Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Sughra Wahid"'
Genetic analysis of osteopetrosis in Pakistani families identifies novel and known sequence variants
Autor:
Chunyu Liu, Muhammad Ajmal, Zaineb Akram, Tariq Ghafoor, Muhammad Farhan, Sobia Shafique, Sughra Wahid, Shahar Bano, Jianqiu Xiao, Humayoon Shafique Satti, Feng Zhang, Tahir Naeem Khan
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-9 (2021)
Abstract Osteopetrosis is a genetically heterogenous, fatal bone disorder characterized by increased bone density. Globally, various genetic causes are reported for osteopetrosis with all forms of inheritance patterns. A precise molecular diagnosis i
Externí odkaz:
https://doaj.org/article/2bf5b2c415524ca4aafc8083fa1e385f
Publikováno v:
European Medical Journal (2022)
Multisystem inflammatory syndrome (MIS-C) is a challenging disease associated with COVID-19. Clinical manifestation of MIS-C may mimic many endemic illnesses of tropical and subtropical countries, making early diagnosis more difficult. The authors pr
Externí odkaz:
https://doaj.org/article/96ef238596c445739a6abf2056881170
Autor:
Anam Zafar, Nahdia Zaman, Muhammad Salman Shafique, Shahzadi Sumbal Ghazi, Maryam Amjad, Sughra Wahid
Publikováno v:
Journal of Rawalpindi Medical College, Vol 25, Iss 3 (2021)
Objective: This study was conducted to compare epinephrine and salbutamol nebulization in emergency management of moderately ill children less than one and a half years old with bronchiolitis in terms of mean change in respiratory distress assessment
Externí odkaz:
https://doaj.org/article/c0194eb2cc88422d8087a652804c6b93
Autor:
Muhammad Ajmal, Asif Mir, Sughra Wahid, Chiea Chuen Khor, Jia Nee Foo, Saima Siddiqi, Mehran Kauser, Salman Akbar Malik, Muhammad Nasir
Publikováno v:
BMC Medical Genetics, Vol 18, Iss 1, Pp 1-9 (2017)
Abstract Background Osteopetrosis is a rare inherited bone disorder mainly described as an increased bone density caused by defective osteoclastic bone resorption. To date, genetic variants of eleven genes have been reported so far to be associated w
Externí odkaz:
https://doaj.org/article/76525fde385343eb99a2f450e8ff2350
Publikováno v:
Pakistan Armed Forces Medical Journal. 72:1392-96
Objectives: To study the impact of applying topical Chlorhexidine compared with Methylated spirit on umbilical cord sloughing time in neonates. Study Design: Quasi-experimental study. Place and Duration of Study: Paediatric Department, KRL Hospital,
Publikováno v:
Pakistan Armed Forces Medical Journal. 72:811-15
Objective: To study the abnormality of alanine aminotransferase (ALT) in enteric fever among children and to test the association between raised alanine aminotransferase with antibiotics resistance. Study Design: A descriptive prospective study. Plac
Autor:
Asma Tayyab, Alvina Asif, Shaista Qazi, Sughra Wahid, Anam Zafar, Michael Halim, Irshad Hussain, Hassan Mumtaz
Publikováno v:
Annals of Medicine & Surgery. 84
Asthma is one of the most common chronic diseases in children and worldwide its prevalence has increased dramatically in the last three decades. We aimed to compare single dose oral dexamethasone versus multiple doses of oral prednisolone in children
Genetic analysis of osteopetrosis in Pakistani families identifies novel and known sequence variants
Autor:
Tahir N. Khan, Chunyu Liu, Shahar Bano, Zaineb Akram, Muhammad Farhan, Sughra Wahid, Feng Zhang, Tariq Ghafoor, Jianqiu Xiao, Humayoon Shafique Satti, Muhammad Ajmal, Sobia Shafique
Publikováno v:
BMC Medical Genomics
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-9 (2021)
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-9 (2021)
Osteopetrosis is a genetically heterogenous, fatal bone disorder characterized by increased bone density. Globally, various genetic causes are reported for osteopetrosis with all forms of inheritance patterns. A precise molecular diagnosis is necessa
Autor:
Sughra Wahid, Maryam Amjad, Shahzadi Sumbal Ghazi, Muhammad Salman Shafique, Nahdia Zaman, Anam Zafar
Publikováno v:
Journal of Rawalpindi Medical College, Vol 25, Iss 3 (2021)
Objective: This study was conducted to compare epinephrine and salbutamol nebulization in emergency management of moderately ill children less than one and a half years old with bronchiolitis in terms of mean change in respiratory distress assessment
Autor:
Saima Siddiqi, Asif Mir, Muhammad Nasir, Chiea Chuen Khor, Salman Akbar Malik, Muhammad Ajmal, Mehran Kauser, Sughra Wahid, Jia Nee Foo
Publikováno v:
BMC Medical Genetics, Vol 18, Iss 1, Pp 1-9 (2017)
BMC Medical Genetics
BMC Medical Genetics
Background Osteopetrosis is a rare inherited bone disorder mainly described as an increased bone density caused by defective osteoclastic bone resorption. To date, genetic variants of eleven genes have been reported so far to be associated with diffe