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Functioning of peripheral Ia pathways in infants with MyelomeningoceleLEE, Dokyeong; TEULIER, Caroline; ULRICH, Beverly D et al.Infant behavior & development. 2013, Vol 36, Num 1, pp 147-161, issn 0163-6383, 15 p.Article
The posterior reversible encephalopathy syndrome: what's certain, what's new?ROTH, C; FERBERT, A.Practical neurology (Print). 2011, Vol 11, Num 3, pp 136-144, issn 1474-7758, 9 p.Article
Work out where the problem is in the brainstem using 'the rule of 4'GATES, Peter.Practical neurology (Print). 2011, Vol 11, Num 3, pp 167-172, issn 1474-7758, 6 p.Article
THE EFFECT OF PAIRED STIMULI ON BLINK REFLEX LATENCIES IN NORMAL SUBJECTSRUBIN, Devon I; DIMBERG, Elliot L; KENNELLY, Kathleen D et al.Muscle & nerve. 2011, Vol 44, Num 2, pp 235-240, issn 0148-639X, 6 p.Article
Sinus dermiques compliqués = Complication of congenital dermal sinusesLOUATI, H; DOUIRA, W; OUESLATI, H et al.Feuillets de radiologie. 2010, Vol 50, Num 4, pp 179-183, issn 0181-9801, 5 p.Article
THE FEASIBILITY OF RECORDING BLINK REFLEXES UNDER GENERAL ANESTHESIADELETIS, Vedran; URRIZA, Javier; ULKATAN, Sedat et al.Muscle & nerve. 2009, Vol 39, Num 5, pp 642-646, issn 0148-639X, 5 p.Article
Facial expression of affect in children with Cornelia de Lange syndromeCOLLIS, L; MOSS, J; JUTLEY, J et al.JIDR. Journal of intellectual disability research (Print). 2008, Vol 52, pp 207-215, issn 0964-2633, 9 p., 3Article
Consciousness without a cerebral cortex: A challenge for neuroscience and medicine. Commentaries. Author's replyMERKER, Bjorn; ABOITIZ, Francisco; COENEN, Anton M. L et al.Behavioral and brain sciences (Print). 2007, Vol 30, Num 1, pp 63-134, issn 0140-525X, 72 p.Article
Medykkary infarcts may cause ipsilateral masseter reflex abnormalitiesTHÖMKE, Frank; MARX, Jürgen J; CRUCCU, Giorgio et al.Muscle & nerve. 2007, Vol 36, Num 4, pp 477-481, issn 0148-639X, 5 p.Article
Delineation of a 2.2 Mb microdeletion at 5q35 associated with microcephaly and congenital heart diseaseBAEKVAD-HANSEN, Marie; TÜMER, Zeynep; DELICADO, Alicia et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 5, pp 427-433, issn 1552-4825, 7 p.Article
Prenatal diagnosis of episodic tachypnea in an infant with OFD VIMCPHERSON, Elizabeth; ZALESKI, Christina; MASCOLA, Maria et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 19, pp 2146-2149, issn 1552-4825, 4 p.Article
Homozygosity mapping of a third Joubert syndrome locus to 6q23LAGIER-TOURENNE, C; BOLTSHAUSER, E; BREIVIK, N et al.Journal of medical genetics. 2004, Vol 41, Num 4, pp 273-277, issn 0022-2593, 5 p.Article
Mutations in the AHI1 gene, encoding jouberin, cause Joubert syndrome with cortical polymicrogyriaDIXON-SALAZAR, Tracy; SILHAVY, Jennifer L; GLEESON, Joseph G et al.American journal of human genetics. 2004, Vol 75, Num 6, pp 979-987, issn 0002-9297, 9 p.Article
Congenital abnormalities of the central nervous systemVERITY, Christopher; FIRTH, Helen; FFRENCH-CONSTANT, Charles et al.Neurology in practice. 2003, Vol 74, Num 1, pp i3-i8, issn 1473-7086Article
Children with growth hormone deficiency and Chiari I malformation: A morphometric analysis of the posterior cranial fossaTUBBS, R. Shane; WELLONS, John C; SMYTH, Matthew D et al.Pediatric neurosurgery. 2003, Vol 38, Num 6, pp 324-328, issn 1016-2291, 5 p.Article
Mouse models of Angelman syndrome, a neurodevelopmental disorder, display different brain regional GABAA receptor alterationsSINKKONEN, S. T; HOMANICS, G. E; KORPI, E. R et al.Neuroscience letters. 2003, Vol 340, Num 3, pp 205-208, issn 0304-3940, 4 p.Article
Pathophysiology of headache associated with cough in patients with Chiari I malformationSANSUR, Charles A; HEISS, John D; DEVROOM, Hetty L et al.Journal of neurosurgery. 2003, Vol 98, Num 3, pp 453-458, issn 0022-3085, 6 p.Article
Previously undescribed nonsense mutation in SHH caused autosomal dominant holoprosencephaly with wide intrafamilial variabilityMARINI, Monica; CUSANO, Roberto; DE BIASIO, Pierangela et al.American journal of medical genetics. 2003, Vol 117A, Num 2, pp 112-115, issn 0148-7299, 4 p.Article
Proton MR spectroscopy demonstration of taurine peaks in megalencephalic leukoencephalopathy with cystsSENER, R. N.Computerized medical imaging and graphics. 2003, Vol 27, Num 1, pp 23-26, issn 0895-6111, 4 p.Article
Sphenoid encephalocele without hypothalamic-pituitary and optic nerve dysfunctionMORIMOTO, Kazuyoshi; TAKEMOTO, Osamu; NISHIKAWA, Masanori et al.Pediatric neurosurgery. 2003, Vol 38, Num 3, pp 160-161, issn 1016-2291, 2 p.Article
La neuropathie sensitivomotrice héréditaire avec agénésie du corps calleux = Severe neuropathy with agenesis of the corpus callosumHOWARD, Heidi C; DUPRE, Nicolas; MATHIEU, Jean et al.MS. Médecine sciences. 2003, Vol 19, Num 4, pp 414-416, issn 0767-0974, 3 p.Article
Problems in detecting mosaic DNA methylation in Angelman syndromeHORSTHEMKE, Bernhard; LICH, Christina; JANSSEN, Bart et al.European journal of human genetics. 2003, Vol 11, Num 12, pp 913-915, issn 1018-4813, 3 p.Article
The molar tooth signMCGRAW, Peter.Radiology. 2003, Vol 229, Num 3, pp 671-672, issn 0033-8419, 2 p.Article
Somatic mosaicism and variable penetrance in doublecortin-associated migration disordersAIGNER, L; UYANIK, G; WOERLE, H et al.Neurology. 2003, Vol 60, Num 2, pp 329-332, issn 0028-3878, 4 p.Article
Ultrasonographic screening in infants with isolated spinal strawberry neviALLEN, Rebecca M; SANDQUIST, Michael A; PIATT, Joseph H et al.Journal of neurosurgery. 2003, Vol 98, Num 3, pp 247-250, issn 0022-3085, 4 p., SUPArticle