Zobrazeno 1 - 10
of 589
pro vyhledávání: '"Kamal Nain"'
Autor:
Kamal Nain Rattan, Deepak Kumar Garg
Publikováno v:
Journal of Neonatal Surgery, Vol 5, Iss 4 (2020)
Background: Type III and IV jejunoileal atresias are associated with loss of significant length of the gut and can lead to short gut syndrome if further resection of proximal dilated gut is done. We modified the anastomotic technique so that proximal
Externí odkaz:
https://doaj.org/article/98aa3c312b8a4aafbda432a3fc235706
Publikováno v:
Journal of Neonatal Surgery, Vol 5, Iss 4 (2020)
Please see fulltext
Externí odkaz:
https://doaj.org/article/1e8afa51c1934efea52321730a845527
Publikováno v:
Interdisciplinary Neurosurgery, Vol 17, Iss , Pp 49-51 (2019)
With the availability of advanced diagnostic and therapeutic modalities, late presentation of hydrocephalus is a very uncommon occurrence in the present era. Here, we report an 11-months infant with late presenting hydrocephalus with spontaneous rupt
Externí odkaz:
https://doaj.org/article/6bd6c5f5de7548c6abf1cdd09f35f5d6
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 20, Iss 2, Pp 174-176 (2019)
Verrucous hemangioma is an uncommon capillary or cavernous hemangioma with reactive epidermal changes of hyperkeratosis, acanthosis, and papillomatosis. Lesions are mostly seen at birth or appear during childhood. These growths are usually located on
Externí odkaz:
https://doaj.org/article/e2be5f3c658f45499fc5f9200de5e33f
Publikováno v:
Iranian Journal of Pediatric Surgery, Vol 3, Iss 1, Pp 46-50 (2017)
Congenital mesoblasticnephroma (CMN) is a benign and very rare renal tumor, typically occurring in utero or during infancy. We are reporting a very young case of left sided classical congenital mesoblasticnephroma in a full term, small for gestationa
Externí odkaz:
https://doaj.org/article/2974acb2b43748399ed590cd17acdf20
Publikováno v:
Middle East Journal of Cancer, Vol 8, Iss 3, Pp 143-150 (2017)
Background: Wilms’ tumor is the most common malignant renal tumor in the pediatric age group. This tumor is classically managed by multimodal treatment which involves surgery, radiotherapy and chemotherapy. While there is plenty of data in world
Externí odkaz:
https://doaj.org/article/192e75534f0049219cc30b21963d9b4b
Publikováno v:
Journal of Pediatric and Neonatal Individualized Medicine, Vol 9, Iss 1, Pp e090105-e090105 (2019)
Despite significant advances, the management of giant omphalocele (GO) still remains a challenging job for neonatologists and pediatric surgeons. Early surgical treatment of GO may not be undertaken in every patient due to the risk of fatal hemodynam
Externí odkaz:
https://doaj.org/article/beb71db0432f4f3b94b3da3edf947c01
Publikováno v:
Proceedings of Singapore Healthcare, Vol 28 (2019)
Recent advances in the perinatal interventions for neonates with congenital diaphragmatic hernia have remarkably improved the outcome in developed countries, but high mortality for such cases continues to be a challenge in resource-poor settings. Thi
Externí odkaz:
https://doaj.org/article/6a3a6913eab74d49bec040c4b953d120
Publikováno v:
Iranian Journal of Pediatric Surgery, Vol 2, Iss 1, Pp 36-39 (2016)
Introduction: Foregut duplication cysts along with vertebral anomalies are called neurenteric cyst. About 30 cases have been reported in the literature so far. Posterior mediastinal neurenteric cysts are very rare and few studies could be found in th
Externí odkaz:
https://doaj.org/article/3b78241029ab46d19198c60d1219ca50