Literature DB >> 30145825

Increased substantia nigra echogenicity in LRRK2 family members without mutations.

Mariel Pullman1,2, Roberto Ortega2, Amanda Glickman2, Andres Deik1,3, Deborah Raymond2, Karen Marder4, Nir Giladi5, Susan Bressman1,2, Johann Hagenah6, Norbert Brüggemann7, Rachel Saunders-Pullman1,2.   

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Year:  2018        PMID： 30145825      PMCID： PMC6346431          DOI： 10.1002/mds.27443

Source DB:  PubMed          Journal:  Mov Disord        ISSN： 0885-3185            Impact factor:   10.338


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  7 in total

1.  Substantia nigra hyperechogenicity with LRRK2 G2019S mutations.

Authors:  Norbert Brüggemann; Johann Hagenah; Kaili Stanley; Christine Klein; Cuiling Wang; Deborah Raymond; Laurie Ozelius; Susan Bressman; Rachel Saunders-Pullman
Journal:  Mov Disord       Date:  2011-02-10       Impact factor: 10.338

Review 2.  The curious case of phenocopies in families with genetic Parkinson's disease.

Authors:  Christine Klein; Rosalind Chuang; Connie Marras; Anthony E Lang
Journal:  Mov Disord       Date:  2011-07-06       Impact factor: 10.338

3.  Olfaction and imaging biomarkers in premotor LRRK2 G2019S-associated Parkinson disease.

Authors:  Maria Sierra; Pascual Sánchez-Juan; María Isabel Martínez-Rodríguez; Isabel González-Aramburu; Inés García-Gorostiaga; María Remedios Quirce; Enrique Palacio; José Manuel Carril; José Berciano; Onofre Combarros; Jon Infante
Journal:  Neurology       Date:  2013-01-16       Impact factor: 9.910

4.  Echogenicity of the substantia nigra: association with increased iron content and marker for susceptibility to nigrostriatal injury.

Authors:  Daniela Berg; Wolfgang Roggendorf; Ute Schröder; Rüdiger Klein; Thomas Tatschner; Peter Benz; Oliver Tucha; Michael Preier; Klaus W Lange; Karlheinz Reiners; Manfred Gerlach; Georg Becker
Journal:  Arch Neurol       Date:  2002-06

5.  Transcranial sonography findings in a large family with homozygous and heterozygous PINK1 mutations.

Authors:  J M Hagenah; B Becker; N Brüggemann; A Djarmati; K Lohmann; A Sprenger; C Klein; G Seidel
Journal:  J Neurol Neurosurg Psychiatry       Date:  2008-05-09       Impact factor: 10.154

6.  Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance.

Authors:  Steven J Lubbe; Valentina Escott-Price; J Raphael Gibbs; Mike A Nalls; Jose Bras; T Ryan Price; Aude Nicolas; Iris E Jansen; Kin Y Mok; Alan M Pittman; James E Tomkins; Patrick A Lewis; Alastair J Noyce; Suzanne Lesage; Manu Sharma; Elena R Schiff; Adam P Levine; Alexis Brice; Thomas Gasser; John Hardy; Peter Heutink; Nicholas W Wood; Andrew B Singleton; Nigel M Williams; Huw R Morris
Journal:  Hum Mol Genet       Date:  2016-12-15       Impact factor: 6.150

7.  Olfactory identification in LRRK2 G2019S mutation carriers: a relevant marker?

Authors:  Rachel Saunders-Pullman; Anat Mirelman; Cuiling Wang; Roy N Alcalay; Marta San Luciano; Robert Ortega; Deborah Raymond; Helen Mejia-Santana; Laurie Ozelius; Lorraine Clark; Avi Orr-Utreger; Karen Marder; Nir Giladi; Susan B Bressman
Journal:  Ann Clin Transl Neurol       Date:  2014-09-30       Impact factor: 4.511
  7 in total

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