Hematopoietic stem cell transplantation for patients with Wiskott-Aldrich syndrome

Autor: Wietstruck P, María Angélica, Zúñiga C, Pamela, Talesnik G, Eduardo, Méndez R, Cecilia, Barriga C, Francisco

Publikováno v: Revista médica de Chile, Volume: 135, Issue: 7, Pages: 917-923, Published: JUL 2007

Background: Wiskott-Aldrich syndrome (WAS) is an X linked congenital disease that presents as eczema, thrombocytopenia and immune deficiency. The only curative procedure for this illness is hematopoietic stem cell transplant (HSCT), preferably from a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______614::581e85b86497a8555eaf791d86a889d2
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872007000700013&lng=en&tlng=en

Pruebas cutáneas de hipersensibilidad inmediata en una población pediátrica seleccionada

Autor: Martínez G, Javiera, Méndez R, Cecilia, Talesnik G, Eduardo, Campos R, Eugenia, Viviani G, Paola, Sánchez D, Ignacio

Publikováno v: Revista médica de Chile, Volume: 133, Issue: 2, Pages: 195-201, Published: FEB 2005

Background: Skin prick test (SPT) of immediate hypersensitivity is a main instrument in the diagnosis of allergy. Aim: To demonstrate the applicability of skin prick test in different age groups. Patients and Methods: We studied children and adolesce

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______614::3cfafbcac8f32535a742b69403ce7970
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872005000200007&lng=en&tlng=en

Enfrentamiento clínico de la osteoporosis en el niño

Autor: Hernández C.,María Isabel, Talesnik G.,Eduardo, García B.,Cristián, Reyes G.,María Loreto

Publikováno v: Revista chilena de pediatría v.74 n.6 2003
SciELO Chile
CONICYT Chile
instacron:CONICYT

La osteoporosis es una enfermedad cada día más frecuente en el niño, debido al aumento del diagnóstico y tratamiento de enfermedades crónicas, tanto genéticas como adquiridas. Se requiere un alto nivel de sospecha para un diagnóstico precoz y

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3056::222bd49e9b77ba8e18f224a5327bb726
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0370-41062003000600002

Deficiencia de vitamina D en niños con enfermedades crónicas evaluados por osteopenia

Autor: Reyes G, María Loreto, Hernández C, María Isabel, Palisson E, Francis, Talesnik G, Eduardo

Publikováno v: Revista médica de Chile, Volume: 130, Issue: 6, Pages: 645-650, Published: JUN 2002

Background: Chronic diseases in children may determine limited sun exposure, use of drugs, and other risk factors of osteopenia. Objective: to evaluate vitamin D deficiency and their risk factor, in children with chronic diseases with suspected osteo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______614::d34c2764a5c6a0b7beede76d104ff824
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872002000600007&lng=en&tlng=en

Clinical heterogeneity of the chromosome 22q11 microdeletion syndrome

Autor: Muñoz C,Sebastián, Garay G,Francisco, Flores C,Ingrid, Heusser R,Felipe, Talesnik G,Eduardo, Aracena A,Mariana, Mellado S,Cecilia, Méndez R,Cecilia, Arnaiz G,Pilar, Repetto L,Gabriela

Publikováno v: Revista médica de Chile, Volume: 129, Issue: 5, Pages: 515-521, Published: MAY 2001
Revista médica de Chile v.129 n.5 2001
SciELO Chile
CONICYT Chile
instacron:CONICYT

Background: DiGeorge anomaly, velocardiofacial syndrome and conotruncal anomaly face syndrome are part of a group of congenital malformations of the chromosome 22q11 microdeletion syndrome, since they share certain phenotypic features as well as a co

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::d10c357a4e0791d5f7a48dc6ea191913
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872001000500007&lng=en&tlng=en