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Clinical Chemistry|September 1, 1994
Molecular diagnosis of acute intermittent porphyria by analysis of DNA extracted from hair rootsW E Schreiber, F Fong, A JamaniThe Medical Journal of Malaysia|January 28, 2022
The bleeding umbilicus: An uncommon presentation of endometriosisN A Jamani, Z Nusee, I HamizahHuman Genetics|May 1, 1994
Frameshift mutations in exons 9 and 10 of the porphobilinogen deaminase gene produce a crossreacting immunological material (CRIM)-negative form of acute intermittent porphyriaW E Schreiber, F Fong, A JamaniAmerican Journal of Clinical Pathology|June 1, 1995
Acute intermittent porphyria in a native North American family. Biochemical and molecular analysisW E Schreiber, A Jamani, J G ArmstrongAmerican Journal of Clinical Pathology|November 1, 1989
Screening tests for porphobilinogen are insensitive. The problem and its solutionW E Schreiber, A Jamani, M R PudekClinical Chemistry|June 1, 1991
Quantitative fluorometric screening test for fecal porphyrinsM R Pudek, W E Schreiber, A JamaniMalaysian Family Physician : the Official Journal of the Academy of Family Physicians of Malaysia|August 27, 2020
An infant with kwashiorkor: The forgotten diseaseN A Kamaruzaman, N A Jamani, A H SaidThe Medical Journal of Malaysia|September 11, 2021
It is tuberculosis or melioidosis? A clinical diagnostic dilemmaN A Jamani, F H Mohd Nor, Y YatimThe Medical Journal of Malaysia|July 31, 2025
Impact of structured physical exercise during pregnancy on maternal health and fetal outcomes: A systematic reviewF H MohdNor, N A Jamani, K H AbdAzizHuman Mutation|January 1, 1997
Hereditary coproporphyria: exon screening by heteroduplex analysis detects three novel mutations in the coproporphyrinogen oxidase geneW E Schreiber, X Zhang, J Senz, et al.Pageof 2