Prati
Karin Alvarez
Karin Alvarez
Clínica Universidad de los Andes
Potvrđena adresa e-pošte na clinicauandes.cl
Naslov
Citirano
Citirano
Godina
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database
M Dominguez-Valentin, JR Sampson, TT Seppälä, SW Ten Broeke, ...
Genetics in Medicine 22 (1), 15-25, 2020
5312020
Increase in decorin and biglycan in Duchenne Muscular Dystrophy: role of fibroblasts as cell source of these proteoglycans in the disease
R Fadic, V Mezzano, K Alvarez, D Cabrera, J Holmgren, E Brandan
Journal of cellular and molecular medicine 10 (3), 758-769, 2006
1192006
The relationship between chemokines CCL2, CCL3, and CCL4 with the tumor microenvironment and tumor-associated macrophage markers in colorectal cancer
M De la Fuente López, G Landskron, D Parada, K Dubois-Camacho, ...
Tumor Biology 40 (11), 1010428318810059, 2018
1152018
Immune system, microbiota, and microbial metabolites: the unresolved triad in colorectal cancer microenvironment
M Hanus, D Parada-Venegas, G Landskron, AM Wielandt, C Hurtado, ...
Frontiers in immunology 12, 612826, 2021
1052021
PIASγ represses the transcriptional activation induced by the nuclear receptor Nurr1
D Galleguillos, A Vecchiola, JA Fuentealba, V Ojeda, K Alvarez, A Gómez, ...
Journal of Biological Chemistry 279 (3), 2005-2011, 2004
912004
Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study
AK Win, JG Dowty, JC Reece, G Lee, AS Templeton, JP Plazzer, ...
The Lancet Oncology 22 (7), 1014-1022, 2021
752021
Augmented synthesis and differential localization of heparan sulfate proteoglycans in Duchenne muscular dystrophy
K Alvarez, R Fadic, E Brandan
Journal of cellular biochemistry 85 (4), 703-713, 2002
712002
Pyruvate dehydrogenase deficiency presenting as isolated paroxysmal exercise induced dystonia successfully reversed with thiamine supplementation. Case report and mini-review
C Castiglioni, D Verrigni, C Okuma, A Diaz, K Alvarez, T Rizza, ...
European Journal of Paediatric Neurology 19 (5), 497-503, 2015
602015
A survey of the clinicopathological and molecular characteristics of patients with suspected Lynch syndrome in Latin America
BM Rossi, EI Palmero, F López-Kostner, C Sarroca, CA Vaccaro, ...
Bmc Cancer 17, 1-26, 2017
442017
Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report
M Dominguez-Valentin, EJ Crosbie, C Engel, S Aretz, F Macrae, I Winship, ...
Genetics in Medicine 23 (4), 705-712, 2021
362021
Detection using molecular biology techniques of Mycoplasma hominis and Ureaplasma urealyticum in urogenital samples
C Fernandez, K Alvarez, L Muy, M Martinez
Revista Argentina De Microbiologia 30 (2), 53-58, 1998
321998
Mutation spectrum in South American Lynch syndrome families
M Dominguez-Valentin, M Nilbert, P Wernhoff, F López-Köstner, ...
Hereditary cancer in clinical practice 11, 1-9, 2013
292013
From colorectal cancer pattern to the characterization of individuals at risk: Picture for genetic research in Latin America
CA Vaccaro, F López‐Kostner, DV Adriana, EI Palmero, BM Rossi, ...
International journal of cancer 145 (2), 318-326, 2019
272019
Medical genetics and genetic counseling in Chile
SB Margarit, M Alvarado, K Alvarez, G Lay-Son
Journal of Genetic Counseling 22, 869-874, 2013
242013
Observations from a nationwide vigilance program in medical care for spinal muscular atrophy patients in Chile
K Alvarez, B Suarez, MA Palomino, C Hervias, G Calcagno, ...
Arquivos de Neuro-Psiquiatria 77, 470-477, 2019
222019
A snapshot of current genetic testing practice in Lynch syndrome: The results of a representative survey of 33 Latin American existing centres/registries
A Della Valle, BM Rossi, EI Palmero, M Antelo, CA Vaccaro, ...
European Journal of Cancer 119, 112-121, 2019
212019
Spectrum of MLH1 and MSH2 mutations in Chilean families with suspected Lynch syndrome
K Alvarez, C Hurtado, MA Hevia, AM Wielandt, M De La Fuente, J Church, ...
Diseases of the colon & rectum 53 (4), 450-459, 2010
212010
Activating PIK3CA somatic mutation in congenital unilateral isolated muscle overgrowth of the upper extremity
C Castiglioni, E Bertini, P Orellana, C Villarroel, F Las Heras, D Hinzpeter, ...
American Journal of Medical Genetics Part A 164 (9), 2365-2369, 2014
202014
Mutational Screening of the APC Gene in Chilean Families with Familial Adenomatous Polyposis: Nine Novel Truncating Mutations
MK De la Fuente, KP Alvarez, AJ Letelier, F Bellolio, ML Acuña, FS León, ...
Diseases of the Colon & Rectum 50, 2142-2148, 2007
192007
LBSL: case series and DARS2 variant analysis in early severe forms with unexpected presentations
MD Stellingwerff, S Figuccia, E Bellacchio, K Alvarez, C Castiglioni, ...
Neurology: Genetics 7 (2), e559, 2021
182021
Sustav trenutno ne može provesti ovu radnju. Pokušajte ponovo kasnije.
Članci 1–20