Works matching Kearns-Sayre syndrome


Results: 264
    1
    2
    3
    4
    5

    “Bartter-like” phenotype in Kearns–Sayre syndrome.

    Published in:
    Pediatric Nephrology, 2006, v. 21, n. 3, p. 355, doi. 10.1007/s00467-005-2092-5
    By:
    • Emma, Francesco;
    • Pizzini, Carla;
    • Tessa, Alessandra;
    • di Giandomenico, Silvia;
    • Onetti-Muda, Andrea;
    • Santorelli, Filippo M.;
    • Bertini, Enrico;
    • Rizzoni, Gianfranco
    Publication type:
    Article
    6
    7

    Sinus Dysrhythmia in Kearns-Sayre Syndrome.

    Published in:
    Pacing & Clinical Electrophysiology, 1994, v. 17, n. 5, p. 991, doi. 10.1111/j.1540-8159.1994.tb01445.x
    By:
    • Ulicny Jr., Karl S.;
    • Detterbeck, Frank C.;
    • Hall, Colin D.
    Publication type:
    Article
    8
    9
    10
    11
    12
    13
    14
    15
    16
    17
    18
    19
    20
    21
    22
    23
    24
    25

    Spinal cord involvement in Kearns-Sayre syndrome: a neuroimaging study.

    Published in:
    Neuroradiology, 2020, v. 62, n. 10, p. 1315, doi. 10.1007/s00234-020-02501-0
    By:
    • Luca, Pasquini;
    • Alessia, Guarnera;
    • Camilla, Rossi-Espagnet Maria;
    • Antonio, Napolitano;
    • Diego, Martinelli;
    • Federica, Deodato;
    • Daria, Diodato;
    • Rosalba, Carrozzo;
    • Carlo, Dionisi-Vici;
    • Daniela, Longo
    Publication type:
    Article
    26
    27
    28
    29
    30
    31
    32
    33
    34
    35
    36
    37
    38
    39

    Kearns-Sayre Syndrome: A Rare Mitochondrial Disorder.

    Published in:
    Journal of Medicine, 2018, v. 19, n. 1, p. 66
    By:
    • TARIKUL ISLAM, QUAZI;
    • HOSSAIN, HOMAYRA TAHSEEN;
    • KHANDAKER, MD. ABUL KASHEM;
    • AHASAN, HAM NAZMUL;
    • MAJUMDER, MAKSUDUL;
    • REZA, ISHRAT BINTE;
    • JABEEN, TAJNUVA;
    • ALAM, KHADDOKER MORSHEDUL
    Publication type:
    Article
    40
    41
    42
    43
    44
    45
    46

    Follow-up of folinic acid supplementation for patients with cerebral folate deficiency and Kearns-Sayre syndrome.

    Published in:
    Orphanet Journal of Rare Diseases, 2014, v. 9, n. 1, p. 551, doi. 10.1186/s13023-014-0217-2
    By:
    • Quijada-Fraile, Pilar;
    • O?Callaghan, MMar;
    • Mart?n-Hern?ndez, Elena;
    • Montero, Raquel;
    • Garcia-Cazorla, ?ngels;
    • Mart?nez de Arag?n, Ana;
    • Muchart, Jordi;
    • M?laga, Ignacio;
    • Pardo, Rafael;
    • Garc?a-Gonzalez, Pedro;
    • Jou, Cristina;
    • Montoya, Julio;
    • Emperador, Sonia;
    • Ruiz-Pesini, Eduardo;
    • Arenas, Joaqu?n;
    • Martin, Miguel Angel;
    • Ormazabal, Aida;
    • Pineda, Merc?;
    • Garc?a-Silva, Mar?a T.;
    • Artuch, Rafael
    Publication type:
    Article
    47
    48
    49
    50