Suchergebnisse - "Archer NM"

Multi-centric origins and gene flow shape the diversity of β-thalassemia mutations in Southern East Asia.

Autoren: Zhang, Qianqian Li, Jialong Huang, Haoyang et al.

Quelle: Nature Communications; 11/20/2025, Vol. 16 Issue 1, p1-14, 14p

Schlagwörter: BETA-Thalassemia, GENE flow, GENETIC mutation, SOUTHEAST Asians, HAPLOTYPES, CLADISTIC analysis, POPULATION differentiation

Geografische Kategorien: CHINA, HAINAN Sheng (China), SOUTHEAST Asia

Safety and efficacy of ketamine use in patients with vaso‐occlusive crisis: A systematic review and meta‐analysis.

Autoren: Calderon Martinez, Ernesto Zachariah Saji, Stephin Campos Carmona, Thomas et al.

Quelle: EJHaem; Dec2024, Vol. 5 Issue 6, p1312-1321, 10p

Association between mean corpuscular hemoglobin concentration and mortality in ICU patients with acute kidney injury: a retrospective multicenter cohort study.

Autoren: Chen, Sheng Ye, Xuejin Guo, Lin et al.

Quelle: European Journal of Medical Research; 9/29/2025, Vol. 30 Issue 1, p1-15, 15p

Schlagwörter: MORTALITY, ACUTE kidney failure, SURVIVAL analysis (Biometry), AT-risk people, COHORT analysis, INTENSIVE care patients, RETROSPECTIVE studies

Burden of hemoglobinopathies and hemolytic anemias in the World Health Organization African region, 2000–2021: Findings from the Global Burden of Disease 2021 study.

Autoren: Ojo, Temitope T Amegbor, Prince M Islam, Farha et al.

Quelle: PLoS Global Public Health; 9/22/2025, Vol. 5 Issue 9, p1-31, 31p

Diabetes and metabolic syndrome in adults with malaria and associations with severe disease: results from two tertiary hospitals in Cameroon.

Autoren: Awungafac, George Njonnou, Sylvain Raoul Simeni Noubom, Michel et al.

Quelle: BMC Infectious Diseases; 8/22/2025, Vol. 25 Issue 1, p1-12, 12p

Schlagwörter: DIABETES, METABOLIC syndrome, SUB-Saharan Africans, ACUTE diseases, MALARIA, CHRONIC diseases, OBESITY

Geografische Kategorien: AFRICA, CAMEROON

Fetal hemoglobin enables malaria parasite growth in sickle cells but augments production of transmission stage parasites.

Autoren: Lavazec, Catherine Loucoubar, Cheikh Dupuy, Florian et al.

Quelle: PLoS ONE; 7/8/2025, Vol. 20 Issue 7, p1-14, 14p

Schlagwörter: SICKLE cell trait, FETAL hemoglobin, LOCUS (Genetics), SICKLE cell anemia, ERYTHROCYTES

Variability in the Recommendations for Management of Vaso-occlusive Crisis and Acute Chest Syndrome in Sickle Cell Disease: Review of Institutional Algorithms of Pediatric Hospitals Across the United States.

Autoren: Elgehiny, Amr Quraishi, Mariam Z. Yadav, Aravind et al.

Quelle: Journal of Pediatric Hematology/Oncology; Jul2025, Vol. 47 Issue 5, pe155-e160, 6p

Assessing germline TP53 mutations in cancer patients: insights into Li-Fraumeni syndrome and genetic testing guidelines.

Autoren: Danishevich, Anastasiia Fedorova, Daria Bodunova, Natalia et al.

Quelle: Hereditary Cancer in Clinical Practice; 2/17/2025, Vol. 23 Issue 1, p1-13, 13p

Schlagwörter: WHOLE genome sequencing, MEDICAL sciences, HEREDITARY cancer syndromes, LI-Fraumeni syndrome, GENETIC testing

Findings supporting neonatal screening for sickle cell disease: an observational study in Senegal.

Autoren: Petigas, Lucie Seck, Ndiogou Doupa, Dominique et al.

Quelle: Frontiers in Pediatrics; 2025, p1-10, 10p

Malaria infection confounds inflammation-adjusted micronutrient biomarker concentrations in children and women in Malawi: a secondary analysis of the 2015/2016 Malawi micronutrient survey.

Autoren: Sandalinas, Fanny Joy, Edward J. M. Hopkins, Heidi et al.

Quelle: British Journal of Nutrition; 5/14/2025, Vol. 133 Issue 9, p1276-1286, 11p

Schlagwörter: SECONDARY analysis, FERRITIN, TRANSFERRIN, MALARIA, FOLIC acid, MULTIPLE regression analysis, MICRONUTRIENTS, CHILD nutrition, RAPID diagnostic tests, ZINC, HEMOGLOBINOPATHY, DESCRIPTIVE statistics, NUTRITIONAL status, INFLAMMATION, WOMEN'S health, CONFIDENCE intervals, BIOMARKERS, SICKLE cell trait, CHILDREN

Geografische Kategorien: MALAWI

Diagnosis and management of intraparenchymal rhabdomyosarcoma.

Autoren: Lannon, Melissa Al-Sajee, Dhuha Bourgeois, Jacqueline et al.

Quelle: British Journal of Neurosurgery; Apr2025, Vol. 39 Issue 2, p232-239, 8p

Schlagwörter: RHABDOMYOSARCOMA, DIAGNOSIS, PATHOGENESIS, TUMORS, CRANIAL nerves

"I was very scared when I found out my son had sickle cell": Caregiver knowledge and attitudes toward early intervention for young children with sickle cell disease: Implications for policy and practice from a multi‐site study.

Autoren: Hoyt, Catherine R. MacArthur, Erin Leaver, Hayes et al.

Quelle: Pediatric Blood & Cancer; Nov2024, Vol. 71 Issue 11, p1-8, 8p

TP53 germline pathogenic variant frequency in anaplastic rhabdomyosarcoma: A Children's Oncology Group report.

Autoren: Fair, Douglas Maese, Luke Chi, Yueh‐Yun et al.

Quelle: Pediatric Blood & Cancer; Sep2023, Vol. 70 Issue 9, p1-4, 4p

Newborn screening for sickle cell disease in Caluquembe, southwestern Angola, 2024–2025.

Autoren: Su, Jasmine J. Kupua, Vasco S. Cummings, Daniel et al.

Quelle: PLoS ONE; 10/30/2025, Vol. 20 Issue 10, p1-8, 8p

Schlagwörter: NEWBORN screening, SICKLE cell anemia, COUNTRIES, PUBLIC health, EPIDEMIOLOGY, RURAL health, POINT-of-care testing

Geografische Kategorien: ANGOLA

Cytolytic circumsporozoite-specific memory CD4⁺ T cell clones are expanded during Plasmodium falciparum infection.

Autoren: Furtado, Raquel Paul, Mahinder Zhang, Jinghang et al.

Quelle: Nature Communications; 11/25/2023, Vol. 14 Issue 1, p1-20, 20p

Schlagwörter: IMMUNOLOGIC memory, T cells, PLASMODIUM falciparum, T helper cells, HUMORAL immunity, CIRCUMSPOROZOITE protein, TH1 cells, T cell receptors

Geografische Kategorien: MALAWI

Assessment of cancer predisposition syndromes in children with leukemia and solid tumors: germline-genomic profiling and clinical features in a series of cases.

Autoren: Singh, Minu Bhatia, Prateek Sharma, Pankaj et al.

Quelle: Pediatric Hematology & Oncology; Nov2024, Vol. 41 Issue 8, p620-632, 13p

Schlagwörter: CANCER patients, GENETIC counseling, FAMILY counseling, GENETIC disorders, CHILDHOOD cancer

Perinatal risk factors and neurocognitive outcomes in children and adolescents with sickle cell disease.

Autoren: Longoria, Jennifer N. Dandar, Christina M. Semko, Joshua H. et al.

Quelle: Pediatric Blood & Cancer; Oct2024, Vol. 71 Issue 10, p1-9, 9p

Adaptive assessment based on fractional CBCT images for cervical cancer.

Autoren: Chang, Yankui Liang, Yongguang Wu, Haotian et al.

Quelle: Journal of Applied Clinical Medical Physics; Oct2024, Vol. 25 Issue 10, p1-12, 12p

Schlagwörter: CONE beam computed tomography, IMAGE registration, ARTISTIC creation, ARTIFICIAL intelligence, CERVICAL cancer, DEEP learning

Potential for a large‐scale newborn screening strategy for sickle cell disease in Mali: A comparative diagnostic performance study of two rapid diagnostic tests (SickleScan® and HemotypeSC®) on cord blood.

Autoren: Guindo, Aldiouma Cisse, Zenab Keita, Ibrahima et al.

Quelle: British Journal of Haematology; Jan2024, Vol. 204 Issue 1, p337-345, 9p

Schlagwörter: RAPID diagnostic tests, SICKLE cell anemia, NEWBORN screening, CORD blood, HIGH performance liquid chromatography

Geografische Kategorien: MALI

Human genetic variations conferring resistance to malaria.

Autoren: Zhang, Xiaokun Wu, Jie Peng, Yunxing et al.

Quelle: Journal of Translational Medicine; 9/24/2025, Vol. 23 Issue 1, p1-25, 25p

Schlagwörter: MALARIA, GENETIC variation, HEMOGLOBINOPATHY, NATURAL immunity, SICKLE cell trait, THALASSEMIA, IMMUNOREGULATION, EPIDEMIOLOGY