Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Fibhaa Syed"'
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 98, Iss 5, Pp 580-586 (2023)
Abstract Background Ectodermal dysplasia syndactyly syndrome 1 (EDSS1) is a rare hereditary disorder characterized by defects in teeth, hair, and nails in association with a fusion of the digits. Genetically, the disease phenotypes are caused by homo
Externí odkaz:
https://doaj.org/article/9da5350d3906421fa84ae0ce4524d6bc
Autor:
Nida Zeb Abbasi, Kainaat Baig, Muhammad Hassan, Fibhaa Syed, Muhammad Anas Waheed Jami, Muhammad Usman
Publikováno v:
Journal of the Pakistan Medical Association, Vol 74, Iss 4 (2024)
Objectives: To evaluate the quality of sleep in patients hospitalised with coronavirus disease-2019, and its impact on hospitalisation duration, need for intensive care unit admission and mortality. Methods: The cross-sectional study was conducted
Externí odkaz:
https://doaj.org/article/bfa7934b6b5e41fbbfc0e50c1b4bf863
Autor:
Valeed Bin Mansoor, Saad Yunus Khan, Muhammad Arsalan Khan, Shafat Khatoon, Muhammad Arqam Miraj, Fibhaa Syed, Mohammad Ali Arif
Publikováno v:
Journal of the Pakistan Medical Association, Vol 74, Iss 1 (2023)
Wilson’s disease is a rare inherited disorder of copper metabolism. If left untreated, it can turn into a multi systemic disease with copper deposition in the liver, brain, and other tissues. Diagnosis of Wilson’s is delayed in Pakistan by many y
Externí odkaz:
https://doaj.org/article/d4e18d9b56204ae1aeb55a907fd6370f
Autor:
Muhammad Hassan, Fibhaa Syed, Naveed Ullah Khan, Zakir Jan, Hafiza Faiza Mushtaq, Nadir Hussain, Mazhar Badshah
Publikováno v:
The Egyptian Journal of Bronchology, Vol 16, Iss 1, Pp 1-3 (2022)
Abstract The pandemic of severe acute respiratory virus (SARS-CoV-2) is characterized by respiratory symptoms with serious consequences, mainly associated with pneumonia and extreme ARDS. There is a lack of data about pneumothorax associated with COV
Externí odkaz:
https://doaj.org/article/da75c61141d749c3853bd01f8931dc3b
Autor:
Muhammad Hassan, Fibhaa Syed, Liaqat Ali, Haris Majid Rajput, Farhan Faisal, Waleed Shahzad, Mazhar Badshah
Publikováno v:
Journal of Movement Disorders, Vol 14, Iss 3, Pp 245-247 (2021)
Externí odkaz:
https://doaj.org/article/ca6c2eaec7bf48e194b5cb00a9cc6a76
Autor:
Muhammad Hassan, Fibhaa Syed, Haris Majid Rajput, Hafiza Faiza Mushtaq, Naveed Ullah Khan, Mazhar Badshah
Publikováno v:
Brain Hemorrhages, Vol 2, Iss 3, Pp 134-136 (2021)
The pandemic of severe acute respiratory virus (SARS-CoV-2) is characterized by respiratory symptoms with serious consequences, mainly associated with pneumonia and extreme ARDS. There is a lack of data about specific neurological manifestations of c
Externí odkaz:
https://doaj.org/article/9d637bab56354475b348445b7ebd451b
Autor:
Fibhaa Syed, Muhammad Hassan, Aamir Shehzad, Salman Shafi Koul, Mohammad Ali Arif, Rebecca Susan Dewey, Tanwir Khaliq
Publikováno v:
Clinical eHealth, Vol 4, Iss , Pp 50-53 (2021)
Background: Telemedicine involves the innovative application of technology to provide remote patient healthcare services especially those relating to emergency care and contagious disease spread. Telemedicine is less developed in low-and-middle-incom
Externí odkaz:
https://doaj.org/article/68e5b689cc0347e1b3eba17006dbb69e
Autor:
Muhammad Hassan, Fibhaa Syed, Fatima Mustafa, Hafiza Faiza Mushtaq, Naveed Ullah Khan, Mazhar Badshah
Publikováno v:
Brain Hemorrhages, Vol 2, Iss 2, Pp 88-90 (2021)
Background: Covid-19 pandemic has been manifested mainly as respiratory and constitutional symptoms. Though, it may demonstrate the involvement of other systems i.e. cardiovascular system (CVS), central nervous system (CNS) or gastrointestinal system
Externí odkaz:
https://doaj.org/article/73420e82a363401eaf128e75410596d2
Autor:
Fibhaa Syed, Mohammad Ali Arif, Adil Ramzan, Rauf Niazi, Muhammad Irfan Murtaza, Ayesha Javed
Publikováno v:
Journal of the Pakistan Medical Association (2022)
Objective: To identify patient practices and knowledge pertaining to Ramadan fasting and to see whether physicians were providing adequate counselling and adjusting medications accordingly. Methods: The cross-sectional study was conducted at the Paki
Externí odkaz:
https://doaj.org/article/0fed93d762644639886a45482b80a166
Autor:
Asmat Ullah, Abid Ali Shah, Fibhaa Syed, Arif Mahmood, Hassan Ur Rehman, Beenish Khurshid, Abdus Samad, Wasim Ahmad, Sulman Basit
Publikováno v:
Medicina, Vol 59, Iss 2, p 379 (2023)
Background and Objective: Mutations in the CYB5R3 gene cause reduced NADH-dependent cytochrome b5 reductase enzyme function and consequently lead to recessive congenital methemoglobinemia (RCM). RCM exists as RCM type I (RCM1) and RCM type II (RCM2).
Externí odkaz:
https://doaj.org/article/e49e79e4c018435aa4e4c534e0a986e8