Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Zafar Fayyaz"'
Autor:
Huma Arshad Cheema, Zafar Fayyaz, Anjum Saeed, Muhammad Nadeem Anjum, Sadaqat Ijaz, Muhammad Arshad Alvi, Syeda Sara Batool
Publikováno v:
The Turkish Journal of Gastroenterology, Vol 34, Iss 10, Pp 1088-1098 (2023)
Externí odkaz:
https://doaj.org/article/68d61de177bf4b8782e9d1a0c799ef5f
Autor:
Muhammad Salman Khoso, Anjum Saeed, Muhammad Nadeem Anjum, Zafar Fayyaz, Muhammad Arshad Alvi, Hiba Kokab, Hooria Rehman
Publikováno v:
Pakistan Armed Forces Medical Journal, Vol 74, Iss 2 (2024)
Objective: To determine the endoscopic findings and its correlation with outcome in oesophageal battery button ingestion in children. Study Design: Cross sectional study. Place and duration of study: Department of Paediatric Gastroenterology, Hep
Externí odkaz:
https://doaj.org/article/78217b9b4f304d1eb412b64d46c3422b
Autor:
Huma Arshad Cheema, Nadia Waheed, Anjum Saeed, Muhammad Nadeem Anjum, Zafar Fayyaz, Sadaqat Ijaz
Publikováno v:
Journal of the Pakistan Medical Association, Vol 73, Iss 8 (2023)
Objective: To report the mutational landscape of a clinically diagnosed cohort of paediatric patients with cholestasis liver diseases. Method: The retrospective study was conducted at the University of Child Health Sciences, The Children Hospital,
Externí odkaz:
https://doaj.org/article/a4f927d51a0748578e6b62bfddcc8fc0
Autor:
Hooria Rehman, Huma Arshad Cheema, Muhammad Arshad Alvi, Muhammad Nadeem Anjum, Zafar Fayyaz, Syeda Sara Batool, Anjum Saeed
Publikováno v:
Pakistan Armed Forces Medical Journal, Vol 72, Iss 5 (2022)
Objective: To evaluate the quality of life among children with inflammatory bowel disease (IBD) by the inflammatory bowel disease questionnaire. Study Design: Cross-sectional study. Place and Duration of the Study: Department of Pediatric Gastr
Externí odkaz:
https://doaj.org/article/b47c8b4ac8684400b5ab2c58e1dde2ae
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 22, Iss 1, Pp 1-6 (2021)
Abstract Background Methylmalonic acidemia with homocystinuria is caused by a rare inborn error of vitamin B12 (cobalamin) metabolism. There are four complementation classes of cobalamin defects cblC, cblD, cblF, and cblJ that are responsible for com
Externí odkaz:
https://doaj.org/article/439b09fde72b41a08174148dc62af136
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 22, Iss 1, Pp 1-10 (2021)
Abstract Background Chanarin–Dorfman syndrome (CDS; OMIM # 275630) is a rare neutral lipid storage disorder caused by mutation in ABHD5 (a/b hydrolase domain containing 5″) a cofactor for adipose triglyceride lipase (ATGL) resulting in intracellu
Externí odkaz:
https://doaj.org/article/8a3d04d7ea5948b4adc48306637a579b
Autor:
Muhammad Bilal Mirza, Asim Shahzad, Nasir Mahmood, Ahmed Imran, Mahvish Hussain, Zafar Fayyaz, Nabila Talat
Publikováno v:
Annals of Pediatric Surgery, Vol 16, Iss 1, Pp 1-7 (2020)
Abstract Background Alimentary tract duplications are rare anomalies and any delay in the diagnosis may develop various complications. Infection, hemorrhage, or perforation of the duplication cyst may lead to an acute presentation. Occasionally, it m
Externí odkaz:
https://doaj.org/article/27d81f601e0b479095ec0d6ec927670a
Autor:
Huma Arshad Cheema, Nadia Waheed, Anjum Saeed, Zafar Fayyaz, Muhammad Nadeem Anjum, Muhammad Arshad Alvi, Syeda Sara Batool
Publikováno v:
Journal of the Pakistan Medical Association, Vol 71, Iss 10 (2021)
Background: Very early-onset inflammatory bowel disease (VEO-IBD) is defined as diagnosis of Ulcerative Colitis (UC) or Crohn’s Disease (CD) in children under six years of age. Genome wide association studies have linked a strong genetic componen
Externí odkaz:
https://doaj.org/article/ea18184265594636ad70779376afdfb7
Autor:
Anjum Saeed, Syeda Sara Batool, Zafar Fayyaz, Muhammad Nadeem Anjum, Muhammad Arshad Alvi, Huma Arshad Cheema, Hooria Rehman
Publikováno v:
Pakistan Armed Forces Medical Journal. 72:1698-1702
Objective: To evaluate the quality of life among children with inflammatory bowel disease (IBD) by the inflammatory bowel disease questionnaire. Study Design: Cross-sectional study. Place and Duration of the Study: Department of Pediatric Gastroenter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::93eddf72ad0e2c4ab5f6d02e73d8809d
https://doi.org/10.51253/pafmj.v72i5.6845
https://doi.org/10.51253/pafmj.v72i5.6845
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 22, Iss 1, Pp 1-6 (2021)
Background Methylmalonic acidemia with homocystinuria is caused by a rare inborn error of vitamin B12 (cobalamin) metabolism. There are four complementation classes of cobalamin defects cblC, cblD, cblF, and cblJ that are responsible for combined met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bfc29b12e130c7a0beda50dfd4f5d1a
https://doaj.org/article/439b09fde72b41a08174148dc62af136
https://doaj.org/article/439b09fde72b41a08174148dc62af136