Results 11 to 20 of about 1,180,087 (300)

Periventricular magnetisation transfer abnormalities in early multiple sclerosis

open access: yesNeuroImage: Clinical, 2022
Objective: Recent studies suggested that CSF-mediated factors contribute to periventricular (PV) T2-hyperintense lesion formation in multiple sclerosis (MS) and this in turn correlates with cortical damage.
Lukas Pirpamer   +9 more
doaj   +1 more source

Multiple corticosteroid abnormalities in cats with hyperaldosteronism

open access: yesJournal of Veterinary Internal Medicine, 2021
Background The frequency with which multiple corticosteroid abnormalities occur in cats with aldosterone secreting adrenocortical tumors is unknown. Objectives To evaluate adrenal‐derived corticosteroids in cats in which blood samples were submitted for ...
Daniel K. Langlois   +3 more
doaj   +1 more source

A practical method for prenatal diagnosis of anal atresia by second trimester ultrasound screening - A retrospective study

open access: yesTaiwanese Journal of Obstetrics & Gynecology, 2023
Objectives: The study aimed to demonstrate the performance of anal atresia ultrasound screening in the second trimester and to describe associated experiences in a primary care fetal medicine clinic. Materials and methods: We retrospectively analyzed the
Hsuan Ko   +3 more
doaj   +1 more source

Genetic Abnormalities in Multiple Myeloma: Prognostic and Therapeutic Implications

open access: yesCells, 2021
Some genetic abnormalities of multiple myeloma (MM) detected more than two decades ago remain major prognostic factors. In recent years, the introduction of cutting-edge genomic methodologies has enabled the extensive deciphering of genomic events in MM.
Ignacio J. Cardona-Benavides   +2 more
doaj   +1 more source

Una variación anatómica: la desembocadura aberrante del conducto torácico

open access: yesBiomédica: revista del Instituto Nacional de Salud, 2009
En uno de los cadáveres disecados durante el primer semestre de 2006 en el anfiteatro del Departamento de Morfología de la Universidad del Valle en Cali (Colombia), se encontró una variación anatómica poco descrita en la literatura científica mundial. Se
Elizabeth Peña, Janneth Zuñiga
doaj   +1 more source

Chromosomal aberrations in transitional cell carcinoma that are predictive of disease outcome are independent of polyploidy [PDF]

open access: yes, 1999
Objective To determine whether aneusomy for chromosomes 7, 9 and 17 (reported to predict recurrence in up to 65% of patients with superficial transitional cell bladder cancer and thus providing the opportunity for early and effective treatment) reflects ...
Adie, L.   +4 more
core   +1 more source

Neuroimaging Evidence of Major Morpho-Anatomical and Functional Abnormalities in the BTBR T+TF/J Mouse Model of Autism [PDF]

open access: yes, 2013
BTBR T+tf/J (BTBR) mice display prominent behavioural deficits analogous to the defining symptoms of autism, a feature that has prompted a widespread use of the model in preclinical autism research.
A Gozzi   +78 more
core   +3 more sources

Halothane hepatitis with renal failure treated with hemodialysis and exchange transfusion [PDF]

open access: yes, 1974
A 38-year-old white female, hepatitis B antigen negative, developed fluminating hepatic failure associated with oliguria and severe azotemia after two halothane anesthesia and without exposure to other hepatotoxic drugs or blood transfusions.
A. G. Redeker   +14 more
core   +1 more source

The strong association of left-side heart anomalies with Kabuki syndrome [PDF]

open access: yesKorean Journal of Pediatrics, 2015
PurposeKabuki syndrome is a multiple congenital malformation syndrome, with characteristic facial features, mental retardation, and skeletal and congenital heart anomalies.
Ja Kyoung Yoon   +6 more
doaj   +1 more source

Atypical miRNA expression in temporal cortex associated with dysregulation of immune, cell cycle, and other pathways in autism spectrum disorders. [PDF]

open access: yes, 2015
BackgroundAutism spectrum disorders (ASDs) likely involve dysregulation of multiple genes related to brain function and development. Abnormalities in individual regulatory small non-coding RNA (sncRNA), including microRNA (miRNA), could have profound ...
Ander, Bradley P   +4 more
core   +1 more source

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