Results 111 to 120 of about 46,311 (239)
ABSTRACT Marden–Walker syndrome (MWS; OMIM 248700) is an extremely rare congenital disorder characterized by multiple joint contractures, craniofacial dysmorphism, neurological abnormalities, and multisystem involvement. Although historically diagnosed on clinical grounds, only a few cases have been molecularly confirmed.
Guilherme Sotto Battiston +35 more
wiley +1 more source
Applications of aerospace technology in biology and medicine [PDF]
Utilization of National Aeronautics and Space Administration (NASA) technology in medicine is discussed. The objective is best obtained by stimulation of the introduction of new or improved commercially available medical products incorporating aerospace ...
Bass, B. +7 more
core +1 more source
Intracranial Hemorrhage Due to Secondary Hypertension from Intracranial Large Vessel Occlusion [PDF]
Simultaneous hemorrhagic and ischemic strokes have been previously reported in the literature. Typically, these occur in patients secondary to dialysis, cerebral amyloid angiopathy, or thrombotic thrombocytopenic purpura.1,2,3 However, this is the unique
Khan, Asif A. +3 more
core
Ventriculoperitoneal Shunt Malfunction: The Importance of Topogram Image Observation
ABSTRACT Disconnection of a ventriculoperitoneal shunt is a serious complication. The “sunset eye” sign is an important indicator of hydrocephalus. Observation of a CT topogram is an important diagnostic measure and should not be overlooked, and good care of the ventriculoperitoneal shunt should also be taken.
Yantao Du +3 more
wiley +1 more source
Neuropsychological profile of patients with normal pressure hydrocephalus and Alzheimer's disease [PDF]
RIGHTS : This article is licensed under the BioMed Central licence at http://www.biomedcentral.com/about/license which is similar to the 'Creative Commons Attribution Licence'.
Gelling, L +4 more
core
The EUROmediCAT Network and Databases: A Resource for Pharmacovigilance in Pregnancy
ABSTRACT Background The evidence gap relating to the risk of congenital anomalies (CA) associated with first trimester medication exposure in pregnancy is well recognized. Aims We describe the EUROmediCAT network and databases, and the methodological approach to pregnancy pharmacovigilance.
Helen Dolk +27 more
wiley +1 more source
Abstract Carrier screening for genetic conditions performed preconception or during pregnancy allows identification of fetal risk for inherited autosomal recessive and X‐linked conditions. The goal is to identify at‐risk patients/couples and offer them reproductive options such as preimplantation genetic diagnosis, prenatal testing, or targeted newborn
Emily B. Rosenfeld +5 more
wiley +1 more source
Spatial model of convective solute transport in brain extracellular space does not support a "glymphatic" mechanism. [PDF]
A "glymphatic system," which involves convective fluid transport from para-arterial to paravenous cerebrospinal fluid through brain extracellular space (ECS), has been proposed to account for solute clearance in brain, and aquaporin-4 water channels in ...
Jin, Byung-Ju +2 more
core
Watching the eye with Mars in sight
Experimental Physiology, EarlyView.
Peter zu Eulenburg +2 more
wiley +1 more source
ABSTRACT Introduction Children with medical complexity are at risk of pulmonary injury due to chronic pulmonary aspiration. Our study aimed to determine the effect of multidisciplinary evaluation and periodic follow‐up of aerodigestive disorders on the final status of the respiratory conditions.
Füsun Ünal +9 more
wiley +1 more source

