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Mark   Year Entries
Autopsy -- Methods.   19
Autopsy -- Miscellanea. : Notes of an anatomist / F. Gonzalez-Crussi  1986 1
Autopsy -- Periodicals : Autopsy & case reports  2011 1
Autopsy -- Religious aspects -- Congresses. : Autopsie und Religion: Die Sektion aus medizinischer, ethischer und religiöser Sicht  2014 1
Autopsy -- Social aspects.   2
Autopsy -- standards.   2
Autopsy -- Standards -- Australia. : Requirements for the facilities and operation of mortuaries / National Pathology Accreditation Advisory Council  2009 1
Autopsy -- Technique. : Scope: CSI Science  2009 1
Autopsy -- veterinary : Necropsy guide for dogs, cats, and small mammals / edited by Sean P. McDonough, Teresa L. Southard  2017 1
Autoradiography.   5
Autoradiography -- Technique. : Techniques of autoradiography / by Andrew W. Rogers  1979 1
Literatura estadounidense -- Autoras hispanoestadounidenses -- Historia y crítica. : Mujer y literatura mexicana y chicana : culturas en contacto : primer coloquio fronterizo, 22, 23 y 24 de abril de 1987  1988 1
Autoras mexicanas -- Crítica e interpretación -- Congresos, conferencias, etc. : Mujer y literatura mexicana y chicana : culturas en contacto : primer coloquio fronterizo, 22, 23 y 24 de abril de 1987  1988 1
Autoras mexicano-americanas -- Crítica e interpretación. : Mujer y literatura mexicana y chicana : culturas en contacto : primer coloquio fronterizo, 22, 23 y 24 de abril de 1987  1988 1
Autoregression (Statistics)   12
Autoregression (Statistics) -- Econometric models. : Colombia : selected issues / [prepared by a staff team consisting of Lisandro Abrego and others]  2008 1
 

Autoregressive integrated moving average -- See Box-Jenkins forecasting


  1
 

Autoregulation -- See Homeostasis


The processes whereby the internal environment of an organism tends to remain balanced and stable
  1
 

Autoreinfusion of blood -- See Blood Transfusion, Autologous


  1
Literatura estadounidense -- Autores negros : Creating memory and cultural identity in African American trauma fiction / by Patricia San José Rico  2019 1
 

Autoridad de Tránsito del Area Metropolitana de Washington -- See Washington Metropolitan Area Transit Authority


  1
 

Autoridad internacional de los fondos marinos -- See International Seabed Authority


  1
 

Autoridad Sueca para el Desarrollo Internacional -- See Sweden. Styrelsen för internationellt utvecklingssamarbete


  1
Autorin Motiv : Modernism, fashion and interwar women writers / Vike Martina Plock  2017 1
Autoritärer Staat   3
Autorität   2
 

Autorité internationale des fonds marins -- See International Seabed Authority


  1
Autorités administratives indépendantes. : The rise of the unelected : democracy and the new separation of powers / Frank Vibert  2007 1
 

Autos (Automobiles) -- See Automobiles



--headings beginning with the word Automobile
  1
 

Autos-da-fé -- See Also Inquisition


  1
Autos sacramentales -- History and criticism. : The Cultural Politics of Twentieth-Century Spanish Theater : Representing the Auto Sacramental  2012 1
 

Autoscopic phenomena -- See Doppelgängers


  1
 

Autoscopy -- See Doppelgängers


  1
 

Autosegmental phonology -- See Autosegmental theory (Linguistics)


  1
Autosegmental theory (Linguistics)   5
 

Autosomal Chromosome Disorder -- See Chromosome Disorders


Clinical conditions caused by an abnormal chromosome constitution in which there is extra or missing chromosome material (either a whole chromosome or a chromosome segment). (from Thompson et al., Genetics in Medicine, 5th ed, p429)
  1
 

Autosomal Chromosome Disorders -- See Chromosome Disorders


Clinical conditions caused by an abnormal chromosome constitution in which there is extra or missing chromosome material (either a whole chromosome or a chromosome segment). (from Thompson et al., Genetics in Medicine, 5th ed, p429)
  1
 

Autosomal Dominant Cerebellar Ataxia, Type II -- See Spinocerebellar Ataxias


A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
  1
 

Autosomal Dominant Familial Dystonia -- See Dystonic Disorders


Acquired and inherited conditions that feature DYSTONIA as a primary manifestation of disease. These disorders are generally divided into generalized dystonias (e.g., dystonia musculorum deformans) and focal dystonias (e.g., writer's cramp). They are also classified by patterns of inheritance and by age of onset
  1
 

Autosomal Dominant Form of Kallmann Syndrome -- See Kallmann Syndrome


A genetically heterogeneous disorder caused by hypothalamic GNRH deficiency and OLFACTORY NERVE defects. It is characterized by congenital HYPOGONADOTROPIC HYPOGONADISM and ANOSMIA, possibly with additional midline defects. It can be transmitted as an X-linked (GENETIC DISEASES, X-LINKED), an autosomal dominant, or an autosomal recessive trait
  1
 

Autosomal Dominant Juvenile Parkinson Disease -- See Parkinsonian Disorders


A group of disorders which feature impaired motor control characterized by bradykinesia, MUSCLE RIGIDITY; TREMOR; and postural instability. Parkinsonian diseases are generally divided into primary parkinsonism (see PARKINSON DISEASE), secondary parkinsonism (see PARKINSON DISEASE, SECONDARY) and inherited forms. These conditions are associated with dysfunction of dopaminergic or closely related motor integration neuronal pathways in the BASAL GANGLIA
  1
 

Autosomal Dominant Juvenile Parkinsonism -- See Parkinsonian Disorders


A group of disorders which feature impaired motor control characterized by bradykinesia, MUSCLE RIGIDITY; TREMOR; and postural instability. Parkinsonian diseases are generally divided into primary parkinsonism (see PARKINSON DISEASE), secondary parkinsonism (see PARKINSON DISEASE, SECONDARY) and inherited forms. These conditions are associated with dysfunction of dopaminergic or closely related motor integration neuronal pathways in the BASAL GANGLIA
  1
 

Autosomal Dominant Opitz G-Bbb Syndrome -- See DiGeorge Syndrome


Congenital syndrome characterized by a wide spectrum of characteristics including the absence of the THYMUS and PARATHYROID GLANDS resulting in T-cell immunodeficiency, HYPOCALCEMIA, defects in the outflow tract of the heart, and craniofacial anomalies
  1
 

Autosomal Dominant Osteopetrosis Type 2 -- See Osteopetrosis


Excessive formation of dense trabecular bone leading to pathological fractures; OSTEITIS; SPLENOMEGALY with infarct; ANEMIA; and extramedullary hemopoiesis (HEMATOPOIESIS, EXTRAMEDULLARY)
  1
 

Autosomal Dominant Parkinsonism -- See Parkinsonian Disorders


A group of disorders which feature impaired motor control characterized by bradykinesia, MUSCLE RIGIDITY; TREMOR; and postural instability. Parkinsonian diseases are generally divided into primary parkinsonism (see PARKINSON DISEASE), secondary parkinsonism (see PARKINSON DISEASE, SECONDARY) and inherited forms. These conditions are associated with dysfunction of dopaminergic or closely related motor integration neuronal pathways in the BASAL GANGLIA
  1
 

Autosomal dominant polycystic kidney disease -- See Polycystic kidney disease


  1
 

Autosomal Hemophilia A -- See Hemophilia A


The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage
  1
 

Autosomal Hemophilia As -- See Hemophilia A


The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage
  1
 

Autosomal Recessive Familial Dystonia -- See Dystonic Disorders


Acquired and inherited conditions that feature DYSTONIA as a primary manifestation of disease. These disorders are generally divided into generalized dystonias (e.g., dystonia musculorum deformans) and focal dystonias (e.g., writer's cramp). They are also classified by patterns of inheritance and by age of onset
  1
 

Autosomal Recessive Form of Kallmann Syndrome -- See Kallmann Syndrome


A genetically heterogeneous disorder caused by hypothalamic GNRH deficiency and OLFACTORY NERVE defects. It is characterized by congenital HYPOGONADOTROPIC HYPOGONADISM and ANOSMIA, possibly with additional midline defects. It can be transmitted as an X-linked (GENETIC DISEASES, X-LINKED), an autosomal dominant, or an autosomal recessive trait
  1
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