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Publications 2013

Andlauer, O., Moore, H., Jouhier, L., Drake, C., Peppard, P.E., Han, F., Hong, S.-C., Poli, F., Plazzi, G., and O’Hara, R. (2013a). Nocturnal rapid eye movement sleep latency for identifying patients with narcolepsy/hypocretin deficiency. JAMA Neurology 70, 891–902.
Andlauer, O., Van Effenterre, A., Haffen, E., Sechter, D., Farooq, K., Lydall, G., Malik, A., and Bhugra, D. (2013b). Encouraging French medical students to choose a career in psychiatry: How and why? International Review of Psychiatry 25, 460–465.
Baroin, A., Chopard, G., Siliman, G., Michoudet, C., Vivot, A., Vidal, C., Mokadym, H., Lavier, A., Berger, É., and Rumbach, L. (2013). Validation of a new quality of life scale related to multiple sclerosis and relapses. Quality of Life Research 22, 1943–1954.
Bennabi, D., Vandel, P., Papaxanthis, C., Pozzo, T., and Haffen, E. (2013). Psychomotor Retardation in Depression: A Systematic Review of Diagnostic, Pathophysiologic, and Therapeutic Implications. BioMed Research International 2013, 1–18.
Bogousslavsky, J., and Tatu, L. (2013). French neuropsychiatry in the great war: between moral support and electricity. Journal of the History of the Neurosciences 22, 144–154.
Bonnet, L., Magnin, E., Comte, A., and Rumbach, L. (2013). Hemifacial spasm revealing contralateral peripheral facial palsy. Revue Neurologique 169, 1015.
Buron, G., Hacquemand, R., Pourié, G., Jacquot, L., and Brand, G. (2013). Effects of pyridine inhalation exposure on olfactory epithelium in mice. Experimental and Toxicologic Pathology 65, 159–164.
Callewaert, B., Su, C.-T., Van Damme, T., Vlummens, P., Malfait, F., Vanakker, O., Schulz, B., Mac Neal, M., Davis, E.C., Lee, J.G.H., et al. (2013). Comprehensive Clinical and Molecular Analysis of 12 Families with Type 1 Recessive Cutis Laxa. Human Mutation 34, 111–121.
Cappello, S., Gray, M.J., Badouel, C., Lange, S., Einsiedler, M., Srour, M., Chitayat, D., Hamdan, F.F., Jenkins, Z.A., Morgan, T., et al. (2013). Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development. Nat Genet 45, 1300–1308.
Chamard, L., Wallon, D., Pijoff, A., Berger, E., Viennet, G., Hannequin, D., and Magnin, E. (2013). Amyloid-Related Imaging Abnormalities in AβPP Duplication Carriers. Journal of Alzheimer’s Disease 37, 789–793.
Chocron, S., Vandel, P., Durst, C., Laluc, F., Kaili, D., Chocron, M., and Etievent, J.-P. (2013). Antidepressant Therapy in Patients Undergoing Coronary Artery Bypass Grafting: The MOTIV-CABG Trial. The Annals of Thoracic Surgery 95, 1609–1618.
Clarenccon, F., Di Maria, F., Biondi, A., Chiras, J., and Sourour, N.-A. (2013a). Distant and Delayed (> 7 Days) Hemorrhage after Treatment by Flow-Diverter Stents in Intracranial Aneurysms: A Rare but Potentially Serious Complication. American Journal of Neuroradiology 34, E81–E82.
Clarenccon, F., Biondi, A., Sourour, N.-A., Di Maria, F., Iosif, C., Nouet, A., Navarro, S., Le Jean, L., and Chiras, J. (2013b). Spontaneous closure of intracranial dural arteriovenous fistulas: A report of 3 cases. Clinical Neurology and Neurosurgery 115, 971–975.
Crabben, S.N. van der, Verhoeven-Duif, N.M., Brilstra, E.H., Maldergem, L.V., Coskun, T., Rubio-Gozalbo, E., Berger, R., and Koning, T.J. de (2013). An update on serine deficiency disorders. J Inherit Metab Dis 36, 613–619.
Debray, F.-G., Baguette, C., Colinet, S., Van Maldergem, L., and Verellen-Dumouin, C. (2013). Early infantile cardiomyopathy and liver disease: A multisystemic disorder caused by congenital lipodystrophy. Molecular Genetics and Metabolism 109, 227–229.
Deltenre, P., and Van Maldergem, L. (2013). Hearing loss and deafness in the pediatric population: causes, diagnosis, and rehabilitation. Handb Clin Neurol 113, 1527–1538.
Dimopoulou, A., Fischer, B., Gardeitchik, T., Schröter, P., Kayserili, H., Schlack, C., Li, Y., Brum, J.M., Barisic, I., Castori, M., et al. (2013). Genotype-phenotype spectrum of PYCR1-related autosomal recessive cutis laxa. Mol. Genet. Metab. 110, 352–361.
Duvignau, K., Manchon, M., Méligne, D., Moulin, T., and Démonet, J.-F. (2013). Lexical difficulties in degenerative language disorders: An exploratory study of the forms and functions of reformulation. Information Grammaticale 138, 38–47.
Funk, F., Ceuterick-de Groote, C., Martin, J.-J., Meinhardt, A., Taratuto, A.L., De Bleecker, J., Van Coster, R., De Paepe, B., Schara, U., Vorgerd, M., et al. (2013). Morphological spectrum and clinical features of myopathies with tubular aggregates. Histol. Histopathol. 28, 1041–1054.
Galliot, E., Comte, A., Magnin, E., Tatu, L., Moulin, T., and Millot, J.-L. (2013). Effects of an ambient odor on brain activations during episodic retrieval of objects. Brain Imaging and Behavior 7, 213–219.
Gentric, J.C., Biondi, A., Piotin, M., Mounayer, C., Lobotesis, K., Bonafé, A., and Costalat, V. (2013). Safety and efficacy of Neuroform for treatment of intracranial aneurysms: a prospective, consecutive, French multicentric study. American Journal of Neuroradiology 34, 1203–1208.
Glangeaud-Freudenthal, N.M.-C., Sutter-Dallay, A.-L., Thieulin, A.-C., Dagens, V., Zimmermann, M.-A., Debourg, A., Amzallag, C., Cazas, O., Cammas, R., Klopfert, M.-E., et al. (2013). Predictors of infant foster care in cases of maternal psychiatric disorders. Soc Psychiatry Psychiatr Epidemiol 48, 553–561.
Grond-Ginsbach, C., Giossi, A., Aksay, S.S., Engelter, S.T., Lyrer, P.A., Metso, T.M., Metso, A.J., Tatlisumak, T., Debette, S., Leys, D., et al. (2013). Elevated peripheral leukocyte counts in acute cervical artery dissection. European Journal of Neurology 20, 1405–1410.
Guala, A., Massa, P., Foscolo, A.M., Olivero, F., Van Maldergem, L., and Danesino, C. (2013). Association of iniencephaly, anencephaly, and fusion of cervical vertebral bodies: a new autosomal recessive syndrome? Clinical Dysmorphology 22, 29–32.
Hacquemand, R., Choffat, N., Jacquot, L., and Brand, G. (2013). Comparison between low doses of TMT and cat odor exposure in anxiety-and fear-related behaviors in mice. Behavioural Brain Research 238, 227–231.
Jacquot, L., Berthaud, L., Sghaïr, A., Diep, C., and Brand, G. (2013). The Influence of “Tastiness” and “Healthiness” Labels in Cheese Flavor Perception. Chemosensory Perception 6, 53–59.
Lyons-Ruth, K., Bureau, J.-F., Easterbrooks, M.A., Obsuth, I., Hennighausen, K., and Vulliez-Coady, L. (2013a). Parsing the construct of maternal insensitivity: distinct longitudinal pathways associated with early maternal withdrawal. Attach Hum Dev 15, 562–582.
Lyons-Ruth, K., Bureau, J.-F., Easterbrooks, M.A., Obsuth, I., Hennighausen, K., and Vulliez-Coady, L. (2013b). Parsing the construct of maternal insensitivity: distinct longitudinal pathways associated with early maternal withdrawal. Attachment & Human Development 15, 562–582.
Magnin, E., Chamard, L., Vuillier, F., Tatu, L., and Berger, E. (2013a). Can Chronic Remote Cortical Hypoperfusion Induced by Thalamic Infarction Cause Damage of Tracts Passing through Those Hypoperfused Regions? Front Neurol 4, 156.
Magnin, E., Chopard, G., Ferreira, S., Sylvestre, G., Dariel, E., Ryff, I., Mertz, C., Lamidieu, C., Hidalgo, J., and Tio, G. (2013b). Initial neuropsychological profile of a series of 20 patients with logopenic variant of primary progressive aphasia. Journal of Alzheimer’s Disease 36, 799–808.
Magnin, E., Decavel, P., Sylvestre, G., Revenco, E., Dariel, E., Haffen, S., Moulin, T., and Rumbach, L. (2013c). Mesencephalic cavernoma, abnormal DAT-SPECT, and corticobasal and crossed cerebellar hypoperfusion. Movement Disorders 28, 442–442.
Magnin, E., Delchev, Y., Chopard, G., Berger, E., Vandel, P., Sechter, D., Rumbach, L., and Haffen, E. (2013d). Transient improvement in sensorimotor conversion during post-anoxic encephalopathy with bilateral medial temporal ischemia. Neurocase 19, 576–582.
Magnin, E., Sylvestre, G., Lenoir, F., Dariel, E., Bonnet, L., Chopard, G., Tio, G., Hidalgo, J., Ferreira, S., and Mertz, C. (2013e). Logopenic syndrome in posterior cortical atrophy. Journal of Neurology 260, 528–533.
Van Maldergem, L., Hou, Q., Kalscheuer, V.M., Rio, M., Doco-Fenzy, M., Medeira, A., de Brouwer, A.P., Cabrol, C., Haas, S.A., and Cacciagli, P. (2013). Loss of function of KIAA2022 causes mild to severe intellectual disability with an autism spectrum disorder and impairs neurite outgrowth. Human Molecular Genetics 22, 3306–3314.
Michel, F., Decavel, P., Toussirot, E., Tatu, L., Aleton, E., Monnier, G., Garbuio, P., and Parratte, B. (2013). Piriformis muscle syndrome: Diagnostic criteria and treatment of a monocentric series of 250 patients. Annals of Physical and Rehabilitation Medicine 56, 371–383.
Moulin, T. (2013a). Doctors in Balzac’s Work. In Frontiers of Neurology and Neuroscience, J. Bogousslavsky, and S. Dieguez, eds. (Basel: S. KARGER AG), pp. 225–235.
Moulin, T. (2013b). Year III of telemedicine in France. European Research in Telemedicine / La Recherche Européenne En Télémédecine 2, 1–4.
Petit, E., Bourdin, H., Mougin, F., Tio, G., and Haffen, E. (2013). Time-of-day effects on psychomotor and physical performances in highly trained cyclists 1, 2. Perceptual & Motor Skills 117, 376–388.
Rodesch, G., Picard, L., Berenstein, A., Biondi, A., Bracard, S., Choi, I.S., Feng, L., Hyogo, T., Lefeuvre, D., Leonardi, M., et al. (2013). Interventional neuroradiology: A neuroscience sub-specialty? Interventional Neuroradiology 19, 519.
Rolet, A., Magnin, E., Millot, J.L., Berger, E., Vidal, C., Sileman, G., and Rumbach, L. (2013). Olfactory dysfunction in multiple sclerosis: evidence of a decrease in different aspects of olfactory function. Eur. Neurol. 69, 166–170.
Rudnik-Schöneborn, S., Senderek, J., Jen, J.C., Houge, G., Seeman, P., Puchmajerová, A., Graul-Neumann, L., Seidel, U., Korinthenberg, R., Kirschner, J., et al. (2013). Pontocerebellar hypoplasia type 1 Clinical spectrum and relevance of EXOSC3 mutations. Neurology 80, 438–446.
Steiner, H., and Van Waes, V. (2013). Addiction-related gene regulation: Risks of exposure to cognitive enhancers vs. other psychostimulants. Progress in Neurobiology 100, 60–80.
Tatton-Brown, K., Murray, A., Hanks, S., Douglas, J., Armstrong, R., Banka, S., Bird, L.M., Clericuzio, C.L., Cormier-Daire, V., Cushing, T., et al. (2013). Weaver syndrome and EZH2 mutations: Clarifying the clinical phenotype. American Journal of Medical Genetics Part A 161, 2972–2980.
Tatu, L., and Bogousslavsky, J. (2013). Madness in blaise cendrars’ novels: moravagine and company. Front Neurol Neurosci 31, 1–9.
Thauvin-Robinet, C., Thomas, S., Sinico, M., Aral, B., Burglen, L., Gigot, N., Dollfus, H., Rossignol, S., Raynaud, M., Philippe, C., et al. (2013). OFD1 mutations in males: phenotypic spectrum and ciliary basal body docking impairment. Clinical Genetics 84, 86–90.
Toriello, H.V., Erick, M., Alessandri, J.-L., Bailey, D., Brunetti-Pierri, N., Cox, H., Fryer, A., Marty, D., McCurdy, C., Mulliken, J.B., et al. (2013). Maternal vitamin K deficient embryopathy: Association with hyperemesis gravidarum and Crohn disease. American Journal of Medical Genetics Part A 161, 417–429.
Vulliez-Coady, L., Obsuth, I., Torreiro-Casal, M., Ellertsdottir, L., and Lyons-Ruth, K. (2013a). Maternal Role Confusion: Relations to Maternal Attachment and Mother–Child Interaction from Infancy to Adolescence. Infant Mental Health Journal 34, 117–131.
Vulliez-Coady, L., Vidal, C., Vivot, A., Monnin, J., Nezelof, S., and Bifulco, A. (2013b). Anxiety and hospitalization in adolescence: relations to attachment style and parental support. Psychiatr Danub 25 Suppl 2, S135–142.