BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

348 related articles for article (PubMed ID: 34399110)

  • 21. Tuberous Sclerosis Complex: A Review.
    Randle SC
    Pediatr Ann; 2017 Apr; 46(4):e166-e171. PubMed ID: 28414398
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Imaging features of tuberous sclerosis complex with autosomal-dominant polycystic kidney disease: a contiguous gene syndrome.
    Back SJ; Andronikou S; Kilborn T; Kaplan BS; Darge K
    Pediatr Radiol; 2015 Mar; 45(3):386-95. PubMed ID: 25355409
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Tuberous sclerosis complex: the past and the future.
    De Waele L; Lagae L; Mekahli D
    Pediatr Nephrol; 2015 Oct; 30(10):1771-80. PubMed ID: 25533384
    [TBL] [Abstract][Full Text] [Related]  

  • 24. TSC2 c.1864C>T variant associated with mild cases of tuberous sclerosis complex.
    Farach LS; Gibson WT; Sparagana SP; Nellist M; Stumpel CT; Hietala M; Friedman E; Pearson DA; Creighton SP; Wagemans A; Segel R; Ben-Shalom E; Au KS; Northrup H
    Am J Med Genet A; 2017 Mar; 173(3):771-775. PubMed ID: 28211972
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Clinical practice recommendations for kidney involvement in tuberous sclerosis complex: a consensus statement by the ERKNet Working Group for Autosomal Dominant Structural Kidney Disorders and the ERA Genes & Kidney Working Group.
    Mekahli D; Müller RU; Marlais M; Wlodkowski T; Haeberle S; de Argumedo ML; Bergmann C; Breysem L; Fladrowski C; Henske EP; Janssens P; Jouret F; Kingswood JC; Lattouf JB; Lilien M; Maleux G; Rozenberg M; Siemer S; Devuyst O; Schaefer F; Kwiatkowski DJ; Rouvière O; Bissler J
    Nat Rev Nephrol; 2024 Jun; 20(6):402-420. PubMed ID: 38443710
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Identification of TSC2 mosaic mutation limited to cortical tuber with TSC targeted sequencing: a case report and literature review.
    Zhou Y; Wang X; Wang J; Ding Y; Wang Y; Li H; Zhao R; Wu B
    Childs Nerv Syst; 2021 Dec; 37(12):3945-3949. PubMed ID: 33517515
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Isolated cortical tuber in an infant with genetically confirmed tuberous sclerosis complex 1 presenting with symptomatic West syndrome.
    Miyata H; Fushimi S; Ota Y; Vinters HV; Adachi K; Nanba E; Akiyama T
    Neuropathology; 2021 Feb; 41(1):58-64. PubMed ID: 33181865
    [TBL] [Abstract][Full Text] [Related]  

  • 28. TuberOus SClerosis registry to increase disease Awareness (TOSCA) - baseline data on 2093 patients.
    Kingswood JC; d'Augères GB; Belousova E; Ferreira JC; Carter T; Castellana R; Cottin V; Curatolo P; Dahlin M; de Vries PJ; Feucht M; Fladrowski C; Gislimberti G; Hertzberg C; Jozwiak S; Lawson JA; Macaya A; Nabbout R; O'Callaghan F; Benedik MP; Qin J; Marques R; Sander V; Sauter M; Takahashi Y; Touraine R; Youroukos S; Zonnenberg B; Jansen AC;
    Orphanet J Rare Dis; 2017 Jan; 12(1):2. PubMed ID: 28057044
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Diagnosis, monitoring and treatment of tuberous sclerosis complex].
    Reinhard M; Sunde L; Madsen MG; Andersen BN; Bendstrup E; Sommerlund M; Gjørup H; Larsen DA; Møller HU; Nielsen DG; Mortensen UM; Handrup MM; Aagaard NKM; Cortnum S; Khatir DS; Bayat M; Andersen G; Stausbøl-Grøn B; Christensen J
    Ugeskr Laeger; 2019 Nov; 181(45):. PubMed ID: 31791451
    [TBL] [Abstract][Full Text] [Related]  

  • 30. An Australian tuberous sclerosis cohort: are surveillance guidelines being met?
    Chopra M; Lawson JA; Wilson M; Kennedy SE; Taylor P; Buckley MF; Wargon O; Parasivam G; Camphausen C; Yates D; Mowat D
    J Paediatr Child Health; 2011 Oct; 47(10):711-6. PubMed ID: 21449900
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A step-wise approach for establishing a multidisciplinary team for the management of tuberous sclerosis complex: a Delphi consensus report.
    Auvin S; Bissler JJ; Cottin V; Fujimoto A; Hofbauer GFL; Jansen AC; Jóźwiak S; Kerecuk L; Kingswood JC; Moavero R; Torra R; Villanueva V
    Orphanet J Rare Dis; 2019 Apr; 14(1):91. PubMed ID: 31039793
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Presentation and Diagnosis of Tuberous Sclerosis Complex in Infants.
    Davis PE; Filip-Dhima R; Sideridis G; Peters JM; Au KS; Northrup H; Bebin EM; Wu JY; Krueger D; Sahin M;
    Pediatrics; 2017 Dec; 140(6):. PubMed ID: 29101226
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A circuitry and biochemical basis for tuberous sclerosis symptoms: from epilepsy to neurocognitive deficits.
    Feliciano DM; Lin TV; Hartman NW; Bartley CM; Kubera C; Hsieh L; Lafourcade C; O'Keefe RA; Bordey A
    Int J Dev Neurosci; 2013 Nov; 31(7):667-78. PubMed ID: 23485365
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Managing tuberous sclerosis in the Asia-Pacific region: refining practice and the role of targeted therapy.
    Lawson JA; Chan CF; Chi CS; Fan PC; Kim HD; Kim KJ; Likasitwatanakul S; Ortiz M; Riney K; Tay SK; Tham CK
    J Clin Neurosci; 2014 Jul; 21(7):1180-7. PubMed ID: 24518266
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Analysis of genotypes and phenotypes in Chinese children with tuberous sclerosis complex.
    Bai D; Zhao J; Li L; Gao J; Wang X
    Sci China Life Sci; 2017 Jul; 60(7):763-771. PubMed ID: 28623545
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Tuberous sclerosis complex and epilepsy: recent developments and future challenges.
    Holmes GL; Stafstrom CE;
    Epilepsia; 2007 Apr; 48(4):617-30. PubMed ID: 17386056
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Tuberous sclerosis complex: A review].
    Pfirmann P; Combe C; Rigothier C
    Rev Med Interne; 2021 Oct; 42(10):714-721. PubMed ID: 33836894
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Rare familial TSC2 gene mutation associated with atypical phenotype presentation of Tuberous Sclerosis Complex.
    Fox J; Ben-Shachar S; Uliel S; Svirsky R; Saitsu H; Matsumoto N; Fattal-Valevski A
    Am J Med Genet A; 2017 Mar; 173(3):744-748. PubMed ID: 28127866
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Deep phenotyping of patients with Tuberous Sclerosis Complex and no mutation identified in TSC1 and TSC2.
    Peron A; Vignoli A; Briola F; Morenghi E; Tansini L; Alfano RM; Bulfamante G; Terraneo S; Ghelma F; Banderali G; Viskochil DH; Carey JC; Canevini MP;
    Eur J Med Genet; 2018 Jul; 61(7):403-410. PubMed ID: 29432982
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Diagnosis of tuberous sclerosis complex focusing on prenatal period].
    Filipová H; Procházka M; Vrtěl R
    Ceska Gynekol; 2016 Apr; 81(2):147-54. PubMed ID: 27457398
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 18.