| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/MUS.22290 |
| P698 | PubMed publication ID | 22334182 |
| P50 | author | Ichizo Nishino | Q37828689 |
| P2093 | author name string | Shinya Sato | |
| Hideo Sugie | |||
| Takekazu Ohi | |||
| P2860 | cites work | A nonischemic forearm exercise test for McArdle disease | Q34147656 |
| Sensory neuropathy from pyridoxine abuse. A new megavitamin syndrome | Q34254765 | ||
| Pyridoxine-induced toxicity in rats: a stereological quantification of the sensory neuropathy | Q34357424 | ||
| McArdle disease: a clinical review | Q34623690 | ||
| A case of McArdle disease: efficacy of vitamin B6 on fatigability and impaired glycogenolysis | Q37777937 | ||
| McArdle disease: Phosphorylase activity in regenerating muscle fibers | Q40588675 | ||
| McArdle disease: the mystery of reappearing phosphorylase activity in muscle culture--a fetal isoenzyme | Q41420353 | ||
| Genetic analysis of Japanese patients with myophosphorylase deficiency (McArdle's disease): single-codon deletion in exon 17 is the predominant mutation | Q52208872 | ||
| Molecular genetic heterogeneity of myophosphorylase deficiency (McArdle's disease) | Q55670939 | ||
| Effect of vitamin B6 supplementation in McArdle's disease: a strategic case study | Q58023476 | ||
| McArdle's disease: Molecular genetics and metabolic consequences of the phenotype | Q58023486 | ||
| P433 | issue | 3 | |
| P921 | main subject | vitamin B6 | Q205130 |
| pyridoxine | Q423746 | ||
| vitamin | Q34956 | ||
| vitamin B | Q183206 | ||
| P304 | page(s) | 436-440 | |
| P577 | publication date | 2012-02-13 | |
| P1433 | published in | Muscle and Nerve | Q15764281 |
| P1476 | title | Confirmation of the efficacy of vitamin B6 supplementation for McArdle disease by follow-up muscle biopsy | |
| P478 | volume | 45 |
| Q88575072 | A new interpretation of sulfate activation of rabbit muscle glycogen phosphorylase |
| Q34677854 | Feasibility of resistance training in adult McArdle patients: clinical outcomes and muscle strength and mass benefits |
| Q38606830 | Genes and exercise intolerance: insights from McArdle disease |
| Q38443406 | McArdle Disease: Update of Reported Mutations and Polymorphisms in the PYGM Gene |
| Q38229959 | McArdle disease: a unique study model in sports medicine. |
| Q58611601 | Myopathies Related to Glycogen Metabolism Disorders |
| Q48302748 | Probing the catalytic site of rabbit muscle glycogen phosphorylase using a series of specifically modified maltohexaose derivatives. |
| Q40133127 | Sodium valproate increases the brain isoform of glycogen phosphorylase: looking for a compensation mechanism in McArdle disease using a mouse primary skeletal-muscle culture in vitro. |
| Q34663450 | The pathogenomics of McArdle disease--genes, enzymes, models, and therapeutic implications. |
| Q37127561 | Therapeutic advances in the management of Pompe disease and other metabolic myopathies |
| Q45872248 | Treatment Opportunities in Patients With Metabolic Myopathies |
| Q49390517 | Wave of renal impairment. |
Search more.