Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Hinglaj Saha"'
Autor:
Somak Krishna Biswas, Kalyani Saha Basu, Sumitra Kumar Biswas, Hinglaj Saha, Subhankar Chakravorty, Jay Kishor Soren
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 25, Iss 4, Pp 213-218 (2020)
Background: Choledochal cyst is a fairly common hepatobiliary condition in pediatric surgical practice. For the most common type (type I), it is well established that the total excision of the cyst with an wide biliary-enteric anastomosis is key for
Externí odkaz:
https://doaj.org/article/5c039c7b49df4a56a429390719b10644
Autor:
Hinglaj Saha, Dipak Ghosh, Somak Kumar Biswas, Prafulla Kumar Mishra, Kaushik Saha, Uttara Chatterjee
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 24, Iss 1, Pp 52-60 (2019)
Context: Synchronous Bilateral Wilms tumor (sBWT). Aims: This study aimed to assess the outcome of patients with sBWT treated on SIOP protocol. Settings and Design: Retrospective and prospective randomized study. Subjects and Methods: SIOP 93-01 prot
Externí odkaz:
https://doaj.org/article/74612ff160f945d49cfc61750de2d95c
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 23, Iss 4, Pp 206-211 (2018)
Context and Aim: The aim of this study is to highlight the rarity of this disorder and its associated anomalies and our objective was to review our experience in the management of colonic atresia (CA) with respect to staged surgery versus one-step pr
Externí odkaz:
https://doaj.org/article/77bebe9710794f1fb8c061b7fd68d1a9
Autor:
Hinglaj Saha, Ghosh Tapanjyoti, Somak Biswas, Prafulla Kumar Mishra, Kalyani Saha Basu, Uttara Chatterjee
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 24, Iss 1, Pp 75-77 (2019)
Progressive familial intrahepatic cholestasis (PFIC) is a rare bile acid transporter defect and autosomal recessive disorder with type 2 being the most common type. Partial internal or external biliary diversion delays its progression to end-stage li
Externí odkaz:
https://doaj.org/article/b6497afce4d14a88909a9fdf60c271e9
Publikováno v:
Journal of Pediatric Surgery. 54:2291-2299
Purpose To assess the thickness of the intestinal smooth muscle layer and analyze the distribution and density of interstitial cells of Cajal (ICC) and enteric neurons in the proximal and distal segments of neonatal jejuno-ileal atresia. Methods This
Autor:
Madhumita Mukhopadhyay, Hinglaj Saha, Moupali Ghosh, Koushik Saha, Nelofar Islam, Chhanda Datta, Uttara Chatterjee
Publikováno v:
Diagnostic Cytopathology. 46:776-781
Inflammatory myofibroblastic tumor is a tumor of intermediate grade with a low rate of metastasis. The tumor often mimics malignancy. There is sparse literature available describing the cytological findings of this rare condition. It often presents i
Autor:
Kaushik Saha, Hinglaj Saha, Dipak Ghosh, Somak Kumar Biswas, Uttara Chatterjee, Prafulla Kumar Mishra
Publikováno v:
Journal of Indian Association of Pediatric Surgeons
Journal of Indian Association of Pediatric Surgeons, Vol 24, Iss 1, Pp 52-60 (2019)
Journal of Indian Association of Pediatric Surgeons, Vol 24, Iss 1, Pp 52-60 (2019)
Context: Synchronous Bilateral Wilms tumor (sBWT). Aims: This study aimed to assess the outcome of patients with sBWT treated on SIOP protocol. Settings and Design: Retrospective and prospective randomized study. Subjects and Methods: SIOP 93-01 prot
Publikováno v:
International Journal of Human Genetics. 13:1-6
Breast cancer is the most frequent malignancy among women. Since genetic factors such as BRCA1 and BRCA2 as well as reproductive history constitute 30% of the cause, environmental exposure may play a significant role in the development of breast canc
Publikováno v:
Journal of Pediatric Neurosciences. 13:352
Intrathoracic migration of ventriculoperitoneal shunt is a rare complication and usually complicated with pneumonia or cerebrospinal fluid hydrothorax, which leads to diagnosis and early interventions. Very rarely patient remains asymptomatic. Here i
Autor:
Hinglaj Saha
Publikováno v:
INTERNATIONAL JOURNAL OF HUMAN GENETICS. 13