Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Muhammad Almas, Hashmi"'
Autor:
Muhammad Almas Hashmi, Aftab Anwar
Publikováno v:
Pakistan Armed Forces Medical Journal, Vol 68, Iss 3, Pp 627-633 (2018)
Objective: To determine the frequency of different predisposing illnesses and risk factors responsible for spread of chronic viral hepatitis in children. Study Design: Descriptive study. Place and Duration of Study: Department of Pediatric Gastroen
Externí odkaz:
https://doaj.org/article/5efd1e594ca5443cb14605bcf3ea984e
Publikováno v:
Pakistan Armed Forces Medical Journal, Vol 68, Iss 3, Pp 634-638 (2018)
Objective: To describe the presentation and outcome of upper gastrointestinal (GI) foreign bodies in children. Study Design: Descriptive case series. Place and Duration of Study: Department of Pediatric Gastroenterology, Hepatology & Nutrition, the
Externí odkaz:
https://doaj.org/article/00517c4877ff472389906ee11b128b05
Autor:
Kiran Mushtaq Toor, Munir Akmal Lodhi, Muhammad Almas Hashmi, Rabia Aziz, Huma Saleem Khan, Awais Tahir
Publikováno v:
Journal of the College of Physicians and Surgeons Pakistan. 30:1312-1315
Objective To determine the frequency and antimicrobial sensitivity pattern of microbial agents causing neonatal sepsis. Study design Descriptive study. Place and duration of study Neonatal ICU, Fauji Foundation Hospital, Rawalpindi; Foundation Univer
Publikováno v:
Clinical Biochemistry. 69:30-35
Inherited unconjugated hyperbilirubinemias are a group of disorders characterized by increased levels of serum unconjugated bilirubin and arise because of the imbalance between its production and elimination from the body. It includes Crigler-Najjar
Publikováno v:
Journal of Genetics. 97:1445-1449
Monosialotetrahexosylganglioside (GM1) is a rare lysosomal storage disorder caused by the deficiency of beta-galactosidase (β-Gal) encoded by galactose beta 1 (GLB1). It is clinically characterized by developmental delay attributed to multifold accu
Publikováno v:
Journal of the College of Physicians and Surgeons Pakistan. 30:433-434
Wilson's Disease (WD) is a common metabolic disorder predominantly involving liver, brain, and eyes. Pancreatic, renal, psychiatric, and cardiac involvement have also been described. No single investigation can be considered diagnostic of WD; therefo
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEM. 32(11)
Fanconi-Bickel syndrome (FBS) is a rare autosomal recessive carbohydrate metabolism disorder caused by mutations in SLC2A2 encoding the glucose transporter 2 (GLUT2) protein. The clinical manifestations include hepatomegaly, conditional hypo/hypergly
Publikováno v:
The Professional Medical Journal. 23:807-811
3 ORIGINAL PROF-3327 ABSTRACT… Objectives: Probiotics are alive organisms which confer health benefit when taken at an appropriate dosage. This study was done to determine the efficacy of probiotics in decreasing the frequency of diarrhea in childr
Publikováno v:
Journal of genetics. 97(5)
Monosialotetrahexosylganglioside (GM1) is a rare lysosomal storage disorder caused by the deficiency of beta-galactosidase (β-Gal) encoded by galactose beta 1 (
Autor:
Mehmood, Shaikh, Khawaja Ahmad, Irfan Waheed, Sulman, Javaid, Rafia, Gul, Muhammad Almas, Hashmi, Syeda Tehseen, Fatima
Publikováno v:
Journal of Ayub Medical College, Abbottabad : JAMC. 28(3)
Meconium aspiration syndrome (MAS) is respiratory distress in an infant born through meconium stained amniotic fluid (MSAF) whose signs cannot be otherwise explained. MAS is associated with different complications. Many studies have been conducted in