Search Results - "Indaco, Lara"

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  1. 1
    No association between apolipoprotein E polymorphisms and recurrent pregnancy loss

    No association between apolipoprotein E polymorphisms and recurrent pregnancy loss by Bianca, Sebastiano, M.D., Ph.D, Barrano, Barbara, M.D., Ph.D, Cutuli, Nunzio, M.D, Indaco, Lara, M.D, Cataliotti, Antonella, M.D, Milana, Gabriella, M.D, Barone, Chiara, M.D, Ettore, Giuseppe, M.D

    Published in Fertility and sterility (2010)
    “…Our study does not support the reported association between APOE and recurrent pregnancy loss (RPL) than the clinical management of these patients should not…”
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  2. 2
    Kabuki syndrome and sex chromosomal anomalies: is it really an association?

    Kabuki syndrome and sex chromosomal anomalies: is it really an association? by Bianca, Sebastiano, M.D., Ph.D, Barrano, Barbara, M.D., Ph.D, Cataliotti, Antonella, M.D, Indaco, Lara, M.D, Ingegnosi, Carmela, M.D, Ettore, Giuseppe, M.D

    Published in Fertility and sterility (01-05-2009)
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  3. 3
    Reply of the Authors: Association of apolipoprotein E polymorphisms and recurrent pregnancy loss & Apolipoprotein E4 allele and recurrent pregnancy loss: Is it time to draw a conclusion?

    Reply of the Authors: Association of apolipoprotein E polymorphisms and recurrent pregnancy loss & Apolipoprotein E4 allele and recurrent pregnancy loss: Is it time to draw a conclusion? by Bianca, Sebastiano, M.D., Ph.D, Barrano, Barbara, M.D., Ph.D, Cutuli, Nunzio, M.D, Indaco, Lara, M.D, Cataliotti, Antonella, M.D, Milana, Gabriella, M.D, Barone, Chiara, M.D, Ettore, Giuseppe, M.D

    Published in Fertility and sterility (01-03-2010)
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  4. 4
    Prenatal diagnosis of a fetus with anencephaly and thumb agenesis

    Prenatal diagnosis of a fetus with anencephaly and thumb agenesis by Barone, Chiara, Bartoloni, Giovanni, Cataliotti, Antonella, Indaco, Lara, Pappalardo, Elisa, Barrano, Barbara, Ettore, Giuseppe, Bianca, Sebastiano

    Published in Congenital anomalies (01-03-2012)
    “…ABSTRACT Severe anomalies of the forebrain together with reduction limb anomalies are a rare congenital anomalies association. We report a prenatal diagnosis…”
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  5. 5
    Familial nuchal cystic hygroma without fetal effects: Genetic counselling and further evidence for an autosomal recessive subtype

    Familial nuchal cystic hygroma without fetal effects: Genetic counselling and further evidence for an autosomal recessive subtype by Bianca, Sebastiano, Bartoloni, Giovanni, Boemi, Gustavo, Barrano, Barbara, Barone, Chiara, Cataliotti, Antonella, Indaco, Lara, Ettore, Giuseppe

    Published in Congenital anomalies (01-06-2010)
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  6. 6
    Fetal Eagle-Barrett syndrome and pulmonary atresia with intact ventricular septum

    Fetal Eagle-Barrett syndrome and pulmonary atresia with intact ventricular septum by Bianca, Sebastiano, Bartoloni, Giovanni, Boemi, Gustavo, Barrano, Barbara, Cataliotti, Antonella, Barone, Chiara, Indaco, Lara, Campione, Claudio, Ettore, Giuseppe

    Published in Congenital anomalies (01-03-2010)
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  7. 7
    Fetal upper limb amelia with increased nuchal translucency

    Fetal upper limb amelia with increased nuchal translucency by Bianca, Sebastiano, Bartoloni, Giovanni, Libertini, Claudio, Boemi, Gustavo, Barrano, Barbara, Cataliotti, Antonella, Barone, Chiara, Indaco, Lara, Vallone, Antonino, Ettore, Giuseppe

    Published in Congenital anomalies (01-09-2009)
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  8. 8
    Congenital perineal hernia in a fetus with X monosomy

    Congenital perineal hernia in a fetus with X monosomy by Bianca, Sebastiano, Bartoloni, Giovanni, Barrano, Barbara, Boemi, Gustavo, Barone, Chiara, Cataliotti, Antonella, Indaco, Lara, Ettore, Giuseppe

    Published in Congenital anomalies (01-12-2009)
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  9. 9
    An additional clinical sign of 17q21.31 microdeletion syndrome: Preaxial polydactyly of hands with broad thumbs

    An additional clinical sign of 17q21.31 microdeletion syndrome: Preaxial polydactyly of hands with broad thumbs by Barone, Chiara, Novelli, Antonio, Capalbo, Anna, del Grano, Antonella Cataliotti, Giuffrida, Maria Grazia, Indaco, Lara, Bianca, Sebastiano

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  10. 10
    15q11.2 microdeletion and hypoplastic left heart syndrome

    15q11.2 microdeletion and hypoplastic left heart syndrome by Barone, Chiara, Novelli, Antonio, Bianca, Innocenzo, Cataliotti del Grano, Antonella, Campisi, Marcello, Ettore, Carla, Pappalardo, Elisa, Indaco, Lara, Ettore, Giuseppe, Bartoloni, Giovanni, Bianca, Sebastiano

    Published in European journal of medical genetics (01-11-2015)
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  11. 11
    Mosaic trisomy 20: Considerations for genetic counseling

    Mosaic trisomy 20: Considerations for genetic counseling by Bianca, Sebastiano, Boemi, Gustavo, Barrano, Barbara, Cataliotti, Antonella, Ingegnosi, Carmela, Indaco, Lara, Ettore, Giuseppe

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  12. 12
    Prenatal diagnosis of 45,X/46,XY mosaicism with cleft lip and epispadias

    Prenatal diagnosis of 45,X/46,XY mosaicism with cleft lip and epispadias by Barone, Chiara, Bartoloni, Giovanni, Cataliotti, Antonella, Indaco, Lara, Pappalardo, Elisa, Barrano, Barbara, Ettore, Giuseppe, Bianca, Sebastiano

    Published in Archives of gynecology and obstetrics (01-08-2011)
    “…Introduction 45,X/46,XY mosaicism is an uncommon chromosomal anomaly with a range of phenotypes from normal males to cases of multiple congenital anomalies…”
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  13. 13
    Craniorachischisis and heterotaxia with heart disease in twins: link or change nature?

    Craniorachischisis and heterotaxia with heart disease in twins: link or change nature? by Bianca, Sebastiano, Bartoloni, Giovanni, Barone, Chiara, Barrano, Barbara, Boemi, Gustavo, De Filippo, Vincenzo, Indaco, Lara, Cataliotti, Antonella, Ettore, Giuseppe

    Published in Congenital heart disease (01-09-2010)
    “…Craniorachischisis is a rare neural tube defect in which both acrania and a complete schisis of the vertebral column are present. Heterotaxy results from…”
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  14. 14
    Congenital cataract and heart septal defects: are contiguous or reciprocally influenced genes involved?

    Congenital cataract and heart septal defects: are contiguous or reciprocally influenced genes involved? by Bianca, Sebastiano, Barrano, Barbara, Barone, Chiara, Cataliotti, Antonella, Indaco, Lara, Boemi, Gustavo, Bartoloni, Giovanni, Ettore, Giuseppe

    Published in Congenital heart disease (01-05-2009)
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  15. 15
    Prenatal diagnosis of a fetus with anencephaly and thumb agenesis

    Prenatal diagnosis of a fetus with anencephaly and thumb agenesis by Barone, Chiara, Bartoloni, Giovanni, Cataliotti, Antonella, Indaco, Lara, Pappalardo, Elisa, Barrano, Barbara, Ettore, Giuseppe, Bianca, Sebastiano

    Published in Congenital Anomalies (01-03-2012)
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  16. 16
    Congenital perineal hernia in a fetus with X monosomy

    Congenital perineal hernia in a fetus with X monosomy by Bianca, Sebastiano, Bartoloni, Giovanni, Barrano, Barbara, Boemi, Gustavo, Barone, Chiara, Cataliotti, Antonella, Indaco, Lara, Ettore, Giuseppe

    Published in Congenital anomalies (01-12-2009)
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  17. 17
    Fetal upper limb amelia with increased nuchal translucency

    Fetal upper limb amelia with increased nuchal translucency by Bianca, Sebastiano, Bartoloni, Giovanni, Libertini, Claudio, Boemi, Gustavo, Barrano, Barbara, Cataliotti, Antonella, Barone, Chiara, Indaco, Lara, Vallone, Antonino, Ettore, Giuseppe

    Published in Congenital anomalies (01-09-2009)
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