Search citation statements
Paper Sections
Citation Types
Year Published
Publication Types
Relationship
Authors
Journals
The article contains sections titled: 1. Introduction 2. Anesthetics 2.1. Topical Anesthetics 2.2. Regional Anesthetics 3. Antimicrobial Agents 3.1. Antibacterial Agents 3.1.1. Sulfonamides 3.1.2. β‐Lactam Antibiotics 3.1.2.1. Penicillins 3.1.2.2. Cephalosporins 3.1.3. Tetracycline Antibiotics 3.1.4. Aminoglycoside Antibiotics 3.1.5. Polypeptide Antibiotics 3.1.6. Miscellaneous Antimicrobial Agents 3.2. Antifungal Agents 3.3. Antiprotozoal Agents 3.4. Antiviral Agents 4. Anti‐inflammatory Agents 4.1. Corticosteroids 4.2. Miscellaneous Anti‐inflammatory Agents 5. Antiglaucomatous Agents 5.1. Sympathomimetic Drugs 5.2. β‐Adrenergic Blocking Agents 5.3. Carbonic Anhydrase Inhibitors 5.4. Hyperosmotic Agents 5.5. Miotics (Parasympathomimetic Agents) 5.5.1. Cholinergic Agonists 5.5.2. Anticholinesterases 6. Mydriatics and Cycloplegics 6.1. Sympathomimetics 6.2. Parasympatholytics 7. Vasoactive (Adrenergic) Agents 8. Diagnostic Agents 9. Dry Eye Medications 10. Miscellaneous Ophthalmic and Contact Lens Preparations 10.1. Disinfectants and Preservatives 10.1.1. Biguanides 10.1.2. Mercurial Preservatives 10.1.3. Quaternary Ammonium Compounds 10.1.4. Miscellaneous Disinfectants and Preservatives 10.2. Contact Lens Cleaners and Rewetting Agents 10.2.1. Surfactant Cleaners 10.2.2. Enzymatic Cleaners
The article contains sections titled: 1. Introduction 2. Anesthetics 2.1. Topical Anesthetics 2.2. Regional Anesthetics 3. Antimicrobial Agents 3.1. Antibacterial Agents 3.1.1. Sulfonamides 3.1.2. β‐Lactam Antibiotics 3.1.2.1. Penicillins 3.1.2.2. Cephalosporins 3.1.3. Tetracycline Antibiotics 3.1.4. Aminoglycoside Antibiotics 3.1.5. Polypeptide Antibiotics 3.1.6. Miscellaneous Antimicrobial Agents 3.2. Antifungal Agents 3.3. Antiprotozoal Agents 3.4. Antiviral Agents 4. Anti‐inflammatory Agents 4.1. Corticosteroids 4.2. Miscellaneous Anti‐inflammatory Agents 5. Antiglaucomatous Agents 5.1. Sympathomimetic Drugs 5.2. β‐Adrenergic Blocking Agents 5.3. Carbonic Anhydrase Inhibitors 5.4. Hyperosmotic Agents 5.5. Miotics (Parasympathomimetic Agents) 5.5.1. Cholinergic Agonists 5.5.2. Anticholinesterases 6. Mydriatics and Cycloplegics 6.1. Sympathomimetics 6.2. Parasympatholytics 7. Vasoactive (Adrenergic) Agents 8. Diagnostic Agents 9. Dry Eye Medications 10. Miscellaneous Ophthalmic and Contact Lens Preparations 10.1. Disinfectants and Preservatives 10.1.1. Biguanides 10.1.2. Mercurial Preservatives 10.1.3. Quaternary Ammonium Compounds 10.1.4. Miscellaneous Disinfectants and Preservatives 10.2. Contact Lens Cleaners and Rewetting Agents 10.2.1. Surfactant Cleaners 10.2.2. Enzymatic Cleaners
Although the carbonic anhydrase inhibitors have been used in the treatment of the primary periodic paralyses (PPs), their efficacy has not been demonstrated in double‐blind, placebo‐controlled trials. Therefore, we tested the efficacy of dichlorphenamide (DCP; Daranide), a potent carbonic anhydrase inhibitor, in the treatment of episodic weakness in the primary PPs. We performed two multicenter, randomized, double‐blind, placebo‐controlled crossover trials, one involving 42 subjects with hypokalemic periodic paralysis (HypoPP) and the other involving 31 subjects with potassium‐sensitive periodic paralysis (PSPP). In each trial, two 8‐week treatment periods were separated by an active washout period of at least 9 weeks. The primary outcome variable in the HypoPP trial was the occurrence of an intolerable increase in attack severity or frequency (end point). The primary outcome variable in the PSPP trial was the number of attacks per week. In the HypoPP trial, there were 13 subjects who exhibited a preference (in terms of the end point) for either DCP or placebo, and 11 of these preferred DCP. In the PSPP trial, DCP significantly reduced attack rates relative to placebo. DCP also significantly reduced attack rates relative to placebo in the HypoPP subjects. We conclude that DCP is effective in the prevention of episodic weakness in both HypoPP and PSPP. Ann Neurol 2000; 47:46–53
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.