BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

171 related articles for article (PubMed ID: 34334593)

  • 21. [Type I neurofibromatosis (von Recklinghausen's disease) associated with abdominal neurofibrosarcoma and pheochromocytoma. Apropos of a case].
    De Grez T; Lambert M; Delaere B; Gigot JF; Haot J
    Acta Clin Belg; 1991; 46(2):89-93. PubMed ID: 1649534
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Genetic defects associated with familial and sporadic hyperparathyroidism.
    Hendy GN; Cole DE
    Front Horm Res; 2013; 41():149-65. PubMed ID: 23652676
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Corticotropin-producing pheochromocytoma in multiple endocrine neoplasia type 1].
    Rebrova DV; Grigorova SI; Vorokhobina NV; Zgoda EA; Novokshonov KY; Feofanova SG; Rusakov VF; Krasnov LM; Fedorov EA; Chinchuk IK; Shikhmagomedov SS; Pushkaruk AA; Sleptsov IV
    Probl Endokrinol (Mosk); 2023 Nov; 69(5):55-64. PubMed ID: 37968952
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Multiple endocrine neoplasia (MEN)--an overview and case report--patient with sporadic bilateral pheochromocytoma, hyperparathyroidism and marfanoid habitus.
    Fassbender WJ; Krohn-Grimberghe B; Görtz B; Litzlbauer D; Stracke H; Raue F; Kaiser HE
    Anticancer Res; 2000; 20(6C):4877-87. PubMed ID: 11205236
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Parathyroid carcinoma occurred in two glands in multiple endocrine neoplasia 1: a report on a rare case.
    Omi Y; Horiuchi K; Haniu K; Tokura M; Nagai E; Isozaki O; Nagashima Y; Okamoto T
    Endocr J; 2018 Feb; 65(2):245-252. PubMed ID: 29225207
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Multiple Endocrine Neoplasia].
    Uchino S; Ito A
    Gan To Kagaku Ryoho; 2019 Jul; 46(7):1114-1118. PubMed ID: 31296813
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A kindred with a variant of multiple endocrine neoplasia type 1 demonstrating frequent expression of pituitary tumors but not linked to the multiple endocrine neoplasia type 1 locus at chromosome region 11q13.
    Stock JL; Warth MR; Teh BT; Coderre JA; Overdorf JH; Baumann G; Hintz RL; Hartman ML; Seizinger BR; Larsson C; Aronin N
    J Clin Endocrinol Metab; 1997 Feb; 82(2):486-92. PubMed ID: 9024241
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Atypical clinical manifestations of multiple endocrine neoplasia type 1 syndrome.
    Krysiak R; Kajdaniuk D; Marek B; Okopień B
    Pol Arch Med Wewn; 2009 Mar; 119(3):175-9. PubMed ID: 19514648
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A Novel Missense Mutation of the MEN1 Gene in a Patient with Multiple Endocrine Neoplasia Type 1 with Glucagonoma and Obesity.
    Murakami T; Usui T; Nakajima A; Mochida Y; Saito S; Nambu T; Kato T; Matsuda Y; Yonemitsu S; Muro S; Oki S
    Intern Med; 2015; 54(19):2475-81. PubMed ID: 26424307
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Aldosterone-secreting adrenal adenoma as part of multiple endocrine neoplasia type 1 (MEN1): loss of heterozygosity for polymorphic chromosome 11 deoxyribonucleic acid markers, including the MEN1 locus.
    Beckers A; Abs R; Willems PJ; van der Auwera B; Kovacs K; Reznik M; Stevenaert A
    J Clin Endocrinol Metab; 1992 Aug; 75(2):564-70. PubMed ID: 1639957
    [TBL] [Abstract][Full Text] [Related]  

  • 31. MEN1 gene analysis in patients with primary hyperparathyroidism: 10-year experience of a single institution for thyroid and parathyroid care in Japan.
    Kihara M; Miyauchi A; Ito Y; Yoshida H; Miya A; Kobayashi K; Takamura Y; Fukushima M; Inoue H; Higashiyama T; Tomoda C
    Endocr J; 2009; 56(5):649-56. PubMed ID: 19461164
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Impact of cinacalcet hydrochloride in clinical management of primary hyperparathyroidism in multiple endocrine neoplasia type 1.
    Del Prete M; Marotta V; Ramundo V; Marciello F; Di Sarno A; Esposito R; Carratù AC; De Luca Di Roseto C; Di Somma C; Colao A; Faggiano A
    Minerva Endocrinol; 2013 Dec; 38(4):389-94. PubMed ID: 24285106
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A rare missense variant in RET exon 8 in a Portuguese family with atypical multiple endocrine neoplasia type 2A.
    Martins AF; Martins JM; do Vale S; Dias T; Silveira C; da Silva IR; Carmo-Fonseca M
    Hormones (Athens); 2016 Jul; 15(3):435-440. PubMed ID: 27838608
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Severe hypocalcemia complicated by postsurgical hypoparathyroidism and hungry bone syndrome in a patient with primary hyperparathyroidism, Graves' disease, and acromegaly.
    Tachibana S; Sato S; Yokoi T; Nagaishi R; Akehi Y; Yanase T; Yamashita H
    Intern Med; 2012; 51(14):1869-73. PubMed ID: 22821103
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Germline CDKN1B/p27Kip1 mutation in multiple endocrine neoplasia.
    Georgitsi M; Raitila A; Karhu A; van der Luijt RB; Aalfs CM; Sane T; Vierimaa O; Mäkinen MJ; Tuppurainen K; Paschke R; Gimm O; Koch CA; Gündogdu S; Lucassen A; Tischkowitz M; Izatt L; Aylwin S; Bano G; Hodgson S; De Menis E; Launonen V; Vahteristo P; Aaltonen LA
    J Clin Endocrinol Metab; 2007 Aug; 92(8):3321-5. PubMed ID: 17519308
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Novel 14 base-pair deletion of the MEN1 gene in a patient with recurrent primary hyperparathyroidism.
    Katai M; Sakurai A; Uchino S; Minemura K; Hashizume K; Fukushima Y
    Jpn J Clin Oncol; 2006 Jun; 36(6):395-7. PubMed ID: 16714299
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Peak incidence of pheochromocytoma and primary hyperparathyroidism in multiple endocrine neoplasia 2: need for age-adjusted biochemical screening.
    Machens A; Lorenz K; Dralle H
    J Clin Endocrinol Metab; 2013 Feb; 98(2):E336-45. PubMed ID: 23284010
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [TYPE 1 MULTIPLE ENDOCRINE NEOPLASIA SYNDROME AND FAMILIAL ISOLATED HYPERPARATHYROIDISM].
    Mamedova EO; Pigarova EA; Mokrysheva NG; Kuznetsov SN; Kim IV; Kuznetsov NS; Rozhinskaya LY; Tyul'pakov AN
    Klin Med (Mosk); 2015; 93(11):73-7. PubMed ID: 26987145
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Familial Hyperparathyroidism - Disorders of Growth and Secretion in Hormone-Secretory Tissue.
    Marx SJ; Lourenço DM
    Horm Metab Res; 2017 Nov; 49(11):805-815. PubMed ID: 29136674
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Loss of p27 expression is associated with MEN1 gene mutations in sporadic parathyroid adenomas.
    Borsari S; Pardi E; Pellegata NS; Lee M; Saponaro F; Torregrossa L; Basolo F; Paltrinieri E; Zatelli MC; Materazzi G; Miccoli P; Marcocci C; Cetani F
    Endocrine; 2017 Feb; 55(2):386-397. PubMed ID: 27038812
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.