thiamine has been researched along with Muscular Weakness in 8 studies
thiamine(1+) : A primary alcohol that is 1,3-thiazol-3-ium substituted by (4-amino-2-methylpyrimidin-5-yl)methyl, methyl and 2-hydroxyethyl groups at positions 3, 4 and 5, respectively.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Tenderness in the limb muscles has been reported anecdotally in patients with beriberi neuropathy, but clinical effects of thiamine deficiency on skeletal muscle have received little attention." | 7.73 | Myopathy in thiamine deficiency: analysis of a case. ( Hattori, N; Iijima, M; Inukai, A; Koike, H; Mori, K; Sobue, G; Watanabe, H, 2006) |
| "Acute thiamine deficiency, an uncommon cause of hemodynamic instability in Western countries, may be manifested by acute heart failure and neurological deficits." | 7.72 | Fatal metabolic acidosis caused by thiamine deficiency. ( Gurman, GM; Klein, M; Weksler, N, 2004) |
| "We studied two siblings with a mitochondrial myopathy, familial thiamine deficiency, and an A3243G mutation of the mitochondrial DNA (mtDNA)." | 7.70 | Mitochondrial myopathy and familial thiamine deficiency. ( Higuchi, I; Naito, E; Nakagawa, M; Oizumi, K; Osame, M; Sato, Y, 2000) |
| " This was a diagnostic dilemma until an MRI brain revealed symmetrical signal abnormality and enhancement in the periaqueductal area indicative of Wernicke's encephalopathy, caused by thiamine deficiency from poor nutrition." | 3.91 | Starvation-induced diplopia and weakness: a case of beriberi and Wernicke's encephalopathy. ( Aung, T; Chan Chung, C; Lim, KC; Tan, TXZ, 2019) |
| "Tenderness in the limb muscles has been reported anecdotally in patients with beriberi neuropathy, but clinical effects of thiamine deficiency on skeletal muscle have received little attention." | 3.73 | Myopathy in thiamine deficiency: analysis of a case. ( Hattori, N; Iijima, M; Inukai, A; Koike, H; Mori, K; Sobue, G; Watanabe, H, 2006) |
| "Acute thiamine deficiency, an uncommon cause of hemodynamic instability in Western countries, may be manifested by acute heart failure and neurological deficits." | 3.72 | Fatal metabolic acidosis caused by thiamine deficiency. ( Gurman, GM; Klein, M; Weksler, N, 2004) |
| "We studied two siblings with a mitochondrial myopathy, familial thiamine deficiency, and an A3243G mutation of the mitochondrial DNA (mtDNA)." | 3.70 | Mitochondrial myopathy and familial thiamine deficiency. ( Higuchi, I; Naito, E; Nakagawa, M; Oizumi, K; Osame, M; Sato, Y, 2000) |
| "PDHc deficiency was demonstrated in muscle and fibroblasts without detectable PDHA1 mutations." | 1.36 | Dihydrolipoamide dehydrogenase (DLD) deficiency in a Spanish patient with myopathic presentation due to a new mutation in the interface domain. ( Briones, P; Font, A; Pineda, M; Quintana, E; Ribes, A; Tort, F; Vilaseca, MA, 2010) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (12.50) | 18.2507 |
| 2000's | 3 (37.50) | 29.6817 |
| 2010's | 3 (37.50) | 24.3611 |
| 2020's | 1 (12.50) | 2.80 |
| Authors | Studies |
|---|---|
| Hayano, S | 1 |
| Amamoto, M | 1 |
| Naito, E | 3 |
| Tsao, WC | 1 |
| Ro, LS | 1 |
| Chen, CM | 1 |
| Chang, HS | 1 |
| Kuo, HC | 1 |
| Tan, TXZ | 1 |
| Lim, KC | 1 |
| Chan Chung, C | 1 |
| Aung, T | 1 |
| Quintana, E | 1 |
| Pineda, M | 1 |
| Font, A | 1 |
| Vilaseca, MA | 1 |
| Tort, F | 1 |
| Ribes, A | 1 |
| Briones, P | 1 |
| Klein, M | 1 |
| Weksler, N | 1 |
| Gurman, GM | 1 |
| Koike, H | 1 |
| Watanabe, H | 1 |
| Inukai, A | 1 |
| Iijima, M | 1 |
| Mori, K | 1 |
| Hattori, N | 1 |
| Sobue, G | 1 |
| Kinoshita, H | 1 |
| Sakuragawa, N | 1 |
| Tada, H | 1 |
| Kuroda, Y | 1 |
| Nonaka, I | 1 |
| Sato, Y | 1 |
| Nakagawa, M | 1 |
| Higuchi, I | 1 |
| Osame, M | 1 |
| Oizumi, K | 1 |
8 other studies available for thiamine and Muscular Weakness
| Article | Year |
|---|---|
Thiamine-responsive pyruvate dehydrogenase complex deficiency presenting as recurrent muscle weakness: Identification of a novel mutation (p.T111I) in the PDHA1 gene.
Topics: Humans; Muscle Weakness; Mutation; Pyruvate Dehydrogenase Complex Deficiency Disease; Thiamine | 2023 |
Non-alcoholic Wernicke's encephalopathy with cortical involvement and polyneuropathy following gastrectomy.
Topics: Aged; Cerebral Cortex; Female; Gait Disorders, Neurologic; Gastrectomy; Gastric Bypass; Humans; Magn | 2017 |
Starvation-induced diplopia and weakness: a case of beriberi and Wernicke's encephalopathy.
Topics: Beriberi; Diagnosis, Differential; Diplopia; Humans; Magnetic Resonance Imaging; Male; Middle Aged; | 2019 |
Dihydrolipoamide dehydrogenase (DLD) deficiency in a Spanish patient with myopathic presentation due to a new mutation in the interface domain.
Topics: Acidosis, Lactic; Adult; Amino Acid Sequence; Base Sequence; Biomarkers; Blepharoptosis; Cells, Cult | 2010 |
Fatal metabolic acidosis caused by thiamine deficiency.
Topics: Acidosis; Adult; Diagnostic Errors; Edema; Emergency Medicine; Fatal Outcome; Gastroenteritis; Human | 2004 |
Myopathy in thiamine deficiency: analysis of a case.
Topics: Adult; Biomarkers; Cardiomegaly; Creatine Kinase; Diet; Edema; Female; Fructose-Bisphosphate Aldolas | 2006 |
Recurrent muscle weakness and ataxia in thiamine-responsive pyruvate dehydrogenase complex deficiency.
Topics: Child, Preschool; Humans; Lymphocytes; Male; Muscle Weakness; Muscle, Skeletal; Pyruvate Dehydrogena | 1997 |
Mitochondrial myopathy and familial thiamine deficiency.
Topics: Adult; Atrophy; DNA, Mitochondrial; Electrocardiography; Female; Hemodynamics; Humans; Mitochondria, | 2000 |