Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 30 (of 218 Records) |
Query Trace: Sickle Cell Anemia[original query] |
---|
Analysis of clinical presentation, hematological factors, self-reported bed net usage, and malaria burden in sickle cell disease patients. EClinicalMedicine 2021 8 39 101045. Harp Keri Oxendine, Botchway Felix, Dei-Adomakoh Yvonne, Wilson Michael D, Mubasher Mohamed, Adjei Andrew A, Thompson Winston E, Stiles Jonathan K, Driss Ad |
Vitamin D level, lipid profile, and vitamin D receptor and transporter gene variants in sickle cell disease patients from Kurdistan of Iraq. Journal of clinical laboratory analysis 2021 7 35 (9): e23908. Hama Abdalla Hussein, Shakiba Ebrahim, Rahimi Zohreh, Karimi Mehran, Mozafari Hadi, Abdulkarim Omed Adn |
Genotypic Diversity among Angolan Children with Sickle Cell Anemia. International journal of environmental research and public health 2021 6 18 (10): . Delgadinho Mariana, Ginete Catarina, Santos Brígida, Miranda Armandina, Brito Migu |
Association of KLOTHO polymorphisms with clinical complications of sickle cell anemia. Annals of hematology 2021 Jun . Batista Jéssica V G F, Pereira-Martins Diego A, Falcão Diego A, Domingos Igor F, Arcanjo Gabriela S, Hatzlhofer Betânia L, Weinhäuser Isabel, Batista Thais H C, Cardoso Pablo R G, Dos Anjos Ana C, Hazin Manuela F, Pitta Maira G R, Costa Fernando F, Araujo Aderson S, Lucena-Araujo Antonio R, Bezerra Marcos |
Co-Inheritance of ?-thalassemia gene mutation in patients with sickle cell Disease: Impact on clinical and hematological variables. Nigerian journal of clinical practice 2021 6 24 (6): 874-882. Ali Al-Barazanchi Z A, Abdulateef S S, Hassan Meaad Kadh |
Association of alpha-thalassemia and Glucose-6-Phosphate Dehydrogenase deficiency with transcranial Doppler ultrasonography in Nigerian children with sickle cell anemia. Journal of clinical laboratory analysis 2021 5 35 (6): e23802. Ojewunmi Oyesola Oyewole, Adeyemo Titilope Adenike, Oyetunji Ajoke Idayat, Benn Yewande, Ekpo Mfoniso Godwin, Iwalokun Bamidele Abiod |
Sickle Cell Disease in Jordan: The Experience of a Major Referral Center. Medical archives (Sarajevo, Bosnia and Herzegovina) 2021 5 75 (1): 27-30. Oudat Raida I, Abualruz Heba S, Al-Shiek Nazih Kh Abu, Al-Mashaqba Eman A, Al-Hiari Rawan A, Alsoukhni Hala A, Hammad Ma'mon A A |
Oral microbiota analyses of Saudi sickle cell anemics with dental caries. International dental journal 2022 9 73 (1): 144-150. Alyousef Yousef M, Alonaizan Faisal A, Alsulaiman Ahmed A, Aldarwish Mohammed I, Alali Ali A, Almasood Naif N, Vatte Chittibabu, Cyrus Cyril, Habara Alawi H, Koeleman Bobby P |
Fetal hemoglobin-boosting haplotypes of BCL11A gene and HBS1L-MYB intergenic region in the prediction of clinical and hematological outcomes in a cohort of children with sickle cell anemia. Journal of human genetics 2022 9 67 (12): 701-709. Sales Rahyssa Rodrigues, Nogueira Bárbara Lisboa, Belisário André Rolim, Faria Gabriela, Mendes Fabiola, Viana Marcos Borato, Luizon Marcelo Rizzat |
Fetal hemoglobin regulating genetic variants identified in homozygous (HbSS) and heterozygous (HbSA) subjects from South Mexico. Journal of tropical pediatrics 2022 9 68 (5): . Rizo-de la Torre L C, Borrayo-López F J, Perea-Díaz F J, Aquino E, Venegas M, Hernández-Carbajal C, Espinoza-Mata L L, Ibarra-Cortés |
Genetic modulation of anemia severity, hemolysis level, and hospitalization rate in Angolan children with Sickle Cell Anemia. Molecular biology reports 2022 Sep . Germano Isabel, Santos Brígida, Delgadinho Mariana, Ginete Catarina, Lopes Pedro, Arez Ana Paula, Brito Miguel, Faustino Pau |
Genetic counseling and carrier screening in candidates for gamete donation at a Portuguese center. JBRA assisted reproduction 2022 8 . Soares Célia Azevedo, Tkachenko Natália, Vale-Fernandes Emídio, Barreiro Márcia, Abreu Maria, Reis Cláudia Falcão, Soares Gabriela, Fortuna Ana Maria, Soares Ana Ri |
Transcranial doppler as screening method for sickling crises in children with sickle cell anemia: a latin America cohort study. BMC pediatrics 2022 Jun 22 (1): 368. Modolo Gabriel Pinheiro, Luvizutto Gustavo José, Hamamoto Filho Pedro Tadao, Braga Gabriel Pereira, Bazan Silmeia Garcia Zanati, Ferreira Natalia Cristina, de Souza Juli Thomaz, Winckler Fernanda Cristina, Macedo de Freitas Carlos Clayton, Hokama Newton Key, Vidal Edison Iglesias de Oliveira, Bazan Rodri |
Effects of Senegal haplotype (Xmn1-rs7412844), alpha-thalassemia (3.7kb HBA1/HBA2 deletion), NPRL3-rs11248850 and BCL11A-rs4671393 variants on sickle cell nephropathy. International journal of biochemistry and molecular biology 2022 5 13 (2): 5-16. Ndour El Hadji Malick, Mnika Khuthala, Guèye Tall Fatou, Seck Moussa, Dème Ly Indou, Nembaware Victoria, Sagna-Bassène Hélène Ange Thérèse, Dione Rokhaya, Ndongo Aliou Abdoulaye, Diop Jean Pascal Demba, Barry Nènè Oumou Kesso, Djité Moustapha, Ndiaye Diallo Rokhaya, Guèye Papa Madièye, Diop Saliou, Diagne Ibrahima, Cissé Aynina, Wonkam Ambroise, Lopez Sall Philomè |
Molecular Analysis of Xmn1-Polymorphic Site ´5 to G? of the ?-Globin Gene Cluster in a Saudi Population of Jazan Region in Correlation with Hb F Expression. Evidence-based complementary and alternative medicine : eCAM 2022 3 2022 1717207. Elderdery Abozer Y, Alsrhani Abdullah, Alzahrani Badr, Atif Muhammad, Refaiy Ahmed I, Shiwani Hussain, Abbas Amin, Yahia Dawelbiet |
Fetal hemoglobin modulates neurocognitive performance in sickle cell anemia. Current research in translational medicine 2022 3 70 (3): 103335. Heitzer Andrew M, Longoria Jennifer, Rampersaud Evadnie, Rashkin Sara R, Estepp Jeremie H, Okhomina Victoria I, Wang Winfred C, Raches Darcy, Potter Brian, Steinberg Martin H, King Allison A, Kang Guolian, Hankins Jane |
Relation between haptoglobin polymorphism and oxidative stress status, lipid profile, and cardiovascular risk in sickle cell anemia patients. Health science reports 2022 3 5 (1): e465. Kengne Fotsing Christian Bernard, Pieme Constant Anatole, Biapa Nya Prosper Cabral, Chedjou Jean Paul, Dabou Solange, Nguemeni Carine, Teto Georges, Mbacham Wilfred Fon, Gatsing Donati |
Do Genetic Polymorphisms Affect Fetal Hemoglobin (HbF) Levels in Patients With Sickle Cell Anemia Treated With Hydroxyurea? A Systematic Review and Pathway Analysis. Frontiers in pharmacology 2021 12 779497. Sales Rahyssa Rodrigues, Nogueira Bárbara Lisboa, Tosatti Jéssica Abdo Gonçalves, Gomes Karina Braga, Luizon Marcelo Rizzat |
Biomarkers of sickle cell nephropathy in Senegal. PloS one 2022 11 17 (11): e0273745. Ndour El Hadji Malick, Mnika Khuthala, Tall Fatou Guèye, Seck Moussa, Ly Indou Dème, Nembaware Victoria, Mazandu Gaston Kuzamunu, Sagna Bassène Hélène Ange Thérèse, Dione Rokhaya, Ndongo Aliou Abdoulaye, Diop Jean Pascal Demba, Barry Nènè Oumou Kesso, Djité Moustapha, Ndiaye Diallo Rokhaya, Guèye Papa Madièye, Diop Saliou, Diagne Ibrahima, Cissé Aynina, Wonkam Ambroise, Lopez Sall Philomè |
Molecular Detection of Hemoglobin O-Arab in the Sudanese Population. International journal of general medicine 2023 8 16 3323-3330. Izzeldin Elbashir, Tagwa Yousif Elsayed Yous |
Plasminogen activator inhibitor-2 and impaired fibrinolysis in pregnancy and sickle cell anemia. Archives of gynecology and obstetrics 2023 7 . Durjoy Shome, Lamiaa Al-Jamea, Alexander Woodman, Abdel Halim Salem, Moiz Bakhiet, Safa Taha, Amarjit Kaur Sandhu, Fatimah S Al-Yami, Khawaja Bilal Waheed, Elmoeiz Ali Elnagi, Mohammed Almish, Jenifer Vecina Quiamb |
Are Genetic Modifiers the Answer to Different Responses to Hydroxyurea Treatment?-A Pharmacogenetic Study in Sickle Cell Anemia Angolan Children. International journal of molecular sciences 2023 5 24 (10): . Catarina Ginete, Mariana Delgadinho, Brígida Santos, Vera Pinto, Carina Silva, Armandina Miranda, Miguel Bri |
Clinical and biological profile of Sickle Cell Anemia children in a rural area in Central Africa. Hematology (Amsterdam, Netherlands) 2023 4 28 (1): 2193770. Mbayabo Gloire, Ngole Mamy, Lumbala Paul Kabuyi, Lumaka Aimé, Race Valerie, Matthijs Gert, Mikobi Tite Minga, Devriendt Koenraad, Van Geet Chris, Lukusa Prosper Tshilo |
Leg Ulcers in Sickle Cell Disease: A Multifactorial Analysis Highlights the Hemolytic Profile. Hematology reports 2023 2 15 (1): 119-129. Santos Edvan do Carmo, Santana Paulo Vinícius Bispo, Jesus Laíne Lopes Silva de, Melo Gabriela Imbassahy Valentim, Yahouédéhou Sètondji Cocou Modeste Alexandre, Guarda Caroline Conceição da, Santiago Rayra Pereira, Fiuza Luciana Magalhães, Carvalho Suéllen Pinheiro, Santos Liz Oliveira Dos, Adorno Elisângela Vitória, Aleluia Augusto Cezar Magalhães, Luiz Luciene Cristina Gastalho Campos, Fonseca Teresa Cristina Cardoso, Gonçalves Marilda de Souza, Aleluia Milena Magalhã |
A positive correlation between mutated gene of sickle cell anemia and glucose-6-phosphate dehydrogenase among gond tribes of Chhattisgarh, India. Mutation research 2023 12 828 111849. Ekta Singh, Lohit Raj Shivwanshi, Anil Kum |
A-296G variant of THBS1 gene (rs1478605) is associated with a lower frequency of stroke in a Brazilian population with sickle cell anemia. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2023 11 33 (1): 107474. Jessica M F Oliveira, Gabriela S Arcanjo, Igor F Domingos, Jéssica V G F Batista, Diego A Pereira-Martins, Thais H C Batista, Betânia L D Hatzlhofer, Diego A Falcão, Madi V Diniz, Alexsandro P Silva, Bárbara C V Pires, Ana C Dos Anjos, Fernando F Costa, Aderson S Araujo, Antonio R Lucena-Araujo, Marcos A Bezer |
Polymorphisms and gene expression of metalloproteinases and their inhibitors associated with cerebral ischemic stroke in young patients with sickle cell anemia. Molecular biology reports 2023 1 . do Kleyton Palmeira Ó, da Silva Freire Ana Karla, de Nóbrega Débora Nascimento, Dos Santos Souza Roberta, Farias Isabela Cristina Cordeiro, de Mendonça Belmont Taciana Furtado, da Silva Andreia Soares, da Silva Arcanjo Gabriela, da Silva Araujo Aderson, Dos Anjos Ana Cláudia Mendonça, de Araujo Antônio Roberto Lucena, Bezerra Marcos André Cavalcanti, de Moura Patricia Muniz Mendes Freire, do Socorro Mendonça Cavalcanti Maria, Vasconcelos Luydson Richardson Sil |
[Population characterization of mutations for sickle cell anemia and its treatment: One step towards personalized medicine for the disease]. Andes pediatrica : revista Chilena de pediatria 2024 4 95 (1): 41-52. Bernardita Cayupe, Rafael Bar |
Genetic Variants Associated with the Risk of Stroke in Sickle Cell Anemia: Systematic Review and Meta-Analysis. Hemoglobin 2024 4 48 (2): 101-112. Aradhana Kumari, Ganesh Chauhan, Partha Kumar Chaudhuri, Sushma Kumari, Anupa Pras |
CETP gene polymorphisms and haplotypes are explanatory variables for HDL cholesterol level in sickle cell disease. Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas 2024 1 57 e12879. N R C Cruz, T N S Valente, F O Ferreira, L R Macedo, A R Belisário, C M da Silva, N S Oliveira, A F F Gomides, C Velloso-Rodrigu |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: