Search Results - "Frías, L"

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    Maternal age and prevalence of isolated congenital heart defects in an urban area of the United States by Miller, Assia, Riehle-Colarusso, Tiffany, Siffel, Csaba, Frías, Jaime L., Correa, Adolfo

    “…Although maternal age has been associated with a number of birth defects in several reports, the literature on the association of maternal age with isolated…”
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    Journal Article
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    Non-genetic risk factors for gastroschisis by Rasmussen, Sonja A., Frías, Jaime L.

    “…Gastroschisis is an abdominal wall defect typically located to the right of the umbilical cord in which intestines and occasionally other abdominal contents…”
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    Congenital Heart Defects and Major Structural Noncardiac Anomalies, Atlanta, Georgia, 1968 to 2005 by Miller, Assia, MD, MPH, Riehle-Colarusso, Tiffany, MD, Alverson, C.J., MS, Frías, Jaime L., MD, Correa, Adolfo, MD, PhD

    Published in The Journal of pediatrics (01-07-2011)
    “…Objective To identify the proportion of major structural noncardiac anomalies identified with congenital heart defects (CHDs). Study design Records of infants…”
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    Direct costs of a home parenteral nutrition programme by Arhip, L., García-Peris, P., Romero, R.M., Frías, L., Bretón, I., Camblor, M., Motilla, M., Velasco, C., Morales, A., Carrascal, M.L., Herranz, A., Sanjurjo, M., Cuerda, C.

    Published in Clinical nutrition (Edinburgh, Scotland) (01-08-2019)
    “…Home parenteral nutrition (HPN) is a lifesaving treatment for people with chronic intestinal failure and its cost has been reported to be very high. The…”
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    Orofacial clefts in the National Birth Defects Prevention Study, 1997-2004 by Genisca, Alicia E., Frías, Jaime L., Broussard, Cheryl S., Honein, Margaret A., Lammer, Edward J., Moore, Cynthia A., Shaw, Gary M., Murray, Jeffrey C., Yang, Wei, Rasmussen, Sonja A.

    “…Orofacial clefts are among the most common types of birth defects, but their clinical presentation has not been well described in a geographically diverse US…”
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    Pre-gestational maternal body mass index predicts an increased risk of congenital malformations in infants of mothers with gestational diabetes by Martínez-Frías, M. L., Frías, J. P., Bermejo, E., Rodríguez-Pinilla, E., Prieto, L., Frías, J. L.

    Published in Diabetic medicine (01-06-2005)
    “…Aims  The aim of the present study was to identify characteristics in women diagnosed with gestational diabetes mellitus (GDM) that could be predictive of…”
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    Risk factors for non-syndromic holoprosencephaly in the National Birth Defects Prevention Study by Miller, Eric A., Rasmussen, Sonja A., Siega-Riz, Anna Maria, Frías, Jaime L., Honein, Margaret A.

    “…Holoprosencephaly (HPE) is a complex structural brain anomaly that results from incomplete cleavage of the forebrain. The prevalence of HPE at birth is low,…”
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    Long-Term Survival of Infants with Atrioventricular Septal Defects by Miller, Assia, MD, MPH, Siffel, Csaba, MD, PhD, Lu, Chengxing, PhD, Riehle-Colarusso, Tiffany, MD, Frías, Jaime L., MD, Correa, Adolfo, MD, PhD

    Published in The Journal of pediatrics (01-06-2010)
    “…Objective To examine the variation in survival in infants with atrioventricular septal defects (AVSD) with demographic factors and clinical characteristics,…”
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    Infrequently studied congenital anomalies as clues to the diagnosis of maternal diabetes mellitus by FRIAS, Jaime L, FRIAS, Juan P, FRIAS, Patricio A, MARTINEZ-FRIAS, Maria Luisa

    “…The aim of this study was to identify congenital anomalies (CA) among infants of women with diabetes mellitus (DM) that, even though infrequent or infrequently…”
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    Omissions in the synthetic theory of evolution by Frías L, Daniel

    Published in Biological research (2010)
    “…The Synthetic Theory of Evolution is the most unifying theory of life science. This theory has dominated scientific thought in explaining the mechanisms…”
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    Clinical and pathological effects of different acrylic intracorneal ring segments in corneal additive surgery by Pérez-Merino, P., Parra, F., Ibares-Frías, L., Gallego, P., Vázquez-Lasa, B., Benito, L., San Román, J., Martínez-García, C., Merayo-Lloves, J.

    Published in Acta biomaterialia (01-07-2010)
    “…The objective of this work was to evaluate the potential use of less stiff materials based on acrylic copolymers of methyl methacrylate/2-ethylhexyl acrylate…”
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    Two new patients bearing mutations in the fukutin gene confirm the relevance of this gene in Walker-Warburg syndrome by Cotarelo, RP, Valero, MC, Prados, B, Peña, A, Rodríguez, L, Fano, O, Marco, JJ, Martínez-Frías, ML, Cruces, J

    Published in Clinical genetics (01-02-2008)
    “…Walker–Warburg syndrome (WWS) is an autosomal recessive disorder characterized by congenital muscular dystrophy, brain malformations and structural…”
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    Two unrelated patients with autosomal dominant omodysplasia and FRIZZLED2 mutations by Warren, Hannah E., Louie, Raymond J., Friez, Michael J., Frías, Jaime L., Leroy, Jules G., Spranger, Jürgen W., Skinner, Steven A., Champaigne, Neena L.

    Published in Clinical case reports (01-11-2018)
    “…Key Clinical Message Presented are two patients with autosomal dominant omodysplasia and mutations in the FZD2 gene. The mutations identified have been…”
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