Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Krishna Revanna Gopagondanahalli"'
Autor:
Krishna Revanna Gopagondanahalli, Abdul Alim Abdul Haium, Shrenik Jitendrakumar Vora, Sreekanthan Sundararaghavan, Wei Di Ng, Tze Liang Jonathan Choo, Wai Lin Ang, Nur Qaiyimah Binte Mohamad Taib, Nishanthi Han Ying Wijedasa, Victor Samuel Rajadurai, Kee Thai Yeo, Teng Hong Tan
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
ObjectivesTo evaluate serial tissue Doppler cardiac imaging (TDI) in the evolution of bronchopulmonary dysplasia-associated pulmonary hypertension (BPD-PH) among extremely preterm infants.DesignProspective observational study.SettingSingle-center, te
Externí odkaz:
https://doaj.org/article/ce18b160f8e6406b8b72c760a60c4b8a
Autor:
Monika Kantilal Kotecha, Khurshid Merchant, Charmaine Jiahui Chan, Jonathan Tze Liang Choo, Krishna Revanna Gopagondanahalli, Dyan Zhewei Zhang, Teng Hong Tan, Sreekanthan Sundararaghavan
Publikováno v:
Diagnostics, Vol 13, Iss 8, p 1481 (2023)
Background: Neonatal lupus (NL) is a clinical syndrome that develops in the fetus as a result of maternal autoimmune antibodies. Congenital complete heart block (CHB) is the most common manifestation, while extranodal cardiac manifestations of NL, su
Externí odkaz:
https://doaj.org/article/3ae2d6a534ca49558a8dbbd2419c6637
Autor:
Simrita Kaur Khurana, Krishna Revanna Gopagondanahalli, Victor Samuel Rajadurai, Suresh Chandran
Publikováno v:
Medical Journal of Dr. D.Y. Patil Vidyapeeth, Vol 13, Iss 2, Pp 175-178 (2020)
Oligohydramnios secondary to mid-trimester preterm premature rupture of the membranes can result in a range of abnormalities from functional hypoplasia of the lungs to structural hypoplasia and fetal compression syndrome. Here, we discuss two infants
Externí odkaz:
https://doaj.org/article/f31eb7c64c78415b87165f176a8a671b
Autor:
Krishna Revanna Gopagondanahalli, Annette Chang, Ramesh Nataraja, Kenneth Tan, Suresh Chandran, T R Saiprasad
Publikováno v:
Medical Journal of Dr. D.Y. Patil Vidyapeeth, Vol 13, Iss 3, Pp 285-287 (2020)
Congenital hernia of the umbilical cord (CHUC) is a rare, distinctive anomaly with variable presentation and conflicting terminology. We report two newborn infants who had fetal antenatal diagnosis as umbilical cord cyst and omphalocele, respectively
Externí odkaz:
https://doaj.org/article/a656fe225176499aa2205f549ad66e49
Publikováno v:
Medical Journal of Dr. D.Y. Patil Vidyapeeth, Vol 13, Iss 5, Pp 564-566 (2020)
A premature female neonate born at 27 weeks of gestational age with a birth weight of 1000 g, developed spontaneous pneumoperitoneum on day 10 of life. The baby remained clinically stable with constant serial blood gases and inflammatory markers. In
Externí odkaz:
https://doaj.org/article/1cd7bea63439492990c8da41f138f874
Autor:
Eric Ma, Krishna Revanna Gopagondanahalli, Jenica Su-ern Yong, Chua Mei Chien, Suresh Chandran
Publikováno v:
Data in Brief, Vol 31, Iss , Pp 105689- (2020)
This data describes the modern surgical treatment of congenital vallecular cyst in a term newborn infant who developed neonatal stridor on day 1 of life. Diagnosis was made by nasoendoscopy and the infant underwent successful treatment by marsupializ
Externí odkaz:
https://doaj.org/article/70e2c24e12844c5383f99d571fbe3885
Autor:
Eric Ma, Krishna Revanna Gopagondanahalli, Jenica Su-ern Yong, Chua Mei Chien, Suresh Chandran
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 59, Iss , Pp 101460- (2020)
Vallecular cyst is a rare but observed cause of neonatal stridor that can present with respiratory distress and feeding difficulties arising from upper airway obstruction. Stridor in neonates is usually congenital in nature and most often caused by l
Externí odkaz:
https://doaj.org/article/fb1b54acaa1a420699881125ce0dda51
Williams-Beuren Syndrome and Congenital Lobar Emphysema: Uncommon Association with Common Pathology?
Publikováno v:
Case Reports in Pediatrics, Vol 2017 (2017)
Introduction. Congenital lobar emphysema (CLE) and Williams-Beuren Syndrome are two rare conditions that have only been reported together in a single case study. Case Presentation. We report another case of a male Caucasian newborn with nonspecific i
Externí odkaz:
https://doaj.org/article/eaccbcb749b6416b8a8a5b251f640488
Autor:
Krishna Revanna Gopagondanahalli, Rashmi Arun Mittal, Abdul Alim Abdul Haium, Bin Huey Quek, Pratibha Agarwal, Lourdes Mary Daniel, Mei Chien Chua, Victor Samuel Rajadurai
Publikováno v:
Neonatology. 119:494-500
Introduction: Glucose 6-phosphate dehydrogenase (G6PD) deficiency increases the risk of severe neonatal hyperbilirubinemia. This study evaluates the risk factors predicting the need for phototherapy in G6PD-deficient neonates after 72 h of age and as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec06fc339daa0bb8de02189bf503433e
https://doi.org/10.1159/000524966
https://doi.org/10.1159/000524966
Autor:
Krishna Revanna Gopagondanahalli, Victor Samuel Rajadurai, Suresh Chandran, Simrita Kaur Khurana
Publikováno v:
Medical Journal of Dr. D.Y. Patil Vidyapeeth, Vol 13, Iss 2, Pp 175-178 (2020)
Oligohydramnios secondary to mid-trimester preterm premature rupture of the membranes can result in a range of abnormalities from functional hypoplasia of the lungs to structural hypoplasia and fetal compression syndrome. Here, we discuss two infants
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c0120cd0d6407b67b28534585090e9d
http://www.mjdrdypv.org/article.asp?issn=2589-8302
http://www.mjdrdypv.org/article.asp?issn=2589-8302