نتایج جستجو برای: arthrogryposis
تعداد نتایج: 1172 فیلتر نتایج به سال:
Global satellite validation of SCIAMACHY O3 columns with GOME WFDOAS A. Bracher, M. Weber, K. Bramstedt, M. Coldewey-Egbers, L. N. Lamsal, and J. P. Burrows Institute of Environmental Physics and Remote Sensing (IUP/IFE), University of Bremen, Otto-Hahn-Allee 1, 28334 Bremen, Germany Received: 20 December 2004 – Accepted: 7 February 2005 – Published: 14 February 2005 Correspondence to: A. Brach...
We present a theory of spatial development. Manufacturing and services rms located in a continuous geographic area choose each period how much to innovate. Firms trade subject to transport costs and technology di¤uses spatially across locations. The result is a spatial endogenous growth theory that can shed light on the link between the evolution of economic activity over time and space. We ap...
Arthrogryposis multiplex congenita (AMC) is a symptom complex of congenital joint contractures associated with neurogenic and myopathic disorders. It is diagnosed at birth and often progresses to a state of significant disability. Pregnancy in a woman with AMC is at high risk due to diminished pulmonary reserve, increased risk of thromboembolism and anesthesia. Successful pregnancy in patients ...
The clinical case of a patient with a segmental humeral defect, in the context of an arthrogryposis congenita multiplex and morbid obesity, reconstructed with a pedicled segmental radial bone flap is reported. The use of the pedicled vascularized diaphyseal radial bone flap may be a useful technique for humerus reconstruction in patients with contraindication for microvascular bone transfers an...
We describe Zika virus (ZIKV) vertical transmission in an imported case in Spain, in a 17-week pregnant woman. ZIKV IgG, IgM and RNA were detected in serum in week 17. At 19 weeks, ultrasound scan revealed fetal malformations and ZIKV was detected in the amniotic fluid. Pregnancy was terminated at week 21; autopsy of the fetus revealed bilateral hydrocephalus, brain microcalcifications and arth...
We report a case of a male baby who has characteristic signs of Freeman-Sheldon syndrome, a rare but recognizable, severe autosomal dominant form of distal arthrogryposis. Diagnosis was based on the distinctive clinical characteristics of the syndrome and confirmed by genetic analysis that showed a de novo missense mutation c.2015G>A (p.Arg672His) of the MYH3 gene. We highlight the different fe...
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