Paper · 5317954
The relative efficacy of guanethidine, methyldopa and pargyline as antihypertensive agents.
Oates JA and 4 others. N Engl J Med, 1965. Cited by 63 papers, by iCite.
11 sourcespapers-2026-11-12-0.1.0
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ConductScience Library. The relative efficacy of guanethidine, methyldopa and pargyline as antihypertensive agents. Papers, record 5317954. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/5317954
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Paper
PubMed's record of the paper, with iCite's citation figures. No abstract is shown.
- Title
- The relative efficacy of guanethidine, methyldopa and pargyline as antihypertensive agents.
- PubMed
Topics7
NLM's MeSH indexing of the paper, its major topics first.
| MeSH term | Major |
|---|---|
| Guanethidine | Major topic |
| Hypertension | Major topic |
| Methyldopa | Major topic |
| Pargyline | Major topic |
| Clinical Trials as Topic | |
| Humans | |
| Hypotension, Orthostatic |
Source PubMed
Grants0
Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.
None in this release.
Trials0
The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.
None in this release.
Comments and corrections0
PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.
None in this release.
References0
The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.
None in this release.
Cited by17
The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 63 citations.
| PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|
| 30,255,284 | A reassessment of the safety profile of monoamine oxidase inhibitors: elucidating tired old tyramine myths. | J Neural Transm (Vienna) | 2018 | https://conductscience.org/library/papers/30255284 | PubMed |
| 20,919,347 | Problems with Beta Adrenergic Blocking Drugs and other Antihypertensive Drugs. | Proc R Soc Med | 1977 | https://conductscience.org/library/papers/20919347 | PubMed |
| 20,791,420 | Bethanidine, Guanethidine, and Methyldopa in Treatment of Hypertension: a Within-patient Comparison. | Br Med J | 1968 | https://conductscience.org/library/papers/20791420 | PubMed |
| 20,791,413 | Drugs in control of hypertension. | Br Med J | 1968 | https://conductscience.org/library/papers/20791413 | PubMed |
| 19,821,316 | Methyldopa for primary hypertension. | Cochrane Database Syst Rev | 2009 | https://conductscience.org/library/papers/19821316 | PubMed |
| 18,730,059 | Recent concepts in the clinical pharmacology of anithypertensive drugs. | Calif Med | 1967 | https://conductscience.org/library/papers/18730059 | PubMed |
| 6,025,595 | Double-blind trial of four hypotensive drugs (methyldopa and three sympatholytic agents). | Br Med J | 1967 | https://conductscience.org/library/papers/6025595 | PubMed |
| 5,761,914 | Treatment of hypertension with propranolol. | Br Med J | 1969 | https://conductscience.org/library/papers/5761914 | PubMed |
| 5,381,984 | [Fluorescence histochemical studies on the effect of alpha methyldopa on rat small intestine]. | Klin Wochenschr | 1969 | https://conductscience.org/library/papers/5381984 | PubMed |
| 5,127,116 | Hypertension and depression: interrelated problems in therapy. | J R Coll Physicians Lond | 1971 | https://conductscience.org/library/papers/5127116 | PubMed |
1 to 10 of 17
See all 17 cited byGenes0
The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.
None in this release.
Drugs0
The drugs whose trials, in the Pipelines release, list the paper.
None in this release.
Data0
The data bank entries PubMed's record names. Trial numbers are under Trials.
None in this release.
Data dates
The date of each source this release read.
- Trials
- 2026-11-12
- Gene search
- 2026-11-11
- Pipelines
- 2026-09-18
Sources 11
- ChEMBL, through Open TargetsCC BY-SA 3.0
- ClinicalTrials.govNo license stated
- HGNCCC0
- iCiteCC BY 4.0
- NCBI GenePublic domain (US government)
- NIH RePORTER's grant and paper linksPublic domain
- Open TargetsCC0 1.0
- PMC's ID filePublic domain (US government)
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0
Each source's terms
- ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- ClinicalTrials.govnone stated
- HGNCCC0: https://www.genenames.org/about/license/
- iCiteCC BY 4.0
- NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
- NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
- Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
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