Search Results - "Leonora Luna-Muñoz"

Trisomy 13 and 18—Prevalence and mortality—A multi‐registry population based analysis by Goel, Nitin, Morris, Joan K., Tucker, David, Walle, Hermien E. K., Bakker, Marian K., Kancherla, Vijaya, Marengo, Lisa, Canfield, Mark A., Kallen, Karin, Lelong, Nathalie, Camelo, Jorge L., Stallings, Erin B., Jones, Abbey M., Nance, Amy, Huynh, My‐Phuong, Martínez‐Fernández, Maria‐Luisa, Sipek, Antonin, Pierini, Anna, Nembhard, Wendy N., Goetz, Dorit, Rissmann, Anke, Groisman, Boris, Luna‐Muñoz, Leonora, Szabova, Elena, Lapchenko, Serhiy, Zarante, Ignacio, Hurtado‐Villa, Paula, Martinez, Laura E., Tagliabue, Giovanna, Landau, Danielle, Gatt, Miriam, Dastgiri, Saeed, Morgan, Margery

“…The aim of the study is to determine the prevalence, outcomes, and survival (among live births [LB]), in pregnancies diagnosed with trisomy 13 (T13) and 18…”
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Conjoined twins: A worldwide collaborative epidemiological study of the International Clearinghouse for Birth Defects Surveillance and Research by Mutchinick, Osvaldo M., Luna-Muñoz, Leonora, Amar, Emmanuelle, Bakker, Marian K., Clementi, Maurizio, Cocchi, Guido, da Graça Dutra, Maria, Feldkamp, Marcia L., Landau, Danielle, Leoncini, Emanuele, Li, Zhu, Lowry, Brian, Marengo, Lisa K., Martínez-Frías, María-Luisa, Mastroiacovo, Pierpaolo, Métneki, Julia, Morgan, Margery, Pierini, Anna, Rissman, Anke, Ritvanen, Annukka, Scarano, Gioacchino, Siffel, Csaba, Szabova, Elena, Arteaga-Vázquez, Jazmín

“…Conjoined twins (CT) are a very rare developmental accident of uncertain etiology. Prevalence has been previously estimated to be 1 in 50,000 to 1 in 100,000…”
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Isolated postaxial polydactyly: Epidemiologic characteristics from a multicenter birth defects study by Ortiz‐Cruz, Gabriela, Luna‐Muñoz, Leonora, Arteaga‐Vázquez, Jazmín, Mutchinick, Osvaldo M.

“…Isolated postaxial polydactyly (I‐PAP), as a single defect, is a frequent malformation, characterized by an extra digit placed on the ulnar or fibular side of…”
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Moderate altitude as a risk factor for isolated congenital malformations. Results from a case–control multicenter–multiregional study by Ibarra‐Ibarra, Blanca Rebeca, Luna‐Muñoz, Leonora, Mutchinick, Osvaldo M., Arteaga‐Vázquez, Jazmín

“…Background Living in high‐altitude regions has been associated with a higher prevalence of some birth defects. Moderate altitudes (1500–2500 m) have been…”
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Myelomeningocele genotype–phenotype correlation findings in cilia, HH, PCP, and WNT signaling pathways by Ortiz‐Cruz, Gabriela, Aguayo‐Gómez, Adolfo, Luna‐Muñoz, Leonora, Muñoz‐Téllez, Luis A., Mutchinick, Osvaldo M.

“…Background Myelomeningocele (MMC) is the most severe and frequent type of spina bifida. Its etiology remains poorly understood. The Hedgehog (Hh), Wnt, and…”
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Severe Congenital Neutropenia Type 4: A Rare Disease Harboring a G6pc3 Gene Pathogenic Variant Particular to the Mexican Population by López-Rodríguez, Larissa, Svyryd, Yevgeniya, Benítez-Alonso, Edmar O, Rivero-García, Pamela, Luna-Muñoz, Leonora, Mutchinick, Osvaldo M

“…Severe congenital neutropenia type 4 (SCN4) is a rare autosomal recessive granulopoiesis disorder caused by gene pathogenic variants. The estimated prevalence…”
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OEIS complex: Prevalence, clinical, and epidemiologic findings in a multicenter Mexican birth defects surveillance program by Arteaga‐Vázquez, Jazmín, Luna‐Muñoz, Leonora, Morales‐Suárez, Juan José, Mutchinick, Osvaldo M.

“…OEIS is the acronym of a malformations complex association including omphalocele, exstrophy of bladder or cloaca, imperforate anus, and spinal defects. It has…”
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Telomeres Length Variations in a Rheumatoid Arthritis Patients Cohort at Early Disease Onset and after Follow-Up by Svyryd, Yevgeniya, Pascual-Ramos, Virginia, Contreras-Yañez, Irazú, Muñoz-Tellez, Luís A, Luna-Muñoz, Leonora, López-Hernández, María A, Aguayo-Gómez, Adolfo, Mutchinick, Osvaldo M

“…Rheumatoid arthritis (RA) is an autoimmune disease characterized by chronic synovial joint inflammation, progressive disability, premature immune aging, and…”
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Congenital malformations in the offspring of epileptic mothers with and without anticonvulsant treatment by Arteaga-Vázquez, Jazmín, Luna-Muñoz, Leonora, Mutchinick, Osvaldo M

“…To determine the prevalence at birth and type of congenital malformations (CM) in newborns of epileptic mothers (NEM) treated and not treated with…”
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Acardia: Epidemiologic findings and literature review from the International Clearinghouse for Birth Defects Surveillance and Research by Botto, Lorenzo D., Feldkamp, Marcia L., Amar, Emmanuelle, Carey, John C., Castilla, Eduardo E., Clementi, Maurizio, Cocchi, Guido, de Walle, Hermien E.K., Halliday, Jane, Leoncini, Emanuele, Li, Zhu, Lowry, R. Brian, Marengo, Lisa K., Martínez-Frías, María-Luisa, Merlob, Paul, Morgan, Margery, Muñoz, Leonora Luna, Rissmann, Anke, Ritvanen, Annukka, Scarano, Gioacchino, Mastroiacovo, Pierpaolo

“…Acardia is a severe, complex malformation of monozygotic twinning, but beyond clinical case series, very few epidemiologic data are available. The goals of…”
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Genetic Risk Determinants for Cigarette Smoking Dependence in Mexican Mestizo Families by Svyryd, Yevgeniya, Ramírez-Venegas, Alejandra, Sánchez-Hernández, Beatriz, Aguayo-Gómez, Adolfo, Luna-Muñoz, Leonora, Arteaga-Vázquez, Jazmín, Regalado-Pineda, Justino, Mutchinick, Osvaldo M.

“…Tobacco smoking is a leading cause of mortality in developed and developing countries. Despite antitobacco and smoke-free policies, the prevalence of active…”
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Malformaciones congénitas en hijos de madres epilépticas con y sin tratamiento con anticonvulsivantes by Arteaga-Vázquez, Jazmín, Luna-Muñoz, Leonora, Mutchinick, Osvaldo M

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Malformaciones congénitas en hijos de madres epilépticas con y sin tratamiento con anticonvulsivantes Congenital malformations in the offspring of epileptic mothers with and without anticonvulsant treatment by Jazmín Arteaga-Vázquez, Leonora Luna-Muñoz, Osvaldo M Mutchinick

“…OBJETIVO: Determinar la frecuencia y tipo de malformaciones congénitas (MC) en hijos de madres epilépticas (HME) tratadas y no tratadas con anticonvulsivantes,…”
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Malformaciones congénitas en hijos de madres epilépticas con y sin tratamiento con anticonvulsivantes by Arteaga-Vázquez, Jazmín, Luna-Muñoz, Leonora, Mutchinick, Osvaldo M

“…OBJETIVO: Determinar la frecuencia y tipo de malformaciones congénitas (MC) en hijos de madres epilépticas (HME) tratadas y no tratadas con anticonvulsivantes,…”
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