Psychomotor Disorders
Mostrando 13-24 de 27 artigos, teses e dissertações.
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13. Clinical neuropsychomotor follow up of high neurological risk children / Acompanhamento neuropsicomotor ambulatorial de crianças de alto risco neurológico
Enfatizar a prevenção de distúrbios neuropsicomotores torna-se fundamental à medida que os avanços em obstetrícia e neonatologia promovem maior sobrevivência de bebês de risco. Ambulatórios de Alto Risco em Neonatologia têm sido implementados para proporcionar o acompanhamento dessas crianças, em que geralmente há predomínio de fatores de risco
Publicado em: 2005
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14. Delirium : um estudo comparativo entre adultos jovens, adultos e idosos
This is a descriptive and comparative study of Delirium , a cerebral organic syndrome without specific etiology, characterized by the presence of simultaneous disorders of consciousness, attention, perception , thought, memory, psychomotor manifestations , emotions and of the sleeping-vigil rhythm. The duration of the disease manifestation varies, as well as
Publicado em: 2002
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15. Psychomotor slowing and subcortical-type dysfunction in depression.
Elderly patients with major depression and normal controls completed the Sternberg short-term memory scanning procedure and WAIS Digit Symbol. Depressed patients demonstrated psychomotor slowing on both tasks, but normal response latency as a function of memory set size on the Sternberg procedure. While cognitive-behavioural slowing may be observed in both d
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16. The CHARGE association and athyreosis.
We report on a male infant with congenital hypothyroidism owing to athyreosis occurring with the CHARGE association (bilateral papillary coloboma, congenital heart disease, dysmorphic ears, sensorineural deafness, psychomotor retardation, cryptorchidism, facial palsy, and vesicoureteral reflux). The coexistence of these two disorders has not been described p
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17. Phenytoin dosage in ambulant epileptic patients.
Ambulant patients with recently diagnosed generalised or psychomotor seizure disorders or both were randomly assigned to two dosage regimens of phenytoin. Drug compliance was evaluated with subsequent blood phenytoin levels four to eight weeks after initial enrollment into the study. Although the two groups had similar mg-kg daily dosages of phenytoin, the m
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18. Executive and social behaviors under nicotinic receptor regulation
Nicotine enhances several cognitive and psychomotor behaviors, and nicotinic antagonists cause impairments in tasks requiring cognitive effort. To explore the contribution of nicotinic receptors to complex cognitive functions, we developed an automated method to investigate sequential locomotor behavior in the mouse and an analysis of social behavior. We
National Academy of Sciences.
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19. Congenital rubella syndrome: ophthalmic manifestations and associated systemic disorders.
Congenital rubella syndrome has a wide variety of severe ophthalmic and systemic complications. A worldwide rubella epidemic from 1963 to 1965 affected thousands of infants. This is a 20 year follow up study of patients with congenital rubella syndrome analysing the prevalence of ophthalmic disorders, associated systemic problems, and correlations among thes
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20. Carbohydrate deficient glycoprotein syndrome type II: a deficiency in Golgi localised N-acetyl-glucosaminyltransferase II.
The carbohydrate deficient glycoprotein (CDG) syndromes are a family of genetic multisystemic disorders with severe nervous system involvement. This report is on a child with a CDG syndrome that differs from the classical picture but is very similar to a patient reported in 1991. Both these patients are therefore designated CDG syndrome type II. Compared wit
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21. De novo HRAS and KRAS mutations in two siblings with short stature and neuro‐cardio‐facio‐cutaneous features
Mutations in genes involved in Ras signalling cause Noonan syndrome and other disorders characterised by growth disturbances and variable neuro‐cardio‐facio‐cutaneous features. We describe two sisters, 46 and 31 years old, who presented with dysmorphic features, hypotonia, feeding difficulties, retarded growth and psychomotor retardation early in lif
BMJ Group.
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22. An Australian study of telegraphists' cramp1
Ferguson, D. (1971).Brit. J. industr. Med.,28, 280-285. An Australian study of telegraphists' cramp. An investigation of telegraphists' cramp in an Australian public service organization attempted to assess the prevalance of the disorder, the degree of its transfer from morse to keyboard operating, and possible contributory influences. From an interview of 5
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23. Dolichol phosphate mannose synthase (DPM1) mutations define congenital disorder of glycosylation Ie (CDG-Ie)
Congenital disorders of glycosylation (CDGs) are metabolic deficiencies in glycoprotein biosynthesis that usually cause severe mental and psychomotor retardation. Different forms of CDGs can be recognized by altered isoelectric focusing (IEF) patterns of serum transferrin (Tf). Two patients with these symptoms and similar abnormal Tf IEF patterns were analyz
American Society for Clinical Investigation.
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24. The Caenorhabditis elegans mucolipin-like gene cup-5 is essential for viability and regulates lysosomes in multiple cell types
The misregulation of programmed cell death, or apoptosis, contributes to the pathogenesis of many diseases. We used Nomarski microscopy to screen for mutants containing refractile cell corpses in a C. elegans strain in which all programmed cell death is blocked and such corpses are absent. We isolated a mutant strain that accumulates refractile bodies resemb
The National Academy of Sciences.