Works matching AU Palanduz, Sukru


Results: 52
    1

    WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects.

    Published in:
    Human Mutation, 2017, v. 38, n. 1, p. 7, doi. 10.1002/humu.23128
    By:
    • Yokote, Koutaro;
    • Chanprasert, Sirisak;
    • Lee, Lin;
    • Eirich, Katharina;
    • Takemoto, Minoru;
    • Watanabe, Aki;
    • Koizumi, Naoko;
    • Lessel, Davor;
    • Mori, Takayasu;
    • Hisama, Fuki M.;
    • Ladd, Paula D.;
    • Angle, Brad;
    • Baris, Hagit;
    • Cefle, Kivanc;
    • Palanduz, Sukru;
    • Ozturk, Sukru;
    • Chateau, Antoinette;
    • Deguchi, Kentaro;
    • Easwar, T.K.M;
    • Federico, Antonio
    Publication type:
    Article
    2

    Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis.

    Published in:
    Human Mutation, 2012, v. 33, n. 8, p. 1175, doi. 10.1002/humu.22111
    By:
    • Diggle, Christine P.;
    • Parry, David A.;
    • Logan, Clare V.;
    • Laissue, Paul;
    • Rivera, Carolina;
    • Restrepo, Carlos Martín;
    • Fonseca, Dora J.;
    • Morgan, Joanne E.;
    • Allanore, Yannick;
    • Fontenay, Michaela;
    • Wipff, Julien;
    • Varret, Mathilde;
    • Gibault, Laure;
    • Dalantaeva, Nadezhda;
    • Korbonits, Márta;
    • Zhou, Bowen;
    • Yuan, Gang;
    • Harifi, Ghita;
    • Cefle, Kivanc;
    • Palanduz, Sukru
    Publication type:
    Article
    3
    4
    5
    6

    Evaluation of TMED9, DNAJC1, LMAN2, COPE and KDELR1 Biomarkers in Patients with Monoclonal Gammopathy of Undetermined Significance and Multiple Myeloma.

    Published in:
    UHOD: International Journal of Hematology & Oncology / Uluslararasi Hematoloji Onkoloji Dergisi, 2023, v. 33, n. 2, p. 92, doi. 10.4999/uhod.236990
    By:
    • SARIMAN, Melda;
    • SALMAN YAYLAZ, Burcu;
    • YABACI TAK, Aysegul;
    • AYER, Mesut;
    • SIRMA EKMEKCI, Sema;
    • SUER, Ilknur;
    • CEFLE, Kivanc;
    • PALANDUZ, Sukru;
    • OZTURK, Sukru;
    • NALCACI, Meliha;
    • ABACI, Neslihan
    Publication type:
    Article
    7

    Dysregulation of MS4A3 and PRDX5 Gene Expression in Multiple Myeloma Patients.

    Published in:
    UHOD: International Journal of Hematology & Oncology / Uluslararasi Hematoloji Onkoloji Dergisi, 2021, v. 31, n. 4, p. 205, doi. 10.4999/uhod.215420
    By:
    • SUER, Ilknur;
    • ADAY, Aynur;
    • SARIMAN, Melda;
    • AYER, Mesut;
    • HINDILERDEN, Ipek Yonal;
    • EKMEKCI, Sema Sirma;
    • ABACI, Neslihan;
    • PALANDUZ, Sukru;
    • CEFLE, Kıvanc;
    • OZTURK, Sukru
    Publication type:
    Article
    8
    9
    10
    11

    Clinical Images in Oral Medicine and Maxillofacial Radiology.

    Published in:
    Quintessence International, 2001, v. 32, n. 9, p. 748
    By:
    • Yalçin, Serhat;
    • Aybar, Buket;
    • Palandüz, Sükrü;
    • Haznedaroglu, Faruk;
    • Yazar, Taha Tekin;
    • Emes, Yusuf;
    • Terezhalmy, Geza T.;
    • Riley, Catherine K.;
    • Moore, William S.
    Publication type:
    Article
    12
    13

    ERAP1 Gen İfadesinin Plazma Hücre Diskrazilerinde İncelenmesi.

    Published in:
    Medical Journal of Istanbul Kanuni Sultan Süleyman / İstanbul Kanuni Sultan Süleyman Tıp Dergisi, 2022, v. 14, n. 2, p. 120, doi. 10.14744/iksstd.2021.29494
    By:
    • Sarıman, Melda;
    • Karaçam, Büşra;
    • Ayer, Mesut;
    • Ekmekci, Sema Sırma;
    • Suer, İlknur;
    • Çefle, Kıvanç;
    • Palanduz, Şükrü;
    • Öztürk, Şükrü;
    • Nalçacı, Meliha;
    • Abacı, Neslihan
    Publication type:
    Article
    14
    15

    Atrial and Ventricular Arryhthmogenic Potential in Turner Syndrome.

    Published in:
    Pacing & Clinical Electrophysiology, 2008, v. 31, n. 9, p. 1140, doi. 10.1111/j.1540-8159.2008.01154.x
    By:
    • SOZEN, AHMET B.;
    • CEFLE, KIVANÇ;
    • KUDAT, HASAN;
    • OZTURK, SUKRU;
    • OFLAZ, HUSEYIN;
    • PAMUKCU, BURAK;
    • AKKAYA, VAKUR;
    • ISGUVEN, PINAR;
    • PALANDUZ, SUKRU;
    • OZCAN, MUSTAFA;
    • GOREN, TANER;
    • GUVEN, OZEN
    Publication type:
    Article
    16
    17
    18
    19
    20
    21
    22
    23
    24
    25
    26
    27
    28
    29

    A novel locus for syndromic chronic idiopathic intestinal pseudo-obstruction maps to chromosome 8q23–q24.

    Published in:
    European Journal of Human Genetics, 2007, v. 15, n. 8, p. 889, doi. 10.1038/sj.ejhg.5201844
    By:
    • Deglincerti, Alessia;
    • De Giorgio, Roberto;
    • Cefle, Kivanc;
    • Devoto, Marcella;
    • Pippucci, Tommaso;
    • Castegnaro, Giovanni;
    • Panza, Emanuele;
    • Barbara, Giovanni;
    • Cogliandro, Rosanna F;
    • Mungan, Zeynel;
    • Palanduz, Sukru;
    • Corinaldesi, Roberto;
    • Romeo, Giovanni;
    • Seri, Marco;
    • Stanghellini, Vincenzo
    Publication type:
    Article
    30

    Mutations in NSD1 are responsible for Sotos syndrome, but are not a frequent finding in other overgrowth phenotypes.

    Published in:
    European Journal of Human Genetics, 2003, v. 11, n. 11, p. 858, doi. 10.1038/sj.ejhg.5201050
    By:
    • Türkmen, Seval;
    • Gillessen-Kaesbach, Gabriele;
    • Meinecke, Peter;
    • Albrecht, Beate;
    • Neumann, Luitgard M.;
    • Hesse, Volker;
    • Palanduz, Sükrü;
    • Balg, Stefanie;
    • Majewski, Frank;
    • Fuchs, Sigrun;
    • Zschieschang, Petra;
    • Greiwe, Monika;
    • Mennicke, Kirsten;
    • Kreuz, Friedmar R.;
    • Dehmel, Harald J.;
    • Rodeck, Burkhard;
    • Kunze, Jürgen;
    • Tinschert, Sigrid;
    • Mundlos, Stefan;
    • Horn, Denise
    Publication type:
    Article
    31
    32
    33
    34
    35
    36
    38
    39
    40
    41
    42
    43
    44
    45
    46
    47
    48

    Skeletal and molecular findings in 51 Cleidocranial dysplasia patients from Turkey.

    Published in:
    American Journal of Medical Genetics. Part A, 2021, v. 185, n. 8, p. 2488, doi. 10.1002/ajmg.a.62261
    By:
    • Berkay, Ezgi Gizem;
    • Elkanova, Leyla;
    • Kalaycı, Tuğba;
    • Uludağ Alkaya, Dilek;
    • Altunoğlu, Umut;
    • Cefle, Kıvanç;
    • Mıhçı, Ercan;
    • Nur, Banu;
    • Taşdelen, Elifcan;
    • Bayramoğlu, Zuhal;
    • Karaman, Volkan;
    • Toksoy, Güven;
    • Güneş, Nilay;
    • Öztürk, Şükrü;
    • Palandüz, Şükrü;
    • Kayserili, Hülya;
    • Tüysüz, Beyhan;
    • Uyguner, Zehra Oya
    Publication type:
    Article
    49
    50