Search Results - Longoni, Mauro

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  1. 1
    Use of oxidized regenerated cellulose to achieve hemostasis during laparoscopic cholecystectomy: a retrospective cohort analysis

    Use of oxidized regenerated cellulose to achieve hemostasis during laparoscopic cholecystectomy: a retrospective cohort analysis by Masci, Emilia, Faillace, Giuseppe, Longoni, Mauro

    Published 2018
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  2. 2
    A Review of Donnai-Barrow and Facio-oculo-acoustico-renal (DB/FOAR) Syndrome: Clinical Features and Differential Diagnosis

    A Review of Donnai-Barrow and Facio-oculo-acoustico-renal (DB/FOAR) Syndrome: Clinical Features and Differential Diagnosis by Pober, Barbara R., Longoni, Mauro, Noonan, Kristin M.

    Published 2009
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  3. 3
    Polygenic Causes of Congenital Diaphragmatic Hernia Produce Common Lung Pathologies

    Polygenic Causes of Congenital Diaphragmatic Hernia Produce Common Lung Pathologies by Donahoe, Patricia K., Longoni, Mauro, High, Frances A.

    Published 2016
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  4. 4
    Evaluation of 1p36 markers and clinical outcome in a skull base chordoma study

    Evaluation of 1p36 markers and clinical outcome in a skull base chordoma study by Longoni, Mauro, Orzan, Francesca, Stroppi, Michela, Boari, Nicola, Mortini, Pietro, Riva, Paola

    Published 2008
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  5. 5
    Use of Human Fibrin Glue (Tissucol) Versus Staples for Mesh Fixation in Laparoscopic Transabdominal Preperitoneal Hernioplasty: A Prospective, Randomized Study

    Use of Human Fibrin Glue (Tissucol) Versus Staples for Mesh Fixation in Laparoscopic Transabdominal Preperitoneal Hernioplasty: A Prospective, Randomized Study by Lovisetto, Federico, Zonta, Sandro, Rota, Emanuela, Mazzilli, Massimiliano, Bardone, Marco, Bottero, Luca, Faillace, Giuseppe, Longoni, Mauro

    Published 2007
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  6. 6
    De Novo Frameshift Mutation in COUP-TFII (NR2F2) in Human Congenital Diaphragmatic Hernia

    De Novo Frameshift Mutation in COUP-TFII (NR2F2) in Human Congenital Diaphragmatic Hernia by High, Frances A., Bhayani, Pooja, Wilson, Jay M., Bult, Carol J., Donahoe, Patricia K., Longoni, Mauro

    Published 2016
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  7. 7
    MiR-449a Affects Epithelial Proliferation during the Pseudoglandular and Canalicular Phases of Avian and Mammal Lung Development

    MiR-449a Affects Epithelial Proliferation during the Pseudoglandular and Canalicular Phases of Avian and Mammal Lung Development by Sanford, Ethan L., Choy, Kwong W., Donahoe, Patricia K., Tracy, Adam A., Hila, Regis, Loscertales, Maria, Longoni, Mauro

    Published 2016
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  8. 8
    Type IV collagen drives alveolar epithelial–endothelial association and the morphogenetic movements of septation

    Type IV collagen drives alveolar epithelial–endothelial association and the morphogenetic movements of septation by Loscertales, Maria, Nicolaou, Fotini, Jeanne, Marion, Longoni, Mauro, Gould, Douglas B., Sun, Yunwei, Maalouf, Faouzi I., Nagy, Nandor, Donahoe, Patricia K.

    Published 2016
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  9. 9
    Erratum to: Type IV collagen drives alveolar epithelial–endothelial association and the morphogenetic movements of septation

    Erratum to: Type IV collagen drives alveolar epithelial–endothelial association and the morphogenetic movements of septation by Loscertales, Maria, Nicolaou, Fotini, Jeanne, Marion, Longoni, Mauro, Gould, Douglas B., Sun, Yunwei, Maalouf, Faouzi I., Nagy, Nandor, Donahoe, Patricia K.

    Published 2016
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  10. 10
    Hypercalciuria and nephrolithiasis: expanding the renal phenotype of Donnai-Barrow syndrome

    Hypercalciuria and nephrolithiasis: expanding the renal phenotype of Donnai-Barrow syndrome by Anglani, Franca, Terrin, Liliana, Brugnara, Milena, Battista, Michele, Cantaluppi, Vincenzo, Ceol, Monica, Bertoldi, Loris, Valle, Giorgio, Joy, Maliackal P., Pober, Barbara R, Longoni, Mauro

    Published 2018
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  11. 11
    Dual diagnoses in 152 patients with Turner syndrome: Knowledge of the second condition may lead to modification of treatment and/or surveillance

    Dual diagnoses in 152 patients with Turner syndrome: Knowledge of the second condition may lead to modification of treatment and/or surveillance by Jones, Kelly L., McNamara, Erin A., Longoni, Mauro, Miller, Danny E., Rohanizadegan, Mersedeh, Newman, Laura A., Hayes, Frances, Levitsky, Lynne L., Herrington, Betty L., Lin, Angela E.

    Published 2018
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  12. 12
    Congenital diaphragmatic hernia candidate genes derived from embryonic transcriptomes

    Congenital diaphragmatic hernia candidate genes derived from embryonic transcriptomes by Russell, Meaghan K., Longoni, Mauro, Wells, Julie, Maalouf, Faouzi I., Tracy, Adam A., Loscertales, Maria, Ackerman, Kate G., Pober, Barbara R., Lage, Kasper, Bult, Carol J., Donahoe, Patricia K.

    Published 2012
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  13. 13
    Characterization of the Chromosome 1q41q42.12 region, and the Candidate Gene DISP1, in Patients with CDH

    Characterization of the Chromosome 1q41q42.12 region, and the Candidate Gene DISP1, in Patients with CDH by Kantarci, Sibel, Ackerman, Kate G, Russell, Meaghan N, Longoni, Mauro, Sougnez, Carrie, Noonan, Kristin M, Hatchwell, Eli, Zhang, Xiaoyun, Vanmarcke, Rafael Pieretti, Anyane-Yeboa, Kwame, Dickman, Paul, Wilson, Jay, Donahoe, Patricia K, Pober, Barbara R

    Published 2010
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  14. 14
    Genome-wide enrichment of damaging de novo variants in patients with isolated and complex Congenital Diaphragmatic Hernia

    Genome-wide enrichment of damaging de novo variants in patients with isolated and complex Congenital Diaphragmatic Hernia by Longoni, Mauro, High, Frances A., Qi, Hongjian, Joy, Maliackal P., Hila, Regis, Coletti, Caroline M., Wynn, Julia, Loscertales, Maria, Shan, Linshan, Bult, Carol J., Wilson, Jay M., Shen, Yufeng, Chung, Wendy K., Donahoe, Patricia K.

    Published 2017
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  15. 15
    Systematic analysis of copy number variation associated with congenital diaphragmatic hernia

    Systematic analysis of copy number variation associated with congenital diaphragmatic hernia by Zhu, Qihui, High, Frances A., Zhang, Chengsheng, Cerveira, Eliza, Russell, Meaghan K., Longoni, Mauro, Joy, Maliackal P., Ryan, Mallory, Mil-homens, Adam, Bellfy, Lauren, Coletti, Caroline M., Bhayani, Pooja, Hila, Regis, Wilson, Jay M., Donahoe, Patricia K., Lee, Charles

    Published 2018
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  16. 16
    Molecular pathogenesis of congenital diaphragmatic hernia revealed by exome sequencing, developmental data, and bioinformatics

    Molecular pathogenesis of congenital diaphragmatic hernia revealed by exome sequencing, developmental data, and bioinformatics by Longoni, Mauro, High, Frances A., Russell, Meaghan K., Kashani, Alireza, Tracy, Adam A., Coletti, Caroline M., Hila, Regis, Shamia, Ahmed, Wells, Julie, Ackerman, Kate G., Wilson, Jay M., Bult, Carol J., Lee, Charles, Lage, Kasper, Pober, Barbara R., Donahoe, Patricia K.

    Published 2014
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  17. 17
    Congenital Diaphragmatic Hernia Interval on Chromosome 8p23.1 Characterized by Genetics and Protein Interaction Networks

    Congenital Diaphragmatic Hernia Interval on Chromosome 8p23.1 Characterized by Genetics and Protein Interaction Networks by Longoni, Mauro, Lage, Kasper, Russell, Meaghan K., Loscertales, Maria, Abdul-Rahman, Omar A., Baynam, Gareth, Bleyl, Steven B., Brady, Paul D., Breckpot, Jeroen, Chen, Chih P., Devriendt, Koenraad, Gillessen-Kaesbach, Gabriele, Grix, Arthur W., Rope, Alan F., Shimokawa, Osamu, Strauss, Bernarda, Wieczorek, Dagmar, Zackai, Elaine H., Coletti, Caroline M., Maalouf, Faouzi I., Noonan, Kristin M., Park, Ji H., Tracy, Adam A., Lee, Charles, Donahoe, Patricia K., Pober, Barbara R.

    Published 2012
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  18. 18
    De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders

    De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders by Qi, Hongjian, Yu, Lan, Zhou, Xueya, Wynn, Julia, Zhao, Haoquan, Guo, Yicheng, Zhu, Na, Kitaygorodsky, Alexander, Hernan, Rebecca, Aspelund, Gudrun, Lim, Foong-Yen, Crombleholme, Timothy, Cusick, Robert, Azarow, Kenneth, Danko, Melissa E., Chung, Dai, Warner, Brad W., Mychaliska, George B., Potoka, Douglas, Wagner, Amy J., ElFiky, Mahmoud, Wilson, Jay M., Nickerson, Debbie, Bamshad, Michael, High, Frances A., Longoni, Mauro, Donahoe, Patricia K., Chung, Wendy K., Shen, Yufeng

    Published 2018
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  19. 19
    Truncating Variants in NAA15 Are Associated with Variable Levels of Intellectual Disability, Autism Spectrum Disorder, and Congenital Anomalies

    Truncating Variants in NAA15 Are Associated with Variable Levels of Intellectual Disability, Autism Spectrum Disorder, and Congenital Anomalies by Cheng, Hanyin, Dharmadhikari, Avinash V., Varland, Sylvia, Ma, Ning, Domingo, Deepti, Kleyner, Robert, Rope, Alan F., Yoon, Margaret, Stray-Pedersen, Asbjørg, Posey, Jennifer E., Crews, Sarah R., Eldomery, Mohammad K., Akdemir, Zeynep Coban, Lewis, Andrea M., Sutton, Vernon R., Rosenfeld, Jill A., Conboy, Erin, Agre, Katherine, Xia, Fan, Walkiewicz, Magdalena, Longoni, Mauro, High, Frances A., van Slegtenhorst, Marjon A., Mancini, Grazia M.S., Finnila, Candice R., van Haeringen, Arie, den Hollander, Nicolette, Ruivenkamp, Claudia, Naidu, Sakkubai, Mahida, Sonal, Palmer, Elizabeth E., Murray, Lucinda, Lim, Derek, Jayakar, Parul, Parker, Michael J., Giusto, Stefania, Stracuzzi, Emanuela, Romano, Corrado, Beighley, Jennifer S., Bernier, Raphael A., Küry, Sébastien, Nizon, Mathilde, Corbett, Mark A., Shaw, Marie, Gardner, Alison, Barnett, Christopher, Armstrong, Ruth, Kassahn, Karin S., Van Dijck, Anke, Vandeweyer, Geert, Kleefstra, Tjitske, Schieving, Jolanda, Jongmans, Marjolijn J., de Vries, Bert B.A., Pfundt, Rolph, Kerr, Bronwyn, Rojas, Samantha K., Boycott, Kym M., Person, Richard, Willaert, Rebecca, Eichler, Evan E., Kooy, R. Frank, Yang, Yaping, Wu, Joseph C., Lupski, James R., Arnesen, Thomas, Cooper, Gregory M., Chung, Wendy K., Gecz, Jozef, Stessman, Holly A.F., Meng, Linyan, Lyon, Gholson J.

    Published 2018
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