Browsing by Author Figuera, L.E.

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Issue DateTitleAuthor(s)
2002Inherited hypertrichosesGarcia-Cruz, D.; Figuera, L.E.; Cantu, J.M.; Garcia-Cruz, D., División de Genética, Centro de Investigacion Biomedica, Universidad de Guadalajara, Sierra Mojada 950, C. Indeprendencia, Gudalajara, Jal. 44340, Mexico; Figuera, L.E., División de Genética, Centro de Investigacion Biomedica, Universidad de Guadalajara, Sierra Mojada 950, C. Indeprendencia, Gudalajara, Jal. 44340, Mexico; Cantu, J.M., División de Genética, Centro de Investigacion Biomedica, Universidad de Guadalajara, Sierra Mojada 950, C. Indeprendencia, Gudalajara, Jal. 44340, Mexico
2002Inherited hypertrichosesGarcia-Cruz, D.; Figuera, L.E.; Cantu, J.M.; Garcia-Cruz, D., Divisi�n de Gen�tica, Centro de Investigacion Biomedica, Universidad de Guadalajara, Sierra Mojada 950, C. Indeprendencia, Gudalajara, Jal. 44340, Mexico; Figuera, L.E., Divisi�n de Gen�tica, Centro de Investigacion Biomedica, Universidad de Guadalajara, Sierra Mojada 950, C. Indeprendencia, Gudalajara, Jal. 44340, Mexico; Cantu, J.M., Divisi�n de Gen�tica, Centro de Investigacion Biomedica, Universidad de Guadalajara, Sierra Mojada 950, C. Indeprendencia, Gudalajara, Jal. 44340, Mexico
1996Interstitial deletion 6q16.2q22.2 in a child with ectrodactyly [Deletion interstitielle 6q16.2q22.2 chez un enfant ayant une ectrodactylie]Correa-Cerro, L.; Garcia-Cruz, D.; Diaz-Castanos, L.; Figuera, L.E.; Sanchez-Corona, J.; Correa-Cerro, L., Division de Genetica, CIBO-IMSS, Ap. Postal 1, 3838 Guadalajara, Jalisco, Mexico; Garcia-Cruz, D., Division de Genetica, CIBO-IMSS, Ap. Postal 1, 3838 Guadalajara, Jalisco, Mexico; Diaz-Castanos, L., Division de Genetica, CIBO-IMSS, Ap. Postal 1, 3838 Guadalajara, Jalisco, Mexico; Figuera, L.E., Division de Genetica, CIBO-IMSS, Ap. Postal 1, 3838 Guadalajara, Jalisco, Mexico; Sanchez-Corona, J., Division de Genetica, CIBO-IMSS, Ap. Postal 1, 3838 Guadalajara, Jalisco, Mexico
1996Interstitial deletion 6q16.2q22.2 in a child with ectrodactyly [Deletion interstitielle 6q16.2q22.2 chez un enfant ayant une ectrodactylie]Correa-Cerro, L.; Garcia-Cruz, D.; Diaz-Castanos, L.; Figuera, L.E.; Sanchez-Corona, J.; Correa-Cerro, L., Division de Genetica, CIBO-IMSS, Ap. Postal 1, 3838 Guadalajara, Jalisco, Mexico; Garcia-Cruz, D., Division de Genetica, CIBO-IMSS, Ap. Postal 1, 3838 Guadalajara, Jalisco, Mexico; Diaz-Castanos, L., Division de Genetica, CIBO-IMSS, Ap. Postal 1, 3838 Guadalajara, Jalisco, Mexico; Figuera, L.E., Division de Genetica, CIBO-IMSS, Ap. Postal 1, 3838 Guadalajara, Jalisco, Mexico; Sanchez-Corona, J., Division de Genetica, CIBO-IMSS, Ap. Postal 1, 3838 Guadalajara, Jalisco, Mexico
2006Interstitial deletion of 13q22?q31: Case report and review of the literatureMorales, J.A.; Mendizabal, A.P.; Vasquez, A.I.; Figuera, L.E.; Gonzalez-Garcia, J.R.; Morales, J.A., Human Genetics PhD, University of Guadalajara, Guadalajara, Jalisco, Mexico, Genetics Division of Western Biomedical Research Center (CIBO), Guadalajara, Jalisco, Mexico; Mendizabal, A.P., Human Genetics PhD, University of Guadalajara, Guadalajara, Jalisco, Mexico, Mexican Institute for Social Security (IMSS), Guadalajara, Jalisco, Mexico; V�squez, A.I., Genetics Division of Western Biomedical Research Center (CIBO), Guadalajara, Jalisco, Mexico; Figuera, L.E., Human Genetics PhD, University of Guadalajara, Guadalajara, Jalisco, Mexico, Genetics Division of Western Biomedical Research Center (CIBO), Guadalajara, Jalisco, Mexico; Gonz�lez-Garc�a, J.R., Human Genetics PhD, University of Guadalajara, Guadalajara, Jalisco, Mexico, Genetics Division of Western Biomedical Research Center (CIBO), Guadalajara, Jalisco, Mexico, Centro de Investigaci�n Biom�dica de Occidente (CIBO), IMSS, P.O. Box 1-3838, CP 44100, Guadalajara, Mexico
2006Interstitial deletion of 13q22→q31: Case report and review of the literatureMorales, J.A.; Mendizabal, A.P.; Vasquez, A.I.; Figuera, L.E.; Gonzalez-Garcia, J.R.; Morales, J.A., Human Genetics PhD, University of Guadalajara, Guadalajara, Jalisco, Mexico, Genetics Division of Western Biomedical Research Center (CIBO), Guadalajara, Jalisco, Mexico; Mendizabal, A.P., Human Genetics PhD, University of Guadalajara, Guadalajara, Jalisco, Mexico, Mexican Institute for Social Security (IMSS), Guadalajara, Jalisco, Mexico; Vásquez, A.I., Genetics Division of Western Biomedical Research Center (CIBO), Guadalajara, Jalisco, Mexico; Figuera, L.E., Human Genetics PhD, University of Guadalajara, Guadalajara, Jalisco, Mexico, Genetics Division of Western Biomedical Research Center (CIBO), Guadalajara, Jalisco, Mexico; González-García, J.R., Human Genetics PhD, University of Guadalajara, Guadalajara, Jalisco, Mexico, Genetics Division of Western Biomedical Research Center (CIBO), Guadalajara, Jalisco, Mexico, Centro de Investigación Biomédica de Occidente (CIBO), IMSS, P.O. Box 1-3838, CP 44100, Guadalajara, Mexico
2013Intron 4 VNTR (4a/b) polymorphism of the endothelial nitric oxide synthase gene is associated with breast cancer in Mexican women.Ramirez-Patino, R.; Figuera, L.E.; Puebla-Perez, A.M.; Delgado-Saucedo, J.I.; Legazpi-Macias, M.M.; Mariaud-Schmidt, R.P.; Ramos-Silva, A.; Gutierrez-Hurtado, I.A.; Gomez Flores-Ramos, L.; Zuniga-Gonzalez, G.M.; Gallegos-Arreola, M.P.; Ramírez-Patiño, R., Molecular Genetics Laboratory, Molecular Medicine Division, Western Biomedical Research Center (CIBO), Western National Medical Center (CMNO), Mexican Social Security Institute (IMSS), Guadalajara, Jalisco, Mexico. ; PhD Program in Human Genetics, Health Sciences University Center (CUCS), University of Guadalajara (U de G), Guadalajara, Jalisco, Mexico.; Figuera, L.E.; Puebla-Pérez, A.M.; Delgado-Saucedo, J.I.; Legazpí-Macias, M.M.; Mariaud-Schmidt, R.P.; Ramos-Silva, A.; Gutiérrez-Hurtado, I.A.; Gómez Flores-Ramos, L.; Zúñiga-González, G.M.; Gallegos-Arreola, M.P.
2013Intron 4 VNTR (4a/b) polymorphism of the endothelial nitric oxide synthase gene is associated with breast cancer in Mexican women.Ramirez-Patino, R.; Figuera, L.E.; Puebla-Perez, A.M.; Delgado-Saucedo, J.I.; Legazpi-Macias, M.M.; Mariaud-Schmidt, R.P.; Ramos-Silva, A.; Gutierrez-Hurtado, I.A.; Gomez Flores-Ramos, L.; Zuniga-Gonzalez, G.M.; Gallegos-Arreola, M.P.; Ram�rez-Pati�o, R., Molecular Genetics Laboratory, Molecular Medicine Division, Western Biomedical Research Center (CIBO), Western National Medical Center (CMNO), Mexican Social Security Institute (IMSS), Guadalajara, Jalisco, Mexico. ; PhD Program in Human Genetics, Health Sciences University Center (CUCS), University of Guadalajara (U de G), Guadalajara, Jalisco, Mexico.; Figuera, L.E.; Puebla-P�rez, A.M.; Delgado-Saucedo, J.I.; Legazp�-Macias, M.M.; Mariaud-Schmidt, R.P.; Ramos-Silva, A.; Guti�rrez-Hurtado, I.A.; G�mez Flores-Ramos, L.; Z��iga-Gonz�lez, G.M.; Gallegos-Arreola, M.P.
2014Labeling of HeLa cells using ZrO<inf>2</inf>:Yb3+-Er3+ nanoparticles with upconversion emissionGutierrez-Amavizca, B.E.; Orozco-Castellanos, R.; Padilla-Gutierrez, J.R.; Valle, Y.; Figuera, L.E.; Gutiérrez-Amavizca, B.E., División de Genética, Centro de Investigación Biomédica de Occidente, Instituto Mexicano del Seguro SocialGuadalajara, Jalisco, Mexico, Doctorado en Genética Humana, Centro Universitario de Ciencias de la Salud, Universidad de GuadalajaraGuadalajara, Jalisco, Mexico; Orozco-Castellanos, R., Centro del Rincón Guadalajara, Jalisco, Mexico, División de Nefrología y Trasplantes, Unidad Médica de Alta Especialidad, Centro Médico Nacional de Occidente, Instituto Mexicano del Seguro SocialGuadalajara, Jalisco, Mexico; Padilla-Gutiérrez, J.R., Departamento de Clínicas Médicas, Centro Universitario de Ciencias de la Salud, Universidad de GuadalajaraGuadalajara, Jalisco, Mexico; Valle, Y., Departamento de Clínicas Médicas, Centro Universitario de Ciencias de la Salud, Universidad de GuadalajaraGuadalajara, Jalisco, Mexico; Figuera, L.E., División de Genética, Centro de Investigación Biomédica de Occidente, Instituto Mexicano del Seguro SocialGuadalajara, Jalisco, Mexico, Doctorado en Genética Humana, Centro Universitario de Ciencias de la Salud, Universidad de GuadalajaraGuadalajara, Jalisco, Mexico
1995Mapping of the congenital generalized hypertrichosis locus to chromosome Xq24-q27.1Figuera, L.E.; Pandolfo, M.; Dunne, P.W.; Cantu, J.M.; Patel, P.I.; Figuera, L.E., Department of Neurology, Baylor College of Medicine, Houston, TX 77030, United States, División de Genética, CIBO-IMSS and CUCS, Universidad de Guadalajara, Guadalajara, Jal, Mexico; Pandolfo, M., Department of Neurology, Baylor College of Medicine, Houston, TX 77030, United States, Div. of Biochemistry and Genetics, Istituto Nazionale Neurologico Besta, Milan, Italy; Dunne, P.W., Department of Neurology, Baylor College of Medicine, Houston, TX 77030, United States; Cantú, J.M., División de Genética, CIBO-IMSS and CUCS, Universidad de Guadalajara, Guadalajara, Jal, Mexico; Patel, P.I., Department of Neurology, Baylor College of Medicine, Houston, TX 77030, United States, Dept. of Molec. and Human Genetics, Baylor College of Medicine, Houston, TX 77030, United States, Human Genome Center, Baylor College of Medicine, Houston, TX 77030, United States
1995Mapping of the congenital generalized hypertrichosis locus to chromosome Xq24-q27.1Figuera, L.E.; Pandolfo, M.; Dunne, P.W.; Cantu, J.M.; Patel, P.I.; Figuera, L.E., Department of Neurology, Baylor College of Medicine, Houston, TX 77030, United States, División de Genética, CIBO-IMSS and CUCS, Universidad de Guadalajara, Guadalajara, Jal, Mexico; Pandolfo, M., Department of Neurology, Baylor College of Medicine, Houston, TX 77030, United States, Div. of Biochemistry and Genetics, Istituto Nazionale Neurologico Besta, Milan, Italy; Dunne, P.W., Department of Neurology, Baylor College of Medicine, Houston, TX 77030, United States; Cantú, J.M., División de Genética, CIBO-IMSS and CUCS, Universidad de Guadalajara, Guadalajara, Jal, Mexico; Patel, P.I., Department of Neurology, Baylor College of Medicine, Houston, TX 77030, United States, Dept. of Molec. and Human Genetics, Baylor College of Medicine, Houston, TX 77030, United States, Human Genome Center, Baylor College of Medicine, Houston, TX 77030, United States
2005Methylenetetrahydrofolate reductase C677T polymorphism and Factor V Leiden variant in Mexican women with preeclampsia/eclampsiaDavalos, I.P.; Moran, M.C.; Martinez-Abundis, E.; Gonzalez-Ortiz, M.; Flores-Martinez, S.E.; Machorro, V.; Sandoval, L.; Figuera, L.E.; Mena, J.P.; Oliva, J.M.; Tlacuilo-Parra, J.A.; Sanchez-Corona, J.; Salazar-Paramo, M.; D�valos, I.P., Divisiones de Gen�tica Y Medicina Molecular, Centro de Investigaci�n Biom�dica de Occidente, CMNO, S. Mojada 800, Col. Independencia, CP 44330, Guadalajara, Jal., Mexico, Doctorado en Gen�tica Humana, CVCS, Universidad de Guadalajara, M�xico, Mexico, Divisi�n de Gen�tica, CIBO, CMNO, S. Mojada 800, Col. Independencia, CP 44330, Guadalajara, Jal., Mexico; Moran, M.C., Divisiones de Gen�tica Y Medicina Molecular, Centro de Investigaci�n Biom�dica de Occidente, CMNO, S. Mojada 800, Col. Independencia, CP 44330, Guadalajara, Jal., Mexico, Doctorado en Gen�tica Humana, CVCS, Universidad de Guadalajara, M�xico, Mexico; Mart�nez-Abundis, E., Unidad de Investigaci�n M�dica en Epidemiolog�a Cl�nica, Instituto Mexicano del Seguro Social, Mexico, Mexico; Gonz�lez-Ortiz, M., Unidad de Investigaci�n M�dica en Epidemiolog�a Cl�nica, Instituto Mexicano del Seguro Social, Mexico, Mexico; Flores-Mart�nez, S.E., Divisiones de Gen�tica Y Medicina Molecular, Centro de Investigaci�n Biom�dica de Occidente, CMNO, S. Mojada 800, Col. Independencia, CP 44330, Guadalajara, Jal., Mexico, Doctorado en Gen�tica Humana, CVCS, Universidad de Guadalajara, M�xico, Mexico; Machorro, V., Divisiones de Gen�tica Y Medicina Molecular, Centro de Investigaci�n Biom�dica de Occidente, CMNO, S. Mojada 800, Col. Independencia, CP 44330, Guadalajara, Jal., Mexico; Sandoval, L., Divisiones de Gen�tica Y Medicina Molecular, Centro de Investigaci�n Biom�dica de Occidente, CMNO, S. Mojada 800, Col. Independencia, CP 44330, Guadalajara, Jal., Mexico, Doctorado en Gen�tica Humana, CVCS, Universidad de Guadalajara, M�xico, Mexico; Figuera, L.E., Divisiones de Gen�tica Y Medicina Molecular, Centro de Investigaci�n Biom�dica de Occidente, CMNO, S. Mojada 800, Col. Independencia, CP 44330, Guadalajara, Jal., Mexico, Doctorado en Gen�tica Humana, CVCS, Universidad de Guadalajara, M�xico, Mexico; Mena, J.P., Doctorado en Gen�tica Humana, CVCS, Universidad de Guadalajara, M�xico, Mexico; Oliva, J.M., Doctorado en Gen�tica Humana, CVCS, Universidad de Guadalajara, M�xico, Mexico; Tlacuilo-Parra, J.A., Unidad de Investigaci�n M�dica en Epidemiolog�a Cl�nica, Instituto Mexicano del Seguro Social, Mexico, Mexico; S�nchez-Corona, J., Divisiones de Gen�tica Y Medicina Molecular, Centro de Investigaci�n Biom�dica de Occidente, CMNO, S. Mojada 800, Col. Independencia, CP 44330, Guadalajara, Jal., Mexico, Doctorado en Gen�tica Humana, CVCS, Universidad de Guadalajara, M�xico, Mexico; Salazar-P�ramo, M., Unidad de Investigaci�n M�dica en Epidemiolog�a Cl�nica, Instituto Mexicano del Seguro Social, Mexico, Mexico, Departamento de Fisiolog�a, Centro Universitario Ciencias de la Salud, Universidad de Guadalajara, Mexico, Mexico
2005Methylenetetrahydrofolate reductase C677T polymorphism and Factor V Leiden variant in Mexican women with preeclampsia/eclampsiaDavalos, I.P.; Moran, M.C.; Martinez-Abundis, E.; Gonzalez-Ortiz, M.; Flores-Martinez, S.E.; Machorro, V.; Sandoval, L.; Figuera, L.E.; Mena, J.P.; Oliva, J.M.; Tlacuilo-Parra, J.A.; Sanchez-Corona, J.; Salazar-Paramo, M.; Dávalos, I.P., Divisiones de Genética Y Medicina Molecular, Centro de Investigación Biomédica de Occidente, CMNO, S. Mojada 800, Col. Independencia, CP 44330, Guadalajara, Jal., Mexico, Doctorado en Genética Humana, CVCS, Universidad de Guadalajara, México, Mexico, División de Genética, CIBO, CMNO, S. Mojada 800, Col. Independencia, CP 44330, Guadalajara, Jal., Mexico; Moran, M.C., Divisiones de Genética Y Medicina Molecular, Centro de Investigación Biomédica de Occidente, CMNO, S. Mojada 800, Col. Independencia, CP 44330, Guadalajara, Jal., Mexico, Doctorado en Genética Humana, CVCS, Universidad de Guadalajara, México, Mexico; Martínez-Abundis, E., Unidad de Investigación Médica en Epidemiología Clínica, Instituto Mexicano del Seguro Social, Mexico, Mexico; González-Ortiz, M., Unidad de Investigación Médica en Epidemiología Clínica, Instituto Mexicano del Seguro Social, Mexico, Mexico; Flores-Martínez, S.E., Divisiones de Genética Y Medicina Molecular, Centro de Investigación Biomédica de Occidente, CMNO, S. Mojada 800, Col. Independencia, CP 44330, Guadalajara, Jal., Mexico, Doctorado en Genética Humana, CVCS, Universidad de Guadalajara, México, Mexico; Machorro, V., Divisiones de Genética Y Medicina Molecular, Centro de Investigación Biomédica de Occidente, CMNO, S. Mojada 800, Col. Independencia, CP 44330, Guadalajara, Jal., Mexico; Sandoval, L., Divisiones de Genética Y Medicina Molecular, Centro de Investigación Biomédica de Occidente, CMNO, S. Mojada 800, Col. Independencia, CP 44330, Guadalajara, Jal., Mexico, Doctorado en Genética Humana, CVCS, Universidad de Guadalajara, México, Mexico; Figuera, L.E., Divisiones de Genética Y Medicina Molecular, Centro de Investigación Biomédica de Occidente, CMNO, S. Mojada 800, Col. Independencia, CP 44330, Guadalajara, Jal., Mexico, Doctorado en Genética Humana, CVCS, Universidad de Guadalajara, México, Mexico; Mena, J.P., Doctorado en Genética Humana, CVCS, Universidad de Guadalajara, México, Mexico; Oliva, J.M., Doctorado en Genética Humana, CVCS, Universidad de Guadalajara, México, Mexico; Tlacuilo-Parra, J.A., Unidad de Investigación Médica en Epidemiología Clínica, Instituto Mexicano del Seguro Social, Mexico, Mexico; Sánchez-Corona, J., Divisiones de Genética Y Medicina Molecular, Centro de Investigación Biomédica de Occidente, CMNO, S. Mojada 800, Col. Independencia, CP 44330, Guadalajara, Jal., Mexico, Doctorado en Genética Humana, CVCS, Universidad de Guadalajara, México, Mexico; Salazar-Páramo, M., Unidad de Investigación Médica en Epidemiología Clínica, Instituto Mexicano del Seguro Social, Mexico, Mexico, Departamento de Fisiología, Centro Universitario Ciencias de la Salud, Universidad de Guadalajara, Mexico, Mexico
2003Mucopolysaccharidosis I: A comparative study of haplotypes Eco47III-NspI sites frequencies in patients and healthy subjects of Mexican populationGallegos-Arreola, M.P.; Arnaud-Lopez, L.; Figuera, L.E.; Beltran Jaramillo, T.S.; Rangel-Villalobos, H.; Thomatsu, S.; Zuniga-Gonzalez, G.M.; Gallegos-Arreola, M.P., Divisione de Medicina Molecular, Ctro. Invest. Biomedica Occidente, Guadalajara, Jalisco, Mexico, Ctro. Invest. Biomedica Occidente, Sierra Mojada No. 800, A.P. 1-3838, Guadalajara, Jalisco, Mexico; Arnaud-López, L., Divisione de Medicina Molecular, Ctro. Invest. Biomedica Occidente, Guadalajara, Jalisco, Mexico; Figuera, L.E., Divisione de Genética, Ctro. Invest. Biomedica Occidente, Guadalajara, Jalisco, Mexico; Beltrán Jaramillo, T.S., Servicio de Urgencias, Hospital de Especialidades, CMNO, Guadalajara, Jalisco, Mexico; Rangel-Villalobos, H., Laboratorio de Biologia Molecular, Centro Universitario de la Cienega, Guadalajara, Jalisco, Mexico; Thomatsu, S., E.A. Doisy Dept. of Biochemistry, St. Louis Univ. School of Medicine, 1402 South Grand Boulevard, St. Louis, MO, United States; Zúñiga-González, G.M., Divisione de Medicina Molecular, Ctro. Invest. Biomedica Occidente, Guadalajara, Jalisco, Mexico
2003Mucopolysaccharidosis I: A comparative study of haplotypes Eco47III-NspI sites frequencies in patients and healthy subjects of Mexican populationGallegos-Arreola, M.P.; Arnaud-Lopez, L.; Figuera, L.E.; Beltran Jaramillo, T.S.; Rangel-Villalobos, H.; Thomatsu, S.; Zuniga-Gonzalez, G.M.; Gallegos-Arreola, M.P., Divisione de Medicina Molecular, Ctro. Invest. Biomedica Occidente, Guadalajara, Jalisco, Mexico, Ctro. Invest. Biomedica Occidente, Sierra Mojada No. 800, A.P. 1-3838, Guadalajara, Jalisco, Mexico; Arnaud-López, L., Divisione de Medicina Molecular, Ctro. Invest. Biomedica Occidente, Guadalajara, Jalisco, Mexico; Figuera, L.E., Divisione de Genética, Ctro. Invest. Biomedica Occidente, Guadalajara, Jalisco, Mexico; Beltrán Jaramillo, T.S., Servicio de Urgencias, Hospital de Especialidades, CMNO, Guadalajara, Jalisco, Mexico; Rangel-Villalobos, H., Laboratorio de Biologia Molecular, Centro Universitario de la Cienega, Guadalajara, Jalisco, Mexico; Thomatsu, S., E.A. Doisy Dept. of Biochemistry, St. Louis Univ. School of Medicine, 1402 South Grand Boulevard, St. Louis, MO, United States; Zúñiga-González, G.M., Divisione de Medicina Molecular, Ctro. Invest. Biomedica Occidente, Guadalajara, Jalisco, Mexico
2000Mutations of the gene encoding the transmembrane transporter protein ABC-C6 cause pseudoxanthoma elasticumStruk, B.; Cai, L.; Zach, S.; Ji, W.; Chung, J.; Lumsden, A.; Stumm, M.; Huber, M.; Schaen, L.; Kim, C.-A.; Goldsmith, L.A.; Viljoen, D.; Figuera, L.E.; Fuchs, W.; Munier, F.; Ramesar, R.; Hohl, D.; Richards, R.; Neldner, K.H.; Lindpaintner, K.; Struk, B., Department of Cardiology, Children's Hospital, Brigham and Women's Hospital, Boston, MA 021152, United States, Max Delbruck Ctr. for Molec. Med., 13122 Berlin, Germany, F. Hoffmann-La Roche Ltd, Roche Genetics, Pharmaceuticals Division, 4070 Basel, Switzerland; Cai, L., Department of Cardiology, Children's Hospital, Brigham and Women's Hospital, Boston, MA 021152, United States; ZZapotitlánch, S., Department of Dermatology, University of Lausanne, 1011 Lausanne, Switzerland; Ji, W., Department of Cardiology, Children's Hospital, Brigham and Women's Hospital, Boston, MA 021152, United States, F. Hoffmann-La Roche Ltd, Roche Genetics, Pharmaceuticals Division, 4070 Basel, Switzerland; Chung, J., Department of Cardiology, Children's Hospital, Brigham and Women's Hospital, Boston, MA 021152, United States; Lumsden, A., Dept. of Cytogenet./Molec. Genet., Women's and Children's Hospital, 71 King William Road, North Adelaide, SA 5006, Australia; Stumm, M., Human Genetics Institute, Otto-von-Guericke-University, Magdeburg, Germany; Huber, M., Department of Dermatology, University of Lausanne, 1011 Lausanne, Switzerland; Schaen, L., Department of Dermatology, University of Rochester, Rochester, NY 14642, United States; Kim, C.-A., Department of Cardiology, Children's Hospital, Brigham and Women's Hospital, Boston, MA 021152, United States; Goldsmith, L.A., Department of Dermatology, University of Rochester, Rochester, NY 14642, United States; Viljoen, D., S. African Inst. for Med. Research, Johannesburg, South Africa; Figuera, L.E., Divisions of Genet./Molec. Medicine, CIBO-IMSS, Univ. of Guadalajara Medical School, Guadalajara, Mexico; Fuchs, W., Department of Ophthalmology, Mount Sinai School of Medicine, New York, NY 10029, United States; Munier, F., Department of Ophthalmology, University of Lausanne, 1011 Lausanne, Switzerland; Ramesar, R.; Hohl, D., Department of Dermatology, University of Lausanne, 1011 Lausanne, Switzerland; Richards, R., Dept. of Cytogenet./Molec. Genet., Women's and Children's Hospital, 71 King William Road, North Adelaide, SA 5006, Australia, Department of Genetics, University of Adelaide, Adelaide, SA 5000, Australia; Neldner, K.H., Department of Dermatology, Texas Tech Univ. Hlth. Sci. Center, Lubbock, TX 79430, United States; Lindpaintner, K., Max Delbruck Ctr. for Molec. Med., 13122 Berlin, Germany, F. Hoffmann-La Roche Ltd, Roche Genetics, Pharmaceuticals Division, 4070 Basel, Switzerland
2000Mutations of the gene encoding the transmembrane transporter protein ABC-C6 cause pseudoxanthoma elasticumStruk, B.; Cai, L.; Zach, S.; Ji, W.; Chung, J.; Lumsden, A.; Stumm, M.; Huber, M.; Schaen, L.; Kim, C.-A.; Goldsmith, L.A.; Viljoen, D.; Figuera, L.E.; Fuchs, W.; Munier, F.; Ramesar, R.; Hohl, D.; Richards, R.; Neldner, K.H.; Lindpaintner, K.; Struk, B., Department of Cardiology, Children's Hospital, Brigham and Women's Hospital, Boston, MA 021152, United States, Max Delbruck Ctr. for Molec. Med., 13122 Berlin, Germany, F. Hoffmann-La Roche Ltd, Roche Genetics, Pharmaceuticals Division, 4070 Basel, Switzerland; Cai, L., Department of Cardiology, Children's Hospital, Brigham and Women's Hospital, Boston, MA 021152, United States; Zäch, S., Department of Dermatology, University of Lausanne, 1011 Lausanne, Switzerland; Ji, W., Department of Cardiology, Children's Hospital, Brigham and Women's Hospital, Boston, MA 021152, United States, F. Hoffmann-La Roche Ltd, Roche Genetics, Pharmaceuticals Division, 4070 Basel, Switzerland; Chung, J., Department of Cardiology, Children's Hospital, Brigham and Women's Hospital, Boston, MA 021152, United States; Lumsden, A., Dept. of Cytogenet./Molec. Genet., Women's and Children's Hospital, 71 King William Road, North Adelaide, SA 5006, Australia; Stumm, M., Human Genetics Institute, Otto-von-Guericke-University, Magdeburg, Germany; Huber, M., Department of Dermatology, University of Lausanne, 1011 Lausanne, Switzerland; Schaen, L., Department of Dermatology, University of Rochester, Rochester, NY 14642, United States; Kim, C.-A., Department of Cardiology, Children's Hospital, Brigham and Women's Hospital, Boston, MA 021152, United States; Goldsmith, L.A., Department of Dermatology, University of Rochester, Rochester, NY 14642, United States; Viljoen, D., S. African Inst. for Med. Research, Johannesburg, South Africa; Figuera, L.E., Divisions of Genet./Molec. Medicine, CIBO-IMSS, Univ. of Guadalajara Medical School, Guadalajara, Mexico; Fuchs, W., Department of Ophthalmology, Mount Sinai School of Medicine, New York, NY 10029, United States; Munier, F., Department of Ophthalmology, University of Lausanne, 1011 Lausanne, Switzerland; Ramesar, R.; Hohl, D., Department of Dermatology, University of Lausanne, 1011 Lausanne, Switzerland; Richards, R., Dept. of Cytogenet./Molec. Genet., Women's and Children's Hospital, 71 King William Road, North Adelaide, SA 5006, Australia, Department of Genetics, University of Adelaide, Adelaide, SA 5000, Australia; Neldner, K.H., Department of Dermatology, Texas Tech Univ. Hlth. Sci. Center, Lubbock, TX 79430, United States; Lindpaintner, K., Max Delbruck Ctr. for Molec. Med., 13122 Berlin, Germany, F. Hoffmann-La Roche Ltd, Roche Genetics, Pharmaceuticals Division, 4070 Basel, Switzerland
2012Ophthalmic manifestations in Mexican patients with Fabry disease [Manifestaciones oftalmológicas en pacientes mexicanos con enfermedad de Fabry]Beltran-Becerra, K.J.; Rios-Gonzalez, B.E.; Gutierrez-Amavizca, B.E.; Silva-Noriega, D.A.; Figuera, L.E.; Beltrán-Becerra, K.J., Servicio de Oftalmología, Unidad Médica de Alta Especialidad, Instituto Mexicano Del Seguro Social, Guadalajara, Jalisco, Mexico; Ríos-González, B.E., División de Genética, Centro de Investigación Biomédica de Occidente, Universidad de Guadalajara, Guadalajara, Jalisco, Mexico; Gutiérrez-Amavizca, B.E., División de Genética, Centro de Investigación Biomédica de Occidente, Universidad de Guadalajara, Guadalajara, Jalisco, Mexico; Silva-Noriega, D.A., Servicio de Oftalmología, Unidad Médica de Alta Especialidad, Instituto Mexicano Del Seguro Social, Guadalajara, Jalisco, Mexico; Figuera, L.E., División de Genética, Centro de Investigación Biomédica de Occidente, Universidad de Guadalajara, Guadalajara, Jalisco, Mexico
2012Ophthalmic manifestations in Mexican patients with Fabry disease [Manifestaciones oftalmol�gicas en pacientes mexicanos con enfermedad de Fabry]Beltran-Becerra, K.J.; Rios-Gonzalez, B.E.; Gutierrez-Amavizca, B.E.; Silva-Noriega, D.A.; Figuera, L.E.; Beltr�n-Becerra, K.J., Servicio de Oftalmolog�a, Unidad M�dica de Alta Especialidad, Instituto Mexicano Del Seguro Social, Guadalajara, Jalisco, Mexico; R�os-Gonz�lez, B.E., Divisi�n de Gen�tica, Centro de Investigaci�n Biom�dica de Occidente, Universidad de Guadalajara, Guadalajara, Jalisco, Mexico; Guti�rrez-Amavizca, B.E., Divisi�n de Gen�tica, Centro de Investigaci�n Biom�dica de Occidente, Universidad de Guadalajara, Guadalajara, Jalisco, Mexico; Silva-Noriega, D.A., Servicio de Oftalmolog�a, Unidad M�dica de Alta Especialidad, Instituto Mexicano Del Seguro Social, Guadalajara, Jalisco, Mexico; Figuera, L.E., Divisi�n de Gen�tica, Centro de Investigaci�n Biom�dica de Occidente, Universidad de Guadalajara, Guadalajara, Jalisco, Mexico
2014Pedigree analysis of Mexican families with Fabry disease as a powerful tool for identification of heterozygous femalesGutierrez-Amavizca, B.E.; Orozco-Castellanos, R.; Padilla-Gutierrez, J.R.; Valle, Y.; Figuera, L.E.; Gutiérrez-Amavizca, B.E., División de Genética, Centro de Investigación Biomédica de Occidente, Instituto Mexicano del Seguro SocialGuadalajara, Jalisco, Mexico, Doctorado en Genética Humana, Centro Universitario de Ciencias de la Salud, Universidad de GuadalajaraGuadalajara, Jalisco, Mexico; Orozco-Castellanos, R., Centro del RiñónGuadalajara, Jalisco, Mexico, División de Nefrología y Trasplantes, Unidad Médica de Alta Especialidad, Centro Médico Nacional de Occidente, Instituto Mexicano del Seguro SocialGuadalajara, Jalisco, Mexico; Padilla-Gutiérrez, J.R., Departamento de Clínicas Médicas, Centro Universitario de Ciencias de la Salud, Universidad de GuadalajaraGuadalajara, Jalisco, Mexico; Valle, Y., Departamento de Clínicas Médicas, Centro Universitario de Ciencias de la Salud, Universidad de GuadalajaraGuadalajara, Jalisco, Mexico; Figuera, L.E., División de Genética, Centro de Investigación Biomédica de Occidente, Instituto Mexicano del Seguro SocialGuadalajara, Jalisco, Mexico, Doctorado en Genética Humana, Centro Universitario de Ciencias de la Salud, Universidad de GuadalajaraGuadalajara, Jalisco, Mexico