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Results 1 to 25 of 20343

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ANTECOLLIS AND LEVODOPA-RESPONSIVE PARKINSONISM ARE LATE FEATURES OF DRAVET SYNDROMEFASANO, Alfonso; BORLOT, Felippe; LANG, Anthony E et al.Neurology. 2014, Vol 82, Num 24, pp 2250-2251, issn 0028-3878, 2 p.Article

AUTOSOMAL RECESSIVE CEREBELLAR ATAXIA OF ADULT ONSET DUE TO STUB1 MUTATIONSDEPONDT, Chantal; DONATELLO, Simona; SIMONIS, Nicolas et al.Neurology. 2014, Vol 82, Num 19, pp 1749-1750, issn 0028-3878, 2 p.Article

Child Neurology: PRRT2-associated movement disorders and differential diagnosesEBRAHIMI-FAKHARI, Darius; KANG, Keun-Sun; KOTZAERIDOU, Urania et al.Neurology. 2014, Vol 83, Num 18, pp 1680-1683, issn 0028-3878, 4 p.Article

Clinical Reasoning: A case of slowly progressive painful paraparesisCORBETTO, Marzia; CAPONE, Fioravante; DENARO, Vincenzo et al.Neurology. 2014, Vol 82, Num 16, pp 1476-1479, issn 0028-3878, 4 p.Article

DBS REDUCED HEMICHOREA ASSOCIATED WITH A DEVELOPMENTAL VENOUS ANOMALY AND MICROBLEEDING IN STNTAO XIE; AWAD, Issam; UN JUNG KANG et al.Neurology. 2014, Vol 82, Num 7, pp 636-637, issn 0028-3878, 2 p.Article

Dopamine receptor signaling in the forebrain: Recent insights and clinical implicationsSAVICA, Rodolfo; BENARROCH, Eduardo E.Neurology. 2014, Vol 83, Num 8, pp 758-767, issn 0028-3878, 10 p.Article

Epigenetic regulation: Basic concepts and relevance to neurologic diseaseKLEIN, Christopher J; BENARROCH, Eduardo E.Neurology. 2014, Vol 82, Num 20, pp 1833-1840, issn 0028-3878, 8 p.Article

HETEROGENEITY IN NEUROLOGIC EDUCATION AND CARE IN ASIAN AND OCEANIAN REGIONMAN MOHAN MEHNDIRATTA; MEHNDIRATTA, Prachi; NATASHA SINGH GULATI et al.Neurology. 2014, Vol 83, Num 9, pp 842-844, issn 0028-3878, 3 p.Article

INCLUSION BODY MYOSITIS AND CHRONIC LYMPHOCYTIC LEUKEMIA: A CASE SERIESBECK, Elizabeth H; AMATO, Anthony A; GREENBERG, Steven A et al.Neurology. 2014, Vol 83, Num 1, pp 98-99, issn 0028-3878, 2 p.Article

INCREASED OPTIC NERVE RADIOSENSITIVITY FOLLOWING OPTIC NEURITISSANDA, Nicolae; HERAN, Francoise; DALY-SCHVEITZER, Nicolas et al.Neurology. 2014, Vol 82, Num 16, pp 1474-1475, issn 0028-3878, 2 p.Article

Neural control of the heart: Recent concepts and clinical correlationsPALMA, Jose-Alberto; BENARROCH, Eduardo E.Neurology. 2014, Vol 83, Num 3, pp 261-271, issn 0028-3878, 11 p.Article

Odd harvest: Reflections on the practice of brain collectionGILLMAN, Art; BABIJ, Rachel; LEE, Michelle et al.Neurology. 2014, Vol 82, Num 2, pp 184-186, issn 0028-3878, 3 p.Article

Peripheral hypoxia in restless legs syndrome (Willis-Ekbom disease)SALMINEN, Aaro V; RIMPILÄ, Ville; POLO, Olli et al.Neurology. 2014, Vol 82, Num 21, pp 1856-1861, issn 0028-3878, 6 p.Article

Pseudo-Popeye syndrome: Extramedullary plasmacytoma manifesting in skeletal muscleSCHNEIDER, Ilka; MÜLLER, Tobias; STOLTENBURG, Gisela et al.Neurology. 2014, Vol 82, Num 6, pp 544-545, issn 0028-3878, 2 p.Article

TEACHING NEUROIMAGES: SNAKE EYES APPEARANCE IN MRI IN PATIENT WITH ALSALFAHAD, Tariq B; PRADEEP PANKAJAKSHAN NAIR.Neurology. 2014, Vol 82, Num 9, pp 818-819, issn 0028-3878, 2 p.Article

THE CUSHING RESPONSE EVOKED BY A FOURTH VENTRICULAR BRAINSTEM MASSQUIGG, Mark; SADJADI, Reza; BROWN, Cynthia et al.Neurology. 2014, Vol 83, Num 10, pp 945-947, issn 0028-3878, 3 p.Article

THE INTERNATIONAL INCIDENCE AND PREVALENCE OF NEUROLOGIC CONDITIONS: HOW COMMON ARE THEY?PRINGSHEIM, Tamara; FIEST, Kirsten; JETTE, Nathalie et al.Neurology. 2014, Vol 83, Num 18, pp 1661-1664, issn 0028-3878, 4 p.Article

TWO NOVEL HTRA1 MUTATIONS IN A EUROPEAN CARASIL PATIENTBIANCHI, Silvia; DI PALMA, Chiara; FEDERICO, Antonio et al.Neurology. 2014, Vol 82, Num 10, pp 898-900, issn 0028-3878, 3 p.Article

Tullio phenomenon in superior semicircular canal dehiscence syndromeBASURA, Gregory J; CRONIN, Scott J; HEIDENREICH, Katherine D et al.Neurology. 2014, Vol 82, Num 11, issn 0028-3878, p. 1010Article

Bilateral papilledema associated with spinal schwannomaMATSUBARA, Tomoyasu; SAKODA, Ayako; ARITA, Yukimasa et al.Neurology. 2014, Vol 83, Num 24, pp 2312-2313, issn 0028-3878, 2 p.Article

IVth ventricular neurocysticercal cyst: A rare cause of acute hydrocephalusJAUHARI, Prashant; JITENDRA KUMAR SAHU; VYAS, Sameer et al.Neurology. 2014, Vol 83, Num 21, issn 0028-3878, p. 1990Article

A novel TFG mutation causes Charcot-Marie-Tooth disease type 2 and impairs TFG functionTSAI, Pei-Chien; HUANG, Yen-Hua; YET, Shaw-Fang et al.Neurology. 2014, Vol 83, Num 10, pp 903-912, issn 0028-3878, 10 p.Article

ALS2 mutations: Juvenile amyotrophic lateral sclerosis and generalized dystoniaSHEERIN, Una-Marie; SCHNEIDER, Susanne A; CARR, Lucinda et al.Neurology. 2014, Vol 82, Num 12, pp 1065-1067, issn 0028-3878, 3 p.Article

Agreement between TOAST and CCS ischemic stroke classification: The NINDS SiGN StudyMcARDLE, Patrick F; KITTNER, Steven J; BRENNER, David A et al.Neurology. 2014, Vol 83, Num 18, pp 1653-1660, issn 0028-3878, 8 p.Article

Aldehyde dehydrogenase variation enhances effect of pesticides associated with Parkinson diseaseFITZMAURICE, Arthur G; RHODES, Shannon L; COCKBURN, Myles et al.Neurology. 2014, Vol 82, Num 5, pp 419-426, issn 0028-3878, 8 p.Article

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