Leishmaniasis
What's New
Last Posted: Feb 06, 2024
- Cytokines signatures and susceptibility to cutaneous leishmaniasis in patients from Sistan and Baluchestan province of Iran.
Saeideh Jahanshahi, et al. Gene 2024 0 148224 - Automated Identification of Cutaneous Leishmaniasis Lesions Using Deep-Learning-Based Artificial Intelligence.
José Fabrício de Carvalho Leal et al. Biomedicines 2024 12(1) - Assessment of Deep Learning Models for Cutaneous Leishmania Parasite Diagnosis Using Microscopic Images.
Ali Mansour Abdelmula et al. Diagnostics (Basel) 2024 14(1) - The Association of Human Leucocyte Antigen (HLA) Class I and II Genes with Cutaneous and Visceral Leishmaniasis in Iranian Patients: A Preliminary Case-Control Study.
Mitra Eimanzadeh, et al. Iranian journal of parasitology 2023 0 (2) 155-164 - Vitamin D status, vitamin D receptor gene polymorphism, and haplotype in patients with cutaneous leishmaniasis: Correlation with susceptibility and parasite load index.
Doaa A Salem, et al. PLoS neglected tropical diseases 2023 0 (6) e0011393 - Variants of CARD8 in Leishmania guyanensis-cutaneous leishmaniasis and influence of the variants genotypes on circulating plasma cytokines IL-1?, TNF? and IL-8.
Héctor David Graterol Sequera, et al. PLoS neglected tropical diseases 2023 0 (6) e0011416 - Variants of NOD2 in Leishmania guyanensis-infected patients with cutaneous leishmaniasis and correlations with plasma circulating pro-inflammatory cytokines.
Mesquita Tirza Gabrielle Ramos de, et al. PloS one 2023 0 (2) e0281814 - Relationship between pemphigus and American tegumentary leishmaniasis: insights from serological and genetic profiles.
Walsh Priscilla, et al. Transactions of the Royal Society of Tropical Medicine and Hygiene 2017 0 (8) 345-353 - The NOD2 receptor is crucial for immune responses towards New World Leishmania species.
Dos Santos Jéssica Cristina, et al. Scientific reports 2017 0 (1) 15219 - HLA-DR Class II expression on myeloid and lymphoid cells in relation to HLA-DRB1 as a genetic risk factor for visceral leishmaniasis.
Singh Bhawana, et al. Immunology 2018 0 (2) 174-186
More
About Rare Diseases PHGKB
Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 19, 2024
- Content source: