1-anilino-8-naphthalenesulfonate has been researched along with Muscle Disorders in 48 studies
1-anilino-8-naphthalenesulfonate: RN given refers to parent cpd
8-anilinonaphthalene-1-sulfonic acid : A naphthalenesulfonic acid that is naphthalene-1-sulfonic acid substituted by a phenylamino group at position 8.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Metabolism of triceps, pectoralis (in the vicinity of tumor) and gastrocnemius (away from the tumor) muscles in Swiss albino mice bearing adenocarcinoma has been studied histochemically with regard to content of glycogen, lipids, phosphorylase, aldolase, lipase, succinate dehydrogenase and cytochrome oxidase in the constituent fibres." | 7.67 | Skeletal muscle metabolism in mice bearing adenocarcinoma. I. Histochemical alterations in glycogenolytic, glycolytic, lipolytic and oxidative metabolism. ( Asotra, K; Katoch, SS; Krishan, K; Lata, K; Malhotra, RK, 1985) |
| "Nineteen consecutive LSM patients collected during 1995-2007 in our Neuromuscular Laboratory who were dramatically responsive to riboflavin and presented with proximal muscle weakness, exercise intolerance and elevated serum CK but without episodic encephalopathy were subjected to pathological, biochemical and molecular analysis." | 3.76 | Riboflavin-responsive lipid-storage myopathy caused by ETFDH gene mutations. ( Dai, T; Li, D; Li, H; Li, W; Liu, S; Wen, B; Wu, J; Yan, C; Zhang, C; Zhao, Y, 2010) |
| "Metabolism of triceps, pectoralis (in the vicinity of tumor) and gastrocnemius (away from the tumor) muscles in Swiss albino mice bearing adenocarcinoma has been studied histochemically with regard to content of glycogen, lipids, phosphorylase, aldolase, lipase, succinate dehydrogenase and cytochrome oxidase in the constituent fibres." | 3.67 | Skeletal muscle metabolism in mice bearing adenocarcinoma. I. Histochemical alterations in glycogenolytic, glycolytic, lipolytic and oxidative metabolism. ( Asotra, K; Katoch, SS; Krishan, K; Lata, K; Malhotra, RK, 1985) |
| "Clinical myotonia is uncommon." | 1.91 | Neutral lipid storage disease with myopathy and myotonia associated to pathogenic variants on PNPLA2 and CLCN1 genes: case report. ( Brito, LA; Freitas, HC; Landim, JID; Maia, IHM; Oliveira, EB; Ribeiro, IS; Rodrigues, CL; Távora, DGF, 2023) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 6 (12.50) | 18.7374 |
| 1990's | 1 (2.08) | 18.2507 |
| 2000's | 7 (14.58) | 29.6817 |
| 2010's | 28 (58.33) | 24.3611 |
| 2020's | 6 (12.50) | 2.80 |
| Authors | Studies |
|---|---|
| Tian, Y | 1 |
| Wang, S | 1 |
| Wang, F | 1 |
| Yi, L | 1 |
| Dong, M | 1 |
| Huang, X | 1 |
| Yamada, K | 1 |
| Yaguchi, H | 1 |
| Abe, M | 1 |
| Ishikawa, K | 1 |
| Tanaka, D | 1 |
| Oshima, Y | 1 |
| Kudo, A | 1 |
| Uwatoko, H | 1 |
| Shirai, S | 1 |
| Takahashi-Iwata, I | 1 |
| Matsushima, M | 1 |
| Nishino, I | 3 |
| Yabe, I | 1 |
| Landim, JID | 1 |
| Ribeiro, IS | 1 |
| Oliveira, EB | 1 |
| Freitas, HC | 1 |
| Brito, LA | 1 |
| Maia, IHM | 1 |
| Távora, DGF | 1 |
| Rodrigues, CL | 1 |
| Pegoraro, V | 1 |
| Missaglia, S | 6 |
| Marozzo, R | 1 |
| Tavian, D | 6 |
| Angelini, C | 3 |
| Samukawa, M | 1 |
| Nakamura, N | 1 |
| Hirano, M | 3 |
| Morikawa, M | 1 |
| Sakata, H | 1 |
| Izumi, R | 2 |
| Suzuki, N | 1 |
| Kuroda, H | 2 |
| Shiga, K | 1 |
| Saigoh, K | 1 |
| Aoki, M | 2 |
| Kusunoki, S | 1 |
| Zuccarino, R | 1 |
| Anderson, DM | 1 |
| Holman, C | 1 |
| Feely, S | 1 |
| Gutmann, L | 2 |
| Castagnetta, M | 1 |
| Degiorgio, D | 1 |
| Pennisi, EM | 4 |
| Coleman, RA | 2 |
| Dell'Era, P | 1 |
| Mora, C | 1 |
| Coviello, DA | 1 |
| Arca, M | 6 |
| Bertini, E | 1 |
| Bruno, C | 4 |
| Cassandrini, D | 3 |
| D'amico, A | 1 |
| Garibaldi, M | 1 |
| Gragnani, F | 1 |
| Maggi, L | 2 |
| Massa, R | 2 |
| Morandi, L | 1 |
| Musumeci, O | 1 |
| Pegoraro, E | 1 |
| Rastelli, E | 2 |
| Santorelli, FM | 3 |
| Tasca, E | 1 |
| Toscano, A | 1 |
| Brown, AL | 1 |
| Mark Brown, J | 1 |
| Tan, J | 1 |
| Yang, H | 1 |
| Fan, J | 1 |
| Fan, Y | 1 |
| Xiao, F | 1 |
| Latimer, CS | 1 |
| Schleit, J | 1 |
| Reynolds, A | 1 |
| Marshall, DA | 1 |
| Podemski, B | 1 |
| Wang, LH | 1 |
| Gonzalez-Cuyar, LF | 1 |
| Zheng, S | 1 |
| Liao, W | 1 |
| Garcia, MA | 1 |
| Rojas, JA | 1 |
| Millán, SP | 1 |
| Flórez, AA | 1 |
| Ohno, Y | 1 |
| Nara, A | 1 |
| Nakamichi, S | 1 |
| Kihara, A | 1 |
| Matsumoto, R | 1 |
| Tsunekawa, K | 1 |
| Shoho, Y | 1 |
| Yanagawa, Y | 1 |
| Kotajima, N | 1 |
| Matsumoto, S | 1 |
| Araki, O | 1 |
| Kimura, T | 1 |
| Nakajima, K | 1 |
| Murakami, M | 1 |
| van de Weijer, T | 1 |
| Havekes, B | 1 |
| Bilet, L | 1 |
| Hoeks, J | 1 |
| Sparks, L | 1 |
| Bosma, M | 1 |
| Paglialunga, S | 1 |
| Jorgensen, J | 1 |
| Janssen, MC | 2 |
| Schaart, G | 1 |
| Sauerwein, H | 1 |
| Smeets, JL | 1 |
| Wildberger, J | 1 |
| Zechner, R | 2 |
| Schrauwen-Hinderling, VB | 1 |
| Hesselink, MK | 1 |
| Schrauwen, P | 1 |
| Natali, A | 2 |
| Gastaldelli, A | 1 |
| Camastra, S | 1 |
| Baldi, S | 1 |
| Quagliarini, F | 2 |
| Minicocci, I | 1 |
| Pennisi, E | 2 |
| Schrammel, A | 1 |
| Mussbacher, M | 1 |
| Winkler, S | 1 |
| Haemmerle, G | 1 |
| Stessel, H | 1 |
| Wölkart, G | 1 |
| Mayer, B | 1 |
| Perrin, L | 1 |
| Féasson, L | 1 |
| Furby, A | 1 |
| Laforêt, P | 2 |
| Petit, FM | 1 |
| Gautheron, V | 1 |
| Chabrier, S | 1 |
| Kaneko, K | 1 |
| Tateyama, M | 1 |
| Kato, M | 1 |
| Sugimura, K | 1 |
| Sakata, Y | 1 |
| Ikeda, Y | 1 |
| Hirano, K | 1 |
| Dimauro, S | 3 |
| Bernardi, C | 1 |
| Akman, HO | 1 |
| Xu, C | 1 |
| Zhao, Y | 3 |
| Liu, J | 1 |
| Zhang, W | 1 |
| Wang, Z | 1 |
| Yuan, Y | 1 |
| Xie, M | 1 |
| Roy, R | 1 |
| Pozzessere, S | 1 |
| Serra, L | 1 |
| Terracciano, C | 1 |
| Gibellini, M | 1 |
| Bozzali, M | 1 |
| Muggenthaler, M | 1 |
| Petropoulou, E | 1 |
| Omer, S | 1 |
| Simpson, MA | 1 |
| Sahak, H | 1 |
| Rice, A | 1 |
| Raju, H | 1 |
| Conti, FJ | 1 |
| Bridges, LR | 1 |
| Anderson, LJ | 1 |
| Sharma, S | 1 |
| Behr, ER | 1 |
| Jamshidi, Y | 1 |
| Jousserand, G | 1 |
| Streichenberger, N | 1 |
| Petiot, P | 1 |
| Mora, M | 1 |
| Gibertini, S | 1 |
| Blasevich, F | 1 |
| Agostoni, P | 1 |
| Moro, L | 1 |
| Gerevini, S | 1 |
| Campagna, F | 1 |
| Nanni, L | 1 |
| Michailidis, C | 1 |
| Pierelli, F | 1 |
| Casali, C | 1 |
| Ohkuma, A | 1 |
| Noguchi, S | 1 |
| Sugie, H | 1 |
| Malicdan, MC | 1 |
| Fukuda, T | 1 |
| Shimazu, K | 1 |
| López, LC | 1 |
| Hayashi, YK | 1 |
| Nonaka, I | 1 |
| Wen, B | 2 |
| Dai, T | 1 |
| Li, W | 2 |
| Liu, S | 1 |
| Zhang, C | 1 |
| Li, H | 1 |
| Wu, J | 1 |
| Li, D | 1 |
| Yan, C | 2 |
| Reilich, P | 1 |
| Horvath, R | 1 |
| Krause, S | 1 |
| Schramm, N | 1 |
| Turnbull, DM | 1 |
| Trenell, M | 1 |
| Hollingsworth, KG | 1 |
| Gorman, GS | 1 |
| Hans, VH | 1 |
| Reimann, J | 1 |
| MacMillan, A | 1 |
| Turner, L | 1 |
| Schollen, A | 1 |
| Witte, G | 1 |
| Czermin, B | 1 |
| Holinski-Feder, E | 1 |
| Walter, MC | 1 |
| Schoser, B | 1 |
| Lochmüller, H | 1 |
| Lin, P | 1 |
| Fenster, DS | 1 |
| Wang, Y | 1 |
| Gong, Y | 1 |
| Ash, DB | 1 |
| Papadimitriou, D | 1 |
| Hays, AP | 1 |
| Redaelli, C | 1 |
| Invernici, G | 1 |
| Wessalowski, R | 1 |
| Maiwald, R | 1 |
| Fiorillo, C | 1 |
| Brisca, G | 1 |
| Scapolan, S | 1 |
| Astrea, G | 1 |
| Valle, M | 1 |
| Scuderi, F | 1 |
| Trucco, F | 1 |
| Magnano, G | 1 |
| Gazzerro, E | 1 |
| Minetti, C | 1 |
| van Engelen, B | 1 |
| Kapusta, L | 1 |
| Lammens, M | 1 |
| van Dijk, M | 1 |
| Fischer, J | 2 |
| van der Graaf, M | 1 |
| Wevers, RA | 1 |
| Fahrleitner, M | 1 |
| Zimmermann, R | 1 |
| Morava, E | 2 |
| Lefèvre, C | 1 |
| Mussini, JM | 1 |
| Negre-Salvayre, A | 1 |
| Lathrop, M | 1 |
| Salvayre, R | 2 |
| Akiyama, M | 1 |
| Sakai, K | 1 |
| Ogawa, M | 1 |
| McMillan, JR | 1 |
| Sawamura, D | 1 |
| Shimizu, H | 1 |
| Badeloe, S | 1 |
| van Geel, M | 1 |
| Nagtzaam, I | 1 |
| Rubio-Gozalbo, ME | 1 |
| Oei, RL | 1 |
| Steijlen, PM | 1 |
| van Steensel, MA | 1 |
| Piva, E | 1 |
| Pajola, R | 1 |
| Binotto, G | 1 |
| Plebani, M | 1 |
| Kobayashi, K | 1 |
| Inoguchi, T | 1 |
| Maeda, Y | 1 |
| Nakashima, N | 1 |
| Kuwano, A | 1 |
| Eto, E | 1 |
| Ueno, N | 1 |
| Sasaki, S | 1 |
| Sawada, F | 1 |
| Fujii, M | 1 |
| Matoba, Y | 1 |
| Sumiyoshi, S | 1 |
| Kawate, H | 1 |
| Takayanagi, R | 1 |
| Rodger, HD | 1 |
| Murphy, K | 1 |
| Drinan, EM | 1 |
| Kennedy, G | 1 |
| Scarlato, G | 1 |
| Albizzati, MG | 1 |
| Bassi, S | 1 |
| Cerri, C | 1 |
| Frattola, L | 1 |
| Kar, NC | 1 |
| Pearson, CM | 1 |
| Salaspuro, M | 1 |
| Radom, J | 1 |
| Negre, A | 1 |
| Douste-Blazy, L | 1 |
| Asotra, K | 1 |
| Katoch, SS | 1 |
| Krishan, K | 1 |
| Lata, K | 1 |
| Malhotra, RK | 1 |
| Worsfold, M | 1 |
| Park, DC | 1 |
| Pennington, RJ | 1 |
5 reviews available for 1-anilino-8-naphthalenesulfonate and Muscle Disorders
| Article | Year |
|---|---|
Neutral Lipid Storage Disease Associated with the PNPLA2 Gene: Case Report and Literature Review.
Topics: Frameshift Mutation; Humans; Lipase; Lipid Metabolism, Inborn Errors; Male; Middle Aged; Muscular Di | 2020 |
Critical roles for α/β hydrolase domain 5 (ABHD5)/comparative gene identification-58 (CGI-58) at the lipid droplet interface and beyond.
Topics: 1-Acylglycerol-3-Phosphate O-Acyltransferase; Animals; Energy Metabolism; Humans; Hydrolysis; Ichthy | 2017 |
A novel mutation in PNPLA2 causes neutral lipid storage disease with myopathy and triglyceride deposit cardiomyovasculopathy: a case report and literature review.
Topics: Cardiomyopathies; Coronary Angiography; Coronary Artery Disease; Genotyping Techniques; Humans; Lipa | 2014 |
Neutral lipid-storage disease with myopathy and extended phenotype with novel PNPLA2 mutation.
Topics: Adult; Cognition Disorders; Humans; Lipase; Lipid Metabolism, Inborn Errors; Male; Muscular Diseases | 2016 |
Use of enzymes for the diagnosis of alcohol-related organ damage.
Topics: Alanine Transaminase; Alcoholic Intoxication; Alcoholism; Alkaline Phosphatase; Amylases; Animals; A | 1987 |
43 other studies available for 1-anilino-8-naphthalenesulfonate and Muscle Disorders
| Article | Year |
|---|---|
Late onset of neutral lipid storage disease due to a rare PNPLA2 mutation in a patient with myopathy and cardiomyopathy.
Topics: Acyltransferases; Cardiomyopathies; Humans; Lipase; Lipid Metabolism, Inborn Errors; Lipids; Muscle, | 2022 |
Neutral lipid storage disease with myopathy with a novel homozygous PNPLA2 variant.
Topics: Acyltransferases; Humans; Ichthyosiform Erythroderma, Congenital; Lipase; Lipid Metabolism, Inborn E | 2023 |
Neutral lipid storage disease with myopathy and myotonia associated to pathogenic variants on PNPLA2 and CLCN1 genes: case report.
Topics: Acyltransferases; Chloride Channels; Humans; Lipase; Muscular Diseases; Mutation; Myotonia; Myotonia | 2023 |
MiRNAs as biomarkers of phenotype in neutral lipid storage disease with myopathy.
Topics: Age of Onset; Biomarkers; Female; Humans; Lipase; Lipid Metabolism, Inborn Errors; Liver; Magnetic R | 2020 |
Neutral lipid-storage disease with myopathy and Jordan anomaly.
Topics: Humans; Lipase; Lipid Metabolism, Inborn Errors; Male; Middle Aged; Multienzyme Complexes; Muscular | 2020 |
Generation of induced Pluripotent Stem Cells as disease modelling of NLSDM.
Topics: Cell Culture Techniques; Cell Differentiation; Fibroblasts; Humans; Lipase; Lipid Metabolism, Inborn | 2017 |
Neutral Lipid Storage Diseases: clinical/genetic features and natural history in a large cohort of Italian patients.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Cross-Sectional Studies; Female; Genetic Association Stu | 2017 |
Patients with neutral lipid storage disease with myopathy (NLSDM) in Southwestern China.
Topics: Adult; Asian People; Biopsy; China; Female; Humans; Ichthyosiform Erythroderma, Congenital; Lipase; | 2018 |
Neutral lipid storage disease with myopathy: Further phenotypic characterization of a rare PNPLA2 variant.
Topics: Adult; Female; Humans; Lipase; Lipid Metabolism, Inborn Errors; Muscle, Skeletal; Muscular Diseases; | 2018 |
Novel PNPLA2 gene mutation in a child causing neutral lipid storage disease with myopathy.
Topics: Base Sequence; Cardiomegaly; Cardiomyopathies; Child; Creatine Kinase; DNA Mutational Analysis; Earl | 2018 |
Neutral lipid storage disease with myopathy and dropped head syndrome. Report of a new variant susceptible of treatment with late diagnosis.
Topics: Delayed Diagnosis; Disease Progression; Female; Humans; Lipase; Lipid Metabolism, Inborn Errors; Mid | 2018 |
Molecular mechanism of the ichthyosis pathology of Chanarin-Dorfman syndrome: Stimulation of PNPLA1-catalyzed ω-O-acylceramide production by ABHD5.
Topics: 1-Acylglycerol-3-Phosphate O-Acyltransferase; Ceramides; Endoplasmic Reticulum; HEK293 Cells; HeLa C | 2018 |
Association between skeletal muscle mass and serum concentrations of lipoprotein lipase, GPIHBP1, and hepatic triglyceride lipase in young Japanese men.
Topics: Adolescent; Adult; Athletes; Cholesterol, LDL; Energy Metabolism; Exercise; Female; Genetic Associat | 2019 |
Effects of bezafibrate treatment in a patient and a carrier with mutations in the PNPLA2 gene, causing neutral lipid storage disease with myopathy.
Topics: Adult; Alleles; Bezafibrate; Fatty Acids; Female; Humans; Hypolipidemic Agents; Lipase; Lipid Metabo | 2013 |
Metabolic consequences of adipose triglyceride lipase deficiency in humans: an in vivo study in patients with neutral lipid storage disease with myopathy.
Topics: Adiposity; Adult; Blood Glucose; Body Composition; Body Mass Index; Female; Glucose; Glucose Clamp T | 2013 |
Cardiac oxidative stress in a mouse model of neutral lipid storage disease.
Topics: Animals; Blotting, Western; Disease Models, Animal; Ichthyosiform Erythroderma, Congenital; Lipase; | 2013 |
PNPLA2 mutation: a paediatric case with early onset but indolent course.
Topics: Biopsy; Child, Preschool; Humans; Ichthyosiform Erythroderma, Congenital; Lipase; Lipid Metabolism, | 2013 |
A myopathy with unusual features caused by PNPLA2 gene mutations.
Topics: Aged; Biopsy; Female; Heterozygote; Humans; Lipase; Lipid Metabolism, Inborn Errors; Muscle, Skeleta | 2015 |
Muscle MRI in neutral lipid storage disease with myopathy carrying mutation c.187+1G>A.
Topics: Adult; DNA Mutational Analysis; Humans; Lipase; Lipid Metabolism, Inborn Errors; Magnetic Resonance | 2015 |
The Causative Gene in Chanarian Dorfman Syndrome Regulates Lipid Droplet Homeostasis in C. elegans.
Topics: 1-Acylglycerol-3-Phosphate O-Acyltransferase; Amino Acid Sequence; Animals; Caenorhabditis elegans; | 2015 |
Whole exome sequence analysis reveals a homozygous mutation in PNPLA2 as the cause of severe dilated cardiomyopathy secondary to neutral lipid storage disease.
Topics: Cardiomyopathy, Dilated; Exome; Humans; Lipase; Lipid Metabolism, Inborn Errors; Male; Muscular Dise | 2016 |
[Unusual phenotype of myopathy associated with a new PNPLA2 mutation].
Topics: Biopsy; Cardiomyopathies; Humans; Immunohistochemistry; Lipase; Lipid Metabolism, Inborn Errors; Lip | 2016 |
Late onset of neutral lipid storage disease due to novel PNPLA2 mutations causing total loss of lipase activity in a patient with myopathy and slight cardiac involvement.
Topics: Cardiomyopathies; Female; Humans; Lipase; Lipid Metabolism, Inborn Errors; Middle Aged; Muscles; Mus | 2017 |
Novel mutations in the adipose triglyceride lipase gene causing neutral lipid storage disease with myopathy.
Topics: Adult; Biopsy; Exons; Female; Frameshift Mutation; Humans; Lipase; Lysosomal Storage Diseases, Nervo | 2008 |
Clinical and genetic analysis of lipid storage myopathies.
Topics: Adolescent; Adult; Aged; Child; Child, Preschool; Chromatography, Thin Layer; Death Domain Receptor | 2009 |
Riboflavin-responsive lipid-storage myopathy caused by ETFDH gene mutations.
Topics: Adolescent; Adult; Blotting, Western; Child; Electron-Transferring Flavoproteins; Female; Humans; Ir | 2010 |
The phenotypic spectrum of neutral lipid storage myopathy due to mutations in the PNPLA2 gene.
Topics: Adult; DNA Mutational Analysis; Female; Humans; Ichthyosiform Erythroderma, Congenital; Lipase; Lipi | 2011 |
Novel PNPLA2 gene mutations in Chinese Han patients causing neutral lipid storage disease with myopathy.
Topics: Adult; Asian People; Biopsy; DNA Mutational Analysis; Female; Genetic Association Studies; Humans; L | 2012 |
A novel mutation in PNPLA2 leading to neutral lipid storage disease with myopathy.
Topics: Aged; Humans; Lipase; Lipid Metabolism, Inborn Errors; Male; Muscle, Skeletal; Muscular Diseases; Mu | 2012 |
Contribution of novel ATGL missense mutations to the clinical phenotype of NLSD-M: a strikingly low amount of lipase activity may preserve cardiac function.
Topics: Adult; Aged; Blotting, Western; Cardiomyopathies; Chromatography, Thin Layer; Female; Fibroblasts; H | 2012 |
Subclinical myopathy in a child with neutral lipid storage disease and mutations in the PNPLA2 gene.
Topics: Adolescent; Amino Acid Sequence; Humans; Ichthyosiform Erythroderma, Congenital; Lipase; Lipid Metab | 2013 |
Symptomatic lipid storage in carriers for the PNPLA2 gene.
Topics: Adolescent; Adult; Child; Child, Preschool; Family Health; Female; Heterozygote; Humans; Lipase; Lip | 2013 |
The gene encoding adipose triglyceride lipase (PNPLA2) is mutated in neutral lipid storage disease with myopathy.
Topics: Cells, Cultured; DNA Mutational Analysis; Female; Humans; Lipase; Lipidoses; Muscular Diseases; Muta | 2007 |
Novel duplication mutation in the patatin domain of adipose triglyceride lipase (PNPLA2) in neutral lipid storage disease with severe myopathy.
Topics: Adult; Biopsy; DNA Mutational Analysis; Female; Genetic Markers; Genetic Predisposition to Disease; | 2007 |
Chanarin-Dorfman syndrome caused by a novel splice site mutation in ABHD5.
Topics: 1-Acylglycerol-3-Phosphate O-Acyltransferase; Child; Consanguinity; Diagnosis, Differential; Hepatom | 2008 |
Jordans' anomaly in a new neutral lipid storage disease.
Topics: Aged; Azo Compounds; Coloring Agents; Cytoplasm; Humans; Leukocytes; Lipase; Lipidoses; Lipids; Live | 2009 |
The lack of the C-terminal domain of adipose triglyceride lipase causes neutral lipid storage disease through impaired interactions with lipid droplets.
Topics: Animals; Cells, Cultured; Chlorocebus aethiops; COS Cells; Female; Fibroblasts; Humans; Hydrophobic | 2008 |
Apparent lack of response of salmon affected by pancreas disease to pancreatic enzyme replacement therapy.
Topics: Amylases; Animal Feed; Animals; Aquaculture; Body Weight; Cardiomyopathies; Disease Outbreaks; Fish | 1995 |
A case of lipid storage myopathy with carnitine deficiency. Biochemical and electromyographic correlations.
Topics: Adult; Carnitine; Carnitine O-Acetyltransferase; Carnitine O-Palmitoyltransferase; Cholesterol; Elec | 1977 |
Lipase activity in normal and dystrophic human muscle.
Topics: Adolescent; Adult; Aged; Child; Child, Preschool; Humans; Lipase; Middle Aged; Muscles; Muscular Dis | 1975 |
Metabolism of pyrenedecanoic acid in Epstein-Barr virus-transformed lymphoid cell lines from normal subjects and from a patient with multisystemic lipid storage myopathy.
Topics: Cell Line, Transformed; Decanoic Acids; Herpesvirus 4, Human; Humans; Lipase; Lipid Metabolism; Lipi | 1989 |
Skeletal muscle metabolism in mice bearing adenocarcinoma. I. Histochemical alterations in glycogenolytic, glycolytic, lipolytic and oxidative metabolism.
Topics: Adenocarcinoma; Animals; Electron Transport Complex IV; Fructose-Bisphosphate Aldolase; Glycogen; Gl | 1985 |
Familial "mitochondrial" myopathy. A myopathy associated with disordered oxidative metabolism in muscle fibres. 2. Biochemical findings.
Topics: Adenosine Diphosphate; Adult; Child; Chromatography, Thin Layer; Female; Humans; Lipase; Lipid Metab | 1973 |