Neurology &ndash; Research Output

2019

Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function (Nature Communications, (2018), 9, 1, (2098), 10.1038/s41467-018-04362-x)

Davies, G., Lam, M., Harris, S. E., Trampush, J. W., Luciano, M., Hill, W. D., Hagenaars, S. P., Ritchie, S. J., Marioni, R. E., Fawns-Ritchie, C., Liewald, D. C. M., Okely, J. A., Ahola-Olli, A. V., Barnes, C. L. K., Bertram, L., Bis, J. C., Burdick, K. E., Christoforou, A., DeRosse, P., Djurovic, S. & 202 others, Espeseth, T., Giakoumaki, S., Giddaluru, S., Gustavson, D. E., Hayward, C., Hofer, E., Ikram, M. A., Karlsson, R., Knowles, E., Lahti, J., Leber, M., Li, S., Mather, K. A., Melle, I., Morris, D., Oldmeadow, C., Palviainen, T., Payton, A., Pazoki, R., Petrovic, K., Reynolds, C. A., Sargurupremraj, M., Scholz, M., Smith, J. A., Smith, A. V., Terzikhan, N., Thalamuthu, A., Trompet, S., van der Lee, S. J., Ware, E. B., Windham, B. G., Wright, M. J., Yang, J., Yu, J., Ames, D., Amin, N., Amouyel, P., Andreassen, O. A., Armstrong, N. J., Assareh, A. A., Attia, J. R., Attix, D., Avramopoulos, D., Bennett, D. A., Böhmer, A. C., Boyle, P. A., Brodaty, H., Campbell, H., Cannon, T. D., Cirulli, E. T., Congdon, E., Conley, E. D., Corley, J., Cox, S. R., Dale, A. M., Dehghan, A., Dick, D., Dickinson, D., Eriksson, J. G., Evangelou, E., Faul, J. D., Ford, I., Freimer, N. A., Gao, H., Giegling, I., Gillespie, N. A., Gordon, S. D., Gottesman, R. F., Griswold, M. E., Gudnason, V., Harris, T. B., Hartmann, A. M., Hatzimanolis, A., Heiss, G., Holliday, E. G., Joshi, P. K., Kähönen, M., Kardia, S. L. R., Karlsson, I., Kleineidam, L., Knopman, D. S., Kochan, N. A., Konte, B., Kwok, J. B., Le Hellard, S., Lee, T., Lehtimäki, T., Li, S. C., Lill, C. M., Liu, T., Koini, M., London, E., Longstreth, W. T., Lopez, O. L., Loukola, A., Luck, T., Lundervold, A. J., Lundquist, A., Lyytikäinen, L. P., Martin, N. G., Montgomery, G. W., Murray, A. D., Need, A. C., Noordam, R., Nyberg, L., Ollier, W., Papenberg, G., Pattie, A., Polasek, O., Poldrack, R. A., Psaty, B. M., Reppermund, S., Riedel-Heller, S. G., Rose, R. J., Rotter, J. I., Roussos, P., Rovio, S. P., Saba, Y., Sabb, F. W., Sachdev, P. S., Satizabal, C. L., Schmid, M., Scott, R. J., Scult, M. A., Simino, J., Slagboom, P. E., Smyrnis, N., Soumaré, A., Stefanis, N. C., Stott, D. J., Straub, R. E., Sundet, K., Taylor, A. M., Taylor, K. D., Tzoulaki, I., Tzourio, C., Uitterlinden, A., Vitart, V., Voineskos, A. N., Kaprio, J., Wagner, M., Wagner, H., Weinhold, L., Wen, K. H., Widen, E., Yang, Q., Zhao, W., Adams, H. H. H., Arking, D. E., Bilder, R. M., Bitsios, P., Boerwinkle, E., Chiba-Falek, O., Corvin, A., De Jager, P. L., Debette, S., Donohoe, G., Elliott, P., Fitzpatrick, A. L., Gill, M., Glahn, D. C., Hägg, S., Hansell, N. K., Hariri, A. R., Ikram, M. K., Jukema, J. W., Vuoksimaa, E., Keller, M. C., Kremen, W. S., Launer, L., Lindenberger, U., Palotie, A., Pedersen, N. L., Pendleton, N., Porteous, D. J., Räikkönen, K., Raitakari, O. T., Ramirez, A., Reinvang, I., Rudan, I., Dan Rujescu, R., Schmidt, R., Schmidt, H., Schofield, P. W., Schofield, P. R., Starr, J. M., Steen, V. M., Trollor, J. N., Turner, S. T., Van Duijn, C. M., Villringer, A., Weinberger, D. R., Weir, D. R., Wilson, J. F., Malhotra, A., McIntosh, A. M., Gale, C. R., Seshadri, S., Mosley, T. H., Bressler, J., Lencz, T. & Deary, I. J., Dec 1 2019, In : Nature communications. 10, 1, 2068.

Research output: Contribution to journal › Comment/debate

Open Access

document markup languages

HTML

Genetic Loci

loci

lists

Corrigendum to “Modulation of mitochondrial complex I activity averts cognitive decline in multiple animal models of familial Alzheimer's disease” [EBioMedicine 2 (2015) 294–305] (Modulation of Mitochondrial Complex I Activity Averts Cognitive Decline in Multiple Animal Models of Familial Alzheimer's Disease (2015) 2(4) (294–305), (S2352396415000729), (10.1016/j.ebiom.2015.03.009))

Zhang, L., Zhang, S., Maezawa, I., Trushin, S., Minhas, P., Pinto, M., Jin, L. W., Prasain, K., Nguyen, T. D. T., Yamazaki, Y., Kanekiyo, T., Bu, G. D., Gateno, B., Chang, K. O., Nath, K. A., Nemutlu, E., Dzeja, P. P., Pang, Y-P., Hua, D. H. & Trushina, E. D., Apr 1 2019, In : EBioMedicine. 42, 1 p.

Research output: Contribution to journal › Comment/debate

Open Access

Brain

Alzheimer Disease

Animals

Animal Models

Modulation

Corrigendum to “Porphyria: A rare differential diagnosis of polyradiculoneuropathy” (Journal of the Neurological Sciences (2019) 402 (153–155), (S0022510X19302370), (10.1016/j.jns.2019.05.021))

Ali, F., Kumar, N., Dyck, P. J. B., Klaas, J. & Berini, S., Aug 15 2019, In : Journal of the neurological sciences. 403, 1 p.

Research output: Contribution to journal › Comment/debate

Open Access

Polyradiculoneuropathy

Authorship

Porphyrias

Emotions

Differential Diagnosis

1 Citation (Scopus)

Episodic ataxia in CASPR2 autoimmunity

López Chiriboga, A. S. & Pittock, S. J., Mar 1 2019, In : Neurology: Neuroimmunology and NeuroInflammation. 6, 2, e536.

Research output: Contribution to journal › Comment/debate

Open Access

Autoimmunity

Episodic Ataxia

Erratum: De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias (The American Journal of Human Genetics (2018) 103(5) (666–678), (S0002929718303173), (10.1016/j.ajhg.2018.09.006))

Task Force for Neonatal Genomics & Deciphering Developmental Disorders Study, Mar 7 2019, In : American journal of human genetics. 104, 3, 1 p.

Research output: Contribution to journal › Comment/debate

Megalencephaly

Dyskinesias

Medical Genetics

Brain Diseases

Contracture

Erratum: Rabinstein AA. Lifelong Learning in Neurology(CONTINUUM Lifelong Learning in Neurology (2018) 24:6 (1708-1731) DOI :10.1212/CON.0000000000000666)

Rabinstein, A., Apr 1 2019, In : CONTINUUM Lifelong Learning in Neurology. 25, 2, 1 p.

Research output: Contribution to journal › Comment/debate

Continuity of Patient Care

Brain Death

Neurology

Coma

Learning

1 Citation (Scopus)

Hypertrophic olivary degeneration mimics relapse in neuromyelitis optica spectrum disorder

Sechi, E., Parks, N. E., Koeller, K. K. & Flanagan, E., Feb 12 2019, In : Neurology. 92, 7, p. 343-344 2 p.

Research output: Contribution to journal › Comment/debate

Open Access

Neuromyelitis Optica

Recurrence

Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (Nature Genetics, (2018), 50, 4, (524-537), 10.1038/s41588-018-0058-3)

AFGen Consortium, Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium, International Genomics of Blood Pressure (iGEN-BP) Consortium, INVENT Consortium, STARNET, BioBank Japan Cooperative Hospital Group, COMPASS Consortium, EPIC-CVD Consortium, EPIC-InterAct Consortium, International Stroke Genetics Consortium (ISGC), METASTROKE Consortium, Neurology Working Group of the CHARGE Consortium, NINDS Stroke Genetics Network (SiGN), UK Young Lacunar DNA Study & MEGASTROKE Consortium, Jan 1 2019, In : Nature Genetics.

Research output: Contribution to journal › Comment/debate

Open Access

Genome-Wide Association Study

Stroke

2 Citations (Scopus)

The apnea test in brain death determination using oxygen diffusion method remains safe

Daneshmand, A., Rabinstein, A. & Wijdicks, E. F. M., Feb 19 2019, In : Neurology. 92, 8, p. 386-387 2 p.

Research output: Contribution to journal › Comment/debate

Brain Death

Apnea

Oxygen

Thunderclap Headache and Cerebral Vasoconstriction Secondary to Pheochromocytoma

English, S. W. & Nasr, D., Apr 1 2019, In : JAMA neurology. 76, 4, p. 502-503 2 p.

Research output: Contribution to journal › Comment/debate

Primary Headache Disorders

Pheochromocytoma

Vasoconstriction

2018

4 Citations (Scopus)

Author response: Practice guideline update summary: Mild cognitive impairment: Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of Neurology

Petersen, R. C., Lopez, O., Armstrong, M. J., Getchius, T. S. D., Ganguli, M., Gloss, D., Gronseth, G. S., Marson, D., Pringsheim, T., Day, G. S., Sager, M., Stevens, J. & Rae-Grant, A., Aug 21 2018, In : Neurology. 91, 8, p. 373-374 2 p.

Research output: Contribution to journal › Comment/debate

Practice Guidelines

Guidelines

Cognitive Dysfunction

Corrigendum to “Congenital myasthenic syndromes in Turkey: Clinical clues and prognosis with long term follow-up” [Neuromuscular Disorders 28/4 (2018) 315–322] (Neuromuscular Disorders (2018) 28(4) (315–322), (S0960896617312324) (10.1016/j.nmd.2017.11.013))

Durmus, H., Shen, X. M., Serdaroglu-Oflazer, P., Kara, B., Parman-Gulsen, Y., Ozdemir, C., Brengman, J., Deymeer, F. & Engel, A. G., Oct 1 2018, In : Neuromuscular Disorders. 28, 10, 1 p.

Research output: Contribution to journal › Comment/debate

Congenital Myasthenic Syndromes

Turkey

Emotions

Mutation

corrigendum

Equipoise dumbbell

Kallmes, D. F., Kallmes, K., Goyal, M., Hirsch, J. A., Rabinstein, A., Brinjikji, W. & Derdeyn, C., Jul 1 2018, In : Journal of neurointerventional surgery. 10, 7, p. 609-610 2 p.

Research output: Contribution to journal › Comment/debate

Stroke

boldenone undecylenate

11 Citations (Scopus)

Erratum: The Cancer Genome Atlas Comprehensive Molecular Characterization of Renal Cell Carcinoma (Cell Reports (2018) 23(1) (313–326.e5) (S2211124718304364) (10.1016/j.celrep.2018.03.075))

The Cancer Genome Atlas Research Network & The Cancer Genome Atlas Research Network, Jun 19 2018, In : Cell Reports. 23, 12, 1 p.

Research output: Contribution to journal › Comment/debate

Atlases

Renal Cell Carcinoma

Names

Emotions

Genes

18 Citations (Scopus)

Erratum: Comprehensive Characterization of Cancer Driver Genes and Mutations (ARTICLE (2018) 173(2) (371–385), (S009286741830237X), (10.1016/j.cell.2018.02.060))

The MC3 Working Group & The Cancer Genome Atlas Research Network, Aug 9 2018, In : Cell. 174, 4, p. 1034-1035 2 p.

Research output: Contribution to journal › Comment/debate

Neoplasm Genes

Adenocarcinoma

Genes

Mutation

ethyl-2-methylthio-4-methyl-5-pyrimidine carboxylate

Erratum: When do α-synucleinopathies start? An epidemiological timeline: A review (JAMA Neurology (2018) 75:4 (503-509) DOI: 10.1001/jamaneurol.2017.4243)

Savica, R., Boeve, B. F. & Mielke, M. M., Apr 1 2018, In : JAMA Neurology. 75, 9, 1 p.

Research output: Contribution to journal › Comment/debate

Neurology

Names

TimeLine

Erratum to: Neuroimmune disorders of the central nervous system in children in the molecular era (Nature Reviews Neurology, (2018), 14, 7, (433-445), 10.1038/s41582-018-0024-9)

on behalf of the attendees of the International Neuroimmune Meeting, Jul 1 2018, In : Nature Reviews Neurology. 14, 12, 1 p.

Research output: Contribution to journal › Comment/debate

Central Nervous System Diseases

Neurology

Names

1 Citation (Scopus)

Fitting TDP-43 into the APOE ε4 and neurodegeneration story

Josephs, K. A., Sep 1 2018, In : The Lancet Neurology. 17, 9, p. 735-737 3 p.

Research output: Contribution to journal › Comment/debate

He struggled with walking and talking … But why?

Duffy, J. R., Feb 1 2018, In : ASHA Leader. 23, 2, p. 44-45 2 p.

Research output: Contribution to journal › Comment/debate

Articulation Disorders

Gait

Walking

Referral and Consultation

Less effective and more expensive: Is it time to move on from rectal diazepam?

Nickels, K. C., Jan 1 2018, In : Epilepsy Currents. 18, 1, p. 27-28 2 p.

Research output: Contribution to journal › Comment/debate

Diazepam

NORSE versus FIRES: What’s in a name?

Nickels, K. C., Sep 1 2018, In : Epilepsy Currents. 18, 5, p. 301-303 3 p.

Research output: Contribution to journal › Comment/debate

Names

1 Citation (Scopus)

Quantitative analysis of agrammatism in agrammatic primary progressive aphasia and dominant apraxia of speech

Tetzloff, K. A., Utianski, R. L., Duffy, J. R., Clark, H., Strand, E. A., Josephs, K. A. & Whitwell, J. L., Sep 1 2018, In : Journal of Speech, Language, and Hearing Research. 61, 9, p. 2337-2346 10 p.

Research output: Contribution to journal › Comment/debate

Primary Progressive Aphasia

Broca Aphasia

Apraxias

speech disorder

Linguistics

2 Citations (Scopus)

Rest in peace FTDP-17

Josephs, K. A., Feb 1 2018, In : Brain. 141, 2, p. 324-326 3 p.

Research output: Contribution to journal › Comment/debate

Frontotemporal Dementia

Teaching NeuroImages: Not a typical spinalmass

Singh, T. D., Swanson, A., Burrows, A. M., Clarke, M., Shah, S. M., Ali, F. & Coon, E., Aug 21 2018, In : Neurology. 91, 8, p. e790-e791

Research output: Contribution to journal › Comment/debate

Teaching

3 Citations (Scopus)

The heart-brain team-towards optimal team-based coordinated care

Alkhouli, M., Graff-Radford, J. & Holmes, D., Mar 1 2018, In : JAMA Cardiology. 3, 3, p. 187-188 2 p.

Research output: Contribution to journal › Comment/debate

Brain

The Telephone Interview for Cognitive Status

Knopman, D. S., Sep 1 2018, In : Cognitive and Behavioral Neurology. 31, 3, 1 p.

Research output: Contribution to journal › Comment/debate

Interviews

2 Citations (Scopus)

To be or not 2b? to see or not 2c? Alas, the clock is ticking on TICI

Kallmes, D. F., Rabinstein, A. & Gounis, M. J., Apr 1 2018, In : Journal of NeuroInterventional Surgery. 10, 4, p. 323-324 2 p.

Research output: Contribution to journal › Comment/debate

2017

3 Citations (Scopus)

A diagnostic marker to discriminate childhood apraxia of speech from speech delay: Introduction

Shriberg, L. D., Strand, E. A., Fourakis, M., Jakielski, K. J., Hall, S. D., Karlsson, H. B., Mabie, H. L., McSweeny, J. L., Tilkens, C. M. & Wilson, D. L., Apr 1 2017, In : Journal of Speech, Language, and Hearing Research. 60, 4, p. S1094-S1095

Research output: Contribution to journal › Comment/debate

Language Development Disorders

Apraxias

diagnostic

childhood

Childhood Apraxia of Speech

2 Citations (Scopus)

Appraising ApraxiaWhen a speech-sound disorder is severe, how do you know if it's childhood apraxia of speech?

Strand, E., Mar 1 2017, In : ASHA Leader. 22, 3, p. 50-58 9 p.

Research output: Contribution to journal › Comment/debate

Apraxias

Speech Sound Disorder

1 Citation (Scopus)

Clinical/scientific notes: Dacrystic seizures: A cry for help

Gadoth, A., Singh, J., Britton, J. W., Flanagan, E. P. & Pittock, S. J., 2017, In : Neurology: Neuroimmunology and NeuroInflammation. 4, 4

Research output: Contribution to journal › Comment/debate

Seizures

Clinical commentary on ‘Aquaporin-4-IgG-positive neuromyelitis optica spectrum disorder with recurrent short partial transverse myelitis and favorable prognosis: Two new cases’, by Wang et al.

Flanagan, E., Dec 1 2017, In : Multiple Sclerosis. 23, 14, p. 1954-1955 2 p.

Research output: Contribution to journal › Comment/debate

Transverse Myelitis

Aquaporin 4

Neuromyelitis Optica

Immunoglobulin G

Correction: The complex genetics of gait speed: Genome-wide metaanalysis approach [Aging, (Albany NY), 9, 1, (2017), (209-246)]doi 10.18632/aging.101151

Ben-Avraham, D., Karasik, D., Verghese, J., Lunetta, K. L., Smith, J. A., Eicher, J. D., Vered, R., Deelen, J., Arnold, A. M., Buchman, A. S., Tanaka, T., Faul, J. D., Nethander, M., Fornage, M., Adams, H. H., Matteini, A. M., Callisaya, M. L., Smith, A. V., Yu, L., De Jager, P. L. & 50 others, Evans, D. A., Gudnason, V., Hofman, A., Pattie, A., Corley, J., Launer, L. J., Knopman, D. S., Parimi, N., Turner, S. T., Bandinelli, S., Beekman, M., Gutman, D., Sharvit, L., Mooijaart, S. P., Liewald, D. C., Houwing-Duistermaat, J. J., Ohlsson, C., Moed, M., Verlinden, V. J., Mellström, D., van der Geest, J. N., Karlsson, M., Hernandez, D., McWhirter, R., Liu, Y., Thomson, R., Tranah, G. J., Uitterlinden, A. G., Weir, D. R., Zhao, W., Starr, J. M., Johnson, A. D., Arfan Ikram, M., Bennett, D. A., Cummings, S. R., Deary, I. J., Harris, T. B., Kardia, S. L. R., Mosley, T. H., Srikanth, V. K., Windham, B. G., Newman, A. B., Walston, J. D., Davies, G., Evans, D. S., Slagboom, E. P., Ferrucci, L., Kiel, D. P., Murabito, J. M. & Atzmon, G., Jul 1 2017, In : Aging. 9, 7, p. 1844-1846 3 p.

Research output: Contribution to journal › Comment/debate

Genome

Small Nucleolar RNA

Long Noncoding RNA

Genes

Small Nuclear RNA

4 Citations (Scopus)

Early orthostatic hypotension and orthostatic intolerance-more than an observation or annoyance

Singer, W. & Low, P. A., Sep 1 2017, In : JAMA Internal Medicine. 177, 9, p. 1324-1325 2 p.

Research output: Contribution to journal › Comment/debate

Orthostatic Intolerance

Orthostatic Hypotension

Observation

1 Citation (Scopus)

Erratum: De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies (American Journal of Human Genetics (2014) 95(4) (360–370)(S0002929714003838)(10.1016/j.ajhg.2014.08.013))

Appenzeller, S., Balling, R., Barisic, N., Baulac, S., Caglayan, H., Craiu, D., De Jonghe, P., Depienne, C., Dimova, P., Djémié, T., Gormley, P., Guerrini, R., Helbig, I., Hjalgrim, H., Hoffman-Zacharska, D., Jähn, J., Klein, K. M., Koeleman, B., Komarek, V., Krause, R. & 111 others, Kuhlenbäumer, G., Leguern, E., Lehesjoki, A. E., Lemke, J. R., Lerche, H., Linnankivi, T., Marini, C., May, P., Møller, R. S., Muhle, H., Pal, D., Palotie, A., Pendziwiat, M., Robbiano, A., Roelens, F., Rosenow, F., Selmer, K., Serratosa, J. M., Sisodiya, S., Stephani, U., Sterbova, K., Striano, P., Suls, A., Talvik, T., von Spiczak, S., Weber, Y., Weckhuysen, S., Zara, F., Abou-Khalil, B., Sirven, J., Andermann, E., Andermann, F., Amrom, D., Bautista, J. F., Berkovic, S. F., Bluvstein, J., Boro, A., Cascino, G. D., Consalvo, D., Crumrine, P., Devinsky, O., Dlugos, D., Epstein, M. P., Fiol, M., Fountain, N. B., French, J., Friedman, D., Geller, E. B., Glauser, T., Glynn, S., Haas, K., Haut, S. R., Hayward, J., Helmers, S. L., Joshi, S., Kanner, A., Kirsch, H. E., Knowlton, R. C., Kossoff, E. H., Kuperman, R., Kuzniecky, R., Lowenstein, D. H., McGuire, S. M., Motika, P. V., Novotny, E. J., Ottman, R., Paolicchi, J. M., Parent, J., Park, K., Poduri, A., Sadleir, L., Scheffer, I. E., Shellhaas, R. A., Sherr, E., Shih, J. J., Singh, R., Sirven, J., Smith, M. C., Sullivan, J., Thio, L. L., Venkat, A., Vining, E. P. G., Von Allmen, G. K., Weisenberg, J. L., Widdess-Walsh, P., Winawer, M. R., Allen, A. S., Berkovic, S. F., Cossette, P., Delanty, N., Dlugos, D., Eichler, E. E., Epstein, M. P., Glauser, T., Goldstein, D. B., Han, Y., Heinzen, E. L., Johnson, M. R., Kuzniecky, R., Lowenstein, D. H., Marson, A. G., Mefford, H. C., Nieh, S. E., O'Brien, T. J., Ottman, R., Petrou, S., Petrovski, S., Poduri, A., Ruzzo, E. K., Scheffer, I. E. & Sherr, E., Jan 5 2017, In : American Journal of Human Genetics. 100, 1, p. 179 1 p.

Research output: Contribution to journal › Comment/debate

Medical Genetics

Brain Diseases

Synaptic Transmission

Names

Epilepsy

10 Citations (Scopus)

Intracerebral haemorrhage: no good treatment but treatment helps

Rabinstein, A., Feb 11 2017, In : The Lancet. 389, 10069, p. 575-576 2 p.

Research output: Contribution to journal › Comment/debate

Cerebral Hemorrhage

Stroke

Proptosis: A forgotten observation by Miller Fisher on his syndrome

Braksick, S. A., Rabinstein, A. & Wijdicks, E. F. M., Sep 1 2017, In : Neurology. 89, 11, 1 p.

Research output: Contribution to journal › Comment/debate

Miller Fisher Syndrome

Exophthalmos

Observation

2 Citations (Scopus)

Wild-type TTR neuropathy with cardiomyopathy presenting with burning feet

Visser, A. C. & Klein, C. J., Mar 14 2017, In : Neurology. 88, 11, p. 1101-1102 2 p.

Research output: Contribution to journal › Comment/debate

2016

A comparison of tissue-based and recombinant protein-based assays for detecting PCA-TR/DNER-IGG

Alfugham, N., Roforth, M., Komorowski, L., Ott, A., Meyer, W., Probst, C., Lennon, V. A., Pittock, S. J. & McKeon, A. B., 2016, In : Neurology: Neuroimmunology and NeuroInflammation. 3, 6, e294.

Research output: Contribution to journal › Comment/debate

Passive Cutaneous Anaphylaxis

Recombinant Proteins

21 Citations (Scopus)

Central canal enhancement and the trident sign in spinal cord sarcoidosis

Zalewski, N. L., Krecke, K. N., Weinshenker, B. G., Aksamit, A. J., Conway, B. L., McKeon, A. B. & Flanagan, E. P., Aug 16 2016, In : Neurology. 87, 7, p. 743-744 2 p.

Research output: Contribution to journal › Comment/debate

Sarcoidosis

Spinal Cord

Clinical Reasoning: A 73-year-old man with sarcoidosis and multifocal ischemic strokes

Pichler, M., Klaas, J., Temesgen, Z. & Kantarci, O. H., Sep 20 2016, In : Neurology. 87, 12, p. e119-e121

Research output: Contribution to journal › Comment/debate

Sarcoidosis

Stroke

Comment: Network disruption as a common framework for factors contributing to dementia

Jones, D. T., Mar 22 2016, In : Neurology. 86, 12, p. 1118 1 p.

Research output: Contribution to journal › Comment/debate

2 Citations (Scopus)

Comments

Rabinstein, A., Feb 1 2016, In : Neurosurgery. 78, 2, p. 263-264 2 p.

Research output: Contribution to journal › Comment/debate

1 Citation (Scopus)

Correction: Forecasting seizures using bivariate intracranial EEG measures and SVM in naturally occurring canine epilepsy

Brinkmann, B. H., Patterson, E. E., Vite, C., Vasoli, V. M., Crepeau, D., Stead, S. M., Howbert, J. J., Cherkassky, V., Wagenaar, J. B., Litt, B. & Worrell, G. A., May 1 2016, In : PLoS One. 11, 5, e0156476.

Research output: Contribution to journal › Comment/debate

epilepsy

seizures

Canidae

Epilepsy

Seizures

Corrigendum to “Genome-wide association interaction analysis for Alzheimer's disease.” [Neurobiol. Aging (2014) 35 (2436–2443)] (S0197458014003777)(10.1016/j.neurobiolaging.2014.05.014)

Gusareva, E. S., Carrasquillo, M. M., Bellenguez, C., Cuyvers, E., Colon, S., Graff Radford, N. R., Petersen, R. C., Dickson, D. W., Mahachie John, J. M., Bessonov, K., Van Broeckhoven, C., Ramirez, A., Harold, D., Williams, J., Amouyel, P., Sleegers, K., Taner, N., Lambert, J. C. & Van Steen, K., Jan 1 2016, In : Neurobiology of Aging. 37, p. 211 1 p.

Research output: Contribution to journal › Comment/debate

Genome-Wide Association Study

Germany

Psychiatry

Alzheimer Disease

corrigendum