Compounds > methionine

Page last updated: 2024-08-17

methionine and Charcot-Marie-Tooth Disease

methionine has been researched along with Charcot-Marie-Tooth Disease in 12 studies

Research

Studies (12)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	3 (25.00)	18.2507
2000's	8 (66.67)	29.6817
2010's	1 (8.33)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Alberti, JM; Baloh, RH; Biris, N; Dorn, GW; Franco, A; Gavathiotis, E; Janetka, JW; Kitsis, RN; Knight, WC; Krezel, AM; Mochly-Rosen, D; Rocha, AG; Rumsey, JM; Townsend, RR; Zacharioudakis, E	1
Adachi, A; Adachi, Y; Kurihara, S; Nakashima, K; Ohama, E; Wada, K	1
Arne-Bes, MC; de Seze, J; Dubourg, O; Hache, JC; Stojkovic, T; Tardieu, S; Vermersch, P	1
Abbott, RJ; Rajabally, YA	1
Drac, H; Hausmanowa-Petrusewicz, I; Kabzińska, D; Kochański, A; Palau, F; Pedrola, L; Rowińska-Marcińska, K; Ryniewicz, B	1
Beauvais, K; Furby, A; Latour, P	1
Clark, A; Fischer, RA; Kamholz, J; Kolodny, E; Krajewski, KM; Li, J; Lupski, JR; Saifi, GM; Scavina, MT; Scherer, SS; Shy, ME; Szigeti, K	1
Bellone, E; Biancheri, R; Cassandrini, D; Manganelli, F; Minetti, C; Pedemonte, M; Santoro, L; Schenone, A; Striano, P; Stringara, S; Zara, F	1
Drac, H; Goryunov, D; Hausmanowa-Petrusewicz, I; Kabzińska, D; Kochański, A; Liem, RK; Perez-Olle, R; Ryniewicz, B	1
Adolfsson, R; Holmberg, B; Holmgren, G; Nelis, E; van Broeckhoven, C	1
Ekici, A; Leonardis, L; Peterlin, B; Rautenstrauss, B; Zidar, J	1
Ceuterick, C; De Jonghe, P; De Vriendt, E; Löfgren, A; Martin, JJ; Nelis, E; Timmerman, V; Van Broeckhoven, C; Van Maldergem, L; Vercruyssen, A; Verellen, C	1

Other Studies

12 other study(ies) available for methionine and Charcot-Marie-Tooth Disease

Article	Year
MFN2 agonists reverse mitochondrial defects in preclinical models of Charcot-Marie-Tooth disease type 2A. Science (New York, N.Y.), 2018, 04-20, Volume: 360, Issue:6386 Topics: Amino Acid Substitution; Animals; Arginine; Axons; Charcot-Marie-Tooth Disease; Disease Models, Animal; Drug Design; Glutamine; GTP Phosphohydrolases; Humans; Methionine; Mice; Mice, Inbred C57BL; Mitochondria; Mitochondrial Diseases; Mitochondrial Proteins; Oligopeptides; Phosphorylation; Protein Kinases; Sciatic Nerve; Small Molecule Libraries; Threonine	2018
Axonal and demyelinating forms of the MPZ Thr124Met mutation. Acta neurologica Scandinavica, 2003, Volume: 108, Issue:3 Topics: Adult; Aged; Aged, 80 and over; Autopsy; Axons; Charcot-Marie-Tooth Disease; Consanguinity; Demyelinating Diseases; DNA Mutational Analysis; Female; Humans; Japan; Male; Methionine; Middle Aged; Mutation; Myelin P0 Protein; Pedigree; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Threonine	2003
Autonomic and respiratory dysfunction in Charcot-Marie-Tooth disease due to Thr124Met mutation in the myelin protein zero gene. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology, 2003, Volume: 114, Issue:9 Topics: Adult; Aged; Autonomic Nervous System Diseases; Charcot-Marie-Tooth Disease; DNA Mutational Analysis; Evoked Potentials; Family Health; Female; France; Genetic Linkage; Humans; Male; Methionine; Middle Aged; Muscles; Myelin P0 Protein; Neural Conduction; Point Mutation; Polymerase Chain Reaction; Pupil; Respiration Disorders; Respiratory Tract Diseases; Threonine; Urinary Bladder	2003
Charcot-Marie-Tooth disease due to the Thr124Met mutation in the myelin protein zero gene associated with multiple sclerosis. Journal of the peripheral nervous system : JPNS, 2005, Volume: 10, Issue:4 Topics: Charcot-Marie-Tooth Disease; Female; Humans; Methionine; Middle Aged; Multiple Sclerosis; Mutation; Myelin P0 Protein; Threonine	2005
A novel Met116Thr mutation in the GDAP1 gene in a Polish family with the axonal recessive Charcot-Marie-Tooth type 4 disease. Journal of the neurological sciences, 2006, Feb-15, Volume: 241, Issue:1-2 Topics: Adult; Animals; Charcot-Marie-Tooth Disease; Child; Child, Preschool; Chlorocebus aethiops; COS Cells; DNA Mutational Analysis; Family Health; Gene Expression; Green Fluorescent Proteins; Humans; Indoles; Male; Methionine; Microscopy, Electron, Transmission; Mutation; Nerve Tissue Proteins; Pedigree; Poland; Sural Nerve; Threonine; Transfection	2006
Clinical, electrophysiological and molecular genetic studies in a family with X-linked dominant Charcot-Marie-Tooth neuropathy presenting a novel mutation in GJB1 Promoter and a rare polymorphism in LITAF/SIMPLE. Neuromuscular disorders : NMD, 2006, Volume: 16, Issue:1 Topics: Adolescent; Adult; Aged; Charcot-Marie-Tooth Disease; Child; Connexins; DNA Mutational Analysis; Electromyography; Family Health; Female; Gap Junction beta-1 Protein; Humans; Male; Methionine; Mutation; Neural Conduction; Nuclear Proteins; Peripheral Nerves; Polymorphism, Genetic; Promoter Regions, Genetic; Threonine; Transcription Factors	2006
T118M PMP22 mutation causes partial loss of function and HNPP-like neuropathy. Annals of neurology, 2006, Volume: 59, Issue:2 Topics: Adult; Charcot-Marie-Tooth Disease; Child; Female; Genotype; Humans; Male; Methionine; Middle Aged; Mutation; Myelin Proteins; Neural Conduction; Peripheral Nerves; Phenotype; Threonine	2006
GDAP1 mutation in autosomal recessive Charcot-Marie-Tooth with pyramidal features. Journal of neurology, 2006, Volume: 253, Issue:9 Topics: Adolescent; Arginine; Charcot-Marie-Tooth Disease; Child; DNA Mutational Analysis; Evoked Potentials, Motor; Female; Humans; Male; Methionine; Mutation; Nerve Tissue Proteins; Neural Conduction; Pyramidal Tracts	2006
Is a novel I214M substitution in the NEFL gene a cause of Charcot-Marie-Tooth disease? Functional analysis using cell culture models. Journal of the peripheral nervous system : JPNS, 2006, Volume: 11, Issue:3 Topics: Adolescent; Biological Transport; Blotting, Western; Carcinoma; Cell Line, Tumor; Charcot-Marie-Tooth Disease; Child; DNA Mutational Analysis; Family Health; Female; Humans; Isoleucine; Male; Methionine; Models, Molecular; Mutation; Neurofilament Proteins; Transfection; Vimentin	2006
PMP22 Thr(118)Met: recessive CMT1 mutation or polymorphism? Nature genetics, 1997, Volume: 15, Issue:1 Topics: 3T3 Cells; Animals; Charcot-Marie-Tooth Disease; Female; Humans; Male; Methionine; Mice; Myelin Proteins; Pedigree; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Single-Stranded Conformational; Sweden; Threonine	1997
Autosomal dominant Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies: detection of the recombination in Slovene patients and exclusion of the potentially recessive Thr118Met PMP22 point mutation. International journal of molecular medicine, 1998, Volume: 1, Issue:2 Topics: Charcot-Marie-Tooth Disease; Female; Genes, Dominant; Genes, Recessive; Hereditary Sensory and Motor Neuropathy; Humans; Male; Methionine; Myelin Proteins; Pedigree; Point Mutation; Recombination, Genetic; Slovenia; Threonine	1998
The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot-Marie-Tooth phenotype. Brain : a journal of neurology, 1999, Volume: 122 ( Pt 2) Topics: Aged; Biopsy; Charcot-Marie-Tooth Disease; DNA Mutational Analysis; Electromyography; Family Health; Female; Haplotypes; Humans; Male; Median Nerve; Methionine; Motor Neurons; Myelin P0 Protein; Neurons, Afferent; Pedigree; Phenotype; Point Mutation; Polymorphism, Single-Stranded Conformational; Sural Nerve; Threonine; Ulnar Nerve	1999