Increased substantia nigra echogenicity in LRRK2 family members without mutations

Mariel Pullman; Roberto Ortega; Amanda Glickman; Andres Deik; Deborah Raymond; Karen Marder; Nir Giladi; Susan Bressman; Johann Hagenah; Norbert Brüggemann; Rachel Saunders-Pullman

doi:10.1002/mds.27443

Increased substantia nigra echogenicity in LRRK2 family members without mutations

Mariel Pullman, Roberto Ortega, Amanda Glickman, Andres Deik, Deborah Raymond, Karen Marder, Nir Giladi, Susan Bressman, Johann Hagenah, Norbert Brüggemann, Rachel Saunders-Pullman^*

^*Corresponding author for this work

Clinic of Neurology

2 Citations (Scopus)

Original language	English
Journal	Movement Disorders
Volume	33
Issue number	9
Pages (from-to)	1504-1505
Number of pages	2
ISSN	0885-3185
DOIs	https://doi.org/10.1002/mds.27443
Publication status	Published - 01.09.2018

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

SDG 3 Good Health and Well-being
SDG 10 Reduced Inequalities

Research Areas and Centers

Research Area: Medical Genetics

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10.1002/mds.27443

Cite this

@article{746eb8d7a98a44cb9a7e7a6a62a9194b,

title = "Increased substantia nigra echogenicity in LRRK2 family members without mutations",

author = "Mariel Pullman and Roberto Ortega and Amanda Glickman and Andres Deik and Deborah Raymond and Karen Marder and Nir Giladi and Susan Bressman and Johann Hagenah and Norbert Br{\"u}ggemann and Rachel Saunders-Pullman",

year = "2018",

month = sep,

day = "1",

doi = "10.1002/mds.27443",

language = "English",

volume = "33",

pages = "1504--1505",

journal = "Movement Disorders",

issn = "0885-3185",

publisher = "John Wiley \& Sons Inc.",

number = "9",

}

TY - JOUR

T1 - Increased substantia nigra echogenicity in LRRK2 family members without mutations

AU - Pullman, Mariel

AU - Ortega, Roberto

AU - Glickman, Amanda

AU - Deik, Andres

AU - Raymond, Deborah

AU - Marder, Karen

AU - Giladi, Nir

AU - Bressman, Susan

AU - Hagenah, Johann

AU - Brüggemann, Norbert

AU - Saunders-Pullman, Rachel

PY - 2018/9/1

Y1 - 2018/9/1

UR - https://www.scopus.com/pages/publications/85052395874

U2 - 10.1002/mds.27443

DO - 10.1002/mds.27443

M3 - Letters

C2 - 30145825

AN - SCOPUS:85052395874

SN - 0885-3185

VL - 33

SP - 1504

EP - 1505

JO - Movement Disorders

JF - Movement Disorders

IS - 9

ER -

Increased substantia nigra echogenicity in LRRK2 family members without mutations

UN SDGs

Research Areas and Centers

Access to Document

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Cite this