Zobrazeno 1 - 10
of 155
pro vyhledávání: '"Deepika Jain"'
Autor:
Jayesh Sheth, Aadhira Nair, Frenny Sheth, Manali Ajagekar, Tejasvi Dhondekar, Inusha Panigrahi, Ashish Bavdekar, Sheela Nampoothiri, Chaitanya Datar, Ajit Gandhi, Mamta Muranjan, Anupriya Kaur, Manisha Desai, Mehul Mistri, Chitra Patel, Premal Naik, Maulin Shah, Koumudi Godbole, Seema Kapoor, Neerja Gupta, Sunita Bijarnia-Mahay, Sandeep Kadam, Dhaval Solanki, Soham Desai, Anand Iyer, Ketan Patel, Harsh Patel, Raju C. Shah, Shalmi Mehta, Ruchi Shah, Riddhi Bhavsar, Jhanvi Shah, Mili Pandya, Bhagyadhan Patel, Sudhir Shah, Heli Shah, Shalin Shah, Shruti Bajaj, Siddharth Shah, Nilam Thaker, Umesh Kalane, Mahesh Kamate, Vykunta Raju KN, Naresh Tayade, Sujatha Jagadeesan, Deepika Jain, Mitesh Chandarana, Jitendra Singh, Sanjiv Mehta, Beena Suresh, Harsh Sheth
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-17 (2024)
Abstract Background Rare disorders comprise of ~ 7500 different conditions affecting multiple systems. Diagnosis of rare diseases is complex due to dearth of specialized medical professionals, testing labs and limited therapeutic options. There is sc
Externí odkaz:
https://doaj.org/article/2e11021daa8849e989ed195e21ef0b00
Publikováno v:
BMC Musculoskeletal Disorders, Vol 25, Iss 1, Pp 1-9 (2024)
Abstract Background Superior mesenteric artery (SMA) syndrome, also known as Wilkie’s syndrome, is a rare but serious complication following scoliosis correction surgery. It occurs as a result of mechanical compression of third part of duodenum bet
Externí odkaz:
https://doaj.org/article/fef13eace2134520b6281dd42cfcb050
Publikováno v:
JGH Open, Vol 7, Iss 12, Pp 923-927 (2023)
Abstract Background and Aim Celiac disease (CeD) is mainly reported from the northern and western parts of India. In central India, it is believed to be a disease of children, with limited data among adults diagnosed for the first time after the age
Externí odkaz:
https://doaj.org/article/a61ba39e341a46ffab2e51094c78c688
Autor:
Frenny Sheth, Jhanvi Shah, Deepika Jain, Siddharth Shah, Harshkumar Patel, Ketan Patel, Dhaval I Solanki, Anand S Iyer, Bhargavi Menghani, Priti Mhatre, Sanjiv Mehta, Shruti Bajaj, Vishal Patel, Manoj Pandya, Deepak Dhami, Darshan Patel, Jayesh Sheth, Harsh Sheth
Publikováno v:
BMC Neurology, Vol 23, Iss 1, Pp 1-15 (2023)
Abstract Background Autism spectrum disorder (ASD) affects 1 in 100 children globally with a rapidly increasing prevalence. To the best of our knowledge, no data exists on the genetic architecture of ASD in India. This study aimed to identify the gen
Externí odkaz:
https://doaj.org/article/0a811d51a4c7480ba1bd9d0625f615fe
Publikováno v:
Partial Differential Equations in Applied Mathematics, Vol 8, Iss , Pp 100540- (2023)
The importance of differential equations of integer order and fractional order can be seen in many areas of engineering and applied sciences. The present work involves fractional order heat equations that arise in numerous applications of engineering
Externí odkaz:
https://doaj.org/article/662d245cd2374aafa24abb7212580b62
Autor:
Jayesh Sheth, Siddharth Shah, Chaitanya Datar, Kaveri Bhatt, Pooja Raval, Aadhira Nair, Deepika Jain, Jhanvi Shah, Frenny Sheth, Harsh Sheth
Publikováno v:
BMC Pediatrics, Vol 23, Iss 1, Pp 1-7 (2023)
Abstract Background Multiple sulfatase deficiency (MSD) is a rare lysosomal storage disorder caused due to pathogenic variants in the SUMF1 gene. The SUMF1 gene encodes for formylglycine generating enzyme (FGE) that is involved in the catalytic activ
Externí odkaz:
https://doaj.org/article/962909a055b64f58ad03586371dd8e0c
Publikováno v:
Archives of Medicine and Health Sciences, Vol 11, Iss 2, Pp 194-197 (2023)
Background and Aim: Wearing white coat is a recognizable symbol among dental students. It is associated with dignity and respect. However, students are often spotted wearing white coat/apron in public places, a trait that needs to be explored/rectifi
Externí odkaz:
https://doaj.org/article/d597ed4c28c449e9aa9430358677afa5
Autor:
Frenny Sheth, Jhanvi Shah, Ketan Patel, Darshan Patel, Deepika Jain, Jayesh Sheth, Harsh Sheth
Publikováno v:
BMC Neurology, Vol 23, Iss 1, Pp 1-8 (2023)
Abstract Introduction NEUROG1 gene is yet to be associated with a set of human phenotypes in the OMIM database. Three cases have previously been diagnosed with cranial dysinnervation due to biallelic variants in the NEUROG1 gene. This is the fourth a
Externí odkaz:
https://doaj.org/article/8d3ad35ae5a64309bace6d0909e6712d
Autor:
Shivani Sharma, Sourav K. Mishra, Mohit Bhardwaj, Shilpy Jha, Matthew Geller, Aditi Dewan, Ekta Jain, Mallika Dixit, Deepika Jain, Gauri Munjal, Shivmurti Kumar, Sambit K. Mohanty
Publikováno v:
South Asian Journal of Cancer, Vol 11, Iss 03, Pp 249-255 (2022)
Abstract Sambit K. Mohanty Objective Repressor of Silencing (ROS1) gene rearrangement in the lung adenocarcinomas is one of the targetable mutually exclusive genomic alteration. Fluorescence in situ hybridization (FISH), immunohistochemistry (IHC),
Externí odkaz:
https://doaj.org/article/7f7bcee607de4581b4502dd4dbaa554a
Publikováno v:
BMC Neurology, Vol 21, Iss 1, Pp 1-8 (2021)
Abstract Background Rett syndrome (RTT) is characterized by a normal perinatal period with a normal head size at birth followed by normal development for the first 6 months of life followed by gradual deceleration of head growth, loss of acquired pur
Externí odkaz:
https://doaj.org/article/f714cd61c7c14c2a9478475d1bc45901