Works matching AU Raymond, Deborah

Results: 45

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

Published in:

Annals of Clinical & Translational Neurology, 2014, v. 1, n. 9, p. 670, doi. 10.1002/acn3.95

By:

Saunders‐Pullman, Rachel;
Mirelman, Anat;
Wang, Cuiling;
Alcalay, Roy N.;
San Luciano, Marta;
Ortega, Robert;
Raymond, Deborah;
Mejia‐Santana, Helen;
Ozelius, Laurie;
Clark, Lorraine;
Orr‐Utreger, Avi;
Marder, Karen;
Giladi, Nir;
Bressman, Susan B.

Publication type:

Article

Progression in the LRRK2-Asssociated Parkinson Disease Population.

Published in:

JAMA Neurology, 2018, v. 75, n. 3, p. 312, doi. 10.1001/jamaneurol.2017.4019

By:

Saunders-Pullman, Rachel;
Mirelman, Anat;
Alcalay, Roy N.;
Wang, Cuiling;
Ortega, Roberto A.;
Raymond, Deborah;
Mejia-Santana, Helen;
Orbe-Reilly, Martha;
Johannes, Brooke A.;
Thaler, Avner;
Ozelius, Laurie;
Orr-Urtreger, Avi;
Marder, Karen S.;
Giladi, Nir;
Bressman, Susan B.

Publication type:

Article

Complex and Dynamic Chromosomal Rearrangements in a Family With Seemingly Non-Mendelian Inheritance of Dopa-Responsive Dystonia.

Published in:

JAMA Neurology, 2017, v. 74, n. 7, p. 806, doi. 10.1001/jamaneurol.2017.0666

By:

Lohmann, Katja;
Redin, Claire;
Tönnies, Holger;
Bressman, Susan B.;
Subero, Jose Ignacio Martin;
Wiegers, Karin;
Hinrichs, Frauke;
Hellenbroich, Yorck;
Rakovic, Aleksandar;
Raymond, Deborah;
Ozelius, Laurie J.;
Schwinger, Eberhard;
Siebert, Reiner;
Talkowski, Michael E.;
Saunders-Pullman, Rachel;
Klein, Christine

Publication type:

Article

Clinical profiles and outcomes of deep brain stimulation in G2019S LRRK2 Parkinson disease.

Published in:

Journal of Neurosurgery, 2022, v. 137, n. 1, p. 184, doi. 10.3171/2021.7.jns21190

By:

Leaver, Katherine;
Viser, Aaron;
Kopell, Brian H.;
Ortega, Roberto A.;
Miravite, Joan;
Okun, Michael S.;
Elango, Sonya;
Raymond, Deborah;
Bressman, Susan B.;
Saunders-Pullman, Rachel;
Luciano, Marta San

Publication type:

Article

Mutations in GNAL cause primary torsion dystonia.

Published in:

Nature Genetics, 2013, v. 45, n. 1, p. 88, doi. 10.1038/ng.2496

By:

Fuchs, Tania;
Saunders-Pullman, Rachel;
Masuho, Ikuo;
Luciano, Marta San;
Raymond, Deborah;
Factor, Stewart;
Lang, Anthony E;
Liang, Tsao-Wei;
Trosch, Richard M;
White, Sierra;
Ainehsazan, Edmond;
Hervé, Denis;
Sharma, Nutan;
Ehrlich, Michelle E;
Martemyanov, Kirill A;
Bressman, Susan B;
Ozelius, Laurie J

Publication type:

Article

Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystonia.

Published in:

Nature Genetics, 2009, v. 41, n. 3, p. 286, doi. 10.1038/ng.304

By:

Fuchs, Tania;
Gavarini, Sophie;
Saunders-Pullman, Rachel;
Raymond, Deborah;
Ehrlich, Michelle E.;
Bressman, Susan B.;
Ozelius, Laurie J.

Publication type:

Article

Arm swing as a potential new prodromal marker of Parkinson's disease.

Published in:

2016

By:

Mirelman, Anat;
Bernad‐Elazari, Hagar;
Thaler, Avner;
Giladi‐Yacobi, Eytan;
Gurevich, Tanya;
Gana‐Weisz, Mali;
Saunders‐Pullman, Rachel;
Raymond, Deborah;
Doan, Nancy;
Bressman, Susan B.;
Marder, Karen S.;
Alcalay, Roy N.;
Rao, Ashwini K.;
Berg, Daniela;
Brockmann, Kathrin;
Aasly, Jan;
Waro, Bjørg Johanne;
Tolosa, Eduardo;
Vilas, Dolores;
Pont‐Sunyer, Claustre

Publication type:

journal article

REM sleep behavior disorder, as assessed by questionnaire, in G2019S LRRK2 mutation PD and carriers.

Published in:

2015

By:

Saunders‐Pullman, Rachel;
Alcalay, Roy N.;
Mirelman, Anat;
Wang, Cuiling;
Luciano, Marta San;
Ortega, Roberto A.;
Glickman, Amanda;
Raymond, Deborah;
Mejia‐Santana, Helen;
Doan, Nancy;
Johannes, Brooke;
Yasinovsky, Kira;
Ozelius, Laurie;
Clark, Lorraine;
Orr‐Utreger, Avi;
Marder, Karen;
Giladi, Nir;
Bressman, Susan B.

Publication type:

journal article

Disclosure of research results in genetic studies of Parkinson's disease caused by LRRK2 mutations.

Published in:

Movement Disorders, 2015, v. 30, n. 7, p. 904, doi. 10.1002/mds.26250

By:

Pont‐Sunyer, Claustre;
Bressman, Susan;
Raymond, Deborah;
Glickman, Amanda;
Tolosa, Eduardo;
Saunders‐Pullman, Rachel

Publication type:

Article

Nonmotor symptoms in healthy Ashkenazi Jewish carriers of the G2019S mutation in the LRRK2 gene.

Published in:

Movement Disorders, 2015, v. 30, n. 7, p. 981, doi. 10.1002/mds.26213

By:

Mirelman, Anat;
Alcalay, Roy N.;
Saunders‐Pullman, Rachel;
Yasinovsky, Kira;
Thaler, Avner;
Gurevich, Tanya;
Mejia‐Santana, Helen;
Raymond, Deborah;
Gana‐Weisz, Mali;
Bar‐Shira, Anat;
Ozelius, Laurie;
Clark, Lorraine;
Orr‐Urtreger, Avi;
Bressman, Susan;
Marder, Karen;
Giladi, Nir

Publication type:

Article

Low-variance RNAs identify Parkinson's disease molecular signature in blood.

Published in:

Movement Disorders, 2015, v. 30, n. 6, p. 813, doi. 10.1002/mds.26205

By:

Chikina, Maria D.;
Gerald, Christophe P.;
Li, Xianting;
Ge, Yongchao;
Pincas, Hanna;
Nair, Venugopalan D.;
Wong, Aaron K.;
Krishnan, Arjun;
Troyanskaya, Olga G.;
Raymond, Deborah;
Saunders‐Pullman, Rachel;
Bressman, Susan B.;
Yue, Zhenyu;
Sealfon, Stuart C.

Publication type:

Article

Heterogeneity in primary dystonia: Lessons from THAP1, GNAL, and TOR1A in Amish-Mennonites.

Published in:

Movement Disorders, 2014, v. 29, n. 6, p. 812, doi. 10.1002/mds.25818

By:

Saunders‐Pullman, Rachel;
Fuchs, Tania;
San Luciano, Marta;
Raymond, Deborah;
Brashear, Alison;
Ortega, Robert;
Deik, Andres;
Ozelius, Laurie J.;
Bressman, Susan B.

Publication type:

Article

Parkinson disease phenotype in Ashkenazi jews with and without LRRK2 G2019S mutations.

Published in:

Movement Disorders, 2013, v. 28, n. 14, p. 1966, doi. 10.1002/mds.25647

By:

Alcalay, Roy N.;
Mirelman, Anat;
Saunders‐Pullman, Rachel;
Tang, Ming‐X;
Mejia Santana, Helen;
Raymond, Deborah;
Roos, Ernest;
Orbe‐Reilly, Martha;
Gurevich, Tanya;
Bar Shira, Anat;
Gana Weisz, Mali;
Yasinovsky, Kira;
Zalis, Maayan;
Thaler, Avner;
Deik, Andres;
Barrett, Matthew James;
Cabassa, Jose;
Groves, Mark;
Hunt, Ann L.;
Lubarr, Naomi

Publication type:

Article

Mood and cognition in leucine-rich repeat kinase 2 G2019S Parkinson's disease.

Published in:

Movement Disorders, 2011, v. 26, n. 10, p. 1875, doi. 10.1002/mds.23746

By:

Shanker, Vicki;
Groves, Mark;
Heiman, Gary;
Palmese, Christina;
Saunders-Pullman, Rachel;
Ozelius, Laurie;
Raymond, Deborah;
Bressman, Susan

Publication type:

Article

LRRK2 G2019S mutations may be increased in Puerto Ricans.

Published in:

Movement Disorders, 2011, v. 26, n. 9, p. 1771, doi. 10.1002/mds.23632

By:

Saunders-Pullman, Rachel;
Cabassa, Jose;
San Luciano, Marta;
Stanley, Kaili;
Raymond, Deborah;
Ozelius, Laurie J.;
Bressman, Susan B.

Publication type:

Article

Substantia nigra hyperechogenicity with LRRK2 G2019S mutations.

Published in:

Movement Disorders, 2011, v. 26, n. 5, p. 885, doi. 10.1002/mds.23644

By:

Brüggemann, Norbert;
Hagenah, Johann;
Stanley, Kaili;
Klein, Christine;
Wang, Cuiling;
Raymond, Deborah;
Ozelius, Laurie;
Bressman, Susan;
Saunders-Pullman, Rachel

Publication type:

Article

LRRK2 G2019S mutations are associated with an increased cancer risk in Parkinson disease.

Published in:

Movement Disorders, 2010, v. 25, n. 15, p. 2536, doi. 10.1002/mds.23314

By:

Saunders-Pullman, Rachel;
Barrett, Matthew J.;
Stanley, Kaili M.;
Luciano, Marta San;
Shanker, Vicki;
Severt, Lawrence;
Hunt, Ann;
Raymond, Deborah;
Ozelius, Laurie J.;
Bressman, Susan B.

Publication type:

Article

Genetic evidence for an association of the TOR1A locus with segmental/focal dystonia.

Published in:

Movement Disorders, 2010, v. 25, n. 13, p. 2183, doi. 10.1002/mds.23225

By:

Sharma, Nutan;
Franco, Ramon A.;
Kuster, John K.;
Mitchell, Adele A.;
Fuchs, Tania;
Saunders-Pullman, Rachel;
Raymond, Deborah;
Brin, Mitchell F.;
Blitzer, Andrew;
Bressman, Susan B.;
Ozelius, Laurie J.

Publication type:

Article

Responsiveness to levodopa in epsilon-sarcoglycan deletions.

Published in:

Movement Disorders, 2009, v. 24, n. 3, p. 425, doi. 10.1002/mds.22375

By:

Luciano, Marta San;
Ozelius, Laurie;
Sims, Katherine;
Raymond, Deborah;
Liu, Liu;
Saunders-Pullman, Rachel

Publication type:

Article

Phenotypic spectrum and sex effects in eleven myoclonus-dystonia families with ε-sarcoglycan mutations.

Published in:

Movement Disorders, 2008, v. 23, n. 4, p. 588, doi. 10.1002/mds.21785

By:

Raymond, Deborah;
Saunders-Pullman, Rachel;
de Carvalho Aguiar, Patricia;
Schule, Birgitt;
Kock, Norman;
Friedman, Jennifer;
Harris, Juliette;
Ford, Blair;
Frucht, Steven;
Heiman, Gary A.;
Jennings, Danna;
Doheny, Dana;
Brin, Mitchell F.;
de Leon Brin, Deborah;
Multhaupt-Buell, Trisha;
Lang, Anthony E.;
Kurlan, Roger;
Klein, Christine;
Ozelius, Laurie;
Bressman, Susan

Publication type:

Article

Association of Dual LRRK2 G2019S and GBA Variations With Parkinson Disease Progression.

Published in:

JAMA Network Open, 2021, v. 4, n. 4, p. e215845, doi. 10.1001/jamanetworkopen.2021.5845

By:

Ortega, Roberto A.;
Wang, Cuiling;
Raymond, Deborah;
Bryant, Nicole;
Scherzer, Clemens R.;
Thaler, Avner;
Alcalay, Roy N.;
West, Andrew B.;
Mirelman, Anat;
Kuras, Yuliya;
Marder, Karen S.;
Giladi, Nir;
Ozelius, Laurie J.;
Bressman, Susan B.;
Saunders-Pullman, Rachel

Publication type:

Article

Genetic risk variants in New Yorkers of Puerto Rican and Dominican Republic heritage with Parkinson's disease.

Published in:

NPJ Parkinson's Disease, 2023, v. 9, n. 1, p. 1, doi. 10.1038/s41531-023-00599-6

By:

Miltenberger-Miltenyi, Gabriel;
Ortega, Roberto A.;
Domingo, Aloysius;
Yadav, Rachita;
Nishiyama, Ayumi;
Raymond, Deborah;
Katsnelson, Viktoriya;
Urval, Nikita;
Swan, Matthew;
Shanker, Vicki;
Miravite, Joan;
Walker, Ruth H.;
Bressman, Susan B.;
Ozelius, Laurie J.;
Cabassa, José C.;
Saunders-Pullman, Rachel

Publication type:

Article

The influence of density on frequency-dependent food selection: a comparison of four experiments with wild birds.

Published in:

Oecologia, 2000, v. 124, n. 3, p. 391, doi. 10.1007/s004420000399

By:

Weale, Michael E.;
Whitwell, Diana;
Raison, Helen E.;
Raymond, Deborah L.;
Allen, John A.

Publication type:

Article

Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes.

Published in:

Human Molecular Genetics, 2014, v. 23, n. 17, p. 4693, doi. 10.1093/hmg/ddu158

By:

Vacic, Vladimir;
Ozelius, Laurie J.;
Clark, Lorraine N.;
Bar-Shira, Anat;
Gana-Weisz, Mali;
Gurevich, Tanya;
Gusev, Alexander;
Kedmi, Merav;
Kenny, Eimear E.;
Liu, Xinmin;
Mejia-Santana, Helen;
Mirelman, Anat;
Raymond, Deborah;
Saunders-Pullman, Rachel;
Desnick, Robert J.;
Atzmon, Gil;
Burns, Edward R.;
Ostrer, Harry;
Hakonarson, Hakon;
Bergman, Aviv

Publication type:

Article

Multiple sclerosis in LRRK2 G2019S Parkinson's disease and isolated nigral degeneration in a homozygous variant carrier.

Published in:

Frontiers in Neurology, 2024, p. 01, doi. 10.3389/fneur.2024.1450654

By:

Wise, Adina;
Ortega, Roberto A.;
Raymond, Deborah;
Cervera, Alessandra;
Thorn, Emma;
Leaver, Katherine;
Russell, David S.;
Bressman, Susan B.;
Crary, John F.;
Saunders-Pullman, Rachel

Publication type:

Article

The phenotypic spectrum of rapid-onset dystonia–parkinsonism (RDP) and mutations in the ATP1A3 gene.

Published in:

Brain: A Journal of Neurology, 2007, v. 130, n. 3, p. 828, doi. 10.1093/brain/awl340

By:

Allison Brashear;
William B. Dobyns;
Patricia de Carvalho Aguiar;
Michel Borg;
C. J. M. Frijns;
Seema Gollamudi;
Andrew Green;
João Guimaraes;
Bret C. Haake;
Christine Klein;
Gurutz Linazasoro;
Alexander Münchau;
Deborah Raymond;
David Riley;
Rachel Saunders-Pullman;
Marina A. J. Tijssen;
David Webb;
Jacek Zaremba;
Susan B. Bressman;
Laurie J. Ozelius

Publication type:

Article

The metabolic pathology of dopa‐responsive dystonia.

Published in:

Annals of Neurology, 2005, v. 57, n. 4, p. 596

By:

Kotaro Asanuma;
Yilong Ma;
Chaorui Huang;
Maren Carbon‐Correll;
Christine Edwards;
Deborah Raymond;
Susan B. Bressman;
James R. Moeller;
David Eidelberg

Publication type:

Article

Primary dystonia: Is abnormal functional brain architecture linked to genotype?

Published in:

Annals of Neurology, 2002, v. 52, n. 6, p. 853, doi. 10.1002/ana.10418

By:

Tros̆t, Maja;
Carbon, Maren;
Edwards, Christine;
Ma, Yilong;
Raymond, Deborah;
Mentis, Marc J.;
Moeller, James R.;
Bressman, Susan B.;
Eidelberg, David

Publication type:

Article

Evaluation of the role of the D2 dopamine receptor in myoclonus dystonia.

Published in:

Annals of Neurology, 2000, v. 47, n. 3, p. 369, doi. 10.1002/1531-8249(200003)47:3<369::AID-ANA14>3.0.CO;2-9

By:

Klein, Christine;
Gurvich, Nadia;
Sena-Esteves, Miguel;
Bressman, Susan;
Brin, Mitchell F.;
Ebersole, Barbara J.;
Fink, Stephen;
Forsgren, Lars;
Friedman, Jennifer;
Grimes, David;
Holmgren, Gosta;
Kyllerman, Mårtin;
Lang, Anthony E.;
De Leon, Deborah;
Leung, Joanne;
Prioleau, Cassandra;
Raymond, Deborah;
Sanner, Gunnar;
Saunders-Pullman, Rachel;
Vieregge, Peter

Publication type:

Article

Localization of a gene for myoclonus-dystonia to chromosome 7q21-q31.

Published in:

1999

By:

Nygaard, Torbjoern G.;
Raymond, Deborah;
Chen, Caiping;
Nishino, Ichizo;
Greene, Paul E.;
Jennings, Danna;
Heiman, Gary A.;
Klein, Christine;
Saunders-Pullman, Rachel J.;
Kramer, Patricia;
Ozelius, Laurie J.;
Bressman, Susan B.;
Nygaard, T G;
Raymond, D;
Chen, C;
Nishino, I;
Greene, P E;
Jennings, D;
Heiman, G A;
Klein, C

Publication type:

journal article

Interest in Genetic Testing in Ashkenazi Jewish Parkinson's Disease Patients and Their Unaffected Relatives.

Published in:

Journal of Genetic Counseling, 2015, v. 24, n. 2, p. 238, doi. 10.1007/s10897-014-9756-x

By:

Gupte, Manisha;
Alcalay, Roy;
Mejia-Santana, Helen;
Raymond, Deborah;
Saunders-Pullman, Rachel;
Roos, Ernest;
Orbe-Reily, Martha;
Tang, Ming-X;
Mirelman, Anat;
Ozelius, Laurie;
Orr-Urtreger, Avi;
Clark, Lorraine;
Giladi, Nir;
Bressman, Susan;
Marder, Karen

Publication type:

Article

Genetic Testing in Parkinson's Disease.

Published in:

Movement Disorders, 2023, v. 38, n. 8, p. 1384, doi. 10.1002/mds.29500

By:

Pal, Gian;
Cook, Lola;
Schulze, Jeanine;
Verbrugge, Jennifer;
Alcalay, Roy N.;
Merello, Marcelo;
Sue, Carolyn M.;
Bardien, Soraya;
Bonifati, Vincenzo;
Chung, Sun Ju;
Foroud, Tatiana;
Gatto, Emilia;
Hall, Anne;
Hattori, Nobutaka;
Lynch, Tim;
Marder, Karen;
Mascalzoni, Deborah;
Novaković, Ivana;
Thaler, Avner;
Raymond, Deborah

Publication type:

Article

International Genetic Testing and Counseling Practices for Parkinson's Disease.

Published in:

Movement Disorders, 2023, v. 38, n. 8, p. 1527, doi. 10.1002/mds.29442

By:

Saunders‐Pullman, Rachel;
Raymond, Deborah;
Ortega, Roberto A.;
Shalash, Ali;
Gatto, Emilia;
Salari, Mehri;
Markgraf, Maggie;
Alcalay, Roy N.;
Mascalzoni, Deborah;
Mencacci, Niccolò E.;
Bonifati, Vincenzo;
Merello, Marcelo;
Chung, Sun Ju;
Novakovic, Ivana;
Bardien, Soraya;
Pal, Gian;
Hall, Anne;
Hattori, Nobutaka;
Lynch, Timothy;
Thaler, Avner

Publication type:

Article

Differences in Sex‐Specific Frequency of Glucocerebrosidase Variant Carriers and Familial Parkinsonism.

Published in:

Movement Disorders, 2023, v. 38, n. 4, p. 714, doi. 10.1002/mds.29353

By:

Ortega, Roberto A.;
Bressman, Susan B.;
Raymond, Deborah;
Ozelius, Laurie J.;
Wang, Cuiling;
Bennett, Steffany A.L.;
Saunders‐Pullman, Rachel

Publication type:

Article

Differences in Sex‐Specific Frequency of Glucocerebrosidase Variant Carriers and Familial Parkinsonism.

Published in:

Movement Disorders, 2022, v. 37, n. 11, p. 2217, doi. 10.1002/mds.29197

By:

Ortega, Roberto A.;
Bressman, Susan B.;
Raymond, Deborah;
Ozelius, Laurie J.;
Katsnelson, Viktoriya;
Leaver, Katherine;
Swan, Matthew C.;
Shanker, Vicki;
Miravite, Joan;
Wang, Cuiling;
Bennett, Steffany A.L.;
Saunders‐Pullman, Rachel

Publication type:

Article

Assessment of Glucocerebrosidase Enzyme Activity in Parkinson Disease Using Multiple Approaches.

Published in:

Movement Disorders, 2022, v. 37, n. 3, p. 655, doi. 10.1002/mds.28951

By:

Ortega, Roberto A.;
Bodamer, Olaf;
Peake, Roy W.A.;
Raymond, Deborah;
Bressman, Susan B.;
Saunders‐Pullman, Rachel

Publication type:

Article

Cancer outcomes among Parkinson's disease patients with leucine rich repeat kinase 2 mutations, idiopathic Parkinson's disease patients, and nonaffected controls.

Published in:

2019

By:

Agalliu, Ilir;
Ortega, Roberto A.;
Luciano, Marta San;
Mirelman, Anat;
Pont‐Sunyer, Claustre;
Brockmann, Kathrin;
Vilas, Dolores;
Tolosa, Eduardo;
Berg, Daniela;
Warø, Bjørg;
Glickman, Amanda;
Raymond, Deborah;
Inzelberg, Rivka;
Ruiz‐Martinez, Javier;
Mondragon, Elisabet;
Friedman, Eitan;
Hassin‐Baer, Sharon;
Alcalay, Roy N.;
Mejia‐Santana, Helen;
Aasly, Jan

Publication type:

journal article

Deep Brain Stimulation in Isolated Dystonia With a GNAL Mutation.

Published in:

2019

By:

Sarva, Harini;
Trosch, Richard;
Kiss, Zelma H.T.;
Furtado, Sarah;
Luciano, Marta San;
Glickman, Amanda;
Raymond, Deborah;
Ozelius, Laurie J.;
Bressman, Susan B.;
Saunders‐Pullman, Rachel;
Saunders-Pullman, Rachel

Publication type:

Letter

Increased substantia nigra echogenicity in LRRK2 family members without mutations.

Published in:

2018

By:

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

Publication type:

Letter

Application of the Movement Disorder Society prodromal criteria in healthy G2019S-LRRK2 carriers.

Published in:

2018

By:

Mirelman, Anat;
Saunders‐Pullman, Rachel;
Alcalay, Roy N.;
Shustak, Shiran;
Thaler, Avner;
Gurevich, Tanya;
Raymond, Deborah;
Mejia‐Santana, Helen;
Orbe Reilly, Martha;
Ozelius, Laurie;
Clark, Lorraine;
Gana‐Weisz, Mali;
Bar‐Shira, Anat;
Orr‐Utreger, Avi;
Bressman, Susan B.;
Marder, Karen;
Giladi, Nir;
the AJ LRRK2 Consortium;
Saunders-Pullman, Rachel;
Mejia-Santana, Helen

Publication type:

journal article

IN A NEIGHBORHOOD NEAR YOU: HOW COMMUNITY HEALTH WORKERS HELP PEOPLE OBTAIN HEALTH INSURANCE AND PRIMARY CARE.

Published in:

Journal of Health Care for the Poor & Underserved, 2014, v. 25, n. 1, p. lviii, doi. 10.1353/hpu.2014.0028

By:

Lang, Debi;
Cragin, Linda J.;
Raymond, Deborah;
Kane, Sue

Publication type:

Article

Benign SLC39A14 Course of Dystonia‐Parkinsonism Secondary to Inherited Manganese Accumulation.

Published in:

Movement Disorders Clinical Practice, 2020, v. 7, n. 5, p. 569, doi. 10.1002/mdc3.12947

By:

Namnah, Montaser;
Bauer, Max;
Mor‐Shaked, Hagar;
Bressman, Susan B.;
Raymond, Deborah;
Ozelius, Laurie J.;
Arkadir, David

Publication type:

Article

Cognitive Functioning of Glucocerebrosidase (GBA) Non-manifesting Carriers.

Published in:

Frontiers in Neurology, 2021, v. 11, p. N.PAG, doi. 10.3389/fneur.2021.635958

By:

Moran, Eileen E.;
Bressman, Susan B.;
Ortega, Roberto A.;
Raymond, Deborah;
Nichols, William C.;
Palmese, Christina A.;
Elango, Sonya;
Swan, Matthew;
Shanker, Vicki;
Perera, Imali;
Wang, Cuiling;
Zimmerman, Molly E.;
Saunders-Pullman, Rachel

Publication type:

Article

Plant uptake and leaching of dimethylnitrosamine.

Published in:

Nature, 1976, v. 262, n. 5567, p. 394, doi. 10.1038/262394a0

By:

DEAN-RAYMOND, DEBORAH;
ALEXANDER, M.

Publication type:

Article

DYT1 dystonia increases risk taking in humans.

Published in:

eLife, 2016, p. 1, doi. 10.7554/eLife.14155

By:

Arkadir, David;
Radulescu, Angela;
Raymond, Deborah;
Lubarr, Naomi;
Bressman, Susan B.;
Mazzoni, Pietro;
Niv, Yael

Publication type:

Article