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Auto's.   9
 

Autos (Automobiles) -- See Automobiles



--headings beginning with the word Automobile 		  1
 

Autos-da-fé -- See Also Inquisition


  1
Autos sacramentales : The cultural politics of twentieth-century Spanish theatre : representing the auto sacramental / Carey Kasten  c2012 1
Autos sacramentales -- History and criticism : The cultural politics of twentieth-century Spanish theatre : representing the auto sacramental / Carey Kasten  c2012 1
Calderón de la Barca, Pedro, 1600-1681. Autos sacramentales (Pamplona, Spain) : Dando luces a las sombras : estudios sobre los autos sacramentales de Calderón / Ignacio Arellano  2015 1
 

Autoscopic phenomena -- See Doppelgängers


  1
 

Autoscopy -- See Doppelgängers


  1
 

Autosegmental phonology -- See Autosegmental theory (Linguistics)


  1
Autosegmental theory   3
Autosegmental theory (Linguistics)   10
Autosegmentele fonologie.   4
Autosemantikon : Semi-lexical categories : the function of content words and the content of function words / edited by Norbert Corver, Henk van Riemsdijk  2001 1
 

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
 

Autosomal Recessive 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 Recessive 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 Recesssive 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
 

Autosome Abnormalities -- See Chromosome Aberrations


Abnormal number or structure of chromosomes. Chromosome aberrations may result in CHROMOSOME DISORDERS 		  1
 

Autosome Abnormality -- See Chromosome Aberrations


Abnormal number or structure of chromosomes. Chromosome aberrations may result in CHROMOSOME DISORDERS 		  1
Autostabilisation (Informatique) : Stabilization, safety, and security of distributed systems : 8th international symposium, SSS 2006, Dallas, TX, USA, November 17-19, 2006 : proceedings / Ajoy K. Datta, Maria Gradinariu (eds.)  2006 1
  Autosuggestion -- 2 Related Subjects   2
Autosuggestion   12
Autotechniek.   2
 

Autotomy -- See Also Regeneration (Biology)



--subdivision Regeneration under individual organs and regions of the body, e.g. Foot--Regeneration 		  1
Autotools (Electronic resource)   2
 

Autotransfusion -- See Blood Transfusion, Autologous


Reinfusion of blood or blood products derived from the patient's own circulation. (Dorland, 27th ed) 		  1
 

Autotransfusion of blood -- See Blood Transfusion, Autologous


  1
 

Autotransfusions -- See Blood Transfusion, Autologous


Reinfusion of blood or blood products derived from the patient's own circulation. (Dorland, 27th ed) 		  1
 

Autotransplantation -- See Transplantation, Autologous


Transplantation of an individual's own tissue from one site to another site 		  1
Autotransplantation.   6
Autotransplantation -- Complications : False hope : bone marrow transplantation for breast cancer / Richard A. Rettig [and others]  2007 1
Autotransplantation -- Handbooks, manuals, etc   2
Autotransplantation -- Research -- Case studies. : Investigating Associations Between Glycemic Status and Infections in Autologous Hematopoietic Cell Transplantation Recipients / Hammer  2017 1
Autotransplantation -- United States -- History : False hope : bone marrow transplantation for breast cancer / Richard A. Rettig [and others]  2007 1
 

Autotransplantations -- See Transplantation, Autologous


Transplantation of an individual's own tissue from one site to another site 		  1
 

Autotransplants -- See Autografts


  1
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