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Results: 1 to 20 of 107

Similar articles for PubMed (Select 9706619)

1.

Microlissencephaly: a heterogeneous malformation of cortical development.

Barkovich AJ, Ferriero DM, Barr RM, Gressens P, Dobyns WB, Truwit CL, Evrard P.

Neuropediatrics. 1998 Jun;29(3):113-9.

PMID:
9706619
2.

A case of Norman-roberts syndrome identified from postnatal diagnosis of microlissencephaly.

Tosello B, Brévaut-Malaty V, Chaumoître K, Gire C.

Fetal Pediatr Pathol. 2015 Jun;34(3):197-201. doi: 10.3109/15513815.2015.1031414. Epub 2015 Apr 30.

PMID:
25927602
3.

Fetal brain disruption sequence versus fetal brain arrest: A distinct autosomal recessive developmental brain malformation phenotype.

Abdel-Salam GM, Abdel-Hamid MS, El-Khayat HA, Eid OM, Saba S, Farag MK, Saleem SN, Gaber KR.

Am J Med Genet A. 2015 May;167A(5):1089-99. doi: 10.1002/ajmg.a.37010. Epub 2015 Mar 10.

PMID:
25755095
4.

A young child with seizures and mild developmental delay. Diagnosis: Alexander disease.

Seguias L, Khan M.

Pediatr Ann. 2013 Jun 1;42(6):234-7. doi: 10.3928/00904481-20130522-06. No abstract available.

PMID:
23718245
5.

Progressive atrophy of the cerebrum in 2 Japanese sisters with microcephaly with simplified gyri and enlarged extraaxial space.

Hirose M, Haginoya K, Yokoyama H, Kikuchi A, Hino-Fukuyo N, Munakata M, Uematsu M, Iinuma K, Kato M, Yamamoto T, Tsuchiya S.

Neuropediatrics. 2011 Aug;42(4):163-6. doi: 10.1055/s-0031-1287771. Epub 2011 Sep 19.

PMID:
21932181
6.

Congenital microcephaly with a simplified gyral pattern: associated findings and their significance.

Adachi Y, Poduri A, Kawaguch A, Yoon G, Salih MA, Yamashita F, Walsh CA, Barkovich AJ.

AJNR Am J Neuroradiol. 2011 Jun-Jul;32(6):1123-9. doi: 10.3174/ajnr.A2440. Epub 2011 Mar 31.

7.

Clinical features and outcomes of holoprosencephaly in Korea.

Ko JM, Kim SH.

Pediatr Neurol. 2010 Oct;43(4):245-52. doi: 10.1016/j.pediatrneurol.2010.05.001.

PMID:
20837302
8.

Clinical and imaging heterogeneity of polymicrogyria: a study of 328 patients.

Leventer RJ, Jansen A, Pilz DT, Stoodley N, Marini C, Dubeau F, Malone J, Mitchell LA, Mandelstam S, Scheffer IE, Berkovic SF, Andermann F, Andermann E, Guerrini R, Dobyns WB.

Brain. 2010 May;133(Pt 5):1415-27. doi: 10.1093/brain/awq078. Epub 2010 Apr 19.

9.

Primary microcephaly in Hungary: epidemiology and clinical features.

Szabó N, Pap C, Kóbor J, Svékus A, Túri S, Sztriha L.

Acta Paediatr. 2010 May;99(5):690-3. doi: 10.1111/j.1651-2227.2009.01666.x. Epub 2010 Jan 7.

PMID:
20064139
10.

Characterization of a new X-linked mental retardation syndrome with microcephaly, cortical malformation, and thin habitus.

du Souich C, Chou A, Yin J, Oh T, Nelson TN, Hurlburt J, Arbour L, Friedlander R, McGillivray BC, Tyshchenko N, Rump A, Poskitt KJ, Demos MK, Van Allen MI, Boerkoel CF.

Am J Med Genet A. 2009 Nov;149A(11):2469-78. doi: 10.1002/ajmg.a.33071.

PMID:
19842190
11.

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. doi: 10.1212/WNL.0b013e3181b8799a.

PMID:
19770472
12.

Acquired microcephaly: causes, patterns, motor and IQ effects, and associated growth changes.

Baxter PS, Rigby AS, Rotsaert MH, Wright I.

Pediatrics. 2009 Aug;124(2):590-5. doi: 10.1542/peds.2008-2784. Epub 2009 Jul 27.

PMID:
19651581
13.

Apparent diffusion coefficient on magnetic resonance imaging in pons and in corona radiata and relation with the neurophysiologic measurement and the outcome in very preterm infants.

Kaukola T, Perhomaa M, Vainionpaa L, Tolonen U, Jauhiainen J, Paakko E, Hallman M.

Neonatology. 2010;97(1):15-21. doi: 10.1159/000226603. Epub 2009 Jul 2.

PMID:
19571583
14.

Microcephaly, malformation of brain development and intracranial calcification in sibs: pseudo-TORCH or a new syndrome.

Abdel-Salam GM, Zaki MS, Saleem SN, Gaber KR.

Am J Med Genet A. 2008 Nov 15;146A(22):2929-36. doi: 10.1002/ajmg.a.32549.

PMID:
18925673
15.

Long-term outcome of the ketogenic diet for intractable childhood epilepsy with focal malformation of cortical development.

Jung da E, Kang HC, Kim HD.

Pediatrics. 2008 Aug;122(2):e330-3. doi: 10.1542/peds.2008-0012.

PMID:
18676519
16.

Different features of histopathological subtypes of pediatric focal cortical dysplasia.

Krsek P, Maton B, Korman B, Pacheco-Jacome E, Jayakar P, Dunoyer C, Rey G, Morrison G, Ragheb J, Vinters HV, Resnick T, Duchowny M.

Ann Neurol. 2008 Jun;63(6):758-69. doi: 10.1002/ana.21398.

PMID:
18571798
17.

Primary microcephaly with ASPM mutation shows simplified cortical gyration with antero-posterior gradient pre- and post-natally.

Desir J, Cassart M, David P, Van Bogaert P, Abramowicz M.

Am J Med Genet A. 2008 Jun 1;146A(11):1439-43. doi: 10.1002/ajmg.a.32312.

PMID:
18452193
18.

Diffusion tensor imaging of the pyramidal tracts in infants with motor dysfunction.

Ludeman NA, Berman JI, Wu YW, Jeremy RJ, Kornak J, Bartha AI, Barkovich AJ, Ferriero DM, Henry RG, Glenn OA.

Neurology. 2008 Nov 18;71(21):1676-82. doi: 10.1212/01.wnl.0000304084.59964.e2. Epub 2008 Apr 30.

PMID:
18448871
19.

Delayed neurological signs following isolated parasagittal injury in asphyxia at term.

Sato Y, Hayakawa M, Iwata O, Okumura A, Kato T, Hayakawa F, Kubota T, Maruyama K, Hasegawa M, Sato M, Oshiro M, Kito O, Kojima S.

Eur J Paediatr Neurol. 2008 Sep;12(5):359-65. Epub 2007 Dec 3.

PMID:
18054507
20.

A novel form of lethal microcephaly with simplified gyral pattern and brain stem hypoplasia.

Rajab A, Manzini MC, Mochida GH, Walsh CA, Ross ME.

Am J Med Genet A. 2007 Dec 1;143A(23):2761-7.

PMID:
17975804
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