Search Results - Triot, Alexa

  • Showing 1 - 4 results of 4
Refine Results
  1. 1
    Leptin hormone level in serum of opticospinal, neuromyelitisoptica and multiple sclerosis patients

    Leptin hormone level in serum of opticospinal, neuromyelitisoptica and multiple sclerosis patients by Bahrami, Ehsan, Zarkesh-Esfahani, Sayyed Hamid, Kardi, Mohammad T., Mostajeran, Maryam, Triot, Alexa, Bouzari, Majid, Maghzi, Amir H., Etemadifar, Masoud

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  2. 2
    Inherited biallelic CSF3R mutations in severe congenital neutropenia

    Inherited biallelic CSF3R mutations in severe congenital neutropenia by Triot, Alexa, Järvinen, Päivi M, Arostegui, Juan I, Murugan, Dhaarini, Kohistani, Naschla, Dapena Díaz, José Luis, Racek, Tomas, Puchałka, Jacek, Gertz, E Michael, Schäffer, Alejandro A, Kotlarz, Daniel, Pfeifer, Dietmar, Díaz de Heredia Rubio, Cristina, Ozdemir, Mehmet Akif, Patiroglu, Turkan, Karakukcu, Musa, Sánchez de Toledo Codina, José, Yagüe, Jordi, Touw, Ivo P, Unal, Ekrem, Klein, Christoph

    Published in Blood
    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  3. 3
    Inherited biallelic CSF3Rmutations in severe congenital neutropenia

    Inherited biallelic CSF3Rmutations in severe congenital neutropenia by Triot, Alexa, Järvinen, Päivi M., Arostegui, Juan I., Murugan, Dhaarini, Kohistani, Naschla, Dapena Díaz, José Luis, Racek, Tomas, Puchałka, Jacek, Gertz, E. Michael, Schäffer, Alejandro A., Kotlarz, Daniel, Pfeifer, Dietmar, Díaz de Heredia Rubio, Cristina, Ozdemir, Mehmet Akif, Patiroglu, Turkan, Karakukcu, Musa, Sánchez de Toledo Codina, José, Yagüe, Jordi, Touw, Ivo P., Unal, Ekrem, Klein, Christoph

    Published in Blood
    Get full text
    Article
    Save to List
    Saved in:
  4. 4
    Inherited Biallelic Loss-Of-Function Mutations In CSF3R Define a Novel Type Of Severe Congenital Neutropenia With Full Myeloid Cell Maturation and Refractoriness To RhG-CSF

    Inherited Biallelic Loss-Of-Function Mutations In CSF3R Define a Novel Type Of Severe Congenital Neutropenia With Full Myeloid Cell Maturation and Refractoriness To RhG-CSF by Triot, Alexa, Järvinen, Päivi M, Arostegui, Juan I., Racek, Tomas, Puchalka, Jacek, Díaz, Jose Luis Dapena, Kohistani, Naschla, Gertz, E. Michael, Schäffer, Alejandro A., de Heredia Rubio, Cristina Díaz, Ozdemir, Mehmet A., Patiroglu, Turkan, Karakukcu, Musa, de Toledo Codina, José Sanchez, Yagüe, Jordi, Unal, Ekrem, Klein, Christoph

    Published in Blood
    Get full text
    Article
    Save to List
    Saved in:

Search Tools: