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pro vyhledávání: '"T. Moatter"'
Akademický článek
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Akademický článek
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Autor:
T. Moatter, Z. Ahmed
Publikováno v:
Annals of Oncology. 28:x94-x95
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b7a83ec875698142b3239746390faf4
https://doi.org/10.1093/annonc/mdx664.002
https://doi.org/10.1093/annonc/mdx664.002
Akademický článek
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Publikováno v:
International journal of laboratory hematology. 33(6)
Glucose-6-phosphate dehydrogenase (G6PD; E.C. 1.1.1.49) deficiency is the commonest inborn error of metabolism with more than 140 genetic variants. The incidence of G6PD deficiency is 2-9% in Pakistan, but G6PD variants were never studied comprehensi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::687992d50aee40b89ef8fe217eec289d
https://pubmed.ncbi.nlm.nih.gov/21507207
https://pubmed.ncbi.nlm.nih.gov/21507207
Publikováno v:
American Journal of Physiology-Heart and Circulatory Physiology. 265:H675-H680
The adenine nucleotide, ATP, elicits an elevation in intracellular ionized calcium concentration ([Ca2+]i) and phospholipase C-mediated phosphatidylinositol hydrolysis and stimulates the synthesis of the prostaglandins E2 and I2 in cultured endotheli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c705f34fa05edacf5ea2cfbd8b97069
https://doi.org/10.1152/ajpheart.1993.265.2.h675
https://doi.org/10.1152/ajpheart.1993.265.2.h675
Publikováno v:
JPMA. The Journal of the Pakistan Medical Association. 54(5)
To study the frequency of HLA DR2 status of patients with aplastic anemia and their response to immunosuppressive therapy at a tertiary care hospital.Thirty eight consecutive patients of acquired aplastic anemia were evaluated with respect to demogra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4b34623ebe95c47437b94fc903ae7488
https://pubmed.ncbi.nlm.nih.gov/15270183
https://pubmed.ncbi.nlm.nih.gov/15270183
Autor:
Z, Abbas, T, Moatter
Publikováno v:
JPMA. The Journal of the Pakistan Medical Association. 53(2)
To evaluate the frequency of cytokine gene single nucleotide polymorphisms (SNP) of IL-1beta and IL-10 at promoter sites -115 and -1082 respectively and their association with hepatocellular injury as suggested by alanine aminotransferase (ALT) level
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1e0ed17fca8db03963f54e6745007973
https://pubmed.ncbi.nlm.nih.gov/12705485
https://pubmed.ncbi.nlm.nih.gov/12705485
Publikováno v:
JPMA. The Journal of the Pakistan Medical Association. 52(7)
To characterize specific mutations within the 21-hydroxylase gene (CYP21-B) using ARMS-PCR assay in patients with congenital adrenal hyperplasia (CAH) and to compare it with that reported in other populations.Five families, having an index case with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d6b56cd4a55ec9eeccc45ecdea539173
https://pubmed.ncbi.nlm.nih.gov/12481658
https://pubmed.ncbi.nlm.nih.gov/12481658
Publikováno v:
Indian journal of pathologymicrobiology. 42(4)
We ought to obtain data on the prevalence of the newly discovered tranfusion transmittable hepatitis G virus in polytransfused b- thalassemia major children. Each individual had received multiple blood transfusions, from 12 to 36 per year. No documen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::928284c03c6b096ca0d16392fa45d729
https://pubmed.ncbi.nlm.nih.gov/11127381
https://pubmed.ncbi.nlm.nih.gov/11127381