April 2012, Volume 62, Issue 4
Editorial
Biotinidase deficiency (BD) is a biotin responsive, autosomal recessive inherited neurocutaneous, treatable metabolic disorder. It occurs due to the deficiency of an enzyme biotinidase, which is involved in biotin cycle. As a result of BD the vitamin biotin is not recycled in biot
ORIGINAL ARTICLES
Clinical scenario of primary dyslipidaemia in the paediatric age group; an Egyptian experience
Rania Hosny Tomerak , et al
Poisoning by carbon monoxide in Morocco from 1991 to 2008
Hanane Chaoui , et al
Outcome of surgical treatment of monocular elevation deficiency
Saemah Nuzhat Zafar , et al
RESEARCH ARTICLES
IN THIS ISSUE
Short Communication
Morbidity pattern of sick hospitalized preterm infants in Karachi, Pakistan
Muhammad Rehan Khan , et al
Opinion and Debate
Evidence Based Medicine
Learning Research
REVIEW ARTICLES
CASE REPORTS
Report of Haemoglobin J-Toronto and alpha thalassemia in a family from North of Iran
Mohammad Reza Mahdavi , et al
Minimally invasive endoscopic selective parathyroidectomy
Montasir Junaid , et al
STUDENTS' CORNER
Journal of the Pakistan Medical Association has agreed to receive and publish manuscripts in accordance with the principles of the following committees: