phenytoin has been researched along with Congenital Myotonic Dystrophy in 16 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Myotonic dystrophy is a clinically and genetically heterogeneous multisystem disorder with a prevalence of 1 in 8000 in the general population." | 1.40 | Concurrence of myotonic dystrophy and epilepsy: a case report. ( Worku, DK, 2014) |
| "Three cases of myotonia dystrophica are presented with special problems of diagnosis and treatment." | 1.27 | [The problem of diagnosis and therapy of myotonic dystrophy]. ( Markut, H; Reisecker, F; Tulzer, W, 1983) |
| "The diagnosis of dystrophia myotonica (DM) was apparent on clinical examination and his symptoms responded well to phenytoin therapy." | 1.27 | Dysphagia and dystrophia myotonica. A case report. ( Pettengell, KE; Simjee, AE; Spitaels, JM, 1985) |
| "Myotonic dystrophy is a dominantly-inherited disorder which affects skeletal muscle in combination with several other systems." | 1.26 | Monovalent cation transport in myotonic dystrophy. Na-K pump ratio in erythrocytes. ( Brumback, RA; Festoff, BW; Hobbs, AS, 1979) |
| " Patients with Thomsen's myotonia (9 cases) and with atrophic myotonia (7 cases) were treated by novocainamide with a daily dosage of 0." | 1.26 | [Treatment of patients with different forms of myotonia with diphenin and novocainamide]. ( Biriukov, VB, 1976) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 11 (68.75) | 18.7374 |
| 1990's | 2 (12.50) | 18.2507 |
| 2000's | 1 (6.25) | 29.6817 |
| 2010's | 2 (12.50) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Worku, DK | 1 |
| Chan, BS | 1 |
| Sellors, K | 1 |
| Chiew, AL | 1 |
| Buckley, NA | 1 |
| Sechi, GP | 1 |
| Traccis, S | 1 |
| Durelli, L | 1 |
| Monaco, F | 1 |
| Mutani, R | 1 |
| Silver, L | 1 |
| Reisecker, F | 1 |
| Markut, H | 1 |
| Tulzer, W | 1 |
| Ahmadian, JL | 1 |
| Heller, SL | 1 |
| Nishida, T | 1 |
| Altman, KW | 1 |
| Roses, AD | 1 |
| Butterfield, A | 1 |
| Appel, SH | 1 |
| Chestnut, DB | 1 |
| Hobbs, AS | 1 |
| Brumback, RA | 1 |
| Festoff, BW | 1 |
| Biriukov, VB | 1 |
| Griggs, RC | 1 |
| Davis, RJ | 1 |
| Anderson, DC | 1 |
| Dove, JT | 1 |
| Kwieciński, H | 1 |
| Ryniewicz, B | 1 |
| Ostrzycki, A | 1 |
| Hahn, AF | 1 |
| Parkes, AW | 1 |
| Bolton, CF | 1 |
| Stewart, SA | 1 |
| Pettengell, KE | 1 |
| Spitaels, JM | 1 |
| Simjee, AE | 1 |
| Liedtke, B | 1 |
| Kerschensteiner, M | 1 |
| Brown, JC | 1 |
| Negri, S | 1 |
2 trials available for phenytoin and Congenital Myotonic Dystrophy
| Article | Year |
|---|---|
Carbamazepine versus diphenylhydantoin in the treatment of myotonia.
Topics: Adolescent; Adult; Carbamazepine; Clinical Trials as Topic; Double-Blind Method; Female; Humans; Mal | 1983 |
Treatment of myotonia with antiarrhythmic drugs.
Topics: Adolescent; Adult; Anti-Arrhythmia Agents; Disopyramide; Dose-Response Relationship, Drug; Drug Admi | 1992 |
14 other studies available for phenytoin and Congenital Myotonic Dystrophy
| Article | Year |
|---|---|
Concurrence of myotonic dystrophy and epilepsy: a case report.
Topics: Adult; Anticonvulsants; Electromyography; Epilepsy; Ethiopia; Humans; Male; Myotonic Dystrophy; Phen | 2014 |
Use of multi-dose activated charcoal in phenytoin toxicity secondary to genetic polymorphism.
Topics: Aged; Anticonvulsants; Antidotes; Charcoal; Cytochrome P-450 CYP2C19; Cytochrome P-450 CYP2C9; Femal | 2015 |
Hand abnormalities in the fetal hydantoin syndrome.
Topics: Abnormalities, Drug-Induced; Abnormalities, Multiple; Female; Fingers; Humans; Infant; Infant, Newbo | 1981 |
[The problem of diagnosis and therapy of myotonic dystrophy].
Topics: Adult; Biopsy; Child; Deglutition Disorders; Dysarthria; Electromyography; Female; Humans; Male; Mex | 1983 |
Myotonic dystrophy type 1 (DM1) presenting with laryngeal stridor and vocal fold paresis.
Topics: Airway Obstruction; Anticonvulsants; Dyspnea; Humans; Laryngeal Muscles; Male; Middle Aged; Muscle W | 2002 |
Phenytoin and membrane fluidity in myotonic dystrophy.
Topics: Cell Membrane; Electron Spin Resonance Spectroscopy; Erythrocytes; Humans; Myotonic Dystrophy; Pheny | 1975 |
Monovalent cation transport in myotonic dystrophy. Na-K pump ratio in erythrocytes.
Topics: Carrier Proteins; Cell Membrane Permeability; Erythrocyte Membrane; Erythrocytes; Humans; Insulin; M | 1979 |
[Treatment of patients with different forms of myotonia with diphenin and novocainamide].
Topics: Humans; Myotonia Congenita; Myotonic Dystrophy; Phenytoin; Procainamide | 1976 |
Cardiac conduction in myotonic dystrophy.
Topics: Adolescent; Adult; Electrocardiography; Heart; Humans; Middle Aged; Myotonic Dystrophy; Phenytoin; P | 1975 |
Neuromyotonia in hereditary motor neuropathy.
Topics: Adolescent; Anti-Arrhythmia Agents; Carbamazepine; Child; Electromyography; Female; Humans; Lidocain | 1991 |
Dysphagia and dystrophia myotonica. A case report.
Topics: Adult; Deglutition Disorders; Humans; Male; Myotonic Dystrophy; Phenytoin | 1985 |
[Manifestation of myotonic disturbances of muscle function under continuous intravenous drip treatment with the beta-adrenergic th 1165 a (fenoterolhydrobromide) (author's transl)].
Topics: Adrenergic beta-Agonists; Adult; Bromides; Female; Humans; Metaproterenol; Myotonic Dystrophy; Pheno | 1974 |
Muscle weakness after rest in myotonic disorders; an electrophysiological study.
Topics: Action Potentials; Adult; Edrophonium; Electric Stimulation; Electromyography; Guanidines; Humans; M | 1974 |
An atypical case of Steinert's disease (myotonia dystrophica) in infancy.
Topics: Age Factors; Child; Creatine Kinase; Electroencephalography; Electromyography; Facial Muscles; Femal | 1971 |