Congenital anomalies

Xem 1-20 trên 21 kết quả Congenital anomalies
  • Tham khảo sách 'congenital anomalies – case studies and mechanisms edited by alastair sutcliffe', y tế - sức khoẻ, y học thường thức phục vụ nhu cầu học tập, nghiên cứu và làm việc hiệu quả

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  • Tuyển tập các báo cáo nghiên cứu về sinh học được đăng trên tạp chí hóa học quốc tế đề tài : Impact of a child with congenital anomalies on parents (ICCAP) questionnaire; a psychometric analysis

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  • Tuyển tập các báo cáo nghiên cứu về y học được đăng trên tạp chí y học Critical Care giúp cho các bạn có thêm kiến thức về ngành y học đề tài: Uranium and other contaminants in hair from the parents of children with congenital anomalies in Fallujah, Iraq...

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  • Tuyển tập các báo cáo nghiên cứu về y học được đăng trên tạp chí y học Wertheim cung cấp cho các bạn kiến thức về ngành y đề tài: Primary congenital anomalies of the coronary arteries and relation to atherosclerosis: an angiographic study in Lebanon...

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  • Tuyển tập báo cáo các nghiên cứu khoa học quốc tế ngành y học dành cho các bạn tham khảo đề tài: A new association of multiple congenital anomalies/mental retardation syndrome with bradycardia-tachycardia syndrome: a case report

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  • The programme is indebted to the five hundred plus international nurses from twentythree different countries who have worked and studied with us over the last four years at the Oxford Radcliffe Hospitals NHS Trust, the University Hospitals of Leicester NHS Trust and other hospitals. They have tested our new ideas, suggested improvements and shown honesty, courage and a sense of humour throughout. We are particularly grateful to the international nurses who commented on the first drafts of this book....

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  • The second chapter discusses how DNA bisulfite treatment together with high-throughput sequencing allows determining the DNA methylation on a whole genome scale at single cytosine resolution and introduces software for analysis of bisulfite sequencing data. The third chapter presents analysis of GC3-rich genes that have more methylation targets.

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  • Diabetes Mellitus in Pregnancy: Treatment Pregnancy complicated by diabetes mellitus is associated with higher maternal and perinatal morbidity and mortality rates. Preconception counseling and treatment are important for the diabetic patient contemplating pregnancy and can reduce the risk of congenital malformations and improve pregnancy outcome. Folate supplementation reduces the incidence of fetal neural tube defects, which occur with greater frequency in fetuses of diabetic mothers.

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  • Congenital Anomalies of the Lumbar Spine Spondylolysis is a bony defect in the pars interarticularis (a segment near the junction of the pedicle with the lamina) of the vertebra; the etiology may be a stress fracture in a congenitally abnormal segment. The defect (usually bilateral) is best visualized on oblique projections in plain x-rays, CT scan, or single photon emission CT (SPECT) bone scan and occurs in the setting of a single injury, repeated minor injuries, or growth.

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  • Tuyển tập báo cáo các nghiên cứu khoa học quốc tế ngành y học dành cho các bạn tham khảo đề tài: Retention of foreign body in the gut can be a sign of congenital obstructive anomaly: a case report

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  • I wrote the first edition of this book more than 20 years ago, and the discoveries in genetics since then have been phenomenal. The new knowledge and applications of human genetics to health and to society have made it even more necessary that nurses "think genetically" in their practice and, indeed in their lives. Genetic factors can be responsible in some way for both direct and indirect disease causation; for variation that determines predisposition, susceptibility, and resistance to disease and also for response to therapeutic management.

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  • Tuyển tập các báo cáo nghiên cứu về bệnh học thý y được đăng trên tạp chí Acta Veterinaria Scandinavica cung cấp cho các bạn kiến thức về bệnh thú yđề tài: Congenital Pelger-Huët anomaly in a Danish/ Swedish Farmdog: Case Report...

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  • The association of neurodevelopmental handicaps and congenital anomalies with low birthweight has been well established; low birth-weight infants also may be susceptible to a wide range of other conditions, such as lower respiratory tract infections, learning disorders, behavior problems, and complications of neonatal inten...

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  • Opportunity: Cancer is the leading cause of death in Canadian children beyond the neonatal period. One in 400 Canadian adults are survivors of childhood cancer, and more than two-thirds experience chronic and/or late-occurring health problems, that often are not clinically apparent until decades after treatment. 10 Non-random molecular or cytogenetic events are found in 50% of childhood cancers, and many types of childhood cancers are associated with congenital anomalies, or family cancer history, suggesting a strong genetic basis for the etiology of cancer in children.

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  • Congenital abnormalities of the kidney and urinary tract are reported to occur in 5 to 10% of the population [9]. They represent 25% of the total ultrasonographically diagnosed malformations that occur in 0.25–0.7% of fetuses. About 1/3 to 2/3 of ESRD in children are due to congenital ab- normalities of the kidney and urinary tract. In addition, these abnormalities occur in 23% of patients with chromosomal aberrations, and 2/3 of patients with abnormalities of other organ systems.

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  • Current clinical technologies, especially donor transplants and artificial organs, have been excellent life-saving and life-extending therapies to treat patients who need to reconstitute diseased or devastated organs or tissues as a result of an accident, trauma, and cancer, or to correct congenital structural anomalies. For long, most scientists and clinicians believed that damaged or lost tissues could only be replaced by organ transplantation or with totally artificial parts.

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  • In recent years, there has been a paradigm shift in learning, specifically the manner in which information is gathered and ingested. This is particularly no- table in subject matter that covers great breadth or is rapidly evolving, such as medicine, and more specifically, diagnostic imaging. Students and residents (and for that matter, practicing radiologists) quickly turn to the Internet to “Google™” unknown factoids, rapidly gathering information, in many cases without source validation.

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  • 7 Lip Pits; Orthodontic Treatment, Dentition and Occlusion; Associated Skeletal Structures Samuel Berkowitz 7.1 7.1.1 Lip Pits Pits of the Lower Lip in Cleft Lip and/or Palate – Genetic Considerations 7.1.2 Frequency Pits of the lower lip such as fistulas of lower lip, paramedian sinuses of lower lip, humps of lower lip, or labial cysts are a very rare congenital malformation, first described by Demarquay in 1845 [1]. This minimally deforming anomaly is remarkable chiefly for its association with facial clefts.

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  • Rubella (See also Chap. 186) Rubella virus is a known teratogen; first-trimester rubella carries a high risk of fetal anomalies, though the risk decreases significantly later in pregnancy. Congenital rubella may be diagnosed by percutaneous umbilical blood sampling with the detection of IgM antibodies in fetal blood. All pregnant women should be screened for their immune status to rubella. Indeed, all women of childbearing age, regardless of pregnancy status, should have their immune status for rubella verified and be immunized if necessary.

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  • Blue Lesions Lesions that are blue in color are the result of either vascular ectasias and tumors or melanin pigment in the dermis. Venous lakes (ectasias) are compressible dark-blue lesions that are found commonly in the head and neck region. Venous malformations are also compressible blue papulonodules and plaques that can occur anywhere on the body, including the oral mucosa. When there are multiple rather than single congenital lesions, the patient may have the blue rubber bleb syndrome or Mafucci's syndrome.

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