These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

176 related articles for article (PubMed ID: 29196357)

  • 1. An approach to familial lymphoedema.
    Jones GE; Mansour S
    Clin Med (Lond); 2017 Dec; 17(6):552-557. PubMed ID: 29196357
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetics and lymphoedema: a future yet to be fully discovered.
    Cooper G
    Br J Community Nurs; 2017 Jan; 22(1):646-648. PubMed ID: 28034335
    [No Abstract]   [Full Text] [Related]  

  • 3. Variable clinical presentation in primary lymphoedema: report of two cases.
    Ozyurt A; Sevinc E; Baykan A; Arslan D; Argun M; Pamukcu O; Uzum K
    Clin Dysmorphol; 2014 Jul; 23(3):83-87. PubMed ID: 24619057
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis.
    Fotiou E; Martin-Almedina S; Simpson MA; Lin S; Gordon K; Brice G; Atton G; Jeffery I; Rees DC; Mignot C; Vogt J; Homfray T; Snyder MP; Rockson SG; Jeffery S; Mortimer PS; Mansour S; Ostergaard P
    Nat Commun; 2015 Sep; 6():8085. PubMed ID: 26333996
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Genetics, diagnostics and clinical presentation of primary lymphoedema].
    Hägerling R
    Dermatologie (Heidelb); 2023 Aug; 74(8):594-604. PubMed ID: 37402871
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An additional case of Hennekam lymphangiectasia-lymphedema syndrome caused by loss-of-function mutation in ADAMTS3.
    Scheuerle AE; Sweed NT; Timmons CF; Smith ED; Alcaraz WA; Shinde DN
    Am J Med Genet A; 2018 Dec; 176(12):2858-2861. PubMed ID: 30450763
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hennekam lymphangiectasia syndrome: A rare case of primary lymphedema.
    Sanke S; Garg T; Manickavasagam S; Chander R
    Indian J Dermatol Venereol Leprol; 2021; 87(2):240-244. PubMed ID: 33769747
    [No Abstract]   [Full Text] [Related]  

  • 8. Loss of ADAMTS3 activity causes Hennekam lymphangiectasia-lymphedema syndrome 3.
    Brouillard P; Dupont L; Helaers R; Coulie R; Tiller GE; Peeden J; Colige A; Vikkula M
    Hum Mol Genet; 2017 Nov; 26(21):4095-4104. PubMed ID: 28985353
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Intestinal lymphangiectasia in a 3-month-old girl: A case report of Hennekam syndrome caused by CCBE1 mutation.
    Fattorusso A; Pieri ES; Dell'Isola GB; Prontera P; Mencaroni E; Stangoni G; Esposito S
    Medicine (Baltimore); 2020 Jul; 99(27):e20995. PubMed ID: 32629717
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Expanding the genotypic spectrum of CCBE1 mutations in Hennekam syndrome.
    Crawford J; Bower NI; Hogan BM; Taft RJ; Gabbett MT; McGaughran J; Simons C
    Am J Med Genet A; 2016 Oct; 170(10):2694-7. PubMed ID: 27345729
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A novel mutation in GJA1 causing oculodentodigital syndrome and primary lymphoedema in a three generation family.
    Brice G; Ostergaard P; Jeffery S; Gordon K; Mortimer PS; Mansour S
    Clin Genet; 2013 Oct; 84(4):378-81. PubMed ID: 23550541
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Recurrent prenatal PIEZO1-related lymphatic dysplasia: Expanding molecular and ultrasound findings.
    Mastromoro G; Guadagnolo D; Giancotti A; Di Gregorio MG; Marchionni E; Vena F; Lepri FR; Bargiacchi L; Ventriglia F; Di Gioia C; Novelli A; Pizzuti A
    Eur J Med Genet; 2021 Jan; 64(1):104106. PubMed ID: 33227434
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The VASCERN PPL working group patient pathway for primary and paediatric lymphoedema.
    Devoogdt N; Thomis S; Belva F; Dickinson-Blok J; Fourgeaud C; Giacalone G; Karlsmark T; Kavola H; Keeley V; Marques ML; Mansour S; Nissen CV; Nørregaard S; Oberlin M; Ručigaj TP; Somalo-Barranco G; Suominen S; Van Duinen K; Vignes S; Damstra R
    Eur J Med Genet; 2024 Feb; 67():104905. PubMed ID: 38143023
    [TBL] [Abstract][Full Text] [Related]  

  • 14. CCBE1 mutations can cause a mild, atypical form of generalized lymphatic dysplasia but are not a common cause of non-immune hydrops fetalis.
    Connell FC; Kalidas K; Ostergaard P; Brice G; Murday V; Mortimer PS; Jeffrey I; Jeffery S; Mansour S
    Clin Genet; 2012 Feb; 81(2):191-7. PubMed ID: 22239599
    [No Abstract]   [Full Text] [Related]  

  • 15. A homozygous variant in growth and differentiation factor 2 (GDF2) may cause lymphatic dysplasia with hydrothorax and nonimmune hydrops fetalis.
    Aukema SM; Ten Brinke GA; Timens W; Vos YJ; Accord RE; Kraft KE; Santing MJ; Morssink LP; Streefland E; van Diemen CC; Vrijlandt EJ; Hulzebos CV; Kerstjens-Frederikse WS
    Am J Med Genet A; 2020 Sep; 182(9):2152-2160. PubMed ID: 32618121
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Lymphoedema and cellulitis: chicken or egg?
    Keeley VL
    Br J Dermatol; 2008 Jun; 158(6):1175-6. PubMed ID: 18482406
    [No Abstract]   [Full Text] [Related]  

  • 17. A new classification system for primary lymphatic dysplasias based on phenotype.
    Connell F; Brice G; Jeffery S; Keeley V; Mortimer P; Mansour S
    Clin Genet; 2010 May; 77(5):438-52. PubMed ID: 20447153
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Enigmatic lymphatic diseases involving the lung].
    Khen-Dunlop N; Amiel J; Delacourt C; Révillon Y
    Rev Pneumol Clin; 2013 Oct; 69(5):260-4. PubMed ID: 23561737
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Piezo channels.
    Parpaite T; Coste B
    Curr Biol; 2017 Apr; 27(7):R250-R252. PubMed ID: 28376327
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A Multiplex Kindred with Hennekam Syndrome due to Homozygosity for a CCBE1 Mutation that does not Prevent Protein Expression.
    Jackson CC; Best L; Lorenzo L; Casanova JL; Wacker J; Bertz S; Agaimy A; Harrer T
    J Clin Immunol; 2016 Jan; 36(1):19-27. PubMed ID: 26686525
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.