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Sponges -- Catalogs and collections -- Australia -- New South Wales -- Sydney : Descriptive catalogue of the sponges in the Australian Museum, Sydney / by Robert von Lendenfeld  1888 1
Sponges -- Catalogs and collections -- Australia -- Sydney (N.S.W.) : Descriptive catalogue of the sponges in the Australian Museum, Sydney / by Robert von Lendenfeld  1888 1
Sponges -- Classification. : Systema Porifera : a guide to the classification of sponges / edited by John N.A. Hopper and Rob W.M. Van Soest  2002 1
Sponges -- Congresses : Ancient animals, new challenges : developments in sponge research / editors, Manuel Maldonado, Xavier Turon, Maríaí Jesús Uriz & Mikel Becerro, Center for Advanced Studies of Blanes, Department of Aquatic Ecology, Acces a la Cala S. Francesc 14, 17300 Blanes Gerona, Spain  2012 1
Sponges -- Cytology. : The cell biology of sponges / Tracy L. Simpson  1984 1
Sponges -- Development : The comparative embryology of sponges / Alexander V. Ereskovsky  2010 1
Sponges -- Embryology : The comparative embryology of sponges / Alexander V. Ereskovsky  2010 1
Sponges -- Evolution -- Russia (Federation) -- Baikal, Lake : Biosilica in evolution, morphogenesis, and nanobiotechnology : case study Lake Baikal / Werner E.G. Müller, Mikhael A Grachev, editors  2009 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  2009 1
Sponges -- Juvenile literature   2
Sponges -- Morphology.   2
Sponges -- Morphology -- Atlases. : Atlas of sponge morphology = Atlas de morphologie des éponges / Louis De Vos ... [and others]  1991 1
 

Sponges, Vaginal -- See Contraceptive Devices, Female


Contraceptive devices used by females
  1
 

Spongiform encephalopathies -- See Prion diseases


  1
 

Spongiform Encephalopathies, Subacute -- See Creutzfeldt-Jakob Syndrome


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)
  1
  Spongiform encephalopathy, Bovine -- 2 Related Subjects   2
 

Spongiform Encephalopathy, Subacute -- See Creutzfeldt-Jakob Syndrome


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)
  1
 

Spongioblastoma multiforme -- See Glioblastoma multiforme


  1
Sponsors.   6
Sponsors -- England. : Christianizing kinship : ritual sponsorship in Anglo-Saxon England / Joseph H. Lynch  1998 1
Sponsors -- England -- History. : Baptism and spiritual kinship in early modern England / Will Coster  2016 1
Sponsors -- Europe -- History : Godparents and kinship in early medieval Europe / Joseph H. Lynch  1986 1
Sponsors -- Fiction. : The Unidentified  2011 1
Sponsors -- Italy -- History.   2
Sponsors -- Juvenile fiction. : Marigold in Godmother's house / written & pictured by Joyce Lankester Brisley  1934 1
Sponsors -- Korea (South) : James' may / directed by Kim Dong-won  1986 1
Sponsors -- Mexico -- Tlaxcala (State) : Ritual kinship. Volume II, Ideological and structural integration of the compadrazgo system in rural Tlaxcala / Hugo G. Nutini  2014 1
 

Sponsorship, Corporate -- See Corporate sponsorship


  1
 

Sponsorship of literature -- See Authors and patrons


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
  1
 

Sponsorship of performing arts -- See Performing arts sponsorship


  1
 

Sponsorship of sports -- See Sports sponsorship


  1
Spontaneity : Hume's moral philosophy and contemporary psychology / edited by Philip A. Reed and Rico Vitz  2018 1
Spontaneity (Personaliity trait) : The potent self : a guide to spontaneity / Moshe Feldenkrais ; edited by Michaeleen Kimmey  1985 1
Spontaneity (Personality trait)   6
Spontaneity (Philosophy) in literature   2
  Spontaneous Abortion -- 2 Related Subjects   2
 

Spontaneous Abortions -- See Abortion, Spontaneous


Expulsion of the product of FERTILIZATION before completing the term of GESTATION and without deliberate interference
  1
 

Spontaneous combustion -- See Combustion, Spontaneous


  1
 

Spontaneous dematerialization (Parapsychology) -- See Disappearances (Parapsychology)


  1
 

Spontaneous Fracture -- See Fractures, Spontaneous


Fractures occurring as a result of disease of a bone or from some undiscoverable cause, and not due to trauma. (Dorland, 27th ed)
  1
 

Spontaneous Fractures -- See Fractures, Spontaneous


Fractures occurring as a result of disease of a bone or from some undiscoverable cause, and not due to trauma. (Dorland, 27th ed)
  1
 

Spontaneous generation -- See Also Life Origin


  1
Spontaneous generation.   5
Spontaneous generation -- History. : Creatures born of mud and slime : the wonder and complexity of spontaneous generation / Daryn Lehoux  2017 1
 

Spontaneous human combustion -- See Combustion, Spontaneous human


  1
 

Spontaneous Oto-Acoustic Emission Tinnitus -- See Tinnitus


A nonspecific symptom of hearing disorder characterized by the sensation of buzzing, ringing, clicking, pulsations, and other noises in the ear. Objective tinnitus refers to noises generated from within the ear or adjacent structures that can be heard by other individuals. The term subjective tinnitus is used when the sound is audible only to the affected individual. Tinnitus may occur as a manifestation of COCHLEAR DISEASES; VESTIBULOCOCHLEAR NERVE DISEASES; INTRACRANIAL HYPERTENSION; CRANIOCEREBRAL TRAUMA; and other conditions
  1
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