Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Shradha Salunkhe"'
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 18, Iss 10, Pp 08-10 (2024)
Holt-Oram syndrome is a rare congenital autosomal dominant disorder caused by a mutation in the TBX5 gene. It is characterised by upper limb abnormalities and congenital heart lesions, such as Atrial Septal Defect (ASD), typically affecting children.
Externí odkaz:
https://doaj.org/article/b6b95e5b7df442d1850635036333b3d5
Publikováno v:
Annals of Child Neurology, Vol 32, Iss 2, Pp 135-136 (2024)
Externí odkaz:
https://doaj.org/article/16ddc00a8287467c9a1c8cfbcf0dc341
Autor:
Shailaja Vijaykumar Mane, Shradha Salunkhe, Sharad Agarkhedkar, Priyanka Lakhwani, Sudhir Malwade
Publikováno v:
Medical Journal of Dr. D.Y. Patil Vidyapeeth, Vol 15, Iss 5, Pp 682-686 (2022)
Introduction: Human milk banking (HMB) is a service established for collection, screening, processing, storage, and distribution of donated human milk. HMB is the best way of ensuring a safe supply of human milk to all the needy neonates. It helps to
Externí odkaz:
https://doaj.org/article/8bfda5572dfc428fb4785e50857cda3b
Publikováno v:
Medical Journal of Dr. D.Y. Patil University, Vol 5, Iss 2, Pp 163-164 (2012)
A full-term vigorous baby male, was born at term. His micrognathia and cleft palate were immediately apparent but there was no clinical evidence of upper airway obstruction. Feeding was commenced with no initial problems. Prior to discharge on day 7
Externí odkaz:
https://doaj.org/article/08896da7495a45d68a36d60e2992b39b
Autor:
Shradha Salunkhe
Publikováno v:
MedPulse International Journal of Pediatrics. 17:06-09
Publikováno v:
MedPulse International Journal of Pediatrics. 13:12-15
Autor:
Sharad Agarkhedkar, Renuka Jadhav, Suhas Sodal, Anshuman Singh, Shradha Salunkhe, Sanjay Chavan
Publikováno v:
Pediatric Review: International Journal of Pediatric Research. 5:314-319
Background: To study the derangement of serum lipid profile in children 2 to 12 years with nephrotic syndrome. Methods: 50 children 2 to 12 years with nephrotic syndrome were identified. Patients were classified as remission, relapse and newly diagno
Autor:
Sharad Agarkhedkar, Rasika Bharaswadkar, Shradha Salunkhe, Gaurav Kumar, Shailaja Mane, Manu Batta
Publikováno v:
Pediatric Review: International Journal of Pediatric Research. 5:60-65
Autor:
Vineeta Pande, Shradha Salunkhe, Sharad Agarkhedkar, Rasika Bharaswadkar, Manojkumar Patil, Shailaja Mane
Publikováno v:
Medical Journal of Dr. D.Y. Patil Vidyapeeth. 14:656
Autor:
Shradha Salunkhe, Sudhir Malwade, Sharad Agarkhedkar, Anshuman Singh, Namarata Saini, Geeta Karambelkar
Publikováno v:
Journal of Evidence Based Medicine and Healthcare, Vol 3, Iss 25, Pp 1152-1157 (2016)
BACKGROUND Congenital anomaly of kidney and urinary tract (CAKUT) are among the most common anomalies diagnosed prenatally. Early diagnosis and timely intervention can preserve renal function and avoid morbidity. AIMS AND OBJECTIVES To screen, select