Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Awais Abbas"'
Autor:
Ayaz Ur Rehman, Salman Khan, Awais Abbas, Hamdan Ahmad Pasha, Qalab Abbas, Naveed Ur Rehman Siddiqui
Publikováno v:
Journal of Medical Case Reports, Vol 17, Iss 1, Pp 1-5 (2023)
Abstract Background Deep neck space infections are uncommon in infants. Retropharyngeal abscess (RPA) is a deep space neck infection that can present with subtle signs and symptoms. Delay in diagnosis can lead to life-threatening complications. Here
Externí odkaz:
https://doaj.org/article/892ba2ba1d12433faea04c7c8067a4d1
Autor:
Saadullah Farooq Abbasi, Awais Abbas, Iftikhar Ahmad, Mohammed S. Alshehri, Sultan Almakdi, Yazeed Yasin Ghadi, Jawad Ahmad
Publikováno v:
Heliyon, Vol 9, Iss 11, Pp e22195- (2023)
Sleep is an essential feature of living beings. For neonates, it is vital for their mental and physical development. Sleep stage cycling is an important parameter to assess neonatal brain and physical development. Therefore, it is crucial to administ
Externí odkaz:
https://doaj.org/article/a21a0a891c6e40e7b5e5efb1dfff692f
Autor:
Awais Abbas, Faris Abdul Aziz, Naveed Ur Rehman Siddiqui, Yasmin Hashwani, Iraj Khan, Aniqa Abdul Rasool, Anwar Ul Haque, Qalab Abbas
Publikováno v:
Journal of Pediatric Critical Care, Vol 10, Iss 5, Pp 213-219 (2023)
Background: Patients admitted to critical care need timely interventions after evaluating all clinical parameters. This study aims to assess the impact of the comprehensive rounding checklist on physician compliance and patient-related outcomes in a
Externí odkaz:
https://doaj.org/article/29ebcadc47c541f59c44a92d06f295dd
Autor:
Dr Muhammad Pervaiz Bhatti, Anfal Munir, Aqsa Riaz, Zohaib Saeed, Awais Abbas, Muhammad Imran, Ayoub Rashid, Ahmad Adnan
Publikováno v:
SSRN Electronic Journal.
Autor:
Awais Abbas, Sadaf Sarfraz, Umer Younas, Dr Muhammad Pervaiz Bhatti, Shahid Hussain, Zahid Ali, Mazhar Asjad, Shahid Iqbalf
Publikováno v:
SSRN Electronic Journal.
Publikováno v:
Cureus
Hereditary tyrosinemia type 1 (HT-1) is a rare autosomal recessive disorder caused by a deficiency in the enzyme fumarylacetoacetate hydrolase (FAH), which catalyzes the final step in the tyrosine degradation pathway. Hereditary tyrosinemia is a hete
Publikováno v:
Critical Care Medicine. 50:122-122
Publikováno v:
CCECE
A Nonlinear model predictive control (NMPC) for trajectory tracking with the obstacle avoidance of autonomous road vehicles traveling at realistic speeds is presented in this paper, with a focus on the performance of those controllers with respect to
Publikováno v:
Cureus
Malignant rhabdoid tumor of the kidney (MRTK) is a rare neoplasm of infancy. We report a case of a nine-month-old male infant who presented to the pediatrics outpatient department with the history of fever, lethargy, and abnormal head movements. On g
Publikováno v:
Cureus
Charcot-Marie-Tooth (CMT) disease, also referred to as hereditary motor and sensory neuropathy (HMSN), is a heterogeneous group of disorders which primarily affects the peripheral nervous system. Clinically, the main features are progressive muscle w