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 *

266 related articles for article (PubMed ID: 31771992)

  • 21. X-linked hydrocephalus: a novel missense mutation in the L1CAM gene.
    Sztriha L; Vos YJ; Verlind E; Johansen J; Berg B
    Pediatr Neurol; 2002 Oct; 27(4):293-6. PubMed ID: 12435569
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Cisterna Magna Injection in Rats to Study Glymphatic Function.
    Ramos M; Burdon Bechet N; Battistella R; Pavan C; Xavier ALR; Nedergaard M; Lundgaard I
    Methods Mol Biol; 2019; 1938():97-104. PubMed ID: 30617975
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Compound heterozygous variants in the multiple PDZ domain protein (MPDZ) cause a case of mild non-progressive communicating hydrocephalus.
    Al-Jezawi NK; Al-Shamsi AM; Suleiman J; Ben-Salem S; John A; Vijayan R; Ali BR; Al-Gazali L
    BMC Med Genet; 2018 Mar; 19(1):34. PubMed ID: 29499638
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Glymphatic MRI in idiopathic normal pressure hydrocephalus.
    Ringstad G; Vatnehol SAS; Eide PK
    Brain; 2017 Oct; 140(10):2691-2705. PubMed ID: 28969373
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Congenital idiopathic intestinal pseudo-obstruction and hydrocephalus with stenosis of the aqueduct of sylvius.
    Bott L; Boute O; Mention K; Vinchon M; Boman F; Gottrand F
    Am J Med Genet A; 2004 Sep; 130A(1):84-7. PubMed ID: 15368500
    [TBL] [Abstract][Full Text] [Related]  

  • 26. In Xenopus ependymal cilia drive embryonic CSF circulation and brain development independently of cardiac pulsatile forces.
    Dur AH; Tang T; Viviano S; Sekuri A; Willsey HR; Tagare HD; Kahle KT; Deniz E
    Fluids Barriers CNS; 2020 Dec; 17(1):72. PubMed ID: 33308296
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Hydrocephalus and Hirschsprung's disease with a mutation of L1CAM.
    Okamoto N; Del Maestro R; Valero R; Monros E; Poo P; Kanemura Y; Yamasaki M
    J Hum Genet; 2004; 49(6):334-337. PubMed ID: 15148591
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Neonatal hydrocephalus leads to white matter neuroinflammation and injury in the corpus callosum of Ccdc39 hydrocephalic mice.
    Goulding DS; Vogel RC; Pandya CD; Shula C; Gensel JC; Mangano FT; Goto J; Miller BA
    J Neurosurg Pediatr; 2020 May; 25(5):476-483. PubMed ID: 32032950
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Light sheet fluorescence microscopy of optically cleared brains for studying the glymphatic system.
    Bèchet NB; Kylkilahti TM; Mattsson B; Petrasova M; Shanbhag NC; Lundgaard I
    J Cereb Blood Flow Metab; 2020 Oct; 40(10):1975-1986. PubMed ID: 32525440
    [TBL] [Abstract][Full Text] [Related]  

  • 30. L1CAM mutation in a boy with hydrocephalus and duplex kidneys.
    Liebau MC; Gal A; Superti-Furga A; Omran H; Pohl M
    Pediatr Nephrol; 2007 Jul; 22(7):1058-61. PubMed ID: 17294222
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Dysfunctional cilia lead to altered ependyma and choroid plexus function, and result in the formation of hydrocephalus.
    Banizs B; Pike MM; Millican CL; Ferguson WB; Komlosi P; Sheetz J; Bell PD; Schwiebert EM; Yoder BK
    Development; 2005 Dec; 132(23):5329-39. PubMed ID: 16284123
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A novel L1CAM mutation with L1 spectrum disorders.
    Silan F; Ozdemir I; Lissens W
    Prenat Diagn; 2005 Jan; 25(1):57-9. PubMed ID: 15662685
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Diagnosis of a fetus with X-linked hydrocephalus due to mutation of L1CAM gene].
    Wu Q; Sun L; Xu Y; Yang X; Sun S; Wang W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Sep; 36(9):897-900. PubMed ID: 31515785
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Prenatal molecular diagnosis of a severe type of L1 syndrome (X-linked hydrocephalus).
    Yamasaki M; Nonaka M; Suzumori N; Nakamura H; Fujita H; Namba A; Kamei Y; Yamada T; Pooh RK; Tanemura M; Sudo N; Nagasaka M; Yoshioka E; Shofuda T; Kanemura Y
    J Neurosurg Pediatr; 2011 Oct; 8(4):411-6. PubMed ID: 21961551
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Analysis of L1CAM gene mutation in pedigrees with X-linked genetic hydrocephalus].
    Hu S; Wang L; Liu N; Kong X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 May; 36(5):465-467. PubMed ID: 31030434
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Dysfunction of axonemal dynein heavy chain Mdnah5 inhibits ependymal flow and reveals a novel mechanism for hydrocephalus formation.
    Ibañez-Tallon I; Pagenstecher A; Fliegauf M; Olbrich H; Kispert A; Ketelsen UP; North A; Heintz N; Omran H
    Hum Mol Genet; 2004 Sep; 13(18):2133-41. PubMed ID: 15269178
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Hydrocephalus with Hirschsprung disease: severe end of X-linked hydrocephalus spectrum.
    Takenouchi T; Nakazawa M; Kanemura Y; Shimozato S; Yamasaki M; Takahashi T; Kosaki K
    Am J Med Genet A; 2012 Apr; 158A(4):812-5. PubMed ID: 22354677
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Characterizing the glymphatic influx by utilizing intracisternal infusion of fluorescently conjugated cadaverine.
    Zhang C; Lin J; Wei F; Song J; Chen W; Shan L; Xue R; Wang G; Tao J; Zhang G; Xu GY; Wang L
    Life Sci; 2018 May; 201():150-160. PubMed ID: 29605446
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The role of L1cam in murine corticogenesis, and the pathogenesis of hydrocephalus.
    Itoh K; Fushiki S
    Pathol Int; 2015 Feb; 65(2):58-66. PubMed ID: 25641508
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Strain-dependent brain defects in mouse models of primary ciliary dyskinesia with mutations in Pcdp1 and Spef2.
    Finn R; Evans CC; Lee L
    Neuroscience; 2014 Sep; 277():552-67. PubMed ID: 25073043
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.