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Significado da presença de esquizócitos no sangue periférico de gestantes com pré-eclâmpsia
(2008-08-01)
PURPOSE: to evaluate the significance of schizocytes presence in peripheral blood smear of pregnant women with pre-eclampsia, identifying and correlating them with other markers of hemolysis and of the disease severity. ...
Prenatal diagnosis of congenital syngnathia by 3D ultrasound and pathological correlation
(Springer, 2013-01-01)
Congenital syngnathia is a maxillomandibular fusion, and it can vary in severity from single mucosal bands (synechiae) to complete bony fusion (synostosis). Cases of combinations of bony or soft tissue adhesions between ...
Pathological mutations in PNKP trigger defects in DNA single-strand break repair but not DNA double-strand break repair
(2020)
Hereditary mutations in polynucleotide kinasephosphatase
(PNKP) result in a spectrum of neurological
pathologies ranging from neurodevelopmental
dysfunction in microcephaly with early onset
seizures (MCSZ) to ...
In vitro osteoclastogenesis from Gaucher patients' cells correlates with bone mineral density but not with Chitotriosidase
(Elsevier Science Inc, 2017-10)
Gaucher disease (GD) is caused by mutations on the gene encoding for the lysosomal enzyme glucocerebrosidase. Type I GD (GD1) patients present anemia, hepatosplenomegaly and bone alterations. In spite of treatment, bone ...
Detection of hepatitis C virus RNA in saliva is not related to oral health status or viral load
(2005)
Hepatitis C is a worldwide public health problem and its transmission is clearly associated with the parenteral route, however, the virus has also been isolated from other body fluids. Hepatitis C virus (HCV) RNA has been ...
Canine inflammatory bowel disease: endoscopic, biochemical and pathologic findings in anterior gastrointestinal tractEnfermedad inflamatoria crónica intestinal canina: hallazgos endoscópicos, bioquímicos y anatomopatológicos del tracto gastrointestinal anterior
(Archivos de Medicina Veterinaria, 2015)
Prevalence of different periapical lesions associated with human teeth and their correlation with the presence and extension of apical external root resorption
(Blackwell Publishing, 2002)
Aim The aim of this study was to determine the prevalence of various periapical pathologies and their association with the presence and extent of apical external inflammatory root resorption in human teeth. Methodology One ...
Prevalence of different periapical lesions associated with human teeth and their correlation with the presence and extension of apical external root resorption
(Blackwell Publishing, 2002)
Aim The aim of this study was to determine the prevalence of various periapical pathologies and their association with the presence and extent of apical external inflammatory root resorption in human teeth. Methodology One ...
Genotype-Phenotype Correlations in Non-Finnish Congenital Nephrotic Syndrome
(AMER SOC NEPHROLOGY, 2010)
Mutations in NPHS1, which encodes nephrin, are the main causes of congenital nephrotic syndrome (CNS) in Finnish patients, whereas mutations in NPHS2, which encodes podocin, are typically responsible for childhood-onset ...