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Σε αυτήν τη σελίδα μπορείτε να λάβετε μια λεπτομερή ανάλυση μιας λέξης ή μιας φράσης, η οποία δημιουργήθηκε χρησιμοποιώντας το ChatGPT, την καλύτερη τεχνολογία τεχνητής νοημοσύνης μέχρι σήμερα:
- πώς χρησιμοποιείται η λέξη
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- χρησιμοποιείται πιο συχνά στον προφορικό ή γραπτό λόγο
- επιλογές μετάφρασης λέξεων
- παραδείγματα χρήσης (πολλές φράσεις με μετάφραση)
- ετυμολογία
CMT - translation to ρωσικά
WIKIMEDIA DISAMBIGUATION PAGE
Cmt; CMT (disambiguation)
CMT
общая лексика
Connection Management
управление соединениями
функция кольцевой сети FDDI
peroneal muscular atrophy
![Ankle-foot orthosis]]](https://commons.wikimedia.org/wiki/Special:FilePath/Charcot Marie Tooth CMT.jpg?width=200 "Ankle-foot orthosis]]")
![[[Denervation]] [[atrophy]] of type II [[muscle fibers]]](https://commons.wikimedia.org/wiki/Special:FilePath/Denervation atrophy - atp94 - intermed mag.jpg?width=200 "[[Denervation]] [[atrophy]] of type II [[muscle fibers]]")
![[[Chromosome 17]]](https://commons.wikimedia.org/wiki/Special:FilePath/Human male karyotpe high resolution - Chromosome 17 cropped.png?width=200 "[[Chromosome 17]]")
NEUROMUSCULAR DISEASE THAT IS CHARACTERIZED BY A SLOWLY PROGRESSIVE DEGENERATION OF THE MUSCLES OF THE FOOT, LOWER LEG, HAND AND FOREARM
Charcot-Marie-Tooth; Charcot marie tooth; Charcot-Marie-Tooth Disease; Charcot-marie-tooth disease; Charcot-Marie-Tooth disease, type 1; Charcot-Marie-Tooth disease, type 2; Cmt1a; AR-CMT2; Charcot-Marie Tooth Disease; Charcot-Marie-Tooth disease, type 4; Carcot marie tooth; Peroneal Muscular Atrophy; Hereditary sensorimotor neuropathy type 2; Hereditary sensory-motor neuropathy type 2; HSMN type 2; Peroneal muscular atrophy type 2; Charcot-Marie-Tooth disease (neuronal form); Charcot-Marie-Tooth disease type 2; Hereditary sensorimotor neuropathy type 1; HSMN type 1; Peroneal muscular atrophy type 1; Charcot-Marie-Tooth disease type 1; Hereditary motor and sensory neuropathy type 1; Charcot-Marie-Tooth disease type 1A; Charcot-Marie-Tooth disease type 1B; Charcot-Marie-Tooth disease type 1C; Charcot-Marie-Tooth disease type 2A; Charcot-Marie-Tooth disease type 2C; Charcot-Marie-Tooth disease type 2D; Charcot-Marie-Tooth disease type 4A; Charcot Marie Tooth disease deafness recessive type; Charcot-Marie-Tooth disease deafness recessive type; Charcot-Marie-Tooth disease type 4D; Charcot Marie tooth disease deafness dominant type; Charcot Marie Tooth disease deafness dominant type; Charcot-Marie-Tooth disease deafness dominant type; Charcot-Marie-Tooth disease and deafness deafness dominant type; Charcot-Marie-Tooth peroneal muscular atrophy X-linked; Charcot-Marie-Tooth disease, X-linked type 1; Charcot-Marie-Tooth disease, X-linked type 2, recessive; Charcot-Marie-Tooth disease, X-linked type 3, recessive; Charcot-Marie-Tooth disease, X-linked type 2 recessive; Charcot-Marie-Tooth disease, X-linked type 3 recessive; Charcot-Marie-Tooth peroneal muscular atrophy, X-linked; Charcot-Marie-Tooth disease with ptosis and parkinsonism; Charcot Marie Tooth type 1 aplasia cutis congenita; Charcot-Marie-Tooth type 1 aplasia cutis congenita; Charcot-Marie-Tooth disease type 1 aplasia cutis congenita; Motor sensory neuropathy type 1 aplasia cutis congenita; Charcot-Marie-Tooth syndrome; Peroneal Muscle Atropy; Charcot Marie Tooth disease; Cowchock Syndrome; Charcot-Marie-Tooth disease type 2B1; Charcot-Marie-Tooth disease type 2B2; Charcot-Marie-Tooth disease type 4B; Charcot-Marie-Tooth disease, neuronal, type A; Charcot-Marie-Tooth disease, neuronal, type B; Charcot-Marie-Tooth disease, neuronal, type D; Cowchock syndrome; Charcot Marie tooth disease deafness mental retardation; Charcot Marie tooth disease with deafness and mental retardation; Neuropathy, axonal motor-sensory with deafness and mental retardation; Charcot-Marie-Tooth disease, X-linked recessive, 4; Charcot-Marie-Tooth disease with deafness and mental retardation; Rosenberg-Chutorian syndrome; Charcot-Marie-Tooth disease, X-linked recessive type 5; Charcot-Marie-Tooth neuropathy; CMT2A; CMTD; Charcot-Marie-Tooth disease; Rosenberg Chutorian syndrome; Charcot-Marie-Tooth disease type 2A2; Charcot-Marie-Tooth disease type 2A1; Charcot-Marie-tooth disease; Charcot-Marie-Tooth disease type 1D; Charcot-Marie-Tooth disease type 1E; Charcot-Marie-Tooth disease type 2B; Charcot-Marie-Tooth disease type 1F; Charcot-Marie-Tooth disease type 2E; Charcot-Marie-Tooth disease type 2I; Charcot-Marie-Tooth disease type 2J; Charcot-Marie-Tooth disease type 4C; Charcot-Marie-Tooth disease type 4F; Charcot-Marie-Tooth disease type 4H; Charcot-Marie-Tooth disease type 4J; Peroneal muscular atrophy; Rosenberg–Chutorian syndrome; Charcot–Marie–Tooth disease, type 2; CMT5; CMT6; CMTDI; CMTRI; Charcot–Marie–Tooth syndrome type 1A; Charcot-Marie-Tooth syndrome type 1A; Charcot–Marie–Tooth disease, type 1; Charcot–Marie–Tooth disease, type 4; Charcot–Marie–Tooth disease 2B1; Charcot-Marie-Tooth disease 2B1; CMT disease
медицина
перонеальная мышечная атрофия
Charcot-Marie-Tooth disease
NEUROMUSCULAR DISEASE THAT IS CHARACTERIZED BY A SLOWLY PROGRESSIVE DEGENERATION OF THE MUSCLES OF THE FOOT, LOWER LEG, HAND AND FOREARM
Charcot-Marie-Tooth; Charcot marie tooth; Charcot-Marie-Tooth Disease; Charcot-marie-tooth disease; Charcot-Marie-Tooth disease, type 1; Charcot-Marie-Tooth disease, type 2; Cmt1a; AR-CMT2; Charcot-Marie Tooth Disease; Charcot-Marie-Tooth disease, type 4; Carcot marie tooth; Peroneal Muscular Atrophy; Hereditary sensorimotor neuropathy type 2; Hereditary sensory-motor neuropathy type 2; HSMN type 2; Peroneal muscular atrophy type 2; Charcot-Marie-Tooth disease (neuronal form); Charcot-Marie-Tooth disease type 2; Hereditary sensorimotor neuropathy type 1; HSMN type 1; Peroneal muscular atrophy type 1; Charcot-Marie-Tooth disease type 1; Hereditary motor and sensory neuropathy type 1; Charcot-Marie-Tooth disease type 1A; Charcot-Marie-Tooth disease type 1B; Charcot-Marie-Tooth disease type 1C; Charcot-Marie-Tooth disease type 2A; Charcot-Marie-Tooth disease type 2C; Charcot-Marie-Tooth disease type 2D; Charcot-Marie-Tooth disease type 4A; Charcot Marie Tooth disease deafness recessive type; Charcot-Marie-Tooth disease deafness recessive type; Charcot-Marie-Tooth disease type 4D; Charcot Marie tooth disease deafness dominant type; Charcot Marie Tooth disease deafness dominant type; Charcot-Marie-Tooth disease deafness dominant type; Charcot-Marie-Tooth disease and deafness deafness dominant type; Charcot-Marie-Tooth peroneal muscular atrophy X-linked; Charcot-Marie-Tooth disease, X-linked type 1; Charcot-Marie-Tooth disease, X-linked type 2, recessive; Charcot-Marie-Tooth disease, X-linked type 3, recessive; Charcot-Marie-Tooth disease, X-linked type 2 recessive; Charcot-Marie-Tooth disease, X-linked type 3 recessive; Charcot-Marie-Tooth peroneal muscular atrophy, X-linked; Charcot-Marie-Tooth disease with ptosis and parkinsonism; Charcot Marie Tooth type 1 aplasia cutis congenita; Charcot-Marie-Tooth type 1 aplasia cutis congenita; Charcot-Marie-Tooth disease type 1 aplasia cutis congenita; Motor sensory neuropathy type 1 aplasia cutis congenita; Charcot-Marie-Tooth syndrome; Peroneal Muscle Atropy; Charcot Marie Tooth disease; Cowchock Syndrome; Charcot-Marie-Tooth disease type 2B1; Charcot-Marie-Tooth disease type 2B2; Charcot-Marie-Tooth disease type 4B; Charcot-Marie-Tooth disease, neuronal, type A; Charcot-Marie-Tooth disease, neuronal, type B; Charcot-Marie-Tooth disease, neuronal, type D; Cowchock syndrome; Charcot Marie tooth disease deafness mental retardation; Charcot Marie tooth disease with deafness and mental retardation; Neuropathy, axonal motor-sensory with deafness and mental retardation; Charcot-Marie-Tooth disease, X-linked recessive, 4; Charcot-Marie-Tooth disease with deafness and mental retardation; Rosenberg-Chutorian syndrome; Charcot-Marie-Tooth disease, X-linked recessive type 5; Charcot-Marie-Tooth neuropathy; CMT2A; CMTD; Charcot-Marie-Tooth disease; Rosenberg Chutorian syndrome; Charcot-Marie-Tooth disease type 2A2; Charcot-Marie-Tooth disease type 2A1; Charcot-Marie-tooth disease; Charcot-Marie-Tooth disease type 1D; Charcot-Marie-Tooth disease type 1E; Charcot-Marie-Tooth disease type 2B; Charcot-Marie-Tooth disease type 1F; Charcot-Marie-Tooth disease type 2E; Charcot-Marie-Tooth disease type 2I; Charcot-Marie-Tooth disease type 2J; Charcot-Marie-Tooth disease type 4C; Charcot-Marie-Tooth disease type 4F; Charcot-Marie-Tooth disease type 4H; Charcot-Marie-Tooth disease type 4J; Peroneal muscular atrophy; Rosenberg–Chutorian syndrome; Charcot–Marie–Tooth disease, type 2; CMT5; CMT6; CMTDI; CMTRI; Charcot–Marie–Tooth syndrome type 1A; Charcot-Marie-Tooth syndrome type 1A; Charcot–Marie–Tooth disease, type 1; Charcot–Marie–Tooth disease, type 4; Charcot–Marie–Tooth disease 2B1; Charcot-Marie-Tooth disease 2B1; CMT disease
медицина
наследственная невральная амиотрофия
перонеальная мышечная атрофия
Παραδείγματα από το σώμα κειμένου για CMT
1. It fell to an all–time low of 2.4 million viewers in 2007 and was dropped by CMT.
2. Some 3.1 million viewers watched the live show _ a paltry audience for network television, but a record for CMT.
3. Another is scheduled for Sept. 10 on MTV, VH1 and CMT and will include Green Day, Ludacris and Alicia Keys.
4. CMT picked up the Miss America Pageant after ABC dropped it from its schedule in 2004 because of low ratings.
5. CMT executive vice president Brian Philips cited the network‘s focus on original programming, not ratings, for the decision. As a network, CMT is now in a more aggressive position to build off of existing series and launch more original series and music–centric special events,‘‘ Philips said in a statement.
