Found: 11
Select item for more details and to access through your institution.
CACNA1I gain-of-function mutations differentially affect channel gating and cause neurodevelopmental disorders.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Cytomegalovirus and human herpesvirus 8 DNA detection in peripheral blood monocytic cells of AIDS patients: Correlations with the presence of Kaposi's sarcoma and CMV diseaseAntoinette C. van der Kuyl and Abeltje M. Polstra have contributed equally to this work.
- Published in:
- Journal of Medical Virology, 2005, v. 76, n. 4, p. 541
- By:
- Publication type:
- Article
Retrospective, longitudinal analysis of serum human herpesvirus?8 viral DNA load in AIDS?related kaposi's sarcoma patients before and after diagnosis.
- Published in:
- Journal of Medical Virology, 2004, v. 74, n. 3, p. 390
- By:
- Publication type:
- Article
Latent and lytic HHV-8 mRNA expression in PBMCs and Kaposi's sarcoma skin biopsies of AIDS Kaposi's sarcoma patients.
- Published in:
- Journal of Medical Virology, 2003, v. 70, n. 4, p. 624
- By:
- Publication type:
- Article
5q11.2 deletion syndrome revisited—Further narrowing of the smallest region of overlap for the main clinical characteristics of the syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2021, v. 185, n. 12, p. 3844, doi. 10.1002/ajmg.a.62428
- By:
- Publication type:
- Article
Dynamics of Cytomegalovirus (CMV)--Specific T Cells in HIV-1--Infected Individuals Progressing to AIDS with CMV End-Organ Disease.
- Published in:
- Journal of Infectious Diseases, 2005, v. 191, n. 6, p. 873, doi. 10.1086/427828
- By:
- Publication type:
- Article
Development of real-time NASBA assays with molecular beacon detection to quantify mRNA coding for HHV-8 lytic and latent genes.
- Published in:
- BMC Infectious Diseases, 2002, v. 2, n. 1, p. 18, doi. 10.1186/1471-2334-2-18
- By:
- Publication type:
- Article
Loss-of-function variants in myocardin cause congenital megabladder in humans and mice.
- Published in:
- 2019
- By:
- Publication type:
- journal article
upd(20)mat is a rare cause of the Silver‐Russell‐syndrome‐like phenotype: Two unrelated cases and screening of large cohorts.
- Published in:
- Clinical Genetics, 2020, v. 97, n. 6, p. 902, doi. 10.1111/cge.13727
- By:
- Publication type:
- Article
Capecitabine-based treatment of a patient with a novel DPYD genotype and complete dihydropyrimidine dehydrogenase deficiency.
- Published in:
- International Journal of Cancer, 2018, v. 142, n. 2, p. 424, doi. 10.1002/ijc.31065
- By:
- Publication type:
- Article
Multicentric Castleman's disease and Kaposi's sarcoma in a cyclosporin treated, HIV-1 negative patient: case report.
- Published in:
- BMC Blood Disorders, 2003, v. 3, p. 3
- By:
- Publication type:
- Article