Works by Sarkhail, Peymaneh

Results: 3
    1

    Molecular characterization of a large cohort of mucopolysaccharidosis patients: Iran Mucopolysaccharidosis RE‐diagnosis study (IMPRESsion).

    Published in:
    Human Mutation, 2022, v. 43, n. 4, p. e1, doi. 10.1002/humu.24328
    By:
    • Ghaffari, Saeed R.;
    • Rafati, Maryam;
    • Shadnoush, Mahdi;
    • Pourbabaee, Shokooh;
    • Aghighi, Mohammad;
    • Mirab Samiee, Siamak;
    • Kermanchi, Jamshid;
    • Alaei, Mohammad R.;
    • Salehpour, Shadab;
    • Amirkashani, Davoud;
    • Setoodeh, Aria;
    • Sarkhail, Peymaneh;
    • Badv, Reza Shervin;
    • Aminzadeh, Majid;
    • Shiva, Siamak;
    • Eshraghi, Peyman;
    • Moravej, Hossein;
    • Hashemipour, Mahin;
    • Rostampour, Noushin;
    • Hamidieh, َAmir Ali
    Publication type:
    Article
    2
    3

    Epidemiology of congenital disorders of glycosylation (CDG)—overview and perspectives.

    Published in:
    Journal of Rare Diseases, 2022, v. 1, n. 1, p. 1, doi. 10.1007/s44162-022-00003-6
    By:
    • Piedade, Ana;
    • Francisco, Rita;
    • Jaeken, Jaak;
    • Sarkhail, Peymaneh;
    • Brasil, Sandra;
    • Ferreira, Carlos R.;
    • Rijoff, Tatiana;
    • Pascoal, Carlota;
    • Gil, Alexandre;
    • Lourenço, Ana Beatriz;
    • Abreu, Marta;
    • Gomes, Mafalda;
    • Videira, Paula A.;
    • dos Reis Ferreira, Vanessa
    Publication type:
    Article