Sponges, Fossil. : Fossils and strata, a new Silurian (Llandovery, Telychian) sponge assemblage from Gotland, Sweden / Freek Rhebergen and Joseph P. Botting
2014
1
Sponges, Fossil -- Sweden -- Gotland : Fossils and strata, a new Silurian (Llandovery, Telychian) sponge assemblage from Gotland, Sweden / Freek Rhebergen and Joseph P. Botting
2014
1
Sponges -- Growth. : The algorithmic beauty of seaweeds, sponges, and corals / Jaap A. Kaandorp, Janet E. Kübler
2001
1
Sponges -- Growth -- Molecular aspects : Biosilica in evolution, morphogenesis, and nanobiotechnology : case study Lake Baikal / Werner E.G. Müller, Mikhael A Grachev, editors
A rare transmissible encephalopathy most prevalent between the ages of 50 and 70 years. Affected individuals may present with sleep disturbances, personality changes, ATAXIA; APHASIA, visual loss, weakness, muscle atrophy, MYOCLONUS, progressive dementia, and death within one year of disease onset. A familial form exhibiting autosomal dominant inheritance and a new variant CJD (potentially associated with ENCEPHALOPATHY, BOVINE SPONGIFORM) have been described. Pathological features include prominent cerebellar and cerebral cortical spongiform degeneration and the presence of PRIONS. (From N Engl J Med, 1998 Dec 31;339(27))
1
Spongiform Encephalopathies, Transmissible -- See Prion Diseases
A group of genetic, infectious, or sporadic degenerative human and animal nervous system disorders associated with abnormal PRIONS. These diseases are characterized by conversion of the normal prion protein to an abnormal configuration via a post-translational process. In humans, these conditions generally feature DEMENTIA; ATAXIA; and a fatal outcome. Pathologic features include a spongiform encephalopathy without evidence of inflammation. The older literature occasionally refers to these as unconventional SLOW VIRUS DISEASES. (From Proc Natl Acad Sci USA 1998 Nov 10;95(23):13363-83)
A rare transmissible encephalopathy most prevalent between the ages of 50 and 70 years. Affected individuals may present with sleep disturbances, personality changes, ATAXIA; APHASIA, visual loss, weakness, muscle atrophy, MYOCLONUS, progressive dementia, and death within one year of disease onset. A familial form exhibiting autosomal dominant inheritance and a new variant CJD (potentially associated with ENCEPHALOPATHY, BOVINE SPONGIFORM) have been described. Pathological features include prominent cerebellar and cerebral cortical spongiform degeneration and the presence of PRIONS. (From N Engl J Med, 1998 Dec 31;339(27))
1
Spongiform Encephalopathy, Transmissible -- See Prion Diseases
A group of genetic, infectious, or sporadic degenerative human and animal nervous system disorders associated with abnormal PRIONS. These diseases are characterized by conversion of the normal prion protein to an abnormal configuration via a post-translational process. In humans, these conditions generally feature DEMENTIA; ATAXIA; and a fatal outcome. Pathologic features include a spongiform encephalopathy without evidence of inflammation. The older literature occasionally refers to these as unconventional SLOW VIRUS DISEASES. (From Proc Natl Acad Sci USA 1998 Nov 10;95(23):13363-83)
Sponsors -- Mexico -- Tlaxcala (State) : Ritual kinship. Volume II, Ideological and structural integration of the compadrazgo system in rural Tlaxcala / Hugo G. Nutini
Here are entered works on support of literature by individuals and corporations. Works on support of literature by governments are entered under Government aid to literature
Spontaneous generation -- Early works to 1800 : The primitive origination of mankind considered and examined according to the light of nature / written by the Honourable Sir Matthew Hale ..
1677
1
Spontaneous generation -- History : Creatures born of mud and slime : the wonder and complexity of spontaneous generation / Daryn Lehoux
