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	101.	Prenatal diagnosis of lissencephaly: a case report. [electronic resource] by Aslan, Halil Gungorduk, Kemal Yildirim, Doğukan Aslan, Oğuz Yildirim, Gokhan Ceylan, Yavuz Producer: 20090721 In: Journal of clinical ultrasound : JCU vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	102.	Malformations of cortical development and epilepsy. [electronic resource] by Leventer, Richard J Guerrini, Renzo Dobyns, William B Producer: 20080630 In: Dialogues in clinical neuroscience vol. 10 Availability: No items available. Save to lists Add to cart (remove)
	103.	Recurrent KIF5C mutation leading to frontal pachygyria without microcephaly. [electronic resource] by Cavallin, Mara Hubert, Laurence Cantagrel, Vincent Munnich, Arnold Boddaert, Nathalie Vincent-Delorme, Catherine Cuvellier, Jean Christophe Masson, Cecile Besmond, Claude Bahi-Buisson, Nadia Producer: 20161019 In: Neurogenetics vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	104.	Developmental differences of the major forebrain commissures in lissencephalies. [electronic resource] by Kara, S Jissendi-Tchofo, P Barkovich, A J Producer: 20110222 In: AJNR. American journal of neuroradiology vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	105.	Novel VLDLR microdeletion identified in two Turkish siblings with pachygyria and pontocerebellar atrophy. [electronic resource] by Kolb, Luis E Arlier, Zulfikar Yalcinkaya, Cengiz Ozturk, Ali K Moliterno, Jennifer A Erturk, Ozdem Bayrakli, Fatih Korkmaz, Baris DiLuna, Michael L Yasuno, Katsuhito Bilguvar, Kaya Ozcelik, Tayfun Tuysuz, Beyhan State, Matthew W Gunel, Murat Producer: 20100924 In: Neurogenetics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	106.	Listen carefully: LIS1 and DCX MLPA in lissencephaly and subcortical band heterotopia. [electronic resource] by Delatycki, Martin B Leventer, Richard J Producer: 20090901 In: European journal of human genetics : EJHG vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	107.	Differential activation of mononuclear phagocytes in cerebellar malformation associated with Walker-Warburg syndrome. [electronic resource] by Ulfig, Norbert Steinbrecher, Alice Stoltenburg-Didinger, Gisela Rezaie, Payam Producer: 20080909 In: Neuropathology : official journal of the Japanese Society of Neuropathology vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	108.	Somatic mutation, genomic variation, and neurological disease. [electronic resource] by Poduri, Annapurna Evrony, Gilad D Cai, Xuyu Walsh, Christopher A Producer: 20130716 In: Science (New York, N.Y.) vol. 341 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	109.	A unique case of lissencephaly with Crouzon syndrome heterozygous for FGFR2 mutation. [electronic resource] by Tan, Ai Peng Mankad, Kshitij Producer: 20190529 In: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	110.	New Pachygyria Syndrome Linked to Actin Regulation Identified: When mutated, CTNNA2 leads to a new form of pachygyria that has a diffuse anterior-posterior gradient with cerebellar hypoplasia, thinning corpus callosum, and absent anterior commissure. [electronic resource] Producer: 20190925 In: American journal of medical genetics. Part A vol. 176 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	111.	Congenital pial AVF along the falx cerebri with complete agenesis of the corpus callosum and bilateral parasagittal pachygyria-polymicrogyria secondary to chronic ischemia. [electronic resource] by Ngam, Pei Ing Hussain, Syed Shahzad Tan, Ai Peng Producer: 20200511 In: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	112.	Description of a novel TUBA1A mutation in Arg-390 associated with asymmetrical polymicrogyria and mid-hindbrain dysgenesis. [electronic resource] by Zanni, Ginevra Colafati, Giovanna S Barresi, Sabina Randisi, Francesco Talamanca, Lorenzo Figà Genovese, Elisabetta Bellacchio, Emanuele Bartuli, Andrea Bernardi, Bruno Bertini, Enrico Producer: 20140123 In: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	113.	Functional analyses of lissencephaly-related proteins in Dictyostelium. [electronic resource] by Meyer, Irene Kuhnert, Oliver Gräf, Ralph Producer: 20110328 In: Seminars in cell & developmental biology vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	114.	Novel proximal 14q deletion: clinical and diffusion tensor imaging tractography findings in a patient with lissencephaly, agenesis of the corpus callosum, and septo-optic dysplasia. [electronic resource] by Bravo, E K White, M L Olney, A H McAllister, J L Zhang, Y D Producer: 20120703 In: AJNR. American journal of neuroradiology vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	115.	Prenatal sonographic diagnosis of Dandy-Walker malformation and type III lissencephaly: A novel association. [electronic resource] by Darouich, Sihem Amraoui, Jihen Amraoui, Naima Producer: 20200806 In: Journal of clinical ultrasound : JCU vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	116.	Recurrent KIF2A mutations are responsible for classic lissencephaly. [electronic resource] by Cavallin, Mara Bijlsma, Emilia K El Morjani, Adrienne Moutton, Sébastien Peeters, Els A J Maillard, Camille Pedespan, Jean Michel Guerrot, Anne-Marie Drouin-Garaud, Valérie Coubes, Christine Genevieve, David Bole-Feysot, Christine Fourrage, Cecile Steffann, Julie Bahi-Buisson, Nadia Producer: 20180221 In: Neurogenetics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	117.	The treatment of cerebral salt wasting with fludrocortisone in a child with lissencephaly. [electronic resource] by Ozdemir, Halil Aycan, Zehra Degerliyurt, Aydan Metin, Ayse Producer: 20100430 In: Turkish neurosurgery vol. 20 Availability: No items available. Save to lists Add to cart (remove)
	118.	Is the male Aicardi's characterized by 46 XXY karyotype? [electronic resource] by Saddichha, Sahoo Producer: 20091215 In: Journal of the neurological sciences vol. 284 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	119.	Expanding the spectrum of human ganglionic eminence region anomalies on fetal magnetic resonance imaging. [electronic resource] by Righini, Andrea Cesaretti, Claudia Conte, Giorgio Parazzini, Cecilia Frassoni, Carolina Bulfamante, Gaetano Avagliano, Laura Inverardi, Francesca Izzo, Giana Rustico, Mariangela Producer: 20161219 In: Neuroradiology vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	120.	Evidence for association between structural variants in lissencephaly-related genes and executive deficits in schizophrenia or bipolar patients from a Spanish isolate population. [electronic resource] by Tabarés-Seisdedos, Rafael Mata, Ignacio Escámez, Teresa Vieta, Eduard López-Ilundain, Jose M Salazar, Jose Selva, Gabriel Balanzá, Vicente Rubio, Cristina Martínez-Arán, Anabel Valdés-Sánchez, Lourdes Geijo-Barrientos, Emilio Martínez, Salvador Producer: 20090107 In: Psychiatric genetics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 247 results.