Zobrazeno 1 - 8
of 8
pro vyhledávání: '"T. G. Reilly"'
Publikováno v:
Alimentary Pharmacology & Therapeutics. 9:483-490
SUMMARY Background: Helicobacter pylori eradication for peptic ulcer has been widely taken up. Evidence for the efficacy of different regimens is often derived from small series in clinical trials but there is little reporting of everyday practice wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::642adffdacd8209973d71663ef6c706d
https://doi.org/10.1111/j.1365-2036.1995.tb00410.x
https://doi.org/10.1111/j.1365-2036.1995.tb00410.x
Publikováno v:
Alimentary Pharmacology & Therapeutics. 12:469-474
Background: Amongst the low-dose H2-receptor antagonists available for the self-medication of dyspepsia, both famotidine 10 mg and cimetidine 200 mg have been shown to raise intragastric pH, but there is a delay after ingestion before significant eff
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff0ad9fc58edb615eefd2516a3bc5891
https://doi.org/10.1046/j.1365-2036.1998.00323.x
https://doi.org/10.1046/j.1365-2036.1998.00323.x
Publikováno v:
Gut. 40:454-458
BACKGROUND: A rapid, reliable, and accurate test for the diagnosis of infection with Helicobacter pylori is needed for screening dyspeptic patients before referral for endoscopy. AIM: To compare a new rapid whole blood test (Helisal rapid blood, Cort
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7dd48caa48bb78520a22baa8c34bdf34
https://doi.org/10.1136/gut.40.4.454
https://doi.org/10.1136/gut.40.4.454
Publikováno v:
Alimentary Pharmacology & Therapeutics. 10:749-755
Background : Low-dose H 2 -receptor antagonists are available without prescription for the self-medication of dyspepsia. Methods : To investigate the relative abilities of low doses of famotidine and ranitidine to raise intragastric pH after a single
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::327a6f32016a5944448756553182087e
https://doi.org/10.1046/j.1365-2036.1996.50192000.x
https://doi.org/10.1046/j.1365-2036.1996.50192000.x
Autor:
R. P. Walt, T. G. Reilly
Publikováno v:
Journal of Clinical Pharmacy and Therapeutics. 19:73-80
The treatment of duodenal ulcer has evolved from ineffective medical treatments through an era of surgical management, back to increasingly effective medical treatment. The advent of H2-receptor antagonists changed the outlook for ulcer patients. Mor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4674a47ffca50cabac4ea6668fbc1626
https://doi.org/10.1111/j.1365-2710.1994.tb01115.x
https://doi.org/10.1111/j.1365-2710.1994.tb01115.x
Publikováno v:
Journal of clinical pathology. 57(4)
Hereditary haemochromatosis is the most common inherited disorder in white populations, whereas non-alcoholic steatohepatitis (NASH) is becoming the most common reason for referral for investigation of abnormal liver function tests (LFTs). This repor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bb5c436161558906ca06d1851980e12
https://pubmed.ncbi.nlm.nih.gov/15047754
https://pubmed.ncbi.nlm.nih.gov/15047754
Publikováno v:
Alimentary pharmacologytherapeutics. 12(5)
Amongst the low-dose H2-receptor antagonists available for the self-medication of dyspepsia, both famotidine 10 mg and cimetidine 200 mg have been shown to raise intragastric pH, but there is a delay after ingestion before significant effects can be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a05c1ff6b4168acd4d1ac6d26ecb623a
https://pubmed.ncbi.nlm.nih.gov/9663728
https://pubmed.ncbi.nlm.nih.gov/9663728
Publikováno v:
Gut. 37(3)
To investigate the relative abilities of low doses of famotidine and cimetidine to raise intragastric pH after a single postprandial evening dose, 16 healthy volunteers were recruited to a four period crossover trial of famotidine 10 mg, cimetidine 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2291431d55f6cc338577be2c252cb4a8
https://pubmed.ncbi.nlm.nih.gov/7590425
https://pubmed.ncbi.nlm.nih.gov/7590425