the Major …
… Patients from two Gypsy families were homozygous and haploidentical in a 6-Mb
region of chromosome 4q27. FLJ35630 was selected as a candidate gene, because it was
predicted to encode a …