Literature DB >> 29163746

Genetic Insights into Cerebrovascular Disorders: A Comprehensive Review.

Fawaz Al-Mufti1,2, Ahmed Alkanaq3, Krishna Amuluru4, Rolla Nuoman5, Ahmed Abdulrazzaq6, Tamarah Sami7, Halla Nuoaman7, Caroline Hayes-Rosen5, Charles J Prestigiacomo2, Chirag D Gandhi8.   

Abstract

Entities:  

Keywords:  Cerebrovascular malformations; hereditary diseases

Year:  2017        PMID： 29163746      PMCID： PMC5683023     

Source DB:  PubMed          Journal:  J Vasc Interv Neurol        ISSN： 1941-5893


× No keyword cloud information.
  93 in total

1.  Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage.

Authors:  Daniel Woo; Guido J Falcone; William J Devan; W Mark Brown; Alessandro Biffi; Timothy D Howard; Christopher D Anderson; H Bart Brouwers; Valerie Valant; Thomas W K Battey; Farid Radmanesh; Miriam R Raffeld; Sylvia Baedorf-Kassis; Ranjan Deka; Jessica G Woo; Lisa J Martin; Mary Haverbusch; Charles J Moomaw; Guangyun Sun; Joseph P Broderick; Matthew L Flaherty; Sharyl R Martini; Dawn O Kleindorfer; Brett Kissela; Mary E Comeau; Jeremiasz M Jagiella; Helena Schmidt; Paul Freudenberger; Alexander Pichler; Christian Enzinger; Björn M Hansen; Bo Norrving; Jordi Jimenez-Conde; Eva Giralt-Steinhauer; Roberto Elosua; Elisa Cuadrado-Godia; Carolina Soriano; Jaume Roquer; Peter Kraft; Alison M Ayres; Kristin Schwab; Jacob L McCauley; Joanna Pera; Andrzej Urbanik; Natalia S Rost; Joshua N Goldstein; Anand Viswanathan; Eva-Maria Stögerer; David L Tirschwell; Magdy Selim; Devin L Brown; Scott L Silliman; Bradford B Worrall; James F Meschia; Chelsea S Kidwell; Joan Montaner; Israel Fernandez-Cadenas; Pilar Delgado; Rainer Malik; Martin Dichgans; Steven M Greenberg; Peter M Rothwell; Arne Lindgren; Agnieszka Slowik; Reinhold Schmidt; Carl D Langefeld; Jonathan Rosand
Journal:  Am J Hum Genet       Date:  2014-03-20       Impact factor: 11.025

2.  Lethal genes surviving by mosaicism: a possible explanation for sporadic birth defects involving the skin.

Authors:  R Happle
Journal:  J Am Acad Dermatol       Date:  1987-04       Impact factor: 11.527

Review 3.  Current concepts and clinical applications of stroke genetics.

Authors:  Guido J Falcone; Rainer Malik; Martin Dichgans; Jonathan Rosand
Journal:  Lancet Neurol       Date:  2014-04       Impact factor: 44.182

Review 4.  [131 cases of cavernous angioma (cavernomas) of the CNS, discovered by retrospective analysis of 24,535 autopsies].

Authors:  P Otten; G P Pizzolato; B Rilliet; J Berney
Journal:  Neurochirurgie       Date:  1989       Impact factor: 1.553

5.  Mosaic ACVRL1 and ENG mutations in hereditary haemorrhagic telangiectasia patients.

Authors:  D Hunter Best; Cecily Vaughn; Jamie McDonald; Kristy Damjanovich; James R Runo; Jason M Chibuk; Pinar Bayrak-Toydemir
Journal:  J Med Genet       Date:  2011-03-04       Impact factor: 6.318

6.  Guidelines for the management of spontaneous intracerebral hemorrhage: a guideline for healthcare professionals from the American Heart Association/American Stroke Association.

Authors:  Lewis B Morgenstern; J Claude Hemphill; Craig Anderson; Kyra Becker; Joseph P Broderick; E Sander Connolly; Steven M Greenberg; James N Huang; R Loch MacDonald; Steven R Messé; Pamela H Mitchell; Magdy Selim; Rafael J Tamargo
Journal:  Stroke       Date:  2010-07-22       Impact factor: 7.914

7.  Somatic mosaic activating mutations in PIK3CA cause CLOVES syndrome.

Authors:  Kyle C Kurek; Valerie L Luks; Ugur M Ayturk; Ahmad I Alomari; Steven J Fishman; Samantha A Spencer; John B Mulliken; Margot E Bowen; Guilherme L Yamamoto; Harry P W Kozakewich; Matthew L Warman
Journal:  Am J Hum Genet       Date:  2012-05-31       Impact factor: 11.025

8.  Clinical outcomes of pulmonary arterial hypertension in patients carrying an ACVRL1 (ALK1) mutation.

Authors:  Barbara Girerd; David Montani; Florence Coulet; Benjamin Sztrymf; Azzeddine Yaici; Xavier Jaïs; David Tregouet; Abilio Reis; Valérie Drouin-Garraud; Alain Fraisse; Olivier Sitbon; Dermot S O'Callaghan; Gérald Simonneau; Florent Soubrier; Marc Humbert
Journal:  Am J Respir Crit Care Med       Date:  2010-01-07       Impact factor: 21.405

Review 9.  Malignancy in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).

Authors:  Donna M McDonald-McGinn; Anne Reilly; Carina Wallgren-Pettersson; H Eugene Hoyme; Samuel P Yang; Margaret P Adam; Elaine H Zackai; Kathleen E Sullivan
Journal:  Am J Med Genet A       Date:  2006-04-15       Impact factor: 2.802

10.  Gene microarray analysis of human brain arteriovenous malformations.

Authors:  Tomoki Hashimoto; Michael T Lawton; Gen Wen; Guo-Yuan Yang; Thomas Chaly; Campbell L Stewart; Holly K Dressman; Nicholas M Barbaro; Douglas A Marchuk; William L Young
Journal:  Neurosurgery       Date:  2004-02       Impact factor: 4.654
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.