BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

131 related articles for article (PubMed ID: 32608066)

  • 21. Vascular Stains: Proposal for a Clinical Classification to Improve Diagnosis and Management.
    Rozas-Muñoz E; Frieden IJ; Roé E; Puig L; Baselga E
    Pediatr Dermatol; 2016 Nov; 33(6):570-584. PubMed ID: 27456075
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Capillary malformation-arteriovenous malformation: a clinical review of 45 patients.
    Larralde M; Abad ME; Luna PC; Hoffner MV
    Int J Dermatol; 2014 Apr; 53(4):458-61. PubMed ID: 24168113
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Clinical pitfalls in the diagnosis of segmental overgrowth syndromes: a child with the c.2740G > A mutation in PIK3CA gene.
    Maguolo A; Antoniazzi F; Spano A; Fiorini E; Gaudino R; Mauro M; Cantalupo G; Biban P; Maitz S; Cavarzere P
    Ital J Pediatr; 2018 Sep; 44(1):110. PubMed ID: 30231930
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Mosaic RASopathy due to KRAS variant G12D with segmental overgrowth and associated peripheral vascular malformations.
    Schmidt VF; Wieland I; Wohlgemuth WA; Ricke J; Wildgruber M; Zenker M
    Am J Med Genet A; 2021 Oct; 185(10):3122-3128. PubMed ID: 34114335
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Diffuse capillary malformation in association with fetal pleural effusion: report of five patients.
    Rork JF; Alomari AI; Mulliken JB; Fishman SJ; Liang MG
    Pediatr Dermatol; 2015; 32(1):70-5. PubMed ID: 25644040
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Growth hormone deficiency in megalencephaly-capillary malformation syndrome: An association with activating mutations in PIK3CA.
    Davis S; Ware MA; Zeiger J; Deardorff MA; Grand K; Grimberg A; Hsu S; Kelsey M; Majidi S; Matthew RP; Napier M; Nokoff N; Prasad C; Riggs AC; McKinnon ML; Mirzaa G
    Am J Med Genet A; 2020 Jan; 182(1):162-168. PubMed ID: 31729162
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A novel mutation in RASA1 causes capillary malformation and limb enlargement.
    Hershkovitz D; Bergman R; Sprecher E
    Arch Dermatol Res; 2008 Aug; 300(7):385-8. PubMed ID: 18327598
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Microcephaly-capillary malformation syndrome: Brothers with a homozygous STAMBP mutation, uncovered by exome sequencing.
    Naseer MI; Sogaty S; Rasool M; Chaudhary AG; Abutalib YA; Walker S; Marshall CR; Merico D; Carter MT; Scherer SW; Al-Qahtani MH; Zarrei M
    Am J Med Genet A; 2016 Nov; 170(11):3018-3022. PubMed ID: 27531570
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Capillary malformation of the lower lip, lymphatic malformation of the face and neck, asymmetry and partial/generalized overgrowth (CLAPO): report of six cases of a new syndrome/association.
    López-Gutiérrez JC; Lapunzina P
    Am J Med Genet A; 2008 Oct; 146A(20):2583-8. PubMed ID: 18798326
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Epilepsy with faint capillary malformation or reticulated telangiectasia associated with mosaic AKT3 pathogenic variants.
    De Bortoli M; Ivars M; Revencu N; Nassogne MC; Lavarino C; Paco S; Lammens M; Renders A; Dumitriu D; Helaers R; Boon LM; Baselga E; Vikkula M
    Am J Med Genet A; 2024 Jun; 194(6):e63551. PubMed ID: 38321651
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Fingertip Capillary Malformation and Associated Disorders: Report of 9 Cases.
    López-Gutiérrez JC; Redondo P; Ivars M
    Pediatrics; 2017 Jul; 140(1):. PubMed ID: 28617243
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Update on classification and diagnosis of vascular malformations.
    McCuaig CC
    Curr Opin Pediatr; 2017 Aug; 29(4):448-454. PubMed ID: 28654575
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Phenotypic association of presence of a somatic GNAQ mutation with port-wine stain distribution in capillary malformation.
    Lee KT; Park JE; Eom Y; Lim HS; Ki CS; Lim SY
    Head Neck; 2019 Dec; 41(12):4143-4150. PubMed ID: 31532024
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Capillary malformation--arteriovenous malformation syndrome: review of the literature, proposed diagnostic criteria, and recommendations for management.
    Orme CM; Boyden LM; Choate KA; Antaya RJ; King BA
    Pediatr Dermatol; 2013; 30(4):409-15. PubMed ID: 23662773
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Capillary-venous malformation in the upper limb.
    Uihlein LC; Liang MG; Fishman SJ; Alomari AI; Mulliken JB
    Pediatr Dermatol; 2015; 32(2):287-9. PubMed ID: 25557931
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Histopathological hallmarks of cutaneous lesions of capillary malformation-arteriovenous malformation syndrome.
    Valdivielso-Ramos M; Torrelo A; Martin-Santiago A; Hernández-Nuñez A; Azaña JM; Campos M; Berenguer B; Garnacho G; Moreno R; Colmenero I
    J Eur Acad Dermatol Venereol; 2020 Oct; 34(10):2428-2435. PubMed ID: 32124491
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha (PIK3CA)-related overgrowth spectrum: A brief report.
    Denorme P; Morren MA; Hollants S; Spaepen M; Suaer K; Zutterman N; Labarque V; Legius E; Brems H
    Pediatr Dermatol; 2018 May; 35(3):e186-e188. PubMed ID: 29493003
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Oral sildenafil as a treatment option for lymphatic malformations in PIK3CA-related tissue overgrowth syndromes.
    Horbach SE; Jolink F; van der Horst CM
    Dermatol Ther; 2016 Nov; 29(6):466-469. PubMed ID: 27502552
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Endothelial Cells from Capillary Malformations Are Enriched for Somatic GNAQ Mutations.
    Couto JA; Huang L; Vivero MP; Kamitaki N; Maclellan RA; Mulliken JB; Bischoff J; Warman ML; Greene AK
    Plast Reconstr Surg; 2016 Jan; 137(1):77e-82e. PubMed ID: 26368330
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Macrocephaly-capillary malformation: Analysis of 13 patients and review of the diagnostic criteria.
    Martínez-Glez V; Romanelli V; Mori MA; Gracia R; Segovia M; González-Meneses A; López-Gutierrez JC; Gean E; Martorell L; Lapunzina P
    Am J Med Genet A; 2010 Dec; 152A(12):3101-6. PubMed ID: 21077203
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.