Olfactory neuroblastoma: a single-center experience
Sign Up to like & getrecommendations! Published in 2017 at "Neurosurgical Review"
DOI: 10.1007/s10143-017-0859-3
Abstract: Olfactory neuroblastoma (ONB) is a potentially curable disease, despite being an aggressive malignancy with a poor natural history. Our goal was to evaluate management outcomes for patients with ONB treated at our institution. Our prospective… read more here.
Keywords: surgical margins; tumor size; olfactory neuroblastoma; neuroblastoma single ... See more keywords
Trisomy 21 with t(5; 11) chromosomal translocation as new unfavorable cytogenetic abnormalities in pediatric acute myeloid leukemia type M2: One case report of nine-year follow-up and literature review
Sign Up to like & getrecommendations! Published in 2017 at "Current Medical Science"
DOI: 10.1007/s11596-017-1809-6
Abstract: SummaryWe report one case of pediatric acute myeloid leukemia type 2 (AML-M2) who presented with karyotypic aberration of trisomy 21 with the t(5;11) chromosomal translocation. The patient achieved complete remission after two cycles of chemotherapy… read more here.
Keywords: leukemia type; trisomy chromosomal; myeloid leukemia; acute myeloid ... See more keywords
Clinical significance of understanding lateral and medial circumflex femoral artery origin variability
Sign Up to like & getrecommendations! Published in 2018 at "Anatomical Science International"
DOI: 10.1007/s12565-018-0434-1
Abstract: The common femoral artery (CFA) divides into the superficial femoral artery (SFA) and deep femoral artery (DFA). The lateral circumflex femoral artery (LCFA) and medial circumflex femoral artery (MCFA) are most often branches of the… read more here.
Keywords: dfa; artery; femoral artery; circumflex femoral ... See more keywords
P11-S Co-existence of Juvenile Myoclonic Epilepsy and Neurofibromatosis and the lessons learned from one case report
Sign Up to like & getrecommendations! Published in 2019 at "Clinical Neurophysiology"
DOI: 10.1016/j.clinph.2019.04.551
Abstract: Background Neurofibromatosis type 1 (NF1) is a common autosomal dominant disorder, afflicting 1 in 2500–3000 individuals. These patients harbor cafe-au-lait macules, axillary and inguinal freckling, neurofibromas and optic pathway gliomas. Epilepsy, although not usual, is… read more here.
Keywords: epilepsy; juvenile myoclonic; case; myoclonic epilepsy ... See more keywords
Prevalence of Hemoglobinopathies in Premarital Screening in the Province of Nigde, Turkey.
Sign Up to like & getrecommendations! Published in 2023 at "Hemoglobin"
DOI: 10.1080/03630269.2023.2206971
Abstract: Hemoglobinopathies are one of the most widespread hereditary disorders in Turkey. The present study aimed to determine the prevalence of hemoglobinopathies in the Nigde province of Turkey. This study was conducted with 2013 individuals who… read more here.
Keywords: prevalence hemoglobinopathies; thalassemia; one case; premarital screening ... See more keywords
Fetal Tethered Spinal Cord: Diagnostic Features and Its Association with Congenital Anomalies.
Sign Up to like & getrecommendations! Published in 2023 at "Fetal and pediatric pathology"
DOI: 10.1080/15513815.2023.2172632
Abstract: OBJECTIVE We assessed the frequency and type of associated congenital anomalies encountered with fetal tethered spinal cord (TSC) determined prenatally. METHOD A retrospective review was conducted based on the associated fetal abnormalities following diagnosis of… read more here.
Keywords: spinal cord; fetal tethered; case; congenital anomalies ... See more keywords
The value of lamp to rule out imported malaria diagnosis: a retrospective observational study in Milan, Italy
Sign Up to like & getrecommendations! Published in 2022 at "Infectious Diseases"
DOI: 10.1080/23744235.2021.2023754
Abstract: Abstract Background The diagnosis of malaria in returning travellers could be a challenge in non-endemic settings. We aimed to assess the performance of LAMP in comparison with standard conventional diagnostic methods using real-time-polymerase chain reaction… read more here.
Keywords: lamp; malaria diagnosis; one case; microscopy ... See more keywords
P0246MEMBRANOUS NEPHROPATHY IN THE ELDERLY : EPIDEMIOLOGY, DIAGNOSIS AND MANAGEMENT
Sign Up to like & getrecommendations! Published in 2020 at "Nephrology Dialysis Transplantation"
DOI: 10.1093/ndt/gfaa142.p0246
Abstract: The aging of the population and the increase in life expectancy have led to increasing numbers of elderly patients so greater numbers of elderly patients with chronic kidney diseases are surviving longer. Membranous nephropathy (MN)… read more here.
Keywords: nephrology; diagnosis; management; epidemiology ... See more keywords
AB0778 VENOUS THROMBOSIS IN UNUSUAL SITES
Sign Up to like & getrecommendations! Published in 2021 at "Annals of the Rheumatic Diseases"
DOI: 10.1136/annrheumdis-2021-eular.3332
Abstract: Unusual site venous thrombosis (USVT), which includes venous thromboses of the upper limbs, digestive tract, cellar and brain, are rarely observed compared to those of the lower limbs and require both an etiological approach and… read more here.
Keywords: one case; thrombosis cases; etiology; thrombosis ... See more keywords
P359 Reactive thrombocytosis in children
Sign Up to like & getrecommendations! Published in 2017 at "Archives of Disease in Childhood"
DOI: 10.1136/archdischild-2017-313273.447
Abstract: Background Thrombocytosis can be classified as primary or secondary, also called reactive. If primary thrombocytosis is a very rare condition in children, reactive thrombocytosis occurs commonly in children and it is associated, especially with infections,… read more here.
Keywords: one case; thrombocytosis; thrombocytosis children; reactive thrombocytosis ... See more keywords
P443 Hereditary Thrombophilia in newborn
Sign Up to like & getrecommendations! Published in 2019 at "Archives of Disease in Childhood"
DOI: 10.1136/archdischild-2019-epa.779
Abstract: Background Hereditary Thrombophilia refers to the propensity to develop thrombosis. A homozygous abnormality or combination of two heterozygous abnormal factors can lead to clinically apparent thrombotic disorders at an early age. The aim of our… read more here.
Keywords: one case; hereditary thrombophilia; thrombosis; thrombophilia newborn ... See more keywords