Works matching Hemochromatosis

Results: 2995
    1
    2

    New Mutations in HFE2 and TFR2 Genes Causing Non HFE -Related Hereditary Hemochromatosis.

    Published in:
    2021
    By:
    • Hernández, Gonzalo;
    • Ferrer-Cortès, Xenia;
    • Venturi, Veronica;
    • Musri, Melina;
    • Pilquil, Martin Floor;
    • Torres, Pau Marc Muñoz;
    • Rodríguez, Ines Hernandez;
    • Mínguez, Maria Àngels Ruiz;
    • Kelleher, Nicholas J.;
    • Pelucchi, Sara;
    • Piperno, Alberto;
    • Alberca, Esther Plensa;
    • Ricós, Georgina Gener;
    • Giró, Eloi Cañamero;
    • Pérez-Montero, Santiago;
    • Tornador, Cristian;
    • Villà-Freixa, Jordi;
    • Sánchez, Mayka
    Publication type:
    Case Study
    3
    4
    5
    6
    7
    8
    9
    10

    Longer survival associated with HLA-A*03, B*14 among 212 hemochromatosis probands with HFE C282Y homozygosity and HLA-A and -B typing and haplotyping Longer survival associated with HLA-A*03, B*14 among 212 hemochromatosis probands with HFE C282Y homozygosity and HLA-A and -B typing and haplotyping Barton et al. Hemochromatosis survival and HLA-A*03, B*14

    Published in:
    European Journal of Haematology, 2010, v. 85, n. 5, p. 439, doi. 10.1111/j.1600-0609.2010.01511.x
    By:
    • Barton, James C.;
    • Barton, J. Clayborn;
    • Acton, Ronald T.
    Publication type:
    Article
    11
    12
    13
    14
    15
    16
    17

    Hemochromatosis and osteoporosis, in reference to 4 cases.

    Published in:
    Journal of Osteoporosis & Mineral Metabolism / Revista de Osteoporosis y Metabolismo Mineral (English edition), 2016, v. 8, n. 4, p. 134, doi. 10.4321/s1889-836x2016000400006
    By:
    • Jaramillo, D. Montaño;
    • Curiel, M. Díaz
    Publication type:
    Article
    18

    Measurement of serum hepcidin-25 levels as a potential test for diagnosing hemochromatosis and related disorders.

    Published in:
    Journal of Gastroenterology, 2010, v. 45, n. 11, p. 1163, doi. 10.1007/s00535-010-0259-8
    By:
    • Kaneko, Yoshibumi;
    • Miyajima, Hiroaki;
    • Piperno, Alberto;
    • Tomosugi, Naohisa;
    • Hayashi, Hisao;
    • Morotomi, Natsuko;
    • Tsuchida, Ken-ichi;
    • Ikeda, Takaaki;
    • Ishikawa, Akihisa;
    • Ota, Yusuke;
    • Wakusawa, Shinya;
    • Yoshioka, Kentaro;
    • Kono, Satoshi;
    • Pelucchi, Sara;
    • Hattori, Ai;
    • Tatsumi, Yasuaki;
    • Okada, Toshihide;
    • Yamagishi, Masakazu
    Publication type:
    Article
    19
    20
    21
    22
    23
    24
    25
    26
    27
    28

    Type 4B hereditary hemochromatosis due to heterozygous p.D157A mutation in SLC40A1 complicated with hypopituitarism.

    Published in:
    Medical Molecular Morphology, 2021, v. 54, n. 1, p. 60, doi. 10.1007/s00795-020-00259-1
    By:
    • Honma, Yuichi;
    • Karasuyama, Tsukasa;
    • Kumamoto, Keiichiro;
    • Shimajiri, Shohei;
    • Toki, Yasumichi;
    • Tatsumi, Yasuaki;
    • Sumida, Kazuhiro;
    • Koikawa, Kenji;
    • Morino, Kahori;
    • Oe, Shinji;
    • Miyagawa, Koichiro;
    • Yamasaki, Masahiro;
    • Shibata, Michihiko;
    • Abe, Shintaro;
    • Ikuta, Katsuya;
    • Hayashi, Hisao;
    • Harada, Masaru
    Publication type:
    Article
    29
    30
    31
    32
    33
    34
    35

    Neonatal haemochromatosis with reversible pituitary involvement.

    Published in:
    Transplant International, 2014, v. 27, n. 8, p. e76, doi. 10.1111/tri.12336
    By:
    • Indolfi, Giuseppe;
    • Bèrczes, Rita;
    • Pelliccioli, Isabella;
    • Bosisio, Michela;
    • Agostinis, Cristina;
    • Resti, Massimo;
    • Zambelli, Marco;
    • Lucianetti, Alessandro;
    • Colledan, Michele;
    • D'Antiga, Lorenzo
    Publication type:
    Article
    36
    37

    Surgery for Hepatocellular Carcinoma Arising in Hereditary Hemochromatosis.

    Published in:
    European Surgical Research, 2006, v. 38, n. 4, p. 371, doi. 10.1159/000094532
    By:
    • Sotiropoulos, Georgios C.;
    • Molmenti, Ernesto P.;
    • Lang, Hauke;
    • Beckebaum, Susanne;
    • Kaiser, Gernot M.;
    • Brokalaki, Eirini I.;
    • Frilling, Andrea;
    • Malagó, Massimo;
    • Neuhäuser, Markus;
    • Broelsch, Christoph E.
    Publication type:
    Article
    38
    39
    40
    41
    42
    43

    Impact of hemochromatosis gene mutations on cardiac status in doxorubicin-treated survivors of childhood high-risk leukemia.

    Published in:
    Cancer (0008543X), 2013, v. 119, n. 19, p. 3555, doi. 10.1002/cncr.28256
    By:
    • Lipshultz, Steven E.;
    • Lipsitz, Stuart R.;
    • Kutok, Jeffery L.;
    • Miller, Tracie L.;
    • Colan, Steven D.;
    • Neuberg, Donna S.;
    • Stevenson, Kristen E.;
    • Fleming, Mark D.;
    • Sallan, Stephen E.;
    • Franco, Vivian I.;
    • Henkel, Jacqueline M.;
    • Asselin, Barbara L.;
    • Athale, Uma H.;
    • Clavell, Luis A.;
    • Michon, Bruno;
    • Laverdiere, Caroline;
    • Larsen, Eric;
    • Kelly, Kara M.;
    • Silverman, Lewis B.
    Publication type:
    Article
    44

    Haemochromatosis in children: A national retrospective cohort promoted by the A.I.E.O.P. (Associazione Italiana Emato‐Oncologia Pediatrica) study group.

    Published in:
    British Journal of Haematology, 2024, v. 204, n. 1, p. 306, doi. 10.1111/bjh.19208
    By:
    • Corti, Paola;
    • Ferrari, Giulia Maria;
    • Faraguna, Martha Caterina;
    • Capitoli, Giulia;
    • Longo, Filomena;
    • Corradini, Elena;
    • Casini, Tommaso;
    • Boscarol, Gianluca;
    • Pinto, Valeria Maria;
    • Ghilardi, Roberta;
    • Russo, Giovanna;
    • Colombatti, Raffaella;
    • Mariani, Raffaella;
    • Piperno, Alberto
    Publication type:
    Article
    45
    46
    47
    48
    49
    50