Výsledky vyhledávání - "Claudia Castiglioni T"

Utilidad de la resonancia magnética en el diagnóstico de las enfermedades musculares hereditarias

Autor: Jorge Díaz J, Lionel Suazo R, Claudia Castiglioni T, Jorge A Bevilacqua R

Publikováno v: Revista chilena de radiología v.21 n.4 2015
SciELO Chile
CONICYT Chile
instacron:CONICYT

Las enfermedades musculares hereditarias son patologias raras, debidas a un defecto genetico que causa una alteracion en la estructura o funcionamiento de las fibras musculares. Pueden debutar en cualquier etapa de la vida y su diagnostico definitivo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9285a059a8215ae7fb6ca4bd00197c3e
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-93082015000400005

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[Aripiprazole for the treatment of Tourette syndrome. Experience in 10 patients]

Autor: Marcelo, Miranda C, Claudia, Castiglioni T

Publikováno v: Revista medica de Chile. 135(6)

Tourette syndrome is a neuropsychiatric disorder characterized by motor and vocal tics, attentional deficit, poor control of impulses and obsessive compulsive disorder. Pharmacological treatment is often disappointing due to partial response and freq

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::4b4e7b4b1dc4290c539f6d38697fe372
https://pubmed.ncbi.nlm.nih.gov/17728905

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Aripiprazole en el tratamiento sintomático del síndrome de Gilíes de la Tourette (enfermedad de los tics)

Autor: Claudia Castiglioni T, Marcelo Miranda C

Publikováno v: Revista médica de Chile v.135 n.6 2007
SciELO Chile
CONICYT Chile
instacron:CONICYT

Background: Tourette syndrome is a neuropsychiatric disorder characterized by motor and vocal tics, attentional deficit, poor control of impulses and obsessive compulsive disorder. Pharmacological treatment is often disappointing due to partial respo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01305972eabae4a7a58493ac94718c22
https://doi.org/10.4067/s0034-98872007000600013

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[McLeod syndrome: Multisystem involvement associated with neuroacanthocytosis linked to X chromosome. report of two related cases]

Autor: Marcelo, Miranda C, Claudia, Castiglioni T, Carlos, Regonesi L, Pedro, Aravena A, Lorena, Villagra M, Ana, Quiroz M, Rogelio, Merino G, Ismael, Mena G

Publikováno v: Revista medica de Chile. 134(11)

Neurological abnormalities associated with spiculated, "acanthocytic" red cells in blood have been described as neuroacanthocytosis. This is a heterogeneous group of conditions that can be clearly subdivided on the basis of recent genetic findings. T

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::485a12b348e2ae4e40f2ceddf6f425de
https://pubmed.ncbi.nlm.nih.gov/17277857

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Síndrome de McLeod: compromiso multisistémico asociado a neuroacantocitosis ligada al cromosoma X, en una familia chilena

Autor: Claudia Castiglioni T, Marcelo Miranda C, Rogelio Merino G, Ismael Mena G., Carlos Regonesi L, Ana Quiroz M, Lorena Villagra M, Pedro Aravena A

Publikováno v: Revista médica de Chile v.134 n.11 2006
SciELO Chile
CONICYT Chile
instacron:CONICYT

Neurological abnormalities associated with spiculated,“acanthocytic” red cells in blood have been described as neuroacanthocytosis. This is aheterogeneous group of conditions that can be clearly subdivided on the basis of recent geneticfindings.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::927e72b86bb9018a8e5a4052d2b204aa
https://doi.org/10.4067/s0034-98872006001100011

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