Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Sibnath Gayen"'
Autor:
Sibnath Gayen, Arabinda Kar Chowdhury, Picaso Chowdhury, Pankaj Kumar Halder, Damini Dutta, Partha Chakraborty
Publikováno v:
Journal of the Scientific Society, Vol 50, Iss 1, Pp 121-124 (2023)
Multicystic dysplastic kidney (MCDK) is a congenital somatic maldevelopment in which the renal cortex is replaced by numerous cysts of varying sizes with insinuating dysplastic parenchyma in between. In 76% of cases, it is unilateral occurring on the
Externí odkaz:
https://doaj.org/article/ebbcbb6137b04c8b9d9748cc10d0ebb0
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 18, Iss 1, Pp 60-61 (2017)
Externí odkaz:
https://doaj.org/article/50b259a94fbb45278c3f878e939deeee
Publikováno v:
Oman Journal of Ophthalmology, Vol 4, Iss 2, Pp 101-102 (2011)
Externí odkaz:
https://doaj.org/article/753babf1c7f44be18220c8b3dfa05ddc
Publikováno v:
Oman Journal of Ophthalmology, Vol 3, Iss 3, Pp 153-154 (2010)
Externí odkaz:
https://doaj.org/article/9b8d69650ba9459e9f3be7a329a2e553
Autor:
PankajKumar Halder, Sibnath Gayen, ArabindaKar Chowdhury, Picaso Chowdhury, Damini Dutta, Partha Chakraborty
Publikováno v:
Journal of the Scientific Society. 50:121
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b58a6d639929deb35eb37e9b4dea27b4
https://doi.org/10.4103/jss.jss_137_22
https://doi.org/10.4103/jss.jss_137_22
Publikováno v:
INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH. :57-59
Introduction: Sepsis remains one of the most common causes of neonatal mortality and morbidity in India as also globally. Aim:To evaluate the level of procalcitonin (PCT) in the cord blood of the neonates born with perinatal risk factors for early-on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a721317325e3075e07f3bace99f0a718
https://doi.org/10.36106/0320035
https://doi.org/10.36106/0320035
Autor:
Pradipprava Paria, Saptarshi Das, Sibnath Gayen, Sibarjun Ghosh, Rajarshi Basu, Goutam Bandyopadhyay
Publikováno v:
The Indian journal of chest diseasesallied sciences. 58(1)
Congenital cystic adenomatoid malformation (CCAM) occurs secondary to the cystic adenomatous over-growth of terminal bronchioles, which results in the secondary inhibition of alveolar growth. In most of the cases, respiratory distress is the presenti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a0d7fc6db3eb5c77c46ed5c6bf322b6
https://pubmed.ncbi.nlm.nih.gov/28393565
https://pubmed.ncbi.nlm.nih.gov/28393565
Autor:
Sibarjun Ghosh, Sutirtha Roy, Pradipprava Paria, Indranil Chatterjee, Angshumitra Bandyopadhyay, Sibnath Gayen
Publikováno v:
Volume: 7, Issue: 0
Journal of Pediatric Sciences
Journal of Pediatric Sciences
Penoscrotal transposition, where malposition of penis occur in relation to scrotum. It is frequently associated with malformation of genitourinary, cardiovascular or skeletal system. As it is extremely rare no standard treatment protocol exist. We he
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1d07ddc7c220ea605484a446c317de1
https://dergipark.org.tr/tr/pub/jps/issue/19091/202534
https://dergipark.org.tr/tr/pub/jps/issue/19091/202534
Publikováno v:
International Journal of Research in Medical Sciences. :1733-1734
Dicephalus twins are very rare form of conjoined parapagus twins where there is a common body with two heads. They are subdivided into many groups depending on the number of upper limbs, lower limbs and number of torso. A dicephalus dibrachus dipus c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5215d16d7b2b5fd7d5edc034812449aa
https://doi.org/10.18203/2320-6012.ijrms20161259
https://doi.org/10.18203/2320-6012.ijrms20161259
Publikováno v:
International Journal of Medical Research and Health Sciences, Vol 5, Iss 1, Pp 105-106 (2016)
Harlequin ichthyosis is the most severe form of congenital ichthyosis. It is a rare autosomal recessive disorder (1:300,000). The vast majority of affected individuals are due to mutation in the ABCA12 gene, which cause a deficiency of the epidermal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b5cad154911af7d17f125c3e3b6065a
https://doi.org/10.5958/2319-5886.2016.00022.9
https://doi.org/10.5958/2319-5886.2016.00022.9