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Marie Byrd Land - translation to russian
UNCLAIMED WEST ANTARCTIC REGION
Byrd Land; Mary Byrd Land; Marie Byrd Seamount; Marie Byrd Land Claim; Claim West Antarctica; Protectorate of Managuara Princeland; Marie Byrd land; Marie Byrd; Geography of Marie Byrd Land
Marie Byrd Land
[mə'ri:'bə:d'lænd]
география
Земля Мэри Бэрд
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
Definition
БЕРД
(Byrd) Р., см. Бэрд Р.
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(Byrd) Уильям (ок. 1543-1623), английский композитор, органист, верджинелист, нотоиздатель. Создатель английского мадригала. Фантазии, вариации, танцы для верджинела и виолы, мессы, псалмы и др.
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Чарлз (Карл Николаевич) (1766-1843) , российский инженер, предприниматель, судовладелец. Уроженец Шотландии, с 1786 в России. Первым в России в 1805-06 спроектировал и построил в Петербурге чугунный мост "на дугах". Построил корабельную верфь, основал (1815) пароходство на Неве. Руководил изготовлением и установкой решеток, барельефов, скульптур, фонарей, перекрытий и др. металлических несущих конструкций и элементов. На его первом в России механическом литейном заводе в Петербурге (основан в 1792) изготовлены барельефы Александровской колонны, конструктивные элементы фронтона и купола Исаакиевского собора и др. Изготовил и установил пролетные строения всех висячих мостов Петербурга.
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(Byrd) Уильям (ок. 1543-1623), английский композитор, органист, верджинелист, нотоиздатель. Создатель английского мадригала. Фантазии, вариации, танцы для верджинела и виолы, мессы, псалмы и др.
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Чарлз (Карл Николаевич) (1766-1843) , российский инженер, предприниматель, судовладелец. Уроженец Шотландии, с 1786 в России. Первым в России в 1805-06 спроектировал и построил в Петербурге чугунный мост "на дугах". Построил корабельную верфь, основал (1815) пароходство на Неве. Руководил изготовлением и установкой решеток, барельефов, скульптур, фонарей, перекрытий и др. металлических несущих конструкций и элементов. На его первом в России механическом литейном заводе в Петербурге (основан в 1792) изготовлены барельефы Александровской колонны, конструктивные элементы фронтона и купола Исаакиевского собора и др. Изготовил и установил пролетные строения всех висячих мостов Петербурга.
Wikipedia
Marie Byrd Land
Marie Byrd Land (MBL) is an unclaimed region of Antarctica. With an area of 1,610,000 km2 (620,000 sq mi), it is the largest unclaimed territory on Earth. It was named after the wife of American naval officer Richard E. Byrd, who explored the region in the early 20th century.
The territory lies in West Antarctica, east of the Ross Ice Shelf and the Ross Sea and south of the Pacific Ocean portion of the Antarctic or Southern Ocean, extending eastward approximately to a line between the head of the Ross Ice Shelf and Eights Coast. It stretches between 158°W and 103°24'W. The inclusion of the area between the Rockefeller Plateau and Eights Coast is based upon Byrd's exploration.
