PubMed

Multiple intracranial aneurysms and moyamoya disease associated with microcephalic osteodysplastic primordial dwarfism type II: surgical considerations.

Waldron JS, Hetts SW, Armstrong-Wells J, Dowd CF, Fullerton HJ, Gupta N, Lawton MT.

J Neurosurg Pediatr. 2009 Nov;4(5):439-44.PMID: 19877776 [PubMed - indexed for MEDLINE]Related articles

Hyperekplexia in a neonate: a novel finding in Fukuyama type congenital muscular dystrophy.

Tunc T, Mungan IA, Okulu E, Tiras ST, Tekin M, Atasay B, Arsan S, Turmen T.

Genet Couns. 2009;20(3):275-9.PMID: 19852435 [PubMed - indexed for MEDLINE]Related articles

A Feingold syndrome case with previously undescribed features and a new mutation.

Koçak H, Ozaydin E, Köse G, Marcelis CL, Kamsteeg EJ, Ceylaner S.

Genet Couns. 2009;20(3):261-7.PMID: 19852433 [PubMed - indexed for MEDLINE]Related articles

Seizures in a 9 month old girl.

Armstrong L, Orr V.

BMJ. 2009 Oct 21;339:b4133. doi: 10.1136/bmj.b4133. No abstract available. PMID: 19846480 [PubMed - indexed for MEDLINE]Related articles

Cobblestone-like brain dysgenesis and altered glycosylation in congenital cutis laxa, Debré type.

Morava E, Wevers RA, Willemsen MA, Lefeber D.

Neurology. 2009 Oct 6;73(14):1164; author reply 1164-5. No abstract available. PMID: 19805737 [PubMed - indexed for MEDLINE]Related articles

SLC25A19 mutation as a cause of neuropathy and bilateral striatal necrosis.

Spiegel R, Shaag A, Edvardson S, Mandel H, Stepensky P, Shalev SA, Horovitz Y, Pines O, Elpeleg O.

Ann Neurol. 2009 Sep;66(3):419-24.PMID: 19798730 [PubMed - indexed for MEDLINE]Related articles

Passive range of motion functional magnetic resonance imaging localizing sensorimotor cortex in sedated children.

Ogg RJ, Laningham FH, Clarke D, Einhaus S, Zou P, Tobias ME, Boop FA.

J Neurosurg Pediatr. 2009 Oct;4(4):317-22.PMID: 19795962 [PubMed - indexed for MEDLINE]Related articles

Challenges in the surgical treatment of epilepsy patients with cortical dysplasia.

Mathern GW.

Epilepsia. 2009 Oct;50 Suppl 9:45-50.PMID: 19761453 [PubMed - indexed for MEDLINE]Related articles

Animal models of focal cortical dysplasia and tuberous sclerosis complex: recent progress toward clinical applications.

Wong M.

Epilepsia. 2009 Oct;50 Suppl 9:34-44.PMID: 19761452 [PubMed - indexed for MEDLINE]Related articles

From human tissue to animal models: Insights into the pathogenesis of cortical dysplasia.

D'Arcangelo G.

Epilepsia. 2009 Oct;50 Suppl 9:28-33.PMID: 19761451 [PubMed - indexed for MEDLINE]Related articles

Clinical, functional, and neurophysiologic assessment of dysplastic cortical networks: Implications for cortical functioning and surgical management.

Duchowny M.

Epilepsia. 2009 Oct;50 Suppl 9:19-27. Review.PMID: 19761450 [PubMed - indexed for MEDLINE]Related articles

New directions in clinical imaging of cortical dysplasias.

Madan N, Grant PE.

Epilepsia. 2009 Oct;50 Suppl 9:9-18. Review.PMID: 19761449 [PubMed - indexed for MEDLINE]Related articles

Focal brain malformations: seizures, signaling, sequencing.

Crino PB.

Epilepsia. 2009 Oct;50 Suppl 9:3-8.PMID: 19761448 [PubMed - indexed for MEDLINE]Related articles

Introduction--epileptogenic cortical dysplasia: emerging trends in diagnosis, treatment, and pathogenesis.

Jensen FE.

Epilepsia. 2009 Oct;50 Suppl 9:1-2. No abstract available. PMID: 19761447 [PubMed - indexed for MEDLINE]Related articles

Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutations.

Passemard S, Titomanlio L, Elmaleh M, Afenjar A, Alessandri JL, Andria G, de Villemeur TB, Boespflug-Tanguy O, Burglen L, Del Giudice E, Guimiot F, Hyon C, Isidor B, Mégarbané A, Moog U, Odent S, Hernandez K, Pouvreau N, Scala I, Schaer M, Gressens P, Gerard B, Verloes A.

Neurology. 2009 Sep 22;73(12):962-9.PMID: 19770472 [PubMed - indexed for MEDLINE]Related articles

Practice parameter: Evaluation of the child with microcephaly (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society.

Ashwal S, Michelson D, Plawner L, Dobyns WB; Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society.

Neurology. 2009 Sep 15;73(11):887-97.PMID: 19752457 [PubMed - indexed for MEDLINE]Related articles

Identification of a region required for TSC1 stability by functional analysis of TSC1 missense mutations found in individuals with tuberous sclerosis complex.

Mozaffari M, Hoogeveen-Westerveld M, Kwiatkowski D, Sampson J, Ekong R, Povey S, den Dunnen JT, van den Ouweland A, Halley D, Nellist M.

BMC Med Genet. 2009 Sep 11;10:88.PMID: 19747374 [PubMed - indexed for MEDLINE]Related articlesFree article

Blockage of A2A and A3 adenosine receptors decreases the desensitization of human GABA(A) receptors microtransplanted to Xenopus oocytes.

Roseti C, Palma E, Martinello K, Fucile S, Morace R, Esposito V, Cantore G, Arcella A, Giangaspero F, Aronica E, Mascia A, Di Gennaro G, Quarato PP, Manfredi M, Cristalli G, Lambertucci C, Marucci G, Volpini R, Limatola C, Eusebi F.

Proc Natl Acad Sci U S A. 2009 Sep 15;106(37):15927-31. Epub 2009 Aug 31.PMID: 19721003 [PubMed - indexed for MEDLINE]Related articles

Surgical treatment of the extratemporal epilepsies.

Roper SN.

Epilepsia. 2009 Sep;50 Suppl 8:69-74. Review.PMID: 19702737 [PubMed - indexed for MEDLINE]Related articles

Novel human pathological mutations. Gene symbol: UBE3A. Disease: Angelman Syndrome.

Tzagkaraki E, Christalena S, Helen F, Argyris D, Ariadni M, Emmanuel K.

Hum Genet. 2009 Aug;126(2):331. No abstract available. PMID: 19693993 [PubMed - indexed for MEDLINE]Related articles