BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

175 related articles for article (PubMed ID: 31858400)

  • 1. Acromegaly in the setting of Tatton-Brown-Rahman Syndrome.
    Hage C; Sabini E; Alsharhan H; Fahrner JA; Beckers A; Daly A; Salvatori R
    Pituitary; 2020 Apr; 23(2):167-170. PubMed ID: 31858400
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Acute myeloid leukaemia in a case with Tatton-Brown-Rahman syndrome: the peculiar
    Hollink IHIM; van den Ouweland AMW; Beverloo HB; Arentsen-Peters STCJM; Zwaan CM; Wagner A
    J Med Genet; 2017 Dec; 54(12):805-808. PubMed ID: 28432085
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Aortic root dilatation and dilated cardiomyopathy in an adult with Tatton-Brown-Rahman syndrome.
    Cecchi AC; Haidar A; Marin I; Kwartler CS; Prakash SK; Milewicz DM
    Am J Med Genet A; 2022 Feb; 188(2):628-634. PubMed ID: 34644003
    [TBL] [Abstract][Full Text] [Related]  

  • 4. An adult patient with Tatton-Brown-Rahman syndrome caused by a novel DNMT3A variant and axonal polyneuropathy.
    AlSabah AA; Alsalmi M; Massie R; Bilodeau MC; Campeau PM; McGraw S; D'Agostino MD
    Am J Med Genet A; 2024 Apr; 194(4):e63484. PubMed ID: 38041495
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Skeletal abnormalities in mice with Dnmt3a missense mutations.
    Bell-Hensley A; Beard DC; Feeney K; Zheng H; Jiang Y; Zhang X; Liu J; Gabel H; McAlinden A
    Bone; 2024 Jun; 183():117085. PubMed ID: 38522809
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Perturbed hematopoiesis in individuals with germline DNMT3A overgrowth Tatton-Brown-Rahman syndrome.
    Tovy A; Rosas C; Gaikwad AS; Medrano G; Zhang L; Reyes JM; Huang YH; Arakawa T; Kurtz K; Conneely SE; Guzman AG; Aguilar R; Gao A; Chen CW; Kim JJ; Carter MT; Lasa-Aranzasti A; Valenzuela I; Van Maldergem L; Brunetti L; Hicks MJ; Marcogliese AN; Goodell MA; Rau RE
    Haematologica; 2022 Apr; 107(4):887-898. PubMed ID: 34092059
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The first case report of medulloblastoma associated with Tatton-Brown-Rahman syndrome.
    Sweeney KJ; Mottolese C; Belot A; Szathmari A; Frappaz D; Lesca G; Putoux A; Di Rocco F
    Am J Med Genet A; 2019 Jul; 179(7):1357-1361. PubMed ID: 31066180
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Tatton-Brown-Rahman Syndrome: Case report and DNMT3A variant not previously reported associated to the syndrome].
    Martin M F; Díaz S C; Mira O M
    Andes Pediatr; 2022 Aug; 93(4):561-567. PubMed ID: 37906855
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The spectrum of DNMT3A variants in Tatton-Brown-Rahman syndrome overlaps with that in hematologic malignancies.
    Shen W; Heeley JM; Carlston CM; Acuna-Hidalgo R; Nillesen WM; Dent KM; Douglas GV; Levine KL; Bayrak-Toydemir P; Marcelis CL; Shinawi M; Carey JC
    Am J Med Genet A; 2017 Nov; 173(11):3022-3028. PubMed ID: 28941052
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Novel DNMT3A germline mutations are associated with inherited Tatton-Brown-Rahman syndrome.
    Xin B; Cruz Marino T; Szekely J; Leblanc J; Cechner K; Sency V; Wensel C; Barabas M; Therriault V; Wang H
    Clin Genet; 2017 Apr; 91(4):623-628. PubMed ID: 27701732
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Tatton-Brown-Rahman syndrome: Novel pathogenic variants and new neuroimaging findings.
    Jiménez de la Peña M; Rincón-Pérez I; López-Martín S; Albert J; Martín Fernández-Mayoralas D; Fernández-Perrone AL; Jiménez de Domingo A; Tirado P; Calleja-Pérez B; Porta J; Álvarez S; Fernández-Jaén A
    Am J Med Genet A; 2024 Feb; 194(2):211-217. PubMed ID: 37795572
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Further delineation of neuropsychiatric findings in Tatton-Brown-Rahman syndrome due to disease-causing variants in DNMT3A: seven new patients.
    Tenorio J; Alarcón P; Arias P; Dapía I; García-Miñaur S; Palomares Bralo M; Campistol J; Climent S; Valenzuela I; Ramos S; Monseny AM; Grondona FL; Botet J; Serrano M; Solís M; Santos-Simarro F; Álvarez S; Teixidó-Tura G; Fernández Jaén A; Gordo G; Bardón Rivera MB; Nevado J; Hernández A; Cigudosa JC; Ruiz-Pérez VL; Tizzano EF; ; Lapunzina P
    Eur J Hum Genet; 2020 Apr; 28(4):469-479. PubMed ID: 31685998
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Large-scale second-hit AIP deletion causing a pediatric growth hormone-secreting pituitary adenoma: Case report and review of literature.
    Gummadavelli A; Dinauer C; McGuone D; Vining EM; Erson-Omay EZ; Omay SB
    J Clin Neurosci; 2020 Aug; 78():420-422. PubMed ID: 32336638
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Tatton-Brown-Rahman syndrome due to 2p23 microdeletion.
    Okamoto N; Toribe Y; Shimojima K; Yamamoto T
    Am J Med Genet A; 2016 May; 170A(5):1339-42. PubMed ID: 26866722
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Isolated familial somatotropinoma: 11q13-loh and gene/protein expression analysis suggests a possible involvement of aip also in non-pituitary tumorigenesis.
    Toledo RA; Mendonca BB; Fragoso MC; Soares IC; Almeida MQ; Moraes MB; Lourenço DM; Alves VA; Bronstein MD; Toledo SP
    Clinics (Sao Paulo); 2010 Apr; 65(4):407-15. PubMed ID: 20454499
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Familial acromegaly due to aryl hydrocarbon receptor-interacting protein (AIP) gene mutation in a Turkish cohort.
    Niyazoglu M; Sayitoglu M; Firtina S; Hatipoglu E; Gazioglu N; Kadioglu P
    Pituitary; 2014 Jun; 17(3):220-6. PubMed ID: 23743763
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Acute myeloid leukemia-associated DNMT3A p.Arg882His mutation in a patient with Tatton-Brown-Rahman overgrowth syndrome as a constitutional mutation.
    Kosaki R; Terashima H; Kubota M; Kosaki K
    Am J Med Genet A; 2017 Jan; 173(1):250-253. PubMed ID: 27991732
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Tatton-Brown-Rahman syndrome associated with the DNMT3A gene: a case report and literature review].
    Chen M; Li ST; Cai Y; Xiao X; Shi CC; Hao H
    Zhongguo Dang Dai Er Ke Za Zhi; 2020 Oct; 22(10):1114-1118. PubMed ID: 33059810
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Germline AIP mutations in apparently sporadic pituitary adenomas: prevalence in a prospective single-center cohort of 443 patients.
    Cazabat L; Bouligand J; Salenave S; Bernier M; Gaillard S; Parker F; Young J; Guiochon-Mantel A; Chanson P
    J Clin Endocrinol Metab; 2012 Apr; 97(4):E663-70. PubMed ID: 22319033
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.