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Fame -- Fiction.   12
 

Fame, Halls of -- See Halls of fame


  1
Fame -- History. : Idolizing authorship : literary celebrity and the construction of identity, 1800 to the present / edited by Gaston Franssen and Rick Honings  2017 1
Fame -- History -- 18th century.   3
Fame -- History -- 19th century.   6
Fame -- History -- 20th century.   3
Fame -- History -- Case studies. : Byromania and the birth of celebrity culture / Ghislaine McDayter  2009 1
Fame -- Humor. : Fame in the 20th century / Clive James  1993 1
Fame in literature.   7
Fame -- Juvenile fiction.   7
Fame -- Periodicals : Celebrity studies (Online)  2010- 1
Fame -- Philosophy. : Fame / Mark Rowlands  2008 1
Fame -- Pictorial works -- Juvenile fiction. : The star / Felicity Marshall  2010 1
Fame -- Political aspects.   2
Fame -- Psychological aspects.   5
Fame -- Psychological aspects -- History. : A short history of celebrity / Fred Inglis  2010 1
FAME Recording Studios. : Muscle Shoals / Director: Camalier, Greg  2013 1
Fame -- Social aspects.   37
Fame -- Social aspects -- Brazil -- History -- 20th century : Creating Carmen Miranda : race, camp, and transnational stardom / Kathryn Bishop-Sanchez  2016 1
Fame -- Social aspects -- California -- Los Angeles. : Crane : sex, celebrity, and my father's unsolved murder / Robert Crane and Christopher Fryer  2015 1
Fame -- Social aspects -- Canada. : Celebrity cultures in Canada / Katja Lee and Lorraine York, editors  2016 1
Fame -- Social aspects -- China. : Celebrity in China / edited by Louise Edwards and Elaine Jeffreys  2010 1
Fame -- Social aspects -- Great Britain -- History -- 18th century. : Spectacular disappearances : celebrity and privacy, 1696-1801 / Julia H. Fawcett  2016 1
Fame -- Social aspects -- Handbooks, manuals, etc. : Routledge handbook of celebrity studies / edited by Anthony Elliott  2018 1
Fame -- Social aspects -- History. : A short history of celebrity / Fred Inglis  2010 1
Fame -- Social aspects -- Sweden -- History -- 20th century. : Beauty box : Filmstjärnor och skönhetskultur i det tidiga 1900-talets Sverige / Therése Andersson  2014 1
Fame -- Social aspects -- United States.   10
Fame -- Social aspects -- United States -- Encyclopedias. : Star struck : an encyclopedia of celebrity culture / Sam G. Riley, editor  2010 1
Fame -- Social aspects -- United States -- History -- 20th century   2
Fame -- Social aspects -- United States -- History -- 21st century.   2
Fame -- Sociological aspects.   3
Famechon, John, 1945-   2
Famechon, Johnny, 1945- : "Fammo" / by Johnny Famechon ; with additional material by Frank Quill  1971 1
Familia Cosmovisión Andina Ángeles Custodios : Los Apus : configuración etnomédica en Perú actual / Cástor Saldaña Sousa  2017 1
 

Família Franciscana -- See Franciscans


  1
 

Familial Adenomatous Polyposes -- See Adenomatous Polyposis Coli


A polyposis syndrome due to an autosomal dominant mutation of the APC genes (GENES, APC) on CHROMOSOME 5. The syndrome is characterized by the development of hundreds of ADENOMATOUS POLYPS in the COLON and RECTUM of affected individuals by early adulthood
  1
 

Familial Adenomatous Polyposis -- See Adenomatous Polyposis Coli


A polyposis syndrome due to an autosomal dominant mutation of the APC genes (GENES, APC) on CHROMOSOME 5. The syndrome is characterized by the development of hundreds of ADENOMATOUS POLYPS in the COLON and RECTUM of affected individuals by early adulthood
  1
 

Familial Adenomatous Polyposis Coli -- See Adenomatous Polyposis Coli


A polyposis syndrome due to an autosomal dominant mutation of the APC genes (GENES, APC) on CHROMOSOME 5. The syndrome is characterized by the development of hundreds of ADENOMATOUS POLYPS in the COLON and RECTUM of affected individuals by early adulthood
  1
 

Familial Adenomatous Polyposis of the Colon -- See Adenomatous Polyposis Coli


A polyposis syndrome due to an autosomal dominant mutation of the APC genes (GENES, APC) on CHROMOSOME 5. The syndrome is characterized by the development of hundreds of ADENOMATOUS POLYPS in the COLON and RECTUM of affected individuals by early adulthood
  1
 

Familial Alzheimer Disease (FAD) -- See Alzheimer Disease


A degenerative disease of the BRAIN characterized by the insidious onset of DEMENTIA. Impairment of MEMORY, judgment, attention span, and problem solving skills are followed by severe APRAXIAS and a global loss of cognitive abilities. The condition primarily occurs after age 60, and is marked pathologically by severe cortical atrophy and the triad of SENILE PLAQUES; NEUROFIBRILLARY TANGLES; and NEUROPIL THREADS. (From Adams et al., Principles of Neurology, 6th ed, pp1049-57)
  1
 

Familial Alzheimer Diseases (FAD) -- See Alzheimer Disease


A degenerative disease of the BRAIN characterized by the insidious onset of DEMENTIA. Impairment of MEMORY, judgment, attention span, and problem solving skills are followed by severe APRAXIAS and a global loss of cognitive abilities. The condition primarily occurs after age 60, and is marked pathologically by severe cortical atrophy and the triad of SENILE PLAQUES; NEUROFIBRILLARY TANGLES; and NEUROPIL THREADS. (From Adams et al., Principles of Neurology, 6th ed, pp1049-57)
  1
 

Familial Amaurotic Idiocy -- See Tay-Sachs Disease


An autosomal recessive neurodegenerative disorder characterized by the onset in infancy of an exaggerated startle response, followed by paralysis, dementia, and blindness. It is caused by mutation in the alpha subunit of the HEXOSAMINIDASE A resulting in lipid-laden ganglion cells. It is also known as the B variant (with increased HEXOSAMINIDASE B but absence of hexosaminidase A) and is strongly associated with Ashkenazic Jewish ancestry
  1
Hearing loss, Partial -- Familial and genetic : Genetic and environmental hearing loss : syndromic and non-syndromic : the second annual Symposium on Craniofacial Dysmorphology, held in Chicago, Illinois, June 24, 1979 / sponsored by the Society of Craniofacial Genetics ... [and others] ; editors, L. Stefan Levin, Connie H. Knight, assistant editor, Sue Conde Greene  1980 1
Mental Disorders -- familial & genetic : Origins of mental illness : temperament, deviance, and disorder / Gordon Claridge  1985 1
 

Familial Ataxia, Friedreich -- See Friedreich Ataxia


An autosomal recessive disease, usually of childhood onset, characterized pathologically by degeneration of the spinocerebellar tracts, posterior columns, and to a lesser extent the corticospinal tracts. Clinical manifestations include GAIT ATAXIA, pes cavus, speech impairment, lateral curvature of spine, rhythmic head tremor, kyphoscoliosis, congestive heart failure (secondary to a cardiomyopathy), and lower extremity weakness. Most forms of this condition are associated with a mutation in a gene on chromosome 9, at band q13, which codes for the mitochondrial protein frataxin. (From Adams et al., Principles of Neurology, 6th ed, p1081; N Engl J Med 1996 Oct 17;335(16):1169-75) The severity of Friedreich ataxia associated with expansion of GAA repeats in the first intron of the frataxin gene correlates with the number of trinucleotide repeats. (From Durr et al, N Engl J Med 1996 Oct 17;335(16):1169-75)
  1
 

Familial Ataxia, Friedreich's -- See Friedreich Ataxia


An autosomal recessive disease, usually of childhood onset, characterized pathologically by degeneration of the spinocerebellar tracts, posterior columns, and to a lesser extent the corticospinal tracts. Clinical manifestations include GAIT ATAXIA, pes cavus, speech impairment, lateral curvature of spine, rhythmic head tremor, kyphoscoliosis, congestive heart failure (secondary to a cardiomyopathy), and lower extremity weakness. Most forms of this condition are associated with a mutation in a gene on chromosome 9, at band q13, which codes for the mitochondrial protein frataxin. (From Adams et al., Principles of Neurology, 6th ed, p1081; N Engl J Med 1996 Oct 17;335(16):1169-75) The severity of Friedreich ataxia associated with expansion of GAA repeats in the first intron of the frataxin gene correlates with the number of trinucleotide repeats. (From Durr et al, N Engl J Med 1996 Oct 17;335(16):1169-75)
  1
 

Familial Atrial Fibrillation -- See Atrial Fibrillation


Abnormal cardiac rhythm that is characterized by rapid, uncoordinated firing of electrical impulses in the upper chambers of the heart (HEART ATRIA). In such case, blood cannot be effectively pumped into the lower chambers of the heart (HEART VENTRICLES). It is caused by abnormal impulse generation
  1
 

Familial Atrial Fibrillations -- See Atrial Fibrillation


Abnormal cardiac rhythm that is characterized by rapid, uncoordinated firing of electrical impulses in the upper chambers of the heart (HEART ATRIA). In such case, blood cannot be effectively pumped into the lower chambers of the heart (HEART VENTRICLES). It is caused by abnormal impulse generation
  1
 

Familial Atypical Mycobacterioses -- See Mycobacterium Infections, Nontuberculous


Infections with nontuberculous mycobacteria (atypical mycobacteria): M. kansasii, M. marinum, M. scrofulaceum, M. flavescens, M. gordonae, M. obuense, M. gilvum, M. duvali, M. szulgai, M. intracellulare (see MYCOBACTERIUM AVIUM COMPLEX;), M. xenopi (littorale), M. ulcerans, M. buruli, M. terrae, M. fortuitum (minetti, giae), M. chelonae
  1
 

Familial Atypical Mycobacteriosis -- See Mycobacterium Infections, Nontuberculous


Infections with nontuberculous mycobacteria (atypical mycobacteria): M. kansasii, M. marinum, M. scrofulaceum, M. flavescens, M. gordonae, M. obuense, M. gilvum, M. duvali, M. szulgai, M. intracellulare (see MYCOBACTERIUM AVIUM COMPLEX;), M. xenopi (littorale), M. ulcerans, M. buruli, M. terrae, M. fortuitum (minetti, giae), M. chelonae
  1
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