Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Akshatha Sharma"'
Publikováno v:
BMC Pregnancy and Childbirth, Vol 21, Iss 1, Pp 1-7 (2021)
Abstract Background To evaluate the performance of the Fetal Medicine Foundation (FMF) preterm preeclampsia (PE) screening algorithm in an indigenous South Asian population. Methods This was a prospective observational cohort study conducted in a ter
Externí odkaz:
https://doaj.org/article/0d6bc5e706ac4b50b1820f2dab0494f7
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 26, Iss 3, Pp 162-169 (2021)
Introduction: Isolated fetal ascites is an uncommon finding, and it may be difficult to elucidate the underlying pathology. This is more so when there are limited resources to investigate the patient adequately. This study was undertaken to see the e
Externí odkaz:
https://doaj.org/article/8285cdabb0164c88840edf25c15da405
Autor:
Rachna Gupta, Akshatha Sharma
Publikováno v:
American Journal of Medical Genetics Part A. 188:2178-2183
Publikováno v:
Journal of Ultrasound in Medicine. 41:2877-2883
Autor:
Akshatha Sharma, Anita Kaul
Publikováno v:
Archives of Gynecology and Obstetrics.
Several congenital abnormalities present late in pregnancy necessitating invasive testing to rule out genetic/infectious causes at late gestation. Not many studies have described the indications/safety of a late gestation amniocentesis.All records of
Publikováno v:
Fetal Diagnosis and Therapy. 48:272-278
Objectives: Our study aimed to examine a subset of electively reduced twins and compare their outcomes with those of expectantly managed twins, along with a cohort of singleton pregnancies. The secondary aim was to ascertain the procedure-related mis
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 26, Iss 3, Pp 162-169 (2021)
Journal of Indian Association of Pediatric Surgeons
Journal of Indian Association of Pediatric Surgeons
Introduction: Isolated fetal ascites is an uncommon finding, and it may be difficult to elucidate the underlying pathology. This is more so when there are limited resources to investigate the patient adequately. This study was undertaken to see the e
Publikováno v:
Journal of Fetal Medicine. :301-306
Bardet-Biedl syndrome (BBS) is a rare autosomal recessive disease with a prevalence rate of 1 in 125,000–170,000. BBS can occur as a result of mutation in one of the 19 known genes of the BBS gene complex. The syndrome is mostly diagnosed post-nata
Publikováno v:
The Indian journal of medical research. 154(5)
Down syndrome (DS) is one of the most common causes of developmental delay. In India, there is no protocol for prenatal screening of DS. Second-trimester biochemical screening is still being done by triple test. Quadruple test is with better sensitiv
Autor:
Akshatha Sharma, Vivek Krishnan
Publikováno v:
Journal of Fetal Medicine. :65-71
Pregnant women in the tropics like India are more susceptible to varicella zoster infection due to the lower seroprevalence of varicella as compared to temperate regions. Seronegative pregnant women are highly susceptible following a significant expo