Displaying publications 5901 - 5920 of 25147 in total

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  1. Dutt KA, Velathaun T
    Med J Malaya, 1971 Sep;26(1):65-7.
    PMID: 4258580
    Matched MeSH terms: Female
  2. Menon R
    Med J Malaya, 1971 Sep;26(1):30-3.
    PMID: 4258572
    Matched MeSH terms: Female
  3. Sreenevasan G
    Br J Urol, 1970 Dec;42(6):741.
    PMID: 5497398
    Matched MeSH terms: Female
  4. Dutt AK
    Med J Malaya, 1970 Mar;24(3):234-7.
    PMID: 4246809
    Matched MeSH terms: Female
  5. Dugdale AE
    J Trop Pediatr (1967), 1969 Jun;15(2):34-9.
    PMID: 5306514
    Matched MeSH terms: Female
  6. Roe TN, Lal K, Cawkell WA
    Med J Malaya, 1968 Sep;23(1):78-9.
    PMID: 4237564
    Matched MeSH terms: Female
  7. Chan DP
    Med J Malaya, 1967 Dec;22(2):82-6.
    PMID: 4231983
    Matched MeSH terms: Female
  8. Mendoza-Barker MG
    Med J Malaya, 1965 Jun;19(4):306-10.
    PMID: 4220857
    Matched MeSH terms: Female
  9. Hartini, Y., Mohamed Kamel, A.G.
    Medicine & Health, 2010;5(2):60-65.
    MyJurnal
    A cross-sectional study was carried out in 2006 to determine the prevalence of Ascaris lumbricoides infection among Orang Asli (aborigines) children in Pos Lenjang, Pahang. A total of 71 faecal samples were collected from the children (40 girls and 31 boys) aged between 1-12 years. The samples were examined for the presence of the ova of A. lumbricoides using direct faecal smear and formalin-ether concentration techniques. 42.3%. The prevalence of A. lumbricoides infection was found to be slightly higher in males (45.2%) compared to females (40%) (p>0.05). The school-aged children showed higher prevalence of infection (48.6%) as compared to the preschool children (35.3%) (p
    Matched MeSH terms: Female
  10. Phan, CL, Ong, TC, Chang, KM, Zubaidah, Z., Puteri Jamilatul, N.M.B.
    Medicine & Health, 2010;5(1):45-48.
    MyJurnal
    The t(8;21)(q22;q22) is a frequently occurring aberration in acute myeloid leukemia (AML) (18-20%) and usually correlate with French-America-British (FAB) M2 subtype. Several studies showed that patients carrying this abnormality demonstrated good response to standard chemotherapy but also have a high incidence of disease relapse. Trisomy 4 is a rare and specific chromosomal abnormality occurring in AML M2 or M4 of the FAB subtypes. We report a case of a 33-year-old female with an apparently clinical and hematologic diagnosis of acute promyelocytic leukemia (APL) in whom cytogenetic analysis revealed an abnormal karyotype with trisomy 4, in addition to t(8;21). Trisomy 4 and t(8;21) in a patient with AML is rare. The significance of t(8;21) with trisomy 4 in AML are unclear but patients bearing this abnormality are associated with a poor prognosis.
    Matched MeSH terms: Female
  11. Tamby, M.R., Juliana, M.B., Wan Hamilton, W.H., Masir, N., Hemlata, K.G.
    Medicine & Health, 2011;6(2):139-142.
    MyJurnal
    Primary fallopian tube carcinomas are rare and are difficult to diagnose preoperatively.
    We describe a fallopian tube carcinoma in a 50-year-old lady who presented with symptoms of pelvic inflammatory disease. Ultrasound examination showed bilateral hydrosalphinx. However, CT scan showed features suggestive of a malignant ovarian tumour. At surgery, a markedly dilated left fallopian tube was found and histopathological examination confirmed the presence of a primary serous adenocarcinoma. The uterus and both ovaries were free of tumour. This report highlights that carcinoma of the fallopian tube should be considered as a differential diagnosis in females who present with lower abdominal pain.
    Matched MeSH terms: Female
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