Neurological impact of vasopressin dysregulation and hyponatremia (English)
- New search for: Bhardwaj, A.
- New search for: Bhardwaj, A.
In:
ANNALS OF NEUROLOGY
;
59
, 2
;
229-236
;
2006
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ISSN:
- Article (Journal) / Print
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Title:Neurological impact of vasopressin dysregulation and hyponatremia
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Contributors:Bhardwaj, A. ( author )
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Published in:ANNALS OF NEUROLOGY ; 59, 2 ; 229-236
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Publisher:
- New search for: LITTLE BROWN AND COMPANY
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Publication date:2006-01-01
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Size:8 pages
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ISSN:
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Type of media:Article (Journal)
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Type of material:Print
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Language:English
- New search for: 616.8005 / 161
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Classification:
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© Metadata Copyright the British Library Board and other contributors. All rights reserved.
Table of contents – Volume 59, Issue 2
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 219
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Coxibs and Alzheimer's disease: Should they stay or should they go?Firuzi, Omidreza / Praticò, Domenico et al. | 2006
- 229
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Neurological impact of vasopressin dysregulation and hyponatremiaBhardwaj, Anish et al. | 2006
- 237
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Cleavage of cystatin C in the cerebrospinal fluid of patients with multiple sclerosisIrani, David N. / Anderson, Caroline / Gundry, Rebekah / Cotter, Robert / Moore, Stacy / Kerr, Douglas A. / McArthur, Justin C. / Sacktor, Ned / Pardo, Carlos A. / Jones, Melina et al. | 2006
- 248
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Genotypic and phenotypic spectrum of PANK2 mutations in patients with neurodegeneration with brain iron accumulationHartig, Monika B. / Hörtnagel, Konstanze / Garavaglia, Barbara / Zorzi, Giovanna / Kmiec, Tomasz / Klopstock, Thomas / Rostasy, Kevin / Svetel, Marina / Kostic, Vladimir S. / Schuelke, Markus et al. | 2006
- 257
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Functional role of the basal ganglia in the planning and execution of actionsMonchi, Oury / Petrides, Michael / Strafella, Antonio P. / Worsley, Keith J. / Doyon, Julien et al. | 2006
- 265
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Subcomplexes of human ATP synthase mark mitochondrial biosynthesis disordersCarrozzo, Rosalba / Wittig, Ilka / Santorelli, Filippo M. / Bertini, Enrico / Hofmann, Sabine / Brandt, Ulrich / Schägger, Hermann et al. | 2006
- 276
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Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2Züchner, Stephan / De Jonghe, Peter / Jordanova, Albena / Claeys, Kristl G. / Guergueltcheva, Velina / Cherninkova, Sylvia / Hamilton, Steven R. / Van Stavern, Greg / Krajewski, Karen M. / Stajich, Jeffery et al. | 2006
- 282
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Docosahexaenoic acid reduces levodopa‐induced dyskinesias in 1‐methyl‐4‐phenyl‐1,2,3,6‐tetrahydropyridine monkeysSamadi, Pershia / Grégoire, Laurent / Rouillard, Claude / Bédard, Paul J. / Di Paolo, Thérèse / Lévesque, Daniel et al. | 2006
- 289
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Sarcolemmal reorganization in facioscapulohumeral muscular dystrophyReed, Patrick / Porter, Neil C. / Strong, John / Pumplin, David W. / Corse, Andrea M. / Luther, Paul W. / Flanigan, Kevin M. / Bloch, Robert J. et al. | 2006
- 298
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Clinical heterogeneity of a-synuclein gene duplication in Parkinsons diseaseNishioka, K. / Hayashi, S. / Farrer, M. J. / Singleton, A. B. / Yoshino, H. / Imai, H. / Kitami, T. / Sato, K. / Kuroda, R. / Tomiyama, H. et al. | 2006
- 298
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Clinical heterogeneity of α‐synuclein gene duplication in Parkinson's diseaseNishioka, Kenya / Hayashi, Shin / Farrer, Matthew J. / Singleton, Andrew B. / Yoshino, Hiroyo / Imai, Hisamasa / Kitami, Toshiaki / Sato, Kenichi / Kuroda, Ryu / Tomiyama, Hiroyuki et al. | 2006
- 310
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Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutationVanmolkot, K. R. J. / Stroink, H. / Koenderink, J. B. / Kors, E. E. / van den Heuvel, J. J. M. W. / van den Boogerd, E. H. / Stam, A. H. / Haan, J. / De Vries, B. B. A. / Terwindt, G. M. et al. | 2006
- 315
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Biochemical and pathological characterization of Lrrk2Giasson, Benoit I. / Covy, Jason P. / Bonini, Nancy M. / Hurtig, Howard I. / Farrer, Matthew J. / Trojanowski, John Q. / Van Deerlin, Vivianna M. et al. | 2006
- 323
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Apolipoprotein E and alpha brain rhythms in mild cognitive impairment: A multicentric Electroencephalogram studyBabiloni, Claudio / Benussi, Luisa / Binetti, Giuliano / Cassetta, Emanuele / Dal Forno, Gloria / Del Percio, Claudio / Ferreri, Florinda / Ferri, Raffaele / Frisoni, Giovanni / Ghidoni, Roberta et al. | 2006
- 335
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Functional connectivity networks are disrupted in left temporal lobe epilepsyWaites, Anthony B. / Briellmann, Regula S. / Saling, Michael M. / Abbott, David F. / Jackson, Graeme D. et al. | 2006
- 344
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Defining the response to interferon‐β in relapsing‐remitting multiple sclerosis patientsRío, Jordi / Nos, Carlos / Tintoré, Mar / Téllez, Nieves / Galán, Ingrid / Pelayo, Raúl / Comabella, Manuel / Montalban, Xavier et al. | 2006
- 344
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Defining the response to interferon-b in relapsing-remitting multiple sclerosis patientsRio, J. / Nos, C. / Tintore, M. / Tellez, N. / Galan, I. / Pelayo, R. / Comabella, M. / Montalban, X. et al. | 2006
- 353
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A novel hereditary small vessel disease of the brainVerreault, Steve / Joutel, Anne / Riant, Florence / Neves, Georgina / Rui Silva, Mario / Maciazek, Jacqueline / Tournier‐Lasserve, Elizabeth / Bousser, Marie‐Germaine / Chabriat, Hugues et al. | 2006
- 358
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T118M PMP22 mutation causes partial loss of function and HNPP‐like neuropathyShy, Michael E. / Scavina, Mena T. / Clark, Alisa / Krajewski, Karen M. / Li, Jun / Kamholz, John / Kolodny, Edwin / Szigeti, Kinga / Fischer, Richard A. / Mustafa Saifi, Gulam et al. | 2006
- 365
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Length dependence in polyneuropathy associated with IgM gammopathyFranssen, H. / Notermans, N. C. et al. | 2006
- 372
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Migraine and MTHFR C677T genotype in a population‐based sampleScher, Ann I. / Terwindt, Gisela M. / Verschuren, W. M. Monique / Kruit, Mark C. / Blom, Henk J. / Kowa, Hisanori / Frants, Rune R. / van den Maagdenberg, Arn M. J. M. / van Buchem, Mark / Ferrari, Michel D. et al. | 2006
- 376
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Skin sympathetic adrenergic innervation: An immunofluorescence confocal studyDonadio, Vincenzo / Nolano, Maria / Provitera, Vincenzo / Stancanelli, Annamaria / Lullo, Francesco / Liguori, Rocco / Santoro, Lucio et al. | 2006
- 381
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Increased midbrain gray matter in Tourette's syndromeGarraux, Gaëtan / Goldfine, Andrew / Bohlhalter, Stephan / Lerner, Alicja / Hanakawa, Takashi / Hallett, Mark et al. | 2006
- 385
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Contralateral hand anesthesia transiently improves poststroke sensory deficitsVoller, Bernhard / Flöel, Agnes / Werhahn, Konrad J. / Ravindran, Shashi / Wu, Carolyn W. / Cohen, Leonardo G. et al. | 2006
- 388
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Lrrk2 and Lewy body diseaseRoss, Owen A. / Toft, Mathias / Whittle, Andrew J. / Johnson, Joseph L. / Papapetropoulos, Spiridon / Mash, Deborah C. / Litvan, Irene / Gordon, Mark F. / Wszolek, Zbigniew K. / Farrer, Matthew J. et al. | 2006
- 394
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Cerebral folate deficiency and leukoencephalopathy caused by a mitochondrial DNA deletionPineda, M. / Ormazabal, A. / Lopez-Gallardo, E. / Nascimento, A. / Solano, A. / Herrero, M. D. / Vilaseca, M. A. / Briones, P. / Ibanez, L. / Montoya, J. et al. | 2006
- 398
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Spastic paraplegia type 2 associated with axonal neuropathy and apparent PLP1 position effectLee, Jennifer A. / Madrid, Ricardo E. / Sperle, Karen / Ritterson, Carolyn M. / Hobson, Grace M. / Garbern, James / Lupski, James R. / Inoue, Ken et al. | 2006
- 404
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Association of the PTPN22*R620W polymorphism with autoimmune myasthenia gravisVandiedonck, Claire / Capdevielle, Claire / Giraud, Matthieu / Krumeich, Sophie / Jais, Jean‐Philippe / Eymard, Bruno / Tranchant, Christine / Gajdos, Philippe / Garchon, Henri‐Jean et al. | 2006
- 407
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Low stability of huntington muscle Mitochondria against Ca2+ in R6/2 miceGizatullina, Zemfira Z. / Lindenberg, Katrin S. / Harjes, Phoebe / Chen, Ying / Kosinski, Christoph M. / Landwehrmeyer, Bernhard G. / Ludolph, Albert C. / Striggow, Frank / Zierz, Stephan / Gellerich, Frank N. et al. | 2006
- 411
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Treatment from birth of nonketotic hyperglycinemia due to a novel GLDC mutationKorman, Stanley H. / Wexler, Isaiah D. / Gutman, Alisa / Rolland, Marie‐Odile / Kanno, Junko / Kure, Shigeo et al. | 2006
- 415
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Periventricular leukomalacia specifically affects cortical MEG response to biological motionPavlova, Marina / Marconato, Fabio / Sokolov, Alexander / Braun, Christoph / Birbaumer, Niels / Krägeloh‐Mann, Ingeborg et al. | 2006
- 419
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The human immunodeficiency virus reduces network capacity: Acoustic noise effectTomasi, Dardo / Chang, Linda / de Castro Caparelli, Elisabeth / Telang, Frank / Ernst, Thomas et al. | 2006
- 423
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Periodic electroencephalogram complexes in a patient with variant Creutzfeldt–Jakob diseaseBinelli, Simona / Agazzi, Pamela / Giaccone, Giorgio / Will, Robert G. / Bugiani, Orso / Franceschetti, Silvana / Tagliavini, Fabrizio et al. | 2006
- 428
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Mild‐onset presentation of Canavan's disease associated with novel G212A point mutation in aspartoacylase geneJanson, Christopher G. / Kolodny, Edwin H. / Zeng, Bai‐Jin / Raghavan, Srinivasa / Pastores, Gregory / Torres, Paola / Assadi, Mitra / McPhee, Scott / Goldfarb, Olga / Saslow, Beth et al. | 2006
- 432
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Ictal hemodynamic changes in late‐onset rasmussen encephalitisDi Bonaventura, Carlo / Carnfi, Marco / Vaudano, Anna E. / Pantano, Patrizia / Garreffa, Girolamo / Le Piane, Emilio / Maraviglia, Bruno / Bozzao, Luigi / Manfredi, Mario / Prencipe, Massimiliano et al. | 2006
- 432
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ReplyRosand, Jonathan / Smith, Eric E. / Greenberg, Steven M. et al. | 2006
- 434
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The dominant form of vanishing white matter–like leukoencephalopathy represents autosomal dominant leukodystrophyPtác̆ek, Louis J. / Fu, Ying‐Hui / Koeppen, Arnulf et al. | 2006
- 434
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Optimizing an evidence‐based causative classification system for ischemic strokeSaver, Jeffrey L. et al. | 2006
- 436
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Apoe ϵ2‐ϵ4 genotype is a possible risk factor for primary progressive aphasiaAcciarri, Adele / Masullo, Carlo / Bizzarro, Alessandra / Valenza, Alessandro / Quaranta, Davide / Marra, Camillo / Tiziano, Francesco D. / Brahe, Christina / Seripa, Davide / Matera, Maria G. et al. | 2006
- 437
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Can we identify a CT‐based tissue window for thrombolysis without CTP?Dzialowski, Imanuel / Demchuk, Andrew / Coutts, Shelagh / Hill, Michael / Hudon, Marc / Lee, Ting‐Yim / Von Kummer, Ruediger et al. | 2006
- 438
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Fatigue as a window to the brainDandamudi, Venkata S. R. / Bakshi, Rohit et al. | 2006
- 438
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Toward replacement parts of the brain, implantable biomimetic electronics as neural prosthesesLong, Don M. et al. | 2006
- 439
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Treatment of pediatric neurologic disordersBodensteiner, John et al. | 2006
- 440
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Paediatric movement disorders: Progress in understandingGilbert, Donald L. et al. | 2006
- A11
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ANA Call for Abstracts| 2006
- A12
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CNS Call for Abstracts| 2006