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Fame -- Psychological aspects -- History : A short history of celebrity / Fred Inglis  2010 1
FAME Recording Studios. : Muscle Shoals / Director: Camalier, Greg  2013 1
FAME Recording Studios -- History : Music and mystique in Muscle Shoals / Christopher M. Reali  2022 1
Fame -- Religious aspects -- Christianity. : The devotion and promotion of stigmatics in Europe, c. 1800-1950 : between saints and celebrities / by Tine Van Osselaer, in collaboration with Andrea Graus, Leonardo Rossi and Kristof Smeyers  2021 1
Fame -- Social aspects.   81
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 -- Criticism and interpretation. : Lady Gaga and the sociology of fame : the rise of a pop star in an age of celebrity / Mathieu Deflem  2017 1
Fame -- Social aspects -- England -- London -- History -- 18th century : The Beau monde : fashionable society in Georgian London / Hannah Greig  2013 1
Fame -- Social aspects -- Great Britain -- History -- 18th century   2
Fame -- Social aspects -- Great Britain -- History -- 19th century   3
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 -- Italy : Fame amid the ruins : Italian film stardom in the age of neorealism / Stephen Gundle  2020 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.   16
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   2
Fame -- Social aspects -- United States -- History -- 19th century   2
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- : "Fammo" / by Johnny Famechon ; with additional material by Frank Quill  1971 1
Famechon, Johnny, 1945- : "Fammo" / by Johnny Famechon ; with additional material by Frank Quill  1971 1
Familes of military personnel -- Ohio   2
Família.   9
Família (aspectos legais;sociologia) : Kinship, law and the unexpected : relatives are always a surprise / Marilyn Strathern  2005 1
Família -- Egipte. : Kinship and family in ancient Egypt : archaeology and anthropology in dialogue / Leire Olabarria, University of Birmingham  2020 1
 

Família Franciscana -- See Franciscans


  1
Família -- Grécia antiga;roma antiga. : Plutarch's Advice to the bride and groom, and A consolation to his wife : English translations, commentary, interpretive essays, and bibliography / edited by Sarah B. Pomeroy  1999 1
Família (história). : Families in the expansion of Europe, 1500-1800 / edited by Maria Beatriz Nizza da Silva  2018 1
FAMÍLIA -- ROMA ANTIGA. : The family in late antiquity : the rise of Christianity and the endurance of tradition / Geoffrey S. Nathan  2000 1
Familia (Sociologia)   5
 

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
Familial and genetic Hearing loss, Partial : 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
familial & genetic Mental Disorders : 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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