[Diagnostic clues in atypical hemolytic uremic syndrome: a case report]. [PDF]
An Sist Sanit Navar, 2022 Luquin Irigoyen M +2 more
europepmc +1 more source
IS -94INS/DELATTG POLYMORPHISM IN THE NUCLEAR FACTOR KAPPA-B1 GENE (NFKB1) ASSOCIATED WITH NECROTIZING ENTEROCOLITIS? [PDF]
Arq Bras Cir Dig, 2023 Ferdinando DLT +4 more
europepmc +1 more source
Medisur, 2017 Fundamento: la enfermedad de Wilson se caracteriza por la acumulación de cobre, fundamentalmente en el hígado y cerebro. Se transmite con un patrón de herencia autosómico recesivo. La causa molecular que la provoca son las mutaciones en el gen atp7b, que
Yulia Clark Feoktistova +7 more
doaj
Molecular characterization of Cryptosporidium in ruminants and observation of natural infection by Cryptosporidium andersoni in sheep from Paraná, Brazil. [PDF]
Rev Bras Parasitol Vet, 2023 Holsback L +6 more
europepmc +1 more source
Medisur, 2015 Fundamento: La enfermedad de Wilson se caracteriza por la acumulación de cobre en hígado, cerebro y córnea. La causa molecular que la provoca son las mutaciones en el gen atp7b.
Yulia Clark Feoktistova +5 more
doaj
NOS3 gene intron 4 a/b polymorphism is associated with ESRD in autosomal dominant polycystic kidney disease patients. [PDF]
J Bras Nefrol, 2022 Padhi UN +4 more
europepmc +1 more source
Genetic profiling of HSP70 gene in local Iraqi goats. [PDF]
Braz J Vet Med, 2022 Habib HN, Saleh WMM, Gheni QJ.
europepmc +1 more source
Angiotensin-converting Enzyme Genetic Polymorphism
Arquivos Brasileiros de Cardiologia, 2014 Somsri Wiwanitkit, Viroj Wiwanitkit
doaj +1 more source
Genetic markers for preeclampsia in Peruvian women. [PDF]
Colomb Med (Cali), 2021 Pacheco-Romero J +16 more
europepmc +1 more source
[Review of a series of cases of Creutzfeldt-Jakob disease in a tertiary care hospital]. [PDF]
Rev Neurol, 2023 Villagrán-Sancho D +5 more
europepmc +1 more source