Gilford Motor Co V S Horne(1933) Horne was appointed Managing Director Gilford Motor Co 6-year term. He appointed by a written agreement says he will not solicit customers for their own purposes and whether he is a general manager or after he left. In order to avoid the effect of the agreement‚ Horne left Gilford Motor Co. and started his own company. Johnson’s company provides car accessories of Gilford Motor Co’s car in a weaken price and the shareholder of Gilford Motor being his associate in
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and brought her three Grammys‚ including a Lifetime Achievement Award in 1989; she appeared in 16 feature films and several shorts between 1938 and 1978; she performed occasionally on Broadway‚ including in her own Tony-winning one-woman show‚ Lena Horne: The Lady and Her Music in 1981-1982; and she sang and acted on radio and television. Adding to the challenge of maintaining such a career was her position as an African-American facing discrimination personally and in her profession during a period
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Actress and singer‚ Lena Horne was born June 30‚ 1917‚ in Brooklyn‚ New York. Her parents were Edna Scottron Horne and Edwin "Teddy" Horne. Since her mother traveled as part of various theater troupes‚ Horne alternately accompanied her on the road and stayed with family and friends around the country. Lena Horne was the youngest member of the NAACP. Lena’s photo appeared in the October 1919 issue of the NAACP Branch Bulletin. Lena’s parents divorced‚ when she was three. Due to her mother traveling
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Lena horne BIOGRAPHY! Actress and singer Lena Horne was born June 30‚ 1917‚ in Brooklyn‚ New York. She left school at age 16 to help support her mother and became a dancer at the Cotton Club in Harlem. She later sang at Carnegie Hall and appeared in such films as Stormy Weather and The Wiz. She was also known for her work with civil rights groups‚ and refused to play roles that stereotyped African-American women. Contents Synopsis Early Life Early Career Activism and Blacklists
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Hutchinson-Gilford Disease (Progeria) Only one in every four million kids is known to be diagnosed with Hutchinson-Gilford Progeria Syndrome‚ or most commonly known as Progeria syndrome or “Aging disease.” Progeria syndrome was first founded in 1886 by Dr. Jonathan Hutchinson and by Dr. Hastings Gilford in 1904. Progeria Syndrome is extremely rare and newborns appear to be normal at birth until the first year when the first signs of symptoms begin to appear. Since first found‚ only 130 cases have
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Progeria Progeria‚ also known as HGPS (Hutchinson-Gilford Progeria Syndrome)‚ is a very rare genetic condition. The word Progeria comes from the Greek “progeros” meaning ’prematurely old’. HGPS was named after Dr. Jonathan Hutchinson‚ who first described the disease in 1886‚ and Dr. Hastings Gilford who also discovered it in 1904 (Nordqvist‚ C. (2015‚ April 08). The most frequent type of progeria syndrome is Hutchinson-Gilford progeria syndrome. It’s a rare and terminal genetic disorder. Wiedemann-Rautenstrauch
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Hutchinson-Gilford Progeria Syndrome by Jack Be Nimble Hutchinson-Gilford Progeria Syndrome (HGPS) is a rare‚ fatal genetic condition that is characterized by premature aging in children. Its name is derived from the Greek and means “prematurely old.” There are different forms of Progeria‚ but we will be looking at the classic form that was named after the doctors who first discovered it‚ Dr. Jonathon Hutchinson in 1886 and Dr. Hastings Gilford in 1897. Progeria is a very rare disease and affects
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Progeria‚ also known as Hutchinson-Gilford Progeria Syndrome‚ is a rare‚ fatal genetic condition causing visible appearances of accelerated aging in children. This affects children and makes them look as if they have aged too quickly as well as other characteristics. But when was the first case of this rare disease discovered? And how did they overcome it? Doctors Jonathan Hutchinson (1828 – 1913) and Hastings Gilford (1861 – 1941) were the very first doctors to discover this disease in 1897
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Progeria‚ also known as Hutchinson-Gilford syndrome‚ is a progressive genetic disorder that causes children to age rapidly. Not only is it extremely rare‚ but there is no cure for this chronic condition. This hereditary disease affects the musculoskeletal system and the vasculature system (Mayo Clinic). There are numerous signs and symptoms for this disorder. Within the first year of life‚ the child may be growing slowing. The motor development and intelligence will remain normal at this time though
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Progeria‚ otherwise known as Hutchinson-Gilford syndrome is an extremely rare‚ generic childhood disorder with reported incidence of about one in a million. Hutchinson has reported the syndrome in 1886 when he found the first patient with Progeria. In 1904 Gilford described a second case of Progeria‚ thus creating the term to reflect the syndrome ’s senile features. There are only about a hundred reported cases since the disorder has been discovered over a century ago. Currently‚ there are
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