X-linked agammaglobulinemia with hearing impairment, dystonia-parkinsonism, and progressive neurodegeneration (English)
- New search for: Domingo, Aloysius
- New search for: Schmidt, Thomas G. P. M.
- New search for: Barcelon, Ela
- New search for: Lukban, Marissa
- New search for: Westenberger, Ana
- New search for: Klein, Christine
- New search for: Domingo, Aloysius
- New search for: Schmidt, Thomas G. P. M.
- New search for: Barcelon, Ela
- New search for: Lukban, Marissa
- New search for: Westenberger, Ana
- New search for: Klein, Christine
In:
Journal of Neurology
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261
, 11
; 2225-2227
;
2014
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ISSN:
- Article (Journal) / Electronic Resource
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Title:X-linked agammaglobulinemia with hearing impairment, dystonia-parkinsonism, and progressive neurodegeneration
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Contributors:Domingo, Aloysius ( author ) / Schmidt, Thomas G. P. M. ( author ) / Barcelon, Ela ( author ) / Lukban, Marissa ( author ) / Westenberger, Ana ( author ) / Klein, Christine ( author )
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Published in:Journal of Neurology ; 261, 11 ; 2225-2227
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Publisher:
- New search for: Springer Berlin Heidelberg
- New search for: Steinkopff
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Place of publication:[Darmstadt]
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Publication date:2014
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ISSN:
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ZDBID:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
- New search for: 44.90
- Further information on Basic classification
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Keywords:
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Classification:
BKL: 44.90 Neurologie -
Source:
Table of contents – Volume 261, Issue 11
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.
- 2051
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Deep brain stimulation in Parkinson’s disease: meta-analysis of randomized controlled trialsPerestelo-Pérez, L. / Rivero-Santana, A. / Pérez-Ramos, J. / Serrano-Pérez, P. / Panetta, J. / Hilarion, P. et al. | 2014
- 2061
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Progressing haemorrhagic stroke: categories, causes, mechanisms and managementsChen, Shiyu / Zeng, Liuwang / Hu, Zhiping et al. | 2014
- 2079
-
Endolymphatic space size in patients with vestibular migraine and Ménière’s diseaseNakada, Takafumi / Yoshida, Tadao / Suga, Kenji / Kato, Masahiro / Otake, Hironao / Kato, Ken / Teranishi, Masaaki / Sone, Michihiko / Sugiura, Saiko / Kuno, Kayao et al. | 2014
- 2085
-
Mutation frequency of PRKAR1B and the major familial dementia genes in a Dutch early onset dementia cohortCohn-Hokke, P. E. / Wong, T. H. / Rizzu, P. / Breedveld, G. / van der Flier, W. M. / Scheltens, P. / Baas, F. / Heutink, P. / Meijers-Heijboer, E. J. / van Swieten, J. C. et al. | 2014
- 2093
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Testing the validity of a set of diagnostic criteria for sensory neuronopathies: a francophone collaborative studyAntoine, Jean-Christophe / Robert-Varvat, Florence / Maisonobe, Thierry / Créange, Alain / Franques, Jérôme / Mathis, Stéphane / Delmont, Emilien / Kuntzer, Thierry / Lefaucheur, Jean-Pascal / Pouget, Jean et al. | 2014
- 2101
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A 2-year observational study of patients with relapsing-remitting multiple sclerosis converting to glatiramer acetate from other disease-modifying therapies: the COPTIMIZE trialZiemssen, Tjalf / Bajenaru, Ovidiu A. / Carrá, Adriana / de Klippel, Nina / de Sá, João C. / Edland, Astrid / Frederiksen, Jette L. / Heinzlef, Olivier / Karageorgiou, Klimentini E. / Lander Delgado, Rafael H. et al. | 2014
- 2112
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Dopamine transporter availability in motor subtypes of de novo drug-naïve Parkinson’s diseaseMoccia, Marcello / Pappatà, Sabina / Picillo, Marina / Erro, Roberto / Coda, Anna Rita Daniela / Longo, Katia / Vitale, Carmine / Amboni, Marianna / Brunetti, Arturo / Capo, Giuseppe et al. | 2014
- 2119
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The presence of dysautonomia in different subgroups of myasthenia gravis patientsNikolić, Ana / Perić, Stojan / Nišić, Tanja / Popović, Srdjan / Ilić, Miroljub / Stojanović, Vidosava Rakočević / Lavrnić, Dragana et al. | 2014
- 2128
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Hippocampal damage and affective disorders after treatment of cerebral aneurysmsWostrack, Maria / Friedrich, Benjamin / Hammer, Katrin / Harmening, Kathrin / Stankewitz, Anne / Ringel, Florian / Shiban, Ehab / Boeckh-Behrens, Tobias / Prothmann, Sascha / Zimmer, Claus et al. | 2014
- 2136
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Non-convulsive status epilepticus after ischemic stroke: a hospital-based stroke cohort studyBelcastro, Vincenzo / Vidale, Simone / Gorgone, Gaetano / Pisani, Laura Rosa / Sironi, Luigi / Arnaboldi, Marco / Pisani, Francesco et al. | 2014
- 2143
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Clinical characteristics and outcome of intracerebral hemorrhage in young adultsRutten-Jacobs, Loes CA / Maaijwee, Noortje AM / Arntz, Renate M. / Schoonderwaldt, Hennie C. / Dorresteijn, Lucille D. / van Dijk, Ewoud J. / de Leeuw, Frank-Erik et al. | 2014
- 2150
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New-onset psychiatric disorders after corticosteroid therapy in systemic lupus erythematosus: an observational case-series studyNishimura, Katsuji / Omori, Masako / Sato, Eri / Katsumata, Yasuhiro / Gono, Takahisa / Kawaguchi, Yasushi / Harigai, Masayoshi / Yamanaka, Hisashi / Ishigooka, Jun et al. | 2014
- 2159
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Subcutaneous immunoglobulin in CIDP and MMN: a short-term nationwide studyCocito, Dario / Merola, Aristide / Peci, Erdita / Mazzeo, Anna / Fazio, Raffaella / Francia, Ada / Valentino, Paola / Liguori, Rocco / Filosto, Massimiliano / Siciliano, Gabriele et al. | 2014
- 2165
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Novel EXOSC3 mutation causes complicated hereditary spastic paraplegiaHalevy, Ayelet / Lerer, Israela / Cohen, Rony / Kornreich, Liora / Shuper, Avinoam / Gamliel, Moria / Zimerman, Bat-El / Korabi, Isam / Meiner, Vardiella / Straussberg, Rachel et al. | 2014
- 2170
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Heritability in frontotemporal dementia: more missing pieces?Po, Kieren / Leslie, Felicity V. C. / Gracia, Natalie / Bartley, Lauren / Kwok, John B. J. / Halliday, Glenda M. / Hodges, John R. / Burrell, James R. et al. | 2014
- 2178
-
NADPH oxidase (NOX2) activity is a modifier of survival in ALSMarrali, Giuseppe / Casale, Federico / Salamone, Paolina / Fuda, Giuseppe / Caorsi, Cristiana / Amoroso, Antonio / Brunetti, Maura / Restagno, Gabriella / Barberis, Marco / Bertuzzo, Davide et al. | 2014
- 2184
-
Thinking about the end of life: a common issue for patients with Huntington’s diseaseBooij, Suzanne J. / Tibben, Aad / Engberts, Dick P. / Marinus, Johan / Roos, Raymund A. C. et al. | 2014
- 2192
-
ANO10 mutations cause ataxia and coenzyme $ Q_{10} $ deficiencyBalreira, Andrea / Boczonadi, Veronika / Barca, Emanuele / Pyle, Angela / Bansagi, Boglarka / Appleton, Marie / Graham, Claire / Hargreaves, Iain P. / Rasic, Vedrana Milic / Lochmüller, Hanns et al. | 2014
- 2199
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Spinal axis imaging in non-aneurysmal subarachnoid hemorrhage: a prospective cohort studyGermans, Menno R. / Coert, Bert A. / Majoie, Charles B. L. M. / van den Berg, René / Verbaan, Dagmar / Vandertop, W. Peter et al. | 2014
- 2204
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Screening for dopa-responsive dystonia in patients with scans without evidence of dopaminergic deficiency (SWEDD)De Rosa, Anna / Carducci, Claudia / Carducci, Carla / Peluso, Silvio / Lieto, Maria / Mazzella, Andrea / Saccà, Francesco / Brescia Morra, Vincenzo / Pappatà, Sabina / Leuzzi, Vincenzo et al. | 2014
- 2209
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Concomitant accumulation of α-synuclein and TDP-43 in a patient with corticobasal degenerationYamashita, Satoshi / Sakashita, Naomi / Yamashita, Taro / Tawara, Nozomu / Tasaki, Masayoshi / Kawakami, Kensuke / Komohara, Yoshihiro / Fujiwara, Yukio / Kamikawa, Masashi / Nakagawa, Takenobu et al. | 2014
- 2218
-
Rare variant of unknown significance in POLG1 and diagnostic dilemmaPrasun, Pankaj et al. | 2014
- 2221
-
Intraventricular hemorrhage in reversible cerebral vasoconstriction syndromeWilson, Duncan / Marshall, Charles R. / Solbach, Thomas / Watkins, Laurence / Werring, David J. et al. | 2014
- 2225
-
X-linked agammaglobulinemia with hearing impairment, dystonia-parkinsonism, and progressive neurodegenerationDomingo, Aloysius / Schmidt, Thomas G. P. M. / Barcelon, Ela / Lukban, Marissa / Westenberger, Ana / Klein, Christine et al. | 2014
- 2228
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Visual hallucinations: an unusual manifestation of sporadic Creutzfeldt–Jakob disease termed the ‘Heidenhain variant’Gooriah, R. / Dafalla, B. E. A. / Tun, S. / Venugopalan, T. C. / Lwin, K. K. et al. | 2014
- 2230
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Late onset hereditary sensory and autonomic neuropathy with cognitive impairment associated with Y163X prion mutationThemistocleous, Andreas C. / Kennett, Robin / Husain, Masud / Palace, Jacqueline / Mead, Simon / Bennett, David L. H. et al. | 2014
- 2234
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Inherited disorders of the neuromuscular junction: an updateRodríguez Cruz, Pedro M. / Palace, Jacqueline / Beeson, David et al. | 2014
- 2244
-
Accurate diagnosis of inflammatory neuropathiesIngram, Gillian / Robertson, Neil P. et al. | 2014
- 2247
-
Ernest-Charles Lasègue (1816–1883)Dalfardi, Behnam / Mahmoudi Nezhad, Golnoush Sadat et al. | 2013
- 2249
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Hugo Karl Liepmann (1863–1925)Dalfardi, Behnam / Mahmoudi Nezhad, Golnoush Sadat et al. | 2014