Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Sara Sultana"'
Publikováno v:
Asian Journal of Medical Sciences, Vol 15, Iss 1, Pp 66-70 (2024)
Background: Cataract, a major cause of treatable blindness accounting for 80% of cases, arises from a complex etiology involving various factors. Diabetes notably expedites cataract development, and its potential interaction with electrolyte imbalanc
Externí odkaz:
https://doaj.org/article/cc301d3f93054e20afbe7caf8d200e95
Publikováno v:
Nutrition & Food Science. 50:131-142
Purpose Energy drink (ED) consumption has become a common trend, especially among the youth. Hence, the purpose of this study was undertaken to assess the ED consumption pattern among the university students and investigate the independent predictors
Autor:
Sara Sultana
Publikováno v:
MedPulse International Journal of Ophthalmology. 11:86-89
Publikováno v:
IP International Journal of Ocular Oncology and Oculoplasty. 4:172-173
Aim: To study correlation between clinical features and histopathological exam of ocular surface squamous neoplasia. Materials and Methods: This is a Prospective interventional study conducted at the department of Oculoplasty of Sarojini Devi eye hos
Autor:
Masood Ahmed Shareef, Sara Sultana
Publikováno v:
MedPulse International Journal of Ophthalmology. 11:76-78
Autor:
Sara Sultana, Braj Nandan Kumar Sah
Publikováno v:
International Journal of Medical and Biomedical Studies. 3
Objectives: This present study was done to compare the tolerability and efficacy of tramadol versus aceclofenac in terms of WOMAC Osteoarthritis Index and Visual Analogue Scale of patients with osteoarthritis of knee joint. Methods: A detail history,
Publikováno v:
The International Journal of Electrical Engineering & Education. 54:105-118
The student dropout rate in universities is fascinating, especially among the students of Electrical Engineering. Even the most developed European countries face 40% to 50% dropout rate of engineering students during their first year, and the rate ca
Autor:
Hiba A. Al-Shawafi, Sara Sultana, Miwa Sohda, Saori Makita, Norio Amizuka, Kimimitsu Oda, Ritsuo Takagi
Publikováno v:
Molecular Genetics and Metabolism. 109:282-288
Various loss-of function mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene cause a rare genetic disorder called hypophosphatasia (HPP), which is characterized by defective mineralization in the bones and teeth and a deficiency in
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1822:581-588
Hypophosphatasia (HPP), a rare genetic disease characterized by reduced serum alkaline phosphatase (ALP) activity and failure in bone and tooth mineralization, is caused by mutations in tissue-nonspecific ALP (TNSALP) gene. Two missense mutations (C2
Autor:
Yoko Okada, Kenichiro Kobayashi, Hitomi Ueno, Sara Sultana, Nobutaka Kiyokawa, Takeshi Ishibashi, Shingo Akimoto, Jun-ichi Nagai, Hiroyuki Takahashi, Naoyuki Miyagawa, Masaki Matsuoka, Hiroaki Goto, Kimikazu Matsumoto, Kazumasa Mitsui, Kaori Ootsubo, Akira Ohara, Yasuko Kojima, Hajime Okita
Publikováno v:
Pediatric Blood & Cancer. 62:1058-1060
We report a 10-year-old male with relapsing Ph-like acute lymphoblastic leukemia (ALL) bearing ATF7IP/PDGFRB translocation. He was refractory to conventional therapy, and was finally treated with single-agent second-generation TKI dasatinib. The ther