檢索結果 - Carmelo Salpietro

  • Showing 1 - 11 results of 11
Refine Results
  1. 1
    A homozygousGJA1 gene mutation causes a Hallermann-Streiff/ODDD spectrum phenotype

    A homozygousGJA1 gene mutation causes a Hallermann-Streiff/ODDD spectrum phenotype 由 Antonio Pizzuti, Elisabetta Flex, Rita Mingarelli, Carmelo Salpietro, Leopoldo Zelante, Bruno Dallapiccola

    出版 2004
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  2. 2
    Increase in the Level of Proinflammatory Cytokine HMGB1 in Nasal Fluids of Patients With Rhinitis and its Sequestration by Glycyrrhizin Induces Eosinophil Cell Death

    Increase in the Level of Proinflammatory Cytokine HMGB1 in Nasal Fluids of Patients With Rhinitis and its Sequestration by Glycyrrhizin Induces Eosinophil Cell Death 由 Leonardo Cavone, Caterina Cuppari, Sara Manti, Luisa Grasso, Teresa Arrigo, Luca Calamai, Carmelo Salpietro, Alberto Chiarugi

    出版 2015
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  3. 3
    Recent Developments in United Airways Disease

    Recent Developments in United Airways Disease 由 Giorgio Ciprandi, Davide Caimmi, Michele Miraglia del Giudice, Mario La Rosa, Carmelo Salpietro, Gian Luigi Marseglia

    出版 2012
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  4. 4
    Protective Role of Melatonin in Neonatal Diseases

    Protective Role of Melatonin in Neonatal Diseases 由 Eloisa Gitto, Lucia Marseglia, Sara Manti, Gabriella D’Angelo, Ignazio Barberi, Carmelo Salpietro, Russel J. Reíter

    出版 2013
    獲取全文 獲取全文
    Revisão
    加到收藏夾
    Saved in:
  5. 5
    High-mobility group protein B1: a new biomarker of metabolic syndrome in obese children

    High-mobility group protein B1: a new biomarker of metabolic syndrome in obese children 由 Teresa Arrigo, Valeria Chirico, Vincenzo Salpietro, Caterina Munafò, Valeria Ferraù, Eloisa Gitto, Antonio Lacquaniti, Carmelo Salpietro

    出版 2013
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  6. 6
    Melatonin and Atopy: Role in Atopic Dermatitis and Asthma

    Melatonin and Atopy: Role in Atopic Dermatitis and Asthma 由 Lucia Marseglia, Gabriella D’Angelo, Sara Manti, Carmelo Salpietro, Teresa Arrigo, Ignazio Barberi, Russel J. Reíter, Eloisa Gitto

    出版 2014
    獲取全文 獲取全文
    Revisão
    加到收藏夾
    Saved in:
  7. 7
    Correlation of s-IgA and IL-6 Salivary with Caries Disease and Oral Hygiene Parameters in Children

    Correlation of s-IgA and IL-6 Salivary with Caries Disease and Oral Hygiene Parameters in Children 由 Lo Giudice, Giuseppe, Nicita, Fabiana, Militi, Angela, Bertino, Rossella, Matarese, Marco, Currò, Monica, Damiano, Carmelo Salpietro, Mannucci, Carmen, Calapai, Gioacchino

    出版 2019
    獲取全文 獲取全文 獲取全文
    Text
    加到收藏夾
    Saved in:
  8. 8
    Distinguishing the four genetic causes of jouberts syndrome–related disorders

    Distinguishing the four genetic causes of jouberts syndrome–related disorders 由 Enza Maria Valente, Sarah Marsh, Marco Castori, Tracy Dixon‐Salazar, Enrico Bertini, Lihadh Al‐Gazali, J Messer, Clara Barbot, C. Geoffrey Woods, Eugen Boltshauser, Asma Al-Tawari, Carmelo Salpietro, Hülya Kayserili, László Sztriha, Moez Gribaa, M. Kœnig, Bruno Dallapiccola, Joseph G. Gleeson

    出版 2005
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  9. 9
    <i>MKS3/TMEM67</i>mutations are a major cause of COACH Syndrome, a Joubert Syndrome related disorder with liver involvement

    <i>MKS3/TMEM67</i>mutations are a major cause of COACH Syndrome, a Joubert Syndrome related disorder with liver involvement 由 Francesco Brancati, Miriam Iannicelli, Lorena Travaglini, Annalisa Mazzotta, Enrico Bertini, Eugen Boltshauser, Stefano D’Arrigo, Francesco Emma, Elisa Fazzi, Romina Gallizzi, Mattia Gentile, Damir Lončarević, Vlatka Mejaški‐Bošnjak, Chiara Pantaleoni, Luciana Rigoli, Carmelo Salpietro, Sabrina Signorini, Gilda Stringini, Alain Verloès, Dominika Zabloka, Bruno Dallapiccola, Joseph G. Gleeson, Enza Maria Valente

    出版 2008
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  10. 10
    CEP290 Mutations Are Frequently Identified in the Oculo-Renal Form of Joubert Syndrome–Related Disorders

    CEP290 Mutations Are Frequently Identified in the Oculo-Renal Form of Joubert Syndrome–Related Disorders 由 Francesco Brancati, Giuseppe Barrano, Jennifer L. Silhavy, Sarah Marsh, Lorena Travaglini, Stephanie Bielas, Maria Amorini, Dominika Zablocka, Hülya Kayserili, Lihadh Al‐Gazali, Enrico Bertini, Eugen Boltshauser, Marc D’Hooghe, Elisa Fazzi, Elif Yosunkaya Fenerci, Raoul C. M. Hennekam, Andrea Kiss, Melissa Lees, Elysa Marco, Shubha R. Phadke, Luciana Rigoli, Stéphane Romano, Carmelo Salpietro, Elliott H. Sherr, Sabrina Signorini, Petter Strømme, Bernard Stuart, László Sztriha, David Viskochil, Adnan Yüksel, Bruno Dallapiccola, Enza Maria Valente, Joseph G. Gleeson

    出版 2007
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  11. 11
    Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes

    Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes 由 Enza Maria Valente, Clare V. Logan, Soumaya Mougou-Zerelli, Jeong Ho Lee, Jennifer L. Silhavy, Francesco Brancati, Miriam Iannicelli, Lorena Travaglini, Sveva Romani, Barbara Illi, Matthew Adams, Katarzyna Szymańska, Annalisa Mazzotta, Ji Eun Lee, Jerlyn C. Tolentino, Dominika Swistun, Carmelo Salpietro, Carmelo Fede, Stacey Gabriel, Carsten Russ, Kristian Cibulskis, Carrie Sougnez, Friedhelm Hildebrandt, Edgar A. Otto, Susanne Held, Bill H. Diplas, Erica E. Davis, Mario Mikula, Charles M. Strom, Bruria Ben‐Zeev, Dorit Lev, T. Sagie, Marina Michelson, Yuval Yaron, Amanda Krause, Eugen Boltshauser, Nadia Elkhartoufi, J. Roume, Stavit A. Shalev, Arnold Münnich, Sophie Saunier, Chris F. Inglehearn, Ali Saâd, Adila Al‐Kindy, Sophie Thomas, Michel Vekemans, Bruno Dallapiccola, Nicholas Katsanis, Colin A. Johnson, Tania Attié‐Bitach, Joseph G. Gleeson

    出版 2010
    獲取全文
    Artigo
    加到收藏夾
    Saved in:

檢索工具: