imaps.org
IMAPS 2015, Orlando - 48th International Symposium on Microelectronics
http://www.imaps.org/imaps2015
Session Chair Manual (PDF). Journal of Micro and Elect Pkg. IMAPS 2015 - Orlando. Advanced Packaging and the Internet of Things: The Future of Our Industry. October 27-29, 2015. October 27-28, 2015. Professional Development Courses and. October 26, 2015. Technical Co-Chair - USA:. Technical Co-Chair - Europe:. Technical Co-Chair - Asia:. SK Hynix, Inc. Assistant Technical Co-Chair - USA:. Mary Cristina Ruales Ortega,. Tim Mobley, Triton Micro Tech. Assistant Technical Co-Chairs - Europe:. Download Final ...
mi-rare-cles.blogspot.com
mi-RARE-cles: Spina Bifida, Myelomeningocele
http://mi-rare-cles.blogspot.com/2014/11/spina-bifida-myelomeningocele.html
Monday, November 10, 2014. Spina Bifida, Myelomeningocele. Bifida is the most common permanently disabling birth defect in the United States. Spina Bifida literally means “split spine.” Spina Bifida happens when a baby is in the womb and the spinal column does not close all of the way. Myelomeningocele is the most severe form of Spina Bifida. It happens when parts of the spinal cord and nerves come through the open part of the spine. It causes nerve damage and other disabilities. To relieve the pressure ...
prnewswire.com
NATEL and OnCore Renamed: NEO Tech
http://www.prnewswire.com/news-releases/natel-and-oncore-renamed-neo-tech-300084575.html
All Auto and Transportation. Auto and Transportation Overview. Railroads and Intermodal Transportation. Transportation, Trucking and Railroad. Trucking and Road Transportation. RFID (Radio Frequency ID). Entertainment and Media. All Entertainment and Media. Entertainment and Media Overview. Film and Motion Picture. Publishing and Information Services. Financial Services and Investing. All Financial Services and Investing. Financial Services and Investing Overview. Accounting News and Issues. Sports Eq...
mi-rare-cles.blogspot.com
mi-RARE-cles: Congenital Talipes Equinovarus (CTEV) commonly known as ”Clubfoot”
http://mi-rare-cles.blogspot.com/2014/09/congenital-talipes-equinovarus-ctev.html
Monday, September 8, 2014. Congenital Talipes Equinovarus (CTEV) commonly known as ”Clubfoot”. Clubfoot is diagnosed at birth, or in some instances, by prenatal ultrasound. It cannot be predicted or prevented. When Clubfoot is present in both feet it is called Bilateral Clubfoot. One affected foot is called Unilateral Clubfoot. Treatment Overview: 5 Phases. Correction: Gentle manipulation to align the foot in a normal position with weekly (serial) casting to allow the soft bones to set. Here, the lig...
mi-rare-cles.blogspot.com
mi-RARE-cles: 22q11.2 Deletion Syndrome
http://mi-rare-cles.blogspot.com/2014/09/22q112-deletion-syndrome.html
Monday, September 15, 2014. Missing part of Chromosome 22…can be a random genetic mutation…first in the family…or a person that has it has a 50% chance of passing it on to their children. Gives rise to a variety of symptoms, ranging in severity. Growth, heart, kidney, spine, calcium, feeding, developmental, speech, immune issues. ETC. Needs care by a variety of specialists depending on the particular symptoms (cardiologist, immunologist, speech-language pathologist, feeding therapist, geneticist, ETC).
mi-rare-cles.blogspot.com
mi-RARE-cles: September 2013
http://mi-rare-cles.blogspot.com/2013_09_01_archive.html
Monday, September 16, 2013. PCDH19 Female Limited Epilepsy (FLE). PCDH19 FLE causes severe drug-resistant epilepsy as well as a spectrum of developmental, intellectual, and behavioral problems in girls and women. PCDH19 FLE can occur de novo or can occur within families passed from women to their daughters or asymptomatic sons or from carrier fathers to daughters. PCDH19 FLE is diagnosed via genetic testing. A variety of mutations of PCDH19 (on the X chromosome) can cause the symptoms of PCDH19. Esmé and...
mi-rare-cles.blogspot.com
mi-RARE-cles: February 2014
http://mi-rare-cles.blogspot.com/2014_02_01_archive.html
Monday, February 24, 2014. Long arm : within the 15p15.33 band there is a deletion of 0.133 Mb followed by a duplication of 0.710 Mb followed by a deletion of 0.119 Mb. Short arm: duplication of 5q33.2q35.3. Congenital heart defect, growth failure, failure to thrive, low birth weight, low set of ears, small chin, small jaw, short neck, plagiocephaly, developmental delay in all area. Partial karyotype and FISH studies of both parents it is not inherited it is a de novo event. Contributed by MOM Daniella.
mi-rare-cles.blogspot.com
mi-RARE-cles: Developmentally Cognitively Delayed
http://mi-rare-cles.blogspot.com/2014/05/developmentally-cognitively-delayed.html
Monday, May 5, 2014. 9 years ago, my daughter Grace was born at 24 weeks. She was a micro-preemie. She had a tracheostomy,ventilator, oxygen, and feeing tube. Today, she is mechanically free, but does have DCD. She is in third grade, and is developmentally delayed for her age. Grace still has induced asthma at times, due to her respiratory colds. Grace learns differently at school in her special education classes. She has goals set through her IEP plan through the school district. Follow us on facebook.
mi-rare-cles.blogspot.com
mi-RARE-cles: September 2014
http://mi-rare-cles.blogspot.com/2014_09_01_archive.html
Monday, September 15, 2014. Missing part of Chromosome 22…can be a random genetic mutation…first in the family…or a person that has it has a 50% chance of passing it on to their children. Gives rise to a variety of symptoms, ranging in severity. Growth, heart, kidney, spine, calcium, feeding, developmental, speech, immune issues. ETC. Needs care by a variety of specialists depending on the particular symptoms (cardiologist, immunologist, speech-language pathologist, feeding therapist, geneticist, ETC).
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